Cosmetic Lipids and The Skin Barrier PDF

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Series Introduction
The Cosmetic Science and Technology series was conceived to permit discussion
of a broad range of current theories and knowledge in cosmetic science and tech-
nology. Authorities from industry, academia, and government agencies from
around the world are participating in writing these books. Topics are drawn from
a wide spectrum of disciplines ranging from chemistry, physics, biochemistry,
and analytical and consumer evaluations to safety, efficacy, toxicity, and regula-
tory questions. Organic, inorganic, physical and polymer chemistry, emulsion
and lipid technology, microbiology, dermatology, and toxicology all play a role
in cosmetic science.
There is little commonality among the scientific methods, processes, or
formulations required for the wide variety of cosmetics and toiletries on the
market.
Cosmetics and toiletries represent a highly diversified field involving many
subsections of science and ‘‘art’’. Even in these days of high technology, ‘‘art’’
and intuition continue to play an important part in the development of formula-
tions, their evaluation and the selection of raw materials. The move toward the
application of more sophisticated scientific methodologies that gained momentum
in the 1980s has grown in such areas as claim substantiation, safety testing, prod-
uct testing, and chemical analyses and has led to a better understanding of the
properties of skin and hair. Molecular modeling techniques are beginning to be
applied to data obtained in skin sensory studies.
The Cosmetic Science and Technology series reports the current status of
cosmetic technology and science, changing regulatory climates, and historical
reviews. The series has grown to over 20 books dealing with the constantly chang-
ing technologies and trends in the cosmetic industry, including globalization.
Several books have been translated into Japanese and Chinese. Contributions
range from highly sophisticated and scientific treatises to primers, practical appli-
iii
iv Series Introduction
cations, and pragmatic presentations. Contributors are encouraged to present their

own concepts as well as established theories, and not to shy away from fields
that are in a state of transition or to hesitate to present detailed discussions of
their own work. Our intention is to develop the series into a collection of critical
surveys and ideas covering diverse phases of the cosmetic industry.
Cosmetic Lipids and the Skin Barrier, the twenty-fourth book published in
the series, represents a global effort. Ten chapters are contributed by leading
authorities from European universities and industrial research centers, including
one chapter from Japan. The book covers the chemistry, structure, and biological
functions of skin lipids and their interaction with the lipids formulated into skin
and hair care preparations. Cosmetic emulsions contain high levels of lipids, often
making them the second major component after water. Two chapters discuss body
washes, a relatively new class of products that have appeared on the U.S. market
since the mid-1990s. These are sophisticated surfactant-based formulations con-
taining a relatively high oil load that provide cleaning as well as moisturization
and skin conditioning.
I would like to thank the contributors for participating in this project, partic-
ularly the editor, Dr. Thomas Förster, for conceiving, organizing, and coordinat-
ing this book. Special thanks are extended to Sandra Beberman and the editorial
and production staff at Marcel Dekker, Inc. Finally, I thank my wife, Eva, without
whose constant support and editorial help I would not have undertaken this
project.
Eric Jungermann
Preface
The benefits of lipids in cosmetic treatment of the skin were already known when
Cleopatra took her bath in donkey’s milk. Since ancient times, waxes, oils, and
amphiphilic lipidic materials have been used in various cosmetic formulations
such as creams, rouge, and lipstick to make the skin smooth and supple and
to improve the application properties of cosmetic products. Despite extensive
traditional knowledge about lipids in cosmetic formulations and over 40 years
of intensive research in skin lipid science, a quantitative understanding of the
interaction of topically applied lipids with skin barrier lipids has been lacking.
The primary objective of this book is to describe the most important devel-
opments in understanding the interaction between cosmetic lipids and the skin
barrier over the past 10 years. Emphasis has been placed on connecting the latest
scientific findings and methods with possible applications in cosmetic products.
Each chapter presents the relevant scientific background in a particular area and
an in-depth and up-to-date account of recent research findings.
The first three chapters introduce the fundamentals of lipid chemistry and
recent concepts about the structural arrangement of lipids in the skin barrier.
Chapter 1 describes the chemistry of natural human skin lipids and presents syn-
thetic skin barrier lipid analogs frequently used in skin care creams. Chapter 2
discusses the fate of lipid liposomes applied to the skin. Molecular dynamics
offers a new way to scrutinize the molecular interaction of lipids in lamellar
layers. Chapter 3 presents the state of the art in computer modeling of skin barrier
lipid layers.
The next two chapters deal with the biological function and activity of skin
lipids as studied in vivo and in vitro. Chapter 4 focuses on the role of lipids
in stratum corneum barrier function and barrier repair. Chapter 5 discusses the
expression of skin barrier lipids in in vitro skin models by different ingredients.
The following three chapters review various methods for analyzing the
v
vi Preface
interaction with the skin of topically applied lipids. Chapter 6 scrutinizes the
composition of skin lipids found in humans of different skin types. Chapter 7
reviews several biophysical and analytical methods for assessing lipid status and
the improvement of skin condition. Chapter 8 introduces infrared and Raman
spectroscopy as powerful tools to detect subtle changes in skin surface lipids
after various cosmetic treatments.
The last three chapters are concerned with lipids in cosmetic products and
how they interact with the skin. Chapter 9 gives an overview of different lipid
types used in skin care formulations and their function in the cosmetic product
and on the skin. Chapter 10 discusses the evidence for skin care effects obtained
by lipidic refatters in personal cleansing products. Finally, Chapter 11 relates the
physicochemical properties of various lipid types with the sensorial perception
of these lipids in different leave-on and rinse-off products by consumers.
The contributors represent a cross section of researchers from universities
and industry who are specialists in their particular field. The book provides an
exhaustive, yet concise view of the interaction of cosmetic lipids with the skin
barrier. Students and researchers at universities or in industry who are new to the
field will find this book a valuable introduction. At the other end of the spectrum,
specialists will profit from the current and comprehensive information in each
chapter.
Thomas Förster
Contents
Series Introduction Eric Jungermann iii

Preface v
Contributors ix
PART I. CHEMISTRY AND STRUCTURE OF SKIN LIPIDS
1. The Chemistry of Natural and Synthetic Skin Barrier Lipids 1

Hinrich Möller
2. Structure of Stratum Corneum Lipid Layers and Interactions

with Lipid Liposomes 37
Joke Bouwstra
3. Computer Modeling of Skin Barrier Lipid Layers by Molecular

Dynamics 75
Monika Höltje
PART II. BIOLOGICAL FUNCTION OF SKIN LIPIDS
4. Role of Lipids in Skin Barrier Function 97

Mitsuhiro Denda
5. Investigating Human Skin Barrier Lipids with In Vitro Skin

Models 121
Annie Black, Odile Damour, and Kordula Schlotmann
vii
viii Contents
PART III. ANALYSIS OF SKIN LIPIDS AND THEIR EFFECTS

ON SKIN
6. Analytical Techniques for Skin Lipids 149

Kristien De Paepe and Vera Rogiers
7. Biophysical Methods for Stratum Corneum Characterization 185

Hans Lambers and Hans Pronk
8. Detection of Cosmetic Changes in Skin Surface Lipids by

Infrared and Raman Spectroscopy 227
Thomas Prasch and Thomas Förster
PART IV. LIPIDS IN COSMETIC PRODUCTS
9. Lipidic Ingredients in Skin Care Formulations 255

Ghita Lanzendörfer
10. Benefits of Lipidic Refatters in Surfactant Products 299

Ulrich Issberner
11. Sensory Assessment of Lipids in Leave-On and Rinse-Off

Products 319
Thomas Gassenmeier and Peter Busch
Index 353
Contributors
Annie Black, Ph.D. Laboratoire des Substituts Cutanés, Hôpital Edouard Her-
riot, Lyon, France
Joke Bouwstra, Ph.D. Center for Drug Research, Leiden University, Leiden,
The Netherlands
Peter Busch, Ph.D. Department of Biophysics and Sensorics/Product Perfor-

mance, Cognis Deutschland GmbH, Düsseldorf, Germany
Odile Damour, Ph.D. Director of Laboratoire des Substituts Cutanés, Hôpital

Edouard Herriot, Lyon, France
Kristien De Paepe, Ph.D. Department of Toxicology, Vrije Universiteit Brus-

sel, Brussels, Belgium
Mitsuhiro Denda, Ph.D. Skin Biology Research Laboratory, Shiseido Life

Science Research Center, Yokohama, Japan
Thomas Förster, Ph.D. Department of Cosmetics, Henkel KgaA, Düsseldorf,

Germany
Thomas Gassenmeier, M.D. Department of Skin Biochemistry, Henkel KgaA,

Düsseldorf, Germany
Monika Höltje, Ph.D. Department of Pharmaceutical Chemistry, Institute of

Pharmaceutical Chemistry, Heinrich-Heine University, Düsseldorf, Germany
ix
x Contributors
Ulrich Issberner, M.D. Department of Care Chemicals, Cognis Deutschland

GmbH, Düsseldorf, Germany
Hans Lambers, Ph.D. Department of Innovation Cosmetics, Sara Lee House-

hold and Body Care Research, The Hague, The Netherlands
Ghita Lanzendörfer, Ph.D. Advanced Development, Decorative Cosmetics

Department, Beiersdorf AG, Hamburg, Germany
Hinrich Möller, Ph.D. Department of Cosmetics, Henkel KgaA, Düsseldorf,

Germany
Thomas Prasch, Ph.D. Department of Analytics of Chemical Products, Henkel

KgaA, Düsseldorf, Germany
Hans Pronk, M.Sc. Department of Biophysical Evaluation, Sara Lee House-

hold and Body Care Research, The Hague, The Netherlands
Vera Rogiers, Ph.D. Department of Toxicology, Vrije Universiteit Brussel,

Brussels, Belgium
Kordula Schlotmann, M.D. Department of Skin Biochemistry, Henkel KgaA,

1
The Chemistry of Natural
and Synthetic Skin Barrier Lipids
Hinrich Möller
Henkel KGaA, Düsseldorf, Germany
I. BACKGROUND
As long ago as the mid-1970s, Elias et al. [1] discovered that the intercellular
lipidlike substance of the stratum corneum, which acts as a sort of cement be-
tween the corneocytes, has a lamellar structure. The compound system formed
by the dead cells and the lamellae is the skin’s actual barrier against the environ-
ment. Some years later, the same work group [2] became aware of the relatively
high proportion of ceramides besides cholesterol, free fatty acids, and triacylglyc-
erol in the intercellular lipid layer. The ceramides are credited with playing an
important role in the lamellar lipid structure and in the barrier function of the
stratum corneum.
II. CHEMICAL STRUCTURE
The unusual structure of the ceramides should be explained at this point. They are
derived from sphinganine (d-erythro-2-amino-octadecane-1,3-diol) (see Fig. 1).
This yields sphingosine, an unsaturated compound with a double bond at
the fourth carbon atom. Sphingosine provides the basic structure for the cera-
mides, which are formed from them by N-acylation. Glycosylation of the primary
OH group produces cerebrosides, which are present, mainly in the form of galac-
tosides, in the cell membranes of brain tissue. The final ceramide derivatives are
the sphingomyelins, in which the phosphorylated choline group substitutes the
terminal OH group. They are found in the myelin sheaths of the nerves.
1
2 Möller
Figure 1 Sphinganine derivatives.
Figure 2 Ceramide structures.

Chemistry of Natural and Synthetic Skin Barrier Lipids 3
The most important ceramides found in the stratum corneum lipids have
been assigned numbers in the order of their polarity and are listed in Figure 2 [3].
Structural variation is achieved by changing not only the chain length of the
N-acyl group but also its character, by incorporating 2-hydroxy or ω-acyloxyacyl
groups, as in ceramides of types 1, 4, 5, and 6. On the other hand, the double
bond from the sphingosine group can be hydrated to increase hydrophilicity, as
in ceramides of types 3 and 6a and b. The type 1 ceramide is notable for still
having a linolyloxy group in the ω-position of the C30-acyl group. The structure
of type 6a is the only one that contains three long alkyl chains, but four hydroxy
groups like 6b. It was formerly assigned to a different structure that was derived
from type 1, with the linolyl group being exchanged by the 2-hydroxytetracosa-
noyl group [4]. The cerebrosides are classified similarly.
III. LOCALIZATION AND CREATION
Ceramides, together with other epidermal lipids and water, form intercellular
multilamellar liquid crystalline gel structures. These structures were made visible
in pig epidermis with the help of electron microscopy (Fig. 3) [5].
The individual lipid bilayers between the corneocytes are clearly separate
from each other (a). The effect of a solvent extraction can be seen in part b,
where only residues of these layers are recognizable. Figure 4 shows a model of
the epidermal barrier.
Figure 3 Multiple intercellular lamellae of pig stratum corneum [5].

4 Möller
Figure 4 Barrier model of intercellular horny layer lipids.
The very simplified section of the epidermis shows as the outermost layer
the stratum corneum (horny layer). The enlargement of this section shows the
lamellar structure in the intercellular space between the corneocytes. Further en-
largement reveals the molecular structure of the lipid bilayer in the liquid crystal-
line lipid/water system. The spheres represent the hydrophilic ‘‘heads’’ of the
polar lipid molecules, which are aligned toward the aqueous phase; the lipophilic
hydrocarbon chains are aligned toward the interlayer gap of the lipid bilayers.
Figure 5 Generation of multiple intercellular lipid lamellae in the stratum corneum [4].
These lamellae are directly related to the lamellar bodies in the stratum
granulosum, from which the final epidermal layer, the stratum corneum, is formed
as corneocytes are produced (Fig. 5) [3,4].
These lipid bilayers are preformed as closely packed disks in the lamellar
bodies of the stratum granulosum. Their molecular structure is very similar to
that of the stratum corneum and is shown in model form in the enlargement at
the bottom of the illustration. One major difference is that most of the ceramides
are glycosylated (acyl glycosyl ceramides). In the course of further cytodifferenti-
ation, these lipid disks are relinquished into the intercellular space at the boundary
to the stratum corneum and are absorbed into the extensive lamellar barrier struc-
tures of the stratum corneum while undergoing deglycosylation.
IV. COMPOSITION OF THE EPIDERMAL LIPIDS
Before going into detail of the composition of the epidermal lipids coming up
to the skin surface from the intercellular space after desquamation, it may be of
interest to deal with the second source of lipids on the skin: the sebum. These
lipids are produced by the sebaceous glands and contribute the main part of the
human superficial fat and are nearly uninvolved in barrier function of the skin.
The composition of sebum differs considerably from that of the epidermal origin.
An example is shown in Table 1 [6]. There are found no ceramides, little choles-
terol, but a substantial proportion of squalene that may serve as a marker for
sebum, whereas the free cholesterol and the ceramide content is characteristic of
the stratum corneum lipids.
Table 1 Composition of Lipids from Human

Sebaceous Glands (Scalp) [6]
Component Content [weight %] (S.D.)
Squalene 13.6 (0.6)
Wax esters 19.0 (1.6)
Triacyl glycerols 63.6 (1.1)
94.0
Free fatty acids 1.2 (0.5)
Cholesterol esters 2.0 (0.5)
Cholesterol 0.6 (0.1)
Phospholipids about 6.0
• Phosphatidyl cholin • 3.6
S.D. ⫽ Standard deviation
6 Möller
Triacylglycerols are the main component of the sebaceous lipids—about

60%. After spread to the skin surface, most of the triacylglycerols are split to
free fatty acids and glycerol or to mono- or diacylglycerols. The fatty acids consist
mainly of the C16-, followed by the C18- and C14-, homologues and are saturated
as well as unsaturated. The double bonds in the 6- and 8-position of the mono-
enoic alkanoic acids are unusual. Normally, the double bonds are found in the
9- or in the 9,12-position. It is noteworthy, too, that a considerable portion of
the fatty acids have odd-numbered chain lengths and methyl branching at the
end of the chain [7]. The fairly high squalene content means that in the sebaceous
glands only a small amount is transformed to sterols. Phospholipids, mainly phos-
phatidylcholin, are also present and belong to the polar fraction of lipids. Re-
cently, other authors [8] found varying lipid contents in the sebaceous glands
separated from the chest. They argued that the lipid composition might strongly
depend on the skin area. The origin of the lipids of Table 1 is the scalp.
On the other hand, the lipids of the stratum corneum contain not only the
ceramides but also some other essential components. The functionality of the
above-described lamellar, liquid crystalline lipid structures depends on the pres-
ence of a range of other lipid components as well as the ceramides. Table 2
shows two typical examples of the composition of human stratum corneum lipids
(abdomen [9], lower leg [10]).
In the literature, the results concerning the measurements of the different
components obtained by numerous authors diverge to some degree because it is
very difficult to separate the lipids only of the stratum corneum from the skin
without contamination by lipids from the deeper layer or of the skin surface.
Table 2 Composition of Human Stratum Corneum Lipids [9,10]

Content [weight%]
Component Abdomen Lower leg
Polar lipids 4.9 —
Cholesteryl sulfate 1.5 —
Neutral lipids 74.8 68.1
• Free sterols • 14.0 • 23.7
• Sterol esters • — • 10.2
• Free fatty acids • 19.3 • 25.3
• Triacyl glycerols • 25.2 • 8.9
• Squalene • 4.8 • —
• n-Alkanes • 6.1 • —
Ceramides 18.1 41.8
These latter lipids originate mainly from the sebaceous glands. The skin area also
plays an important role in this respect.
Nevertheless it can be seen that the main components of the neutral lipids
are free sterols (predominantly cholesterol), free fatty acids, and triacylglycerols,
together with a significant proportion of ceramides. Free fatty acids, cholesterol,
and the ceramides that occur mainly in equimolar ratios are especially important
for the formation of stable lamellar structures [11].
At this point, the structures of some major lipidic components of the horny
layer other than ceramides are compiled in order to demonstrate their chemical
features and possible spatial arrangements (Fig. 6).
The different ceramide types in humans have also been studied and ana-
lyzed. The same types were found as in pigs. Table 3 shows a typical composition
[12]. The most abundant ceramide was type 2, making up more than 20%. The
combined values for types 4 and 5, which could not be separated by thin-layer
chromatography, and for types 6a and 6b give a percentage content similar to
type 2. The content of types 1 and 3 is about 10% each.
The research done by Yardley [13] is of interest. He examined changes in
lipid composition during the differentiation of the epidermal cells on their journey
from the basal layer through the stratum granulosum to the stratum corneum.
Figure 6 Chemical structures of some major lipidic components of the stratum corneum,
without ceramides.
8 Möller
Table 3 Composition of Ceramides Found in

Human Stratum Corneum [12]
Ceramide (type) Content [weight %]
1 7.0 (3.2)a
2 21.0 (4.9)
3 13.4 (4.3)
4/5 22.2 (4.5)
6a 9.8 (1.1)
6b 13.6 (4.5)
a
Values in brackets: standard deviation.
Figure 7 very clearly shows the components that undergo the greatest change:
the phospholipids initially increase but are completely absent from the horny
layer. The same applies to the glycosylceramides. They are apparently of impor-
tance for the formation of the lamellar bodies, but their more hydrophilic charac-
ter is reversed to a more hydrophobic one before incorporation into the multila-
mellar structures between the corneocytes.
The marked increase in the content of the hydrophobic ceramides and fatty
acids is also very noticeable, especially in the final differentiation step. The cho-
Figure 7 Change in lipid composition during epidermal cell differentiation [13].

lesterol content also increases strongly. The concentration of the other compo-
nents changes much less, so that this illustration clearly reveals the considerable
significance of the three components—ceramides, cholesterol, and free fatty
acids—for the generation of the lamellar lipid structure in the stratum corneum
that is a basic requirement for the highly efficient barrier function against water
permeability.
V. MODEL STUDIES
On the basis of the above-mentioned lipid analyses, Friberg et al. [14] created a
model horny layer lipid and studied the influence of different individual compo-
nents on the lamellar structure (Table 4). The first major surprise occurred when
they mixed this model lipid with water and were unable to obtain a lamellar
dispersion. Only after the pH of the mixture was adjusted to that of the skin (pH
4.5–6.0) were lamellar structures observed. Moreover the ceramides did not yield
lamellar liquid crystals when mixed only with water, although it had long been
assumed that they would, in view of their structural similarity to the phospholip-
ids. On the other hand, it was found that a mixture of fatty acids and their salts,
together with 30% water, form stable lamellar systems. This occurs most readily
Table 4 Model for Stratum Corneum Lipid [14]

Component Content [weight %]
Free fatty acids 17

• Myristic • 10
• Linolic • 15
• Oleic • 55
80 (unsaturated fatty acids)
• Palmitic • 5
• Palmitoleic • 10
• Stearic • 5
Phosphatidyl ethanolamine 5
Cholesteryl sulfate 4
Cholesterol 17
Triolein 22
Palmityl oleate 5
Squalene 5
Pristane 4
Ceramides 21
10 Möller
at a pH of 4.6, when about 40% of the fatty acids are present as soaps. This
correlation is illustrated in a phase diagram (Fig. 8). The trapezoid in the medium
pH range is the zone of existence of lamellar liquid crystals at between 20% and
70% water content. The other zones contain an aqueous solution, liquid crystals,
crystals, or no structure at all.
Friberg and his colleagues then turned to small angle x-ray scattering
(SAXS) to research the special function of the ceramides. This enabled them to
measure the interlayer distance in lamellar dispersions [16]. Reflections occur
only at polar electron-rich layers, i.e., in the aqueous phase (Fig. 9). The distance
d between the layers can be determined with the help of the Bragg equation. This
yields the sum of the interlayer distances in the aqueous and lipid phases.
On the basis of the above-mentioned basic lamellar system consisting of
a mixture of free fatty acids and their soaps, Friberg and his colleagues then
carried out a systematic study of the influence of the individual components of
the model lipid (Fig. 10) [17]. The interlayer distances were plotted as a function
of the water content. The lowest straight line shows the basic lamellar lipid sys-
tem, which consists of the unsaturated fatty acids of the model lipid system (Table
4). The gradient of the straight line increases slightly as the water content in-
creases. The thickness of the lipid bilayer is obtained by extrapolating to water
content of 0%. If the three saturated fatty acids are now added in sequence, three
Figure 8 Phase diagram of the system: fatty acid–soap–water. (From Ref. 15.)
Figure 9 Scheme of x-ray reflection off lipid bilayers.
Figure 10 Interlayer distance as a function of the water content in the step by step
composed model lipid. (From Ref. 17.)
12 Möller
straight lines are obtained above the original one, each with a similar slope. The
interlayer distances are clearly larger, i.e., incorporation into the lipid bilayer
occurs not so much parallel to the alkyl chains but rather transversal to them in
the zone where the methyl groups of the antipodal alkyl chains meet.
The further addition of phosphatidyl ethanolamine has a similar effect, also
indicating that incorporation occurs between the antipodal monolayers. When
cholesterol is then added, the gradient increases steeply. This variant behavior
is attributed to the lowered water-bonding capacity of the hydrated hydrophilic
heads in the lipid bilayers when cholesterol is added. Some of the added water
is no longer anchored in the lipid bilayer but remains in the aqueous layer, thus
causing a widening of the layers. Extrapolation to a water-free system gives an
interlayer distance that corresponds to the basic system. In this case all of the
components are aligned parallel to the alkyl chains. This unusual effect of the
cholesterol is reversed when ceramide is added, with the gradient of the system
again approximating that of the basic system. The thickness of the layer increases
again. When, finally, the neutral lipids, wax esters, and squalene are added, only
an increase in the interlayer distances is again observed.
Other authors [18] studied a reduced three-component system containing
hexadecanoic acid, ceramide, and cholesterol, which was brought into equilib-
rium with the help of an aqueous buffer solution. They measured the different
effects of ceramides 2 and 5, which differ only by a hydroxy group. Separate
domains for ceramides and fatty acids were detected in the structural pattern of
the lipid bilayers. These mosaic structures, whose presence was recently also
postulated by another research group [19], certainly play a crucial role in regulat-
ing the water permeability of the epidermis.
VI. EFFECTS OF CERAMIDES
The different effects of the ceramides are shown in Table 5.
A. Biophysical Effects
The overriding property of the ceramides revealed by the in vitro measurement
results is their capacity to modulate the lamellar crystalline gel structure of the
horny layer lipids. The studies of Friberg and colleagues and the group around
Bouwstra [20–23] with model lipids show that the ceramides and cholesterol act
as antagonists. This holds true especially in respect to influence on the interlayer
distance of the stratum corneum lamellar structure as demonstrated before. Both
together stabilize the lamellar system, also making it more compatible with other
lipid components. Bouwstra and colleagues found that ceramide 1 and also cera-
Table 5 Activity of Ceramides
Modulation of lamellar gel crystal of the horny layer lipids

• Opponent of cholesterol concerning interlayer distance
• Solution aid for cholesterol
• Augmentation of crystalline parts
• Decrease of membrane fluidity
Influence on the stratum corneum properties
• Decrease of TEWL
• Increase of water content
• Decrease of skin scalines
Biologic activity
• Control of epidermal proliferation
• Induction of cell differentiation
• Stimulation of apoptosis of cancer cells
• Second messenger function
mide 2 possess a pronounced role in building lamellar structures as well as the

molar ratio of cholesterol to ceramides and the composition of the latter.
Our own, not yet published studies have shown that the addition of choles-
terol clearly increases the extent of the layer structure. Addition of ceramides,
on the other hand, partly counteracts this effect and increases the solubility of
cholesterol [24]. The literature also contains reports of a lowering of the mem-
brane fluidity by cholesterol [25], as a result of which the lipid bilayer can be
set to an optimal viscosity.
The barrier properties of the whole stratum corneum are also significantly
influenced by the ceramides and cholesterol and are optimal in the close combina-
tion of horny cells and the complete mixture of stratum corneum lipids. In vitro
and in vivo methods were used to measure the effects. The reduction in transepi-
dermal water loss (TEWL) and the increase in the water-binding capacity demon-
strates the powerful effects of the stratum corneum lipids on the barrier and mois-
turizing function of the epidermis [16,26–28].
This effect is also impressively confirmed in a barrier repair study [29].
The barrier of hairless mice was damaged by washing it with acetone alone and
with acetone containing a substance that inhibits ceramide synthesis, respectively.
In the second case, it was shown that regeneration of the barrier took much longer
and was accompanied by the (also delayed) restoration of the previous ceramide
content.
The in vivo restoration of the barrier of volunteers, whose skin had been
damaged with a surfactant solution or by treatment with Scotch tape stripping,
was significantly better with a synthetic type-2 ceramide than a placebo [30].
14 Möller
Ceramides also help to increase skin moisture as measured on volunteers with a

corneometer [31,32] (for details, see Chapter 4).
A reduction in scaly skin (skin roughness) was also observed when a short-
chain hydroxyacylated phytosphingosine (with another hydroxy group in position
4) was applied to human skin [33].
B. Biological Effects
In addition, biological effects were observed with certain ceramides. For exam-
ple, it was demonstrated that ceramides inhibit the rate of epidermal cell division,
whereas their precursors, the glycosylceramides, which are more highly concen-
trated in the lower layers of the epidermis and do not occur at all in the stratum
corneum, accelerate it [34].
Moreover, it was shown that certain ceramides, such as the cell-permeant
ceramide analogues N-cetyl-(C2-Cer) and N-thioacetylsphingosine, induce cell
differentiation and programmed cell death (apoptosis) in the human epidermis
[35]. C2-Cer, as a second messenger of tumor necrosis factor–alpha (TNF-α)
in follicles of ovaries, is a stimulant of apoptosis [36], initiating the apoptosis
of ovarian cancer cells [37]. Another ceramide analogue (L-threo-1-phenyl-
2-decanoyl-3-morpholino-1-propanol) stimulates cortical neurons and amelio-
rates memory deficits in ischemic rats [38]. Sweeny et al. [39] recently suc-
ceeded in demonstrating that in comparison with nonmethylated sphingosine,
N,N-dimethylsphingosine has a powerful antitumor effect on various human can-
cer cell lines. On the other hand, sphingosine is effective as an anti-inflammatory
agent in the skin via inhibition of protein kinase C, which plays a key role in
inflammation [40]. Also, the antimicrobial activity of a variety of related sphingo-
sines has been observed, and because free sphingosines occur in the stratum cor-
neum and other epidermal layers, they may contribute to the antimicrobial barrier
of the skin [41].
Other authors [42] are studying a second messenger function of the cera-
mides in connection with the epidermal growth factor. Glycosphingolipids (gly-
cosylceramides) with different numbers of monosaccharide units exhibit impor-
tant activities in cell-cell recognition, cellular differentiation, and growth control
[43]. In 1997, Orfanos and coworkers [44] gave an overview of the signaling
role of sphingolipids in human epidermis.
In view of cosmetic applications, interesting recent studies describe utiliza-
tion of ceramide precursors to influence epidermal barrier function. Rawlings
and coworkers [45] found out that the ceramide production in vitro as well as
in vivo could be increased significantly by the application of L-lactic acid. At
the same time, the barrier function of the stratum corneum was ameliorated. The
D-form was nearly ineffective.
In another example, it was demonstrated that the topical application of the

sphingosine derivative tetra-acetylphytosphingosine produced an elevation of
ceramide concentration in the stratum corneum and the barrier function was im-
proved too [46]. Precursors for the biosynthesis of ceramide 1 are linoleic acid
or its derivatives. The known decreased level of this special ceramide in the
stratum corneum causes skin xerosis in winter and could be normalized by topical
application of formulations containing linoleic acid–rich triacylglycerol [47]. Us-
ing human keratinocytes in culture, it was possible to stimulate ceramide biosyn-
thesis in stratum corneum considerably by the action of N-acetyl cysteine. Other
thiols were less active [48].
Additional references concerning biological actions on the barrier function
of the stratum corneum are given in a recently published review article [49].
VII. NONNATURAL CERAMIDES: NATURE-IDENTICAL

CERAMIDES/CERAMIDE ANALOGUES/
PSEUDOCERAMIDES
Now that the special significance of the ceramides for the functioning and appear-
ance of our skin has been explained in detail, it is not difficult to appreciate why
cosmetic chemists in particular show increased interest in this class of substances.
Natural ceramides obtained from the brains of cattle were initially used. They
were, however, very expensive (more than US $1000 per kilogram) and as prod-
ucts isolated from cattle they became increasingly involved in the bovine spongi-
form encephalitis (BSE) debate in recent years. Therefore, it was a logical step
to consider synthetic products with an identical or similar structure.
The term nature-identical ceramides covers nature-identical ceramides and
their racemates, whereas ceramide analogues are usually compounds based on
stereoisomerically pure sphinganine with a different acyl chain length or with a
very similar skeletal structure, and interest is focused on their biological effects.
Pseudoceramides generally have structures that differ more clearly from the basic
structure and are often designed for cosmetic applications. The so-called synthetic
barrier lipids (SBL) are pseudoceramides.
A. Nature-Identical Ceramides and Ceramide Analogues

It is noteworthy, first, that, in the meantime, methods have been developed to
produce nature-identical ceramides biotechnologically. One of these ceramides
is ‘Ceramide III’ from Jan Dekker, obtained by using yeast. But it is not available
at a low price. On the other hand, the synthesis of nature-identical ceramides
has been described [50], but it inevitably involves a large number of steps and
16 Möller
the resulting products are therefore very expensive. A more recent, 7-step synthe-
sis starts from L-serine and yields D-erythro-sphingosine [51]. Figure 11 shows
the synthetic pathway.
This synthesis is also very costly and is difficult to translate onto a commer-
cial scale. This is a major reason why synthesis methods have also been developed
for producing D/L-erythro/threo-sphingosine/sphinganine which contains all
possible stereoisomers. It can subsequently be acylated with suitable fatty acid
derivatives, thus completing a process for synthesizing ceramides that closely
resemble the natural substances on which they are modeled. As an example, the
L’Oreal method [52] for producing 2-oleoylamino-octadecane-1,3-diol is de-
scribed here. The synthetic pathway, which is also suitable for commercial-scale
production, is shown in Figure 12.
This method requires four relatively simple reaction steps leading to the
formation of racemic D/L-erythro/threo-sphinganine, which is subsequently
acylated to the synthetic ceramide. The fact that five different steps have to be
carried out inevitably means that this method, too, is economically unattractive.
Syntheses of ceramide analogues, which are mainly of interest for their
biological effects, often start with natural (commercially available) sphingosine.
To produce C2-, C6-, and C8-ceramides, for example, sphingosine is first com-
pletely O- and N-acylated, and the O-acyl groups are then selectively split by
hydrolysis [53].
Figure 11 Synthesis of D-erythro-sphingosine. (From Ref. 51.)

Figure 12 Synthesis of 2-oleoylamino-octadedecane-1,3-diol. (From Ref. 52.)
B. Pseudoceramides
1. General Remarks
There has been made every effort to synthesize ceramide analogues, pseudocera-
mides, and synthetic barrier lipids (SBL) by simple chemical pathways. There
are now a number of patents in this area, although this is not the place to list
them all in detail. A summary account of new pseudoceramides and special syn-
theses was recently published [54]. By way of illustration, Figure 13 shows a
number of commercially available pseudoceramides with structures that exhibit
clear similarities to the natural ceramide structure.
The first listed product in Figure 13 is the above-mentioned Ceramide III
from Jan Dekker, biotechnologically obtained. The second product from Kao
(SLE) is one of the first pseudoceramides that have been studied in depth [31].
18 Möller
Figure 13 Commercially available pseudoceramides/ceramides.
The C,C double bond of the sphingosine was substituted by an ether group, and
the sphingosine’s primary OH group was substituted by the N-hydroxyethyl
group. This principle is also recognizable in the underlying structure, the cera-
mide H03, although there is no further hydroxy group in the head of the molecule,
but instead several hydroxy groups in the alkyl chain of the acyl group. The
fourth pseudoceramide from Quest [55,56] is similar to the second product insofar
as its hydrophilicity is also due to the N-hydroxyethyl group. Two fatty alkyl
groups and two OH groups are introduced into the molecule through the dicarbox-
ylic acid diamide linkage.
2. Structural and Synthetic Features

The general structure of the above-mentioned pseudoceramides is very similar to
that of the natural type 3 ceramide that was for a long time the only commercially
available one of high purity for purposes of comparison. The fundamental struc-
ture elements for the synthesis of new substances with potential ceramide effects
are shown in Figure 14.
Figure 14 Fundamental structure elements of pseudoceramides.
Two saturated or unsaturated alkyl chains of equal or unequal length are

linked to an oligohydroxy compound to form a nonionic structure. The number
of hydroxy groups should be equal to or greater than two. A poly(ethlenoxy)
group can also represent the hydrophilic part of the molecule. A number of possi-
ble starting materials are shown in Table 6. The individual elements are linked
through CEC, CEN, ester, amide, and ether bonds.
A long-chain alkylamine with one or more hydroxy groups is often pro-
duced as pseudosphingosine/sphinganine, which is then acylated with different
fatty acid derivatives at the nitrogen atom. One or more hydroxy groups can
also be introduced through the fatty acyl group. Methyl esters, acid chlorides,
anhydrides, mixed anhydrides, azolides, and even combinations of carboxylic
acid with carbodi-imides are employed as reactive carboxylic acid derivatives.
3. Syntheses of a Number of Selected Pseudoceramides

a. Pseudoceramides Based on 1-Amino-3-alkoxy-2-propanols. The
synthesis of the most frequently studied pseudoceramide, SLE from Kao (see
Fig. 13), is shown in Figure 15 [57,58].
In the first step, hexadecanol is reacted with 3-chloro-1,2-epoxypropane in
the presence of sodium hydroxide solution and the phase transfer catalyst tetrabu-
tylammonium bromide (TBAB) to obtain 2,3-epoxypropylhexadecyl ether. This
reacts quantitatively with 2-aminoethanol to form a secondary amine. In the third
20 Möller
Table 6 Starting Materials
1 Hydrophiles
Glucose
Alkylglucosides
Hydroxyalkylamines, Oligohydroxyalkylamines
Sorbitylamine
N-Methylsorbitylamine
D-Glucosamine hydrochloride
D-Gluconic acid δ-lactone
Mucic acid
Oligomeric ethylene glycols
2 Lipophiles
Fatty acid chlorides, -methylesters
Alkylsuccinic acid anhydrides, -monoesters
Amino acid esters, amides
Guerbet acid derivatives
Fatty alcohols
Fatty alkylamines
Guerbet-alcohols
Malonic acid derivatives
Hydroxyalkane diacid derivatives
Difattyacyl glycerols
step, the amine undergoes N-acylation with methyl hexadecanoate acid, yielding
the end product SLE.
Unilever has claimed, within a patent application, structures that are based
on the same synthesis principle [59]. These include the 2-hydroxy analogue of
SLE, N-(3-hexadecyloxy-2-hydroxypropyl-N-(2-hydroxyethyl)-2-hydroxyhexa-
decanoic acid amide. In this variant, acylation is carried out with the methyl ester
of 2-hydroxyalkanoic acid in the final step.
b. Pseudoceramides Based on N-Hydroxy/Dihydroxyalkylaminoalkanes.
The structure of the pseudoceramide SLE is more strongly modified in another
Unilever patent [60]. As can be seen in Figure 16, the hydrophilic part of the
molecule also has two hydroxy groups, which are, however, arranged vicinally.
The chain length in the example is shorter. The synthesis is even simpler: dodecyl-
amine reacts with 2,3-epoxypropanol to form 2,3-dihydroxypropyldodecylamine,
which is acylated in the usual way with methyl hexadecanoate to generate a
pseudoceramide. This patent contains another modification of the structure that
is claimed in another patent by Elisabeth Arden [61] as an active ingredient of
a cosmetic product for treating aging skin (at the bottom of Fig. 16). This pseudo-
Figure 15 Synthesis of the pseudoceramide SLE (Kao). (From Ref. 57.)
Figure 16 Synthesis of N-(2,3-dihydroxypropyl)-N-dodecyl-hexadecanoic acid amide.

(From Ref. 60.)
22 Möller
ceramide contains a shortened and hydroxylated acyl group to increase its hydro-
philicity.
A malonic acid bis-(N-2-hydroxyethyl-N-hexadecylamide), Questamide H,
listed among the commercially available pseudoceramides, also falls into this
category and can be obtained in only two reaction steps: hydroxyethylation of
hexadecylamine with ethylene oxide and subsequent reaction with diethyl malo-
nate [56].
c. Pseudoceramides Based on Polyethylene Oxide Adducts. SBL KE
3039 from Henkel [62] is an example of this group of pseudoceramides. The
reaction pathway is shown in Figure 17.
In the first step, hexadecenylsuccinic acid anhydride is obtained in an ene
reaction by addition of 1-hexadecene to maleic acid anhydride. After selective
catalytic hydrogenation, the cyclic anhydride is reacted with behenyl alcohol (do-
cosanol) to give the semiester. In the fourth step, after ethoxylation with 7.5 Mol
ethylene oxide, hexadecylsuccinic acid monobehenyl/polyethyleneglycol ester is
Figure 17 Synthesis of SBL Ke 3039 (Henkel). (From Ref. 62.)

obtained. In this reaction part, the ethylene oxide is additionally inserted into the
already existing ester group.
d. Pseudoceramides Based on Simple Sugar Derivatives. Much work
has recently been carried out on a synthesis concept for pseudoceramides that
makes use of easily accessible sugar derivatives as hydrophilic components and
oleochemical derivatives obtained from natural raw materials as lipophilic ones
[54].
Only glucose and some of its derivatives, all of which are easily accessible,
are shown in Table 6 as examples of oligohydroxy compounds. N-fatty alkyl
glucosylamines, for example, are obtained in a simple reaction by condensing
fatty amines with glucose. The corresponding sorbityl amines are obtained from
them by catalytic hydrogenation. The other substances are commercially avail-
able. The lipophilic substances are mainly fatty acids or other carboxylic acid
derivatives, which have a longer alkyl chain, and dicarboxylic acid derivatives
or fatty alcohols and fatty amines, all of which are also available.
e. Pseudoceramides Based on Amino Acid Derivatives. One general
synthesis concept is based on the use of various commercially obtainable amino
acids. One advantage is that at least two different functional groups are available.
Of relevance in this context are, for example, glycine, alanine, sarcosine, β-
alanine, lysine, serine, aspartic acid, and glutamic acid. The pseudoceramide de-
rived from aspartic acid is obtainable by a two-step synthesis, as shown in Figure
18 [63].
First, the aspartic acid is reacted with cetaryl(C C16/18) alcohol to obtain
the dialkyl ester of aspartic acid. In the second step, this is acylated in a smooth
reaction with D-gluconolactone to give asparagine SBL.
f. Pseudoceramides Based on Succinic Acid Derivatives. Figure 19

shows suggested structures based on succinic acid derivatives. These molecular
structures represent all succinic acid monoamides whose amine component is N-
methylsorbitylamine. The two long alkyl chains that are needed are introduced
on the one hand by C-substitution of the succinic acid and on the other by esteri-
fication of the second carboxyl group [64].
Unsubstituted succinic acid was used in the next three structures, so the
two fatty alkyl groups had to be linked to the hydrophilic part of the molecule
together with the ester group. In these cases—in contrast to the first structure—
the selective introduction of two chains of different length into the target mole-
cule is impossible or can be achieved only with considerable additional effort
[65–67].
The ester components of the final three compounds are formed with the
following hydroxy compounds: C32/36-Guerbet alcohol; 1,3-distearoylglycerol;
and malic acid distearyl ester. Because hexadecylsuccinic acid from the above-
24 Möller
Figure 18 Synthesis of N-gluconoylaspartic acid di-C16/18-alkylester. (From Ref. 63.)
mentioned Henkel pseudoceramide can be used for the first target compound and
different chain lengths can also be selected here, the synthesis of this compound
is an interesting EO-free way of obtaining the above-mentioned pseudoceramide.
The other compounds that are shown are synthesized similarly.
The reaction pathway of the synthesis of C16-alkylsuccinic acid mono-
behenylester N-methylsorbitylamide is shown in Figure 20. The production of
hexadecylsuccinic acid anhydride has already been shown in Figure 17. The acid
anhydride is then, as also described above, neatly reacted with behenyl alcohol
to obtain the semiester, which is converted to the corresponding acid chloride
by reaction with phosphorus trichloride. The acid chloride and an aqueous N-
methylsorbitylamine solution then are reacted under Schotten-Baumann condi-
tions, forming the end product glucamide SBL (Ke 3193). The yield is 70% to
80%, and this synthesis is suitable for production on a commercial scale.
g. Pseudoceramides Based on Different Sugar and Sugar Acid Deriva-

tives. Four typical representatives of this group are shown in Figure 21. The
top two structures are long-chain acylated N-dodecylglucosylamide and N-dode-
cylsorbitylamide, which have already been described in the literature in other
Figure 19 Succinic acid derivatives. (From Refs. 64–67.)
context [68]. The possibility of using these derivatives as synthetic barrier lipids
was recognized at a later stage [69,70].
The third structure in Figure 21 is based on the N-behenylamide of gluconic
acid, which is obtained from the amine with D-gluconolactone and in the next
step receives its second long alkyl chain by acylation with stearoyl chloride [71].
The final compound is the stearic acid ester of dodecylglucoside and, as
such, has been known for a long time. Because the alkyl glycosides, referred to
as APG (alkyl polyglycosides), have been commercially available for some time,
this variant should also be mentioned here. A similar type is derived from 10-
hydroxydecylglucoside and is then acylated at the two primary OH groups to
give the corresponding dilaurate [72]. The syntheses of the two first-mentioned
substances are shown in Figure 22.
In both cases, the synthesis starts with the condensation of glucose and
dodecylamine to give N-alkylglucosylamine. In the first case, the glucosylamine
is hydrogenated to N-sorbitylamine and then acylated. In the second case, the
26 Möller
Figure 20 Synthesis of C16-Alkylsuccinic acid monobehenylester N-methylsorbityl-

amide. (From Ref. 64.)
glucosylamine is directly acylated to stearic acid N-dodecylglucosylamide. Al-

though the second method involves one less step, the hydrogenation yields a
hydrolysis-resistant product with an additional OH group. Both syntheses make
use of favorably priced natural substances.
The compound in the final structure diagram is an especially interesting
prospect for commercial production in view of its simple synthesis [73] (see
Fig. 23).
The C32/36-Guerbet acid, which is obtainable from the corresponding Guer-
bet alcohol through alkali fusion, was converted into the acid chloride. Aminoly-
sis of the chloride in an aqueous environment with N-methylsorbitylamine re-
sulted in the formation of C32/36-Guerbet acid N-methylsorbitylamide. This
synthesis was optimized for production on a commercial scale.
Figure 21 Sugar and sugar acid derivatives.
Figure 22 Syntheses on the basis of N-alkylglucosylamines and -sorbitylamines. (From

Refs. 69,70.)
28 Möller
Figure 23 Synthesis on the basis of C32/36-Guerbet-alkanoic acid. (From Ref. 73.)
VIII. PRECURSOR MOLECULES (SO-CALLED

PRO-DRUGS)
As mentioned at the beginning, the glycosylceramides become deglycosylated

as the differentiation of the keratinocytes proceeds. This gave rise to the idea
that the glycosylceramides themselves could be used as so-called pro-drugs be-
cause they are metabolized to ceramides in the stratum corneum by glycosidases.
Laboratoires Serobiologique was able to demonstrate this for a galactosylcera-
mide, ceramide LS 3773 [74].
In another example, from Unilever, phosphoric acid esters and sulfuric acid
esters of pseudoceramides are claimed as pro-drugs, whose active substance is
said to be liberated by hydrolytic enzymes of the horny layer [75]. Structures
previously described by Kao [57,58] served as the pseudoceramide basis. These
substances can be formulated much better in cosmetic preparations than the un-
derivatized parent compounds because they are more hydrophilic and similar to
emulsifiers.
The sulfonation product of glucamide SBL (Ke 3193) shown in Table 7
[76] also belongs to this group. This sulfate readily forms liposomes in lipid/
water systems. Some structures of the above-mentioned precursor molecules are
given in Table 7.
Table 7 Synthetic Ceramide Precursors
Ceramides 3773
(Lab. Serobiologiques S.A.)
[74]
Phosphoryl-SLE
(Unilever)
[75]
Sulfo-SLE
(Unilever)
[75]
Sulfoglucamid-SBL
(Henkel)
[76]
The development of further pseudoceramide precursors seems to be an in-

teresting task for the future.
IX. PROPERTIES OF SOME PSEUDOCERAMIDES
Table 8 shows a comparison of the typical properties of a few selected pseudocer-

amides and the natural type-3 ceramide. The compared properties are the melting
point and the effect on the lamellar structure of the model lipid mixture after
Friberg [14]. The melting points are all lower than the melting point of the natural
ceramide. For formulation purposes, an optimal melting point is in the range
between 40° and 55°C. The high melting point of the natural ceramide is unusual,
although it should be remembered that it does not occur alone but in mixtures
with other lipids, when it melts at a significantly lower temperature. The final
three substances lie in a favorable melting range. The effect of the pseudocera-
mides on the lamellar structure is in all cases similar to that of the natural cera-
mide—i.e., the thickness of the lipid bilayer of the nonaqueous system is in-
creased and the increase in the total interlayer distance as a function of water
30 Möller
Table 8 Properties of Some Pseudoceramides
Influence on
Structure Melting point lamellar
Name [°C] structurea Source
105 yes standard
Sigma
92 yes pseudo-
ceramide
(Sederma)
36/48 yes pseudo-

ceramide
(Henkel)
55 yes pseudo-
ceramide
(Henkel)
39 — pseudo-
ceramide
(Henkel)
a
added to the lipid model of Friberg [14]
concentration weakens in comparison with a ceramide-free lipid mixture. As the

water content increases, these molecules migrate from the zone between the ends
of the fatty alkyl chains into the parallel-aligned alkyl chain zone. Moreover,
as the water content increases, the liquid crystalline character decreases, thus
modifying the permeability of the barrier layer. In this respect the pseudocera-
mides H03 and glucamide SBL [64] exhibit the greatest similarity to the natural
type-3 ceramide. Guerbet acid N-methylsorbitylamide [73] has a favorable melt-
ing point comparable to that of the Henkel pseudoceramide Ke 3039, but it was
not studied any further.
X. SUMMARY
The special structure and the physical and physiological functions of the epider-
mal lipids with special focus on ceramides were described. Ceramide analogues
were then introduced and a general structural principle for pseudoceramides
based on fatty and oligohydroxy components was explained. A few examples
were selected from the large number of pseudoceramides described in the patent
literature. These examples can be synthesized by simple, technically feasible
methods and are also described as being used in cosmetic applications. In vitro
tests showed that some of them behave very similarly to natural ceramides. Der-
matological studies demonstrated properties such as regeneration of the barrier
function, reduced skin roughness, and improved skin elasticity.
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2
Structure of Stratum Corneum
Lipid Layers and Interactions
with Lipid Liposomes
Joke Bouwstra
Leiden University, Leiden, The Netherlands
I. LIPID ORGANIZATION IN STRATUM CORNEUM

A. Introduction
The natural function of the skin is the protection of the body against the loss of
endogenous substances such as water and against undesired influences from the
environment caused by exogenous substances. The main barrier for diffusion
through the skin is the outermost layer of the skin, the stratum corneum (SC) [1].
The SC consists of keratin-filled dead cells, the corneocytes, which are entirely
surrounded by crystalline lamellar lipid regions. Furthermore, the cell boundary,
the cornified envelope, is a very densely cross-linked protein structure, which
prevents easy absorption of drugs into the cells. This has been illustrated by
confocal studies, in which it was demonstrated that the penetration pathway of
dyes is mainly through the intercellular regions in the SC [2,3]. For these reasons
the lipid regions are considered to be of great importance for the skin barrier
function [4,5]. In the past 20 years, many studies have been carried out to increase
knowledge of the barrier function of the skin. These studies have mainly been
focused on the lipid composition and organization in the SC and the changes
involved in this lipid organization as a consequence of topical application of
drugs in various formulations and patches. This chapter will mainly focus on the
structure in the SC and the changes in this structure as a consequence of water,
surfactants, and liposomes.
37
38 Bouwstra
B. Lipid Organization in Stratum Corneum

The composition of the SC lipids strongly differs from that of cell membranes
of living cells. The major lipid classes [6–8] in the SC are ceramides (CER),
cholesterol (CHOL), and free fatty acids (FFA). The length of the acyl chains
in the CER varies between 16 and 33 carbons; the most abundant acyl chain
lengths of FFA are C22 and C24. These chain lengths are much longer than those
of the phospholipids present in plasma membranes. Furthermore, the CER head
groups are very small and contain several functional groups that can form lateral
hydrogen bonds with adjacent ceramide molecules and with other lipids as well.
The increased chain length and the small size of the head group results in a very
densely packed structure (see below) compared to that present in membranes of
living cells. This is closely related to differences in functionality. In cell mem-
branes, transport across the membrane is required for a proper functioning of the
cells; in SC, however, the lipid lamellae are designed to keep many substances
outside the body and act therefore as permeability barriers. There are at least
eight subclasses of ceramides (HCER) present in human stratum corneum [9].
These HCER, often referred to as HCER 1 to 8, differ from each other by the
head-group architecture (mainly sphingosine or phytosphingosine base linked to
either a fatty acid, an α-hydroxy fatty acid or an ω-hydroxy fatty acid) and the
hydrocarbon chain length. HCER1 and HCER4 both have a very exceptional
molecular structure: a linoleic acid is linked to an ω-hydroxy fatty acid with a
chain length of approximately 30–32 C-atoms. In this respect, the HCER are
different from ceramides isolated from pig SC (pigCER), in which only pigCER1
has this exceptional molecular structure [10] and in which pigCER5 has an un-
usual short chain length (main population around C16–C18).
Many efforts have been undertaken to characterize the lipid lamellar re-
gions. At the end of the 1950s, and early 1960s, the first studies using x-ray
diffraction were carried out with human SC [11,12]. The diffraction patterns of
these excellent measurements were interpreted as being from lipids organized in
tubes surrounding keratin filaments. In the 1970s, however, freeze fracture elec-
tron microscopic studies revealed that the lipids are organized in lamellae [13,14]
located in the intercellular regions in the SC. It took another 10 years before
RuO4 has been introduced as a post-fixating agent to preserve the saturated lipids
in the SC during the embedding procedure. The subsequent electron microscopic
studies revealed an unusual lamellar arrangement of a repeating pattern with elec-
tron translucent bands in a broad-narrow-broad sequence [15–20]. These lipid
lamellae are oriented along the surfaces of the cells. In addition differential scan-
ning calorimetry, Fourier transformed infrared studies, and x-ray diffraction re-
vealed that the lipids are arranged in a crystalline sublattice and that a small
proportion of lipids formed a liquid phase [21–23]. Furthermore, the lipid bilayers
were oriented along the surfaces of the cells. In 1988, a study was reported in
Structure of SC Lipid Layers and Interactions with Lipid Liposomes 39
which x-ray diffraction was used to determine the lipid organization in murine
SC [24]. These studies revealed a lamellar organization of the lipids in the inter-
cellular regions with an unusual long periodicity of the structure being approxi-
mately 13 nm. Furthermore, the lipids in the lamellae are mainly organized in a
crystalline sublattice, which is in agreement with the FTIR studies. In subse-
quent studies, the lipid organization in pig SC and in human SC has also been
assessed [25–28].
In Figure 1A the small angle x-ray diffraction curves of human SC mea-
sured at room temperature are plotted as a function of Q (for a brief explanation
of the technique, see appendix A). Q is a measure for the scattering angle. The
diffraction curve is characterized by a strong and a weak diffraction peak, both
peaks having a shoulder on the right-hand side. The positions of these diffraction
peaks are directly related to the periodicity of the phase by the equation: Q ⫽
2πn/d, in which n is the order of the diffraction peak and d the periodicity of
the lamellar phase. In the diffraction pattern of human SC, the number of peaks
are limited, very broad, and partly overlap, so interpretation of this diffraction
pattern is quite complicated. However, from this curve it is obvious that an in-
crease in the water content from 20% to 60% w/w does not lead to a change in
the peak positions, and therefore not to a change in periodicity of the lamellar
phases. From this observation it was concluded that addition of water to the SC
does not lead to a swelling of the lipid lamellae (for more detailed information
with respect to water, see below). To analyze the diffraction curves in more detail,
additional information was required. For this purpose, the SC lipids were crystal-
lized from 120°C to room temperature, after which the x-ray pattern was moni-
tored. As shown in Figure 1B, the diffraction curves revealed a series of peaks
that were located at the same inter-peak distance. Such a diffraction profile is
characteristic of a lamellar phase. From the positions of the peaks, the periodicity
of the lamellar phase (d) was calculated. These calculations revealed that after
recrystallization, the lipids in SC were organized in a lamellar phase with a peri-
odicity of 13.4 nm. Comparing the peak positions of the diffraction pattern prior
to and after recrystallization revealed that in untreated SC two lamellar phases
are present, one with a periodicity of approximately 6.4 nm, and the other with
a periodicity of approximately 13.4 nm, respectively [10]. Similarly, two lamellar
phases with periodicities of 6 and 13.2 nm were present in pig SC [26]. Because
the 13 nm phase is always present in all the species studied so far, and is very
characteristic for the SC lipid phase behavior, this phase is probably very impor-
tant for the skin barrier function [29].
In addition to the wide angle x-ray diffraction measurements, studies were
carried in which the lateral packing of the lipids was examined. The information
on the lateral packing of the lipids in the lamellae can be gained by wide angle
x-ray diffraction [26]. The spacings of the reflections indicative for the lateral
lipid packing are in the sub-nanometer range and are therefore located at much
(A)
(B)
Figure 1 The diffraction curve of human SC (A) as a function of hydration level varying
between 6% and 60%, (B) prior to and after recrystallization. The diffraction curve is plotted
as a function of Q defined as Q ⫽ 2 π sin θ/λ. The positions of the peaks are directly
related to the periodicity of the lamellar phases by the relation: Qn ⫽ 2 nπ/d; d is the
periodicity and n the order of the reflection; Qn is the position of the nth order reflection.
higher scattering angle in the diffraction pattern (see appendix) than those attrib-
uted to the lamellar phases. With respect to the SC, three sublattices are of impor-
tance: namely, the liquid, the hexagonal, and the orthorhombic lateral packing.
These sublattices are characterized by different sets of reflections. The ortho-
rhombic phase is characterized by spacings at 0.37 and 0.41 nm. The strongest
reflection of the hexagonal phase is located at 0.41 nm. Finally, the pattern of
the liquid phase is characterized by a very broad reflection at 0.46 nm reflecting
the variation in interchain distance in the liquid phase. An example of the wide-
angle x-ray diffraction pattern of human SC is provided in Figure 2.
Several features can be distinguished in this diffraction pattern. Two strong
rings are observed at 0.378 and 0.417 nm, respectively. These reflections indicate
that the lipids are organized in an orthorhombic lattice. However, the strongest
reflection of the hexagonal packing is located at 0.417 nm reflection, so as a
consequence it cannot be concluded from these measurements whether or not a
Figure 2 The wide-angle diffraction pattern of human stratum corneum. The reflections
are indicated in the figure. Large white arrows: the 0.417 and 0.378 nm spacing attributed
to the orthorhombic lateral packing. Black arrows: cholesterol reflections; stars: broad
keratin reflections (at 0.92 and 0.46 nm). Small white arrows: higher order reflections of
the lamellar phases.
42 Bouwstra
hexagonal lateral packing is present as well (see below). The reflections attributed
to the orthorhombic sublattice obscure the reflection of the hexagonal phase. In
addition, several other features are present in the diffraction pattern. Two broad
rings are present at approximately 0.46 and 0.96 nm. These reflections are also
present in extracted SC and are assigned to soft keratin, which is present mainly
in the corneocytes. Whether a population of lipids forms a liquid phase cannot be
concluded from these studies, because the broad reflection of keratin at 0.46 nm
obscures the broad reflection of lipids in a liquid phase. This ring is expected to
be located at 0.46 nm as well. In addition, two reflections are present at 0.36 nm
and 0.72 nm. These reflections are present only approximately 20–30% of the
studies samples and are assigned to proteins. Finally, a series of rings are present
in the diffraction pattern that can be attributed to phase-separated crystalline
cholesterol. The CHOL reflections are present in the diffraction pattern of approx-
imately 50% of the human SC samples.
C. Lipid Organization in Model Membranes

In order to understand the SC lipid phase behavior in normal and diseased skin
in more detail, knowledge of the role the various lipid classes and subclasses
play in the SC lipid organization is required. Because it is impossible to extract
selectively lipids from the SC, these studies have to be carried out with model
membrane systems, in which the lipid composition varies systematically. Several
studies have been carried out in which the model membranes were prepared from
palmitic acid, cholesterol, and bovine-brain ceramides. The choice for palmitic
acid was based on a study by Lampe et al. [30], in which it was stated that the
most abundant fatty acids present in SC have a chain of C16 or C18:1. However,
in more recent studies it has become clear that this was an erroneous observation
and that the main fatty acid chain lengths are C22 and C24 [31,32]. In several
studies, the lateral packing of model membrane mixtures has been studied. NMR
studies carried out with equimolar mixtures of CHOL and bovine-brain ceramide
3 in the absence and presence of palmitic acid revealed that the main population
of lipids formed a crystalline phase, but that also a small proportion of lipids
formed a more mobile phase [33,34]. Upon an increase in the temperature, the
crystalline phase transformed to a liquid phase at around 60°C. This is in contrast
to phospholipid-containing mixtures, in which in the presence of a substantial
amount of cholesterol a liquid-ordered phase has been observed [35–38]. The
presence or absence of this liquid phase may play an important role in the interac-
tions between exogenous substances and the skin because exogenous substances
might more easily mix with a fluid phase than with a crystalline phase [28,39].
In an additional study, it has been shown that sphingomyelin-containing mixtures
form a liquid lateral packing, whereas ceramides having the same chain length
distribution in the presence of cholesterol form a crystalline phase [40]. From
this observation it was concluded that the presence of a liquid phase depends
strongly on the size of the headgroup. The ceramide-containing mixtures were
studied at either pH 5 or 7.4. Slight differences in phase behavior were observed
at these two pH values. Furthermore, in these studies it was shown that more
than 80% of the lipids was in a crystalline state, while a small portion formed
a more mobile phase [41]. A liquid phase was formed at around 50°C. As far as
the lateral packing is concerned, these bovine-brain ceramide mixtures mimic
SC lipid phase behavior quite closely. However, as shown in an additional study
using the x-ray diffraction technique, no lamellar phase was observed with a
periodicity of approximately 12 to 13 nm [42,43]. It seems that in this respect
the bovine-brain ceramide mixtures differ in phase behavior from the lipid organi-
zation in intact SC. In addition, in several studies Fourier transformed infrared
(FTIR) spectroscopy measurements were carried out using mixtures prepared
from either bovine-brain ceramide type III, synthetic ceramide 2, or synthetic
ceramide 5 [44,45]. The ceramides were mixed with cholesterol and perdeuter-
ated palmitic acid. The FTIR spectroscopy measurements were carried out as a
function of temperature and revealed the presence of orthorhombic phases. At
physicological temperature, the CD2 scissoring mode of palmitic acid and the
CH2 scissoring mode of ceramides are each split into two components, indicating
that these molecules are located in different lattices. Increasing the temperature
led to a disordered lattice for palmitic acid at around 40°C and for bovine-brain
ceramide type III at around 60°C, confirming that the components were not prop-
erly mixed in one orthorhombic lattice. A similar behavior was found when mix-
ing fatty acids with either synthetic ceramide 3 or synthetic ceramide 5 [44].
Similarly, in another study using FT-Raman spectroscopy, phase separation was
observed between ceramides and saturated fatty acid in the absence of CHOL.
Again, a single chain length was used [46]. Recently, we observed that addition
of C22 fatty acid to a mixture of isolated CER and CHOL does not mix properly
in the solid state, whereas addition of FFA with a chain length distribution be-
tween 16 and 22 to a CHOL : CER mixture (CER isolated from SC) did not result
in a phase separation (Bouwstra et al., unpublished results). Therefore, it seems
essential when mimicking lipid SC phase behavior that FFA mixtures with a
chain length distribution similar to that present in SC are used instead of a single
chain length of the fatty acids. In several studies, liposomes were used as a model
system for SC lipid lamellae. Although permeation across a bilayer, stability, and
fusion can be studied accurately when using liposomes [47–49], the lamellar
lipid arrangement is expected to be different from that observed in SC. Therefore,
in our opinion, results obtained with liposomes cannot directly be extrapolated
to the situation in stratum corneum. For example, skin lipid liposomes do not
form a stable suspension at around pH 5; the pH at the skin surface is approxi-
mately 5–6.
Several studies have been carried out in which mixtures prepared from
44 Bouwstra
isolated pig ceramides (pigCER) were examined. The first studies, using lipo-
somes, set out to unravel the mechanisms that play a role in the formation of
lamellar phases [50–52].
More recently, mixtures were prepared from either CHOL and pigCER or
from CHOL, pigCER, and FFA [53–58]. A chain length distribution of the FFA
was used according to Wertz and Downing [7]. The composition of these mix-
tures varied systematically. Small- and wide-angle x-ray diffraction studies were
performed. The small-angle x-ray diffraction curve of an equimolar mixture pre-
pared from CHOL and pigCER at a pH of 5 is provided in Figure 3 [57]. In the
x-ray pattern, the presence of a large number of sharp peaks was noticed. The
peaks indicated by I and II have been assigned to a lamellar phase with a periodic-
ity of 5.2 nm, and peaks indicated by 1, 2, 3, 5, and 7 to a lamellar phase with
a periodicity of 12.2 nm. Furthermore, two additional peaks at 3.35 nm and 1.68
Figure 3 The small-angle x-ray diffraction curves of the 1 :1 CHOL :CER and 1 :1 :1
CHOL :CER:FFA lipid mixtures. The arabic numbers indicate the diffraction orders
of the long periodicity phase (repeat distance of 12.2 and 12.8 nm for the equimolar
CHOL :CER and CHOL:CER :FFA mixtures, respectively). The roman numbers indicate
the diffraction orders of the short periodicity phase (repeat distance between 5.2 and 5.5
nm).
nm have been detected, which can be assigned to hydrated crystalline CHOL that
phase separated. Reducing the CHOL/pigCER molar ratio to 0.4 did not change
the phase behavior, except that a smaller amount of CHOL phase-separated. Only
a reduction to a molar ratio of 0.2 or an increase to a molar ratio of 2 weakened
the 12.2 nm phase and increased the proportion of lipids forming the 5.2 nm
lamellar phase. At a molar ratio of 0.2, the periodicity of the 5.2 nm phase in-
creased slightly to 5.6 nm (see Fig. 4). From these observations, it was concluded
that over a wide range the phase behavior is remarkably insensitive to changes
in the CHOL/pigCER molar ratio. Furthermore, it was concluded that mixtures
with CHOL and pigCER mimic lipid phase behavior in intact SC quite closely,
not only with respect to the lateral packing (see below) but also with respect to
the formation of two lamellar phases with periodicities of 5–6 and 12–13 nm.
Addition of long-chain FFA mixture (dominant chain lengths in the mixture C22
and C24), the third class of lipids that is prominently present in SC, did not
change the lipid phase behavior dramatically (see Fig. 3). At an equimolar
CHOL : pigCER: FFA molar ratio, the periodicity of the 12.2 nm phase increased
to approximately 12.8–13.0 nm; the 5.2 nm lameller phase increased its periodic-
ity to 5.4 nm.
The wide-angle x-ray diffraction patterns of CHOL : pigCER mixtures re-
vealed a strong reflection at approximately 0.409 nm, which indicates a hexagonal
lateral packing. Varying the CHOL : pigCER molar ratio between 0.2 to 2 did
not change the lateral packing, except for an increase in the intensities of the
reflections attributed to hydrated crystalline CHOL. Addition of FFA did not
induce changes in the lamellar phase behavior (see above); however, the lateral
packing of the lipids changed drastically. FFA induced a phase transition from
a hexagonal to orthorhombic lateral packing. This means that FFA increase the
packing density of the lipids. This is a very important observation for the skin
barrier function, because it is expected that the permeability through a crystalline
phase is much lower than through a hexagonal phase. The transition from hexago-
nal to orthorhombic phase was observed only after incorporation of long-chain
fatty acids (C22/C24 chain length) and not with short-chain fatty acids (C16/
C18 chain length).
In diseased skin, a deviation in CER composition often has been found
[59–62], so insight in the role of CER subclasses play in SC lipid phase be-
havior is also of great importance. To examine in more detail the role of the
individual ceramides, mixtures prepared from CHOL and pigCER with varying
pigCER composition were examined. For this purpose, mixtures prepared with
pigCER (1–5), pigCER(2–6), or pigCER(1–2) have been used. Because in native
SC, CHOL and CER are present in an approximately equimolar ratio, we first
examined the phase behavior of the equimolar mixtures. These studies revealed
that the lipids were organized in two lamellar phases with periodicities of approxi-
mately 12–13 nm and 5–6 nm, similarly as observed in intact SC (Fig. 4). The
46 Bouwstra
Figure 4 A schematic overview of the lamellar phases of several CHOL:pigCER mix-

tures as function of the molar ratio. Note the similarity in the lamellar phases of the various
CHOL :CER mixtures at an equimolar ratio. The indication weak (w), medium (m) and
strong (s) of the 12–13 nm phase and CHOL denote the presence of these phases compared
to the 5-5.5 nm phase.
exception was found with an equimolar CHOL/CER mixture in which the

pigCER1 was absent. In this mixture, the 12 nm phase was only weakly present
[57], indicating that in equimolar CHOL/CER mixtures the pigCER1 plays a
crucial role in the formation of the 12-13 nm lamellar phase. Similar observations
have been made when FFA was incorporated into CHOL/pigCER mixtures at
an equimolar ratio [63]. This is also in line with the absence of the 12-13 nm
phase in synthetic ceramide mixtures, because none of the synthetic ceramides
used in the studies until now mimic the structure of pigCER1. Again, only
pigCER1 has been found to play a crucial role in the formation of the 12-13 nm
phase. Reduction of the CHOL content made the lipid phase behavior in CHOL/
pigCER mixtures more sensitive to the pigCER composition. For example, in
mixtures with a CHOL :pigCER(1-2) molar ratio of 0.6, the 12.2 nm phase is
hardly present [63]. This means that only a dramatic change in lipid phase behav-
ior can be expected in intact SC when simultaneously the CHOL :pigCER molar
ratio strongly deviates from the equimolar ratio and the pigCER composition
deviates from the composition in normal pig SC. However, whether these findings
can be extrapolated to the in vivo situation in humans is not yet known, because
the CER composition in human SC is slightly different from that in pig SC. For
example, in human SC, two CER are present with a linoleic acid moiety linked
to the ω-hydroxy fatty acid. This might indicate that the role of HCER1 in the
lipid phase behavior in human SC is less prominent than the role of pigCER1
in lipid organization in pig SC.
II. WATER AFFECTS LIPID ORGANIZATION

IN STRATUM CORNEUM
One of the first reports on the interactions between the lipid bilayers and water
has been published by van Duzee using thermal analysis [21]. They detected four
endothermic transitions that were attributed either to lipid-phase transitions or to
protein denaturation. The temperature at which these transitions occur depends
on the water content in the stratum corneum. Such water-dependent thermal tran-
sitions have also been found in phospholipid membranes. However, in phospho-
lipid membranes, the transition temperatures are much more strongly reduced by
water than those observed in the SC. In subsequent studies, the effect of water on
the SC lipid organization was examined by other techniques. The x-ray diffraction
technique revealed that upon increasing the water content, almost no swelling of
the lamellae took place [25–28], indicating that if water is present between the
head groups, it will be present only in very small quantities. Using infrared spec-
troscopy [64], it was found that water did not affect lipid alkyl chain order at
room temperature; with electron spin resonance [65], it was found that an increase
in the water content increased the mobility of the hydrocarbon chains. However,
whether this increase in mobility is due to an indirect effect of the swelling of
the corneocytes or to a very small amount of water located between the head
groups is not clear yet. In a separate publication, it was suggested that the in-
creased chain mobility might be limited to certain domains in the intercellular
regions [22]. This would be in agreement with the observation using freeze frac-
ture electron microscopy. Using this technique, the lipid lamellae can be visual-
ized as smooth areas at the plane of fracture. However, after extensive treatment
with a phosphate buffer saline solution, next to these smooth regions, areas with
a rough surface were present in the intercellular domains, indicating a change in
the lipid structure (see Fig. 5).
48 Bouwstra
Figure 5 After treatment with a phosphate buffer saline solution water pools as well
as rough structures were observed in the intercellular lipid domains in the stratum corneum.
C ⫽ corneocyte; RS ⫽ rough structure; W ⫽ waterpool; IL ⫽ intercellular lipids and
D ⫽ desmosome. Bar represents 100 nm.
Furthermore, this article [66] reports the presence of water domains not
only in the corneocytes but also in the intercellular regions. The water domains
were often present between the bound lipids of the cornified envelope and the
lipid bilayer regions (unpublished observations). The presence of the water do-
mains indicates a phase separation between the lipid lamellae and the water. This
is not unlikely to occur, because the lipids present in the intercellular domains
are quite lipophilic, especially at those pH values at which the FFA are not disso-
ciated. Separate domains of water are also able to change the penetration pathway
of the penetrant and increase its permeability. It is very unlikely that the water
domains are continuous channels across the stratum corneum: this would require
large lipid-water interfacial regions, which would be energetically unfavorable.
III. VESICLES AFFECT DRUG TRANSPORT ACROSS SKIN

A. Introduction
The first publications on interactions between liposomes and skin appeared in
1980 and 1982 [67,68]. In these publications it was reported that liposomes ap-
plied to skin of white rabbits in vivo favored the disposition of drugs in the
epidermis and dermis, whereas the amount of drug found in the various organs
was reduced. Although in these studies it was strongly suggested that vesicles
penetrated the skin, this suggestion was received with a lot of skepticism. After
the first papers by Mezei and Gulasekharam, a large number of studies were
carried out, a description of which will be provided below.
B. Vesicles Affect Skin Penetration in Vitro

After the introduction of liposomes as drug delivery systems for the transdermal
route, Ganesan and Ho [69,70] published two studies. In these studies, liposomes
were prepared from DPPC (dipalmitoyldiphosphatidylcholine) that forms gel-
state bilayers. The authors proposed that the drug could be transported (1) as free
solute, (2) as free solute but also associated with the liposomes, or (3) by a direct
transfer of the drug from liposomal bilayer to SC without partitioning into the
water phase. They assumed that the vesicles were neither absorbed intact nor
fused with the SC surface. The permeation studies were performed in vitro with
mouse skin using glucose, progesterone, and hydrocortisone. The amount of
(model) drug in the receiver compartment was sampled as function of time. No
radiolabeled DPPC was detected in the receiver of the diffusion cell and glucose
entrapped in liposomes resulted in smaller skin permeability than glucose applied
in a normal saline solution. When focusing on the lipophilic drugs the investiga-
tors found almost no release from the liposomes compared to the saline solution.
When applied to the skin, the lipophilic drug penetrated through the skin, sug-
gesting a direct transfer from vesicles to SC. Very convincingly, the results of
these studies did not confirm intact liposome penetration as suggested by Mezei
and Gulasekharam [67,68].
In a study by Knepp et al. [71,72], the vesicles were suspended in an aga-
rose gel. They reported that progesterone release from an agarose gel alone was
very fast compared to the release from liposomes embedded in the agarose gel
and that vesicles reduced the progesterone transport rate across hairless mouse
skin compared to application in an agarose gel alone. As far as the lipid composi-
tion is concerned, progesterone was applied in egg-phosphatidylcholine lipo-
somes, DOPC (dioleoylphosphatidylcholine) liposomes, DMPC (dimirystoyl-
phosphatidyl choline) liposomes, or in DPPC (dipalmitoylphosphatidyl choline)
liposomes. The gel-state DPPC resulted in a slower skin penetration of progester-
one than the egg-phosphatidylcholine liposomes. Furthermore, intercalation of
cis unsaturated fatty acid (oleic acid) in phospholipid bilayers increased the drug
transport rate across the skin by an order of magnitude (see Fig. 6). In two more
recent articles [73,74], it has been reported that a gel immobilizes the liposomes
and therefore might affect the interactions between the liposomes and the skin.
However, the trend observed in the studies of Knepp et al. [28,29]—in which
incorporation of drugs in liquid-state liposomes results in a higher skin perme-
ation rate than when incorporated in gel-state liposomes—was also observed for
gel-free formulations (see below).
50 Bouwstra
Figure 6 Transdermal delivery rate (mean ⫾ SD; n ⫽ 6) of progesterone (PG) across

hairless mouse skin in vitro encapsulated in EPC and DPPC liposomes containing 1%
stearic (SA) acid. (From Ref. 72.)
Several other studies were carried out to evaluate whether liposome compo-
sition affects skin penetration of drugs. In the early 1990s, Dowton et al. [75]
compared the effect of liposomal composition on the disposition of encapsulated
cyclosporin A in mouse skin. They applied the vesicles nonocclusively in vitro.
Two nonionic surfactant vesicles were compared with bovine-brain ceramide li-
posomes and liposomes prepared from saturated and unsaturated phosphatidyl-
choline. The various liposomes were saturated with cyclosporin A. In this way,
an equal thermodynamic activity of cyclosporin A was achieved in all formula-
tions. After 24 hours of application, the distribution of cyclosporin A was deter-
mined. They found that application of the drug in nonionic surfactant vesicles
prepared from glyceryl dilaurate/cholesterol/polyoxyethylene-10 stearyl ether,

the amount of cyclosporin A in deeper skin strata and receiver compartment was
highest compared to the other formulations. These studies confirmed the results
of the studies of Knepp et al. [71,72], although in the studies by Dowton et al. [75]
the vesicles were applied nonocclusively without a gel. The findings of Knepp et
al. [71,72] were also confirmed by studies of Hofland et al. [76]. They found
that estradiol incorporated in gel-state nonionic surfactant resulted in a low drug
transport rate through human SC compared to estradiol in liquid-state bilayers.
These results were obtained with saturated estradiol formulations. In contrast to
the studies of Knepp et al., the studies of Hofland et al. [72] revealed that a drug
applied in liquid-state vesicles resulted in higher penetration rates than when
applied in a phosphate buffer saline solution. This might be caused by a difference
in the study design. Klepp et al. [71,72] incorporated the vesicles in agarose and
used an equal drug concentration in the formulations. Hofland et al. suspended
the vesicles in a buffer solution and used an equal estradiol thermodynamic activ-
ity. In the latter case an equal driving force from formulation to stratum corneum
has been achieved. This difference in study design has a great impact when com-
paring drug permeation in vesicles compared to the control, such as a gel or
buffer solution. In a subsequent study, van Hal et al. [77] reported that a decrease
in cholesterol content in liquid state bilayers, which increases the fluidity of the
vesicles bilayers, resulted in an increase in estradiol transport across SC. Meu-
wissen et al. [78] examined the diffusion depth of the bilayer label fluorescein-
dipalmitoylphosphatidylethanolamine (fluorescein-DPPE) in the skin when ap-
plied in gel-state liposomes and in liquid-state liposomes using confocal laser
scanning microscopy. They reported that fluorescein-DPPE applied in liquid-state
liposomes penetrated deeper in the skin than the label applied in gel-state lipo-
somes. Recently, Fresta and Puglisi [79] reported that corticosteroid dermal deliv-
ery with skin-lipid liposomes was more effective than delivery with phospholipid
vesicles. This concerned the higher drug concentrations in deeper layers of the
skin as well as the therapeutic effectiveness. From all the above-mentioned stud-
ies, it seems very clear that the thermodynamic state of the bilayers of the vesicles
plays a crucial role in the effect of vesicles on drug transport rate across skin in
vitro.
In a few studies, occlusive application was compared to nonocclusive appli-
cation. These studies revealed that occlusive application of vesicle suspensions
was less effective than nonocclusive application [80,81] (see Fig. 7). The results
were somewhat unexpected: it has been reported that water is an effective perme-
ation enhancer. However, in case of nonocclusive application, the increased drug
transport can be caused by (1) a more profound interaction between the liposomal
constituents and the skin and/or (2) the presence of a hydration gradient in the
skin. According to Cevc et al. [80], the water gradient is an important driving
force for drug diffusion. They claim intact vesicle penetration through the skin,
52 Bouwstra
Figure 7 Occlusive versus nonocclusive application of vesicles prepared from dilauryl-

phosphatidylcholine (DLPC) and beptaoxyethylene alkylethers (C12E07). A cross section
of human skin visualized using confocal laser scanning microscopy after 6 or 16 hours
application of fluorescein-phosphatidyl ethanol amine in vesicles.
as long as flexible liposomes, Transfersomes, have been used (see below). In

a few studies, pretreatment with vesicles was compared to application of the drug
associated with the vesicles. In all studies, it was found that drug association
with vesicles was more effective than pretreatment with vesicles. When using an
equal thermodynamic driving force, these findings strongly suggest that the vesi-
cles do not act just as penetration enhancers [76] but that when choosing the
proper vesicle composition, an additional effect can be expected.
The size and lamellarity of liposomes may affect the skin penetration rate.
In a study by du Plessis et al. [82], the effect of vesicle size on drug disposition
was evaluated. They found no favored disposition of the drug in lower skin strata
and the receiver compartment when the drug was applied in small vesicles com-
pared to large vesicles. The authors concluded that intact penetration of liposomes
does not occur. Furthermore, it was found that vehicle lamellarity had little effect
on the disposition of cholesterol and cholesterol sulfate in the various skin strata.
In a more recent study, the role of the size of vesicles on transport was studied
by ESR. They found that smaller vesicles disintegrate faster in the skin than large
liposomes [83].
It seems that the physical parameters such as vesicle size and lamellarity
are less important than the application method and the thermodynamic state of
the bilayers. These findings are in favor of the absence of intact vesicle penetra-
tion across the skin. There are a number of studies [84–88] in which liposomes
have been compared to lotion, creams, or penetration enhancers. Although infor-
mation can be obtained about the relative effectiveness of liposomes compared
with other formulations, no information can be obtained about mechanisms be-
cause in these studies (1) the thermodynamic activity of the drug in the various
formulations might differ quite extensively and (2) the different components in
the liposomes, lotions, or creams might have different interactions with the skin.
Although these studies are of interest because they provide insight into the possi-
ble applications of liposomes as drug formulation compared to other ointments
or creams that might already be on the market, these studies will not be discussed
in this chapter.
Touitou et al. [89] compared penetration enhancers with liposomes; they
found that liposomes mainly deposit the drug in the skin and therefore can act as
an excellent reservoir, whereas the penetration enhancers increased the transcutol
transport through the skin. A few years ago, the terms proliposomes and pronio-
somes were introduced. In the case of proliposomes, lecithin was mixed with
sorbitol particles: in the case of proniosomes, surfactants were mixed with levo-
norgestrel. In both systems, vesicles were formed upon hydration [90,91].
C. Vesicles Affect Skin Penetration in Vivo

In 1986 Komatsu et al. [92] applied butylparaben to the skin in a liposome formu-
lation prepared from egg phosphatidylcholine, cholesterol, and dicetylphosphate.
The liposomes were applied occlusively to the dorsal skin of guinea pig in vivo.
The fate of the liposomes was determined using autoradiography. The radioactive
DPPC (dipalmitoylphosphatidylcholine) was found mainly on the application
site, even after 48 hours; in contrast, the applied 14C butylparaben radioactivity
was found in the small intestine, feces, gallbladder, and urinary bladder. In an
additional in vitro study [93], the mechanisms involved in 14C butylparaben pene-
tration was examined very systematically using a flow-through diffusion cell.
The amount of lipids as well as the amount of 14C butylparaben was varied. The
investigators found that (1) the percentage 14C butylparaben transported across
the skin decreased as a function of increasing amount of lipids, and (2) the trans-
port rate of radioactive phospholipids (DPPC) across guinea pig skin was much
lower than that of 14C butylparaben, indicating that the lipids remain in the SC
and that co-penetration of butylparaben and phospholipids to deeper layers in the
skin did not occur, which confirmed the results of their in vivo experiments [92].
54 Bouwstra
Again it was concluded that most likely the liposomes do not penetrate as intact
entities across the skin. From the finding that the 14C butylparaben flux decreased
at increasing lipid content, it was concluded that only 14C butylparaben dissolved
in the water phase contributed to the percutaneous penetration. However, another
mechanism may also play a role. An increase in the lipid content reduced the
thermodynamic activity of butylparaben in the bilayers, which might lead to a
decrease in the driving force from the lipid phase to either the water phase or
the SC. This may result in a reduced penetration through the skin as well.
In another more recent study [94], double labeling was carried out. 3H phos-
phatidylcholine and 14C tretinoin were intercalated in soybean lecithin. It was
found that the ratio of the labels in SC was approximately constant, and that the
3
H/ 14C ratio in epidermis was lower and decreased steeply until a skin depth of
approximately 200 µm was reached. The authors concluded that co-penetration
of a drug-liposome bilayer is possible in the SC, but that based on the reduced
3
H/ 14C ratio in deeper skin strata, a separate diffusion of the drug and liposomal
bilayers in these layers occurs.
In a series of studies carried out in the early 1990s, it was clearly demon-
strated that the transport of protein across the skin was facilitated by NAT 106
liposomes [95] and that these liposomes also increased the penetration of 35S-
heparine and 99mTc [96]. In a related study, it was shown that these liposome
suspensions also resulted in a decrease in the corneal blood supply as measured
by laser Doppler flowmetry [97], indicating that empty liposomes induce changes
in the lower regions of the skin. When examining the composition of the NAT
106 formulation, in which single and double chain phospholipids are present, it
is possible that these vesicles consist of elastic bilayers and therefore approaches
the properties of Transfersomes (see below).
The group of Cevc published a series of papers on Transfersomes, vesicles
prepared from lipids and an edge activator that might be a single-chain lipid or
surfactant. The edge activator makes the vesicles very elastic. It is stated that as
a result of the hydration force in the skin Transfersomes can be squeezed through
SC lipid lamellar regions [80]. Investigators compared occlusive with nonocclu-
sive application and found nonocclusive application more effective than occlusive
application (see above). This is in line with their theory on lipid transport under
the water gradient based driving force. In order to detect the mass flow across the
skin and the disposition in the animal, they used tritiated DPPC as a radioactive
compound and reported that Transfersomes were much more effective than the
‘‘conventional’’ rigid liposomes when applied nonocclusively. After 8 hours of
Transfersome application in mice, significant amounts were found in blood (ap-
proximately 8% of the applied dose) and liver (20% of the recovered dose). The
group claimed that 50–90% of the dermally deposited lipids can be transported
beyond the level of the SC. Although there is no doubt that their Transfersomes
have clear advantages with respect to increasing the transport of active material
across the skin, it was claimed in these studies that the elastic Transfersomes
penetrated intact through SC and viable skin into the blood circulation. This
statement, in particular, resulted in much skepticism in the research field. In fact,
this statement was and is still not proven. The skepticism is also caused by the
knowledge that such large associates are extremely difficult to transport across
the skin as intact entities, especially because the SC consists of a very tight struc-
ture that is designed to act as a barrier (see previous paragraph). In more recent
studies of this group, several drugs were associated with the vesicles. In the first
published study on drugs associated with Transfersomes [98], the Transfersomes
suspension contained relatively high amounts of lidocaine or tetracaine. The
Transfersomes were tested on rats and on humans and in both studies the Trans-
fersomes appeared to be more efficient than the conventional liposomes or solu-
tions. The differences found using corticosteroids were somewhat less encourag-
ing [99]. In another report, insulin was associated with Transfersomes [100,101].
Blood glucose levels could be lowered after about 3 hours of application. A clear
difference in glucose level in blood was observed between application of insulin
associated with micelles, conventional liposomes, or Transfersomes in the sense
that Transfersomes resulted in a significantly lower glucose level. This was ob-
served in studies of mice, but in more recent studies of humans, a decrease in
glucose level also was observed [102]. Not only relatively large molecules such
as insulin are claimed to be transported but even big molecules such as FITC-
BSA [103] or I-BSA can be transported across the skin when associated with
Transfersomes. The biodistribution of the derived radioactivity after an 8-hour
application to mice skin of I-BSA associated with Transfersomes is very similar
to that of Transfersome-associated I-BSA injected subcutaneously. These results
are very encouraging and certainly show that Transfersomes indeed have advan-
tages over vesicles prepared from only double-chained phospholipids and choles-
terol. It would be of extreme interest to study the mechanisms involved in these
vesicles in more detail.
A very extensive and well-designed study was described by Ogiso et al.
[104], who compared gel systems in which D-limonene or laurocapram was pres-
ent as a penetration enhancer and studied the transport of beta-histine in the pres-
ence or absence of liposomes in the gels. The liposomes were prepared from
either egg phosphatidylcholine or hydrogenated soybean phosphatidylcholine.
The bioavailability of the drug in the presence of the egg PC liposomes was
higher than in the absence of the egg phosphatidylcholine liposomes, confirming
earlier reports. It seems that the fluidity of the membranes is an important factor
for the penetration enhancement, which confirmed the results of earlier studies
[71,72,76–78]. Furthermore, lipid analysis revealed that the amount of ceramides
decreased dramatically in the SC after application of a d-limonene–containing
formulation, indicating extraction of lipids from the skin, and the phospholipid
content in the SC increased after liposomes treatment. This suggests that the
56 Bouwstra
liposomes replace the ceramides in the SC. The investigators assumed that in
their formulations the replacement of ceramides by phospholipids plays an impor-
tant role in the mechanisms involved in the increased penetration of beta-histine.
D. Visualization and Related Studies

Several studies were performed in order to get a detailed insight into the interac-
tions between vesicles and skin. Most studies focused on penetration characteris-
tics of vesicles or vesicle constituents.
The fate of liposomes after application to the skin was studied by γγ angular
correlation spectroscopy with Indium encapsulated in liquid-state vesicles. The
measurements revealed that the vesicles disintegrate on the surface of the skin
and that only a negligible amount of marker penetrated into the deeper layers of
the SC. These results are in agreement with the results of studies carried out by
Lasch et al. [105]: they found, using fluorescence spectroscopy, that no intact
vesicle penetration occurred. In a more recent study, vesicle-skin interactions
were examined using confocal laser scanning microscopy (CLSM) [106]. A large
number of liposome compositions were examined. These studies revealed that
the liposome constituents were present only in the outermost layers of the SC
and that the constituents acted only as penetration enhancers.
In additional studies [107], the interactions between liposomes and skin
were examined by freeze fracture electron microscopy and Fourier transformed
infrared spectroscopy (FTIR). For this purpose, human SC was treated with lipo-
somes prepared from either NAT 106, NAT 50, or NAT 89. The liposomes pre-
pared from NAT 50 fused on the surface of the skin, whereas vesicles prepared
from NAT 89 penetrated between the upper SC cell layers. In addition, quite
frequently distinct regions with a rough surface were detected, indicating a mix-
ing between the SC lipids and the liposomes or separate domains of phospholip-
ids. Application of vesicles prepared from NAT 106 revealed large changes in
the lipid organization in the SC (see Fig. 8). Almost no intact lipid bilayers were
observed between the corneocytes. The intercellular regions were characterized
by ‘‘flattened isolated regions.’’
It seems that liquid-state liposomes prepared from different lipid mixtures
result in different interactions with the SC. Interestingly, the NAT 106 contained
the largest fraction PC. The strong interaction with the SC might be explained by
the presence of a single-chain lipid, lysophosphatidyl choline, in this formulation,
which may act as an edge activator and consequently may increase the elasticity
of the liposomal bilayers. In a related study [108], in vivo skin hydration was
monitored after occlusive application of either NAT 106 liposomes prepared in
D2O or after application of pure D2O. The skin hydration and penetration were
monitored by FTIR. The liposomes were superior compared to pure D2O in driv-
ing D2O into the skin, and the phospholipid components could be detected in
Figure 8 Nat 106 liposomes had a very strong effect on the microstructure of the stratum
corneum. The corneocytes (C) were swollen considerably and the smooth ultrastructure
of the intercellular lipid lamellae (LL) showed flattened spherical structures, see arrow.
The linear arranged keratin filaments along the cell boundary of the corneocytes are absent.
The scale bar indicates 0.1 µm.
deeper layers in the SC. The presence of phospholipids deep in the SC confirmed
the results observed with freeze fracture electronmicroscopy, in which strong
interactions between phospholipid layers and SC were observed. In a study by
Korting et al. [109], liposomes prepared from soya-lecithin were prepared and
applied on reconstructed epidermis. After application, the skin was visualized on
an ultrastructural level using OsO4 staining and fixation. The investigators ob-
served no intact liposomes in the lower layers of the SC, but disposition of lipids
derived from liposomes between and within the corneocytes. These findings are
in agreement with those of Hofland et al. [105]. Korting et al. did not agree with
the interpretations of Foldvari et al. [110], who claimed that intact liposomes
penetrate into the skin. Vrhonik et al. [111] found that dermal delivery increased
when the substance is applied in vesicles with a bilayer domain structure. In
another study, the interaction between vesicles prepared from cholesterol and
surfactants was investigated [112]. When applied occlusively to human skin, the
vesicles absorbed onto the SC surface and frequently changed the lipid organiza-
tion between the SC superfacial cell layers. Occasionally, changes in the deeper
layers of the SC, such as the presence of vesicular structures, were observed. The
authors asserted that penetration of intact vesicles in the SC would be unlikely to
58 Bouwstra
occur and explained the presence of vesicles as the penetration of vesicle constit-
uents that might be able to re-form vesicle in the SC. Various water pools were
observed in the lipid regions between the corneocytes, indicating that phase sepa-
ration between SC lipids and water occurs. This is in agreement with the studies
of van Hal et al., who claimed that also in the absence of surfactants, water pools
were observed. In a more recent study [113], it was found that the vesicles were
only very occasionally present in the deeper layers of the skin and, therefore, are
not expected to affect the diffusion characteristics of drugs across the skin. In
two recent studies, CLSM was used to study the penetration of fluorescent
labels across the skin in more detail. Schätzlein and Cevc [114,115] intercalated
Rhodamine-DHPE (1,2-dihexadecanoyl-sn-glycero-3-phosphatidylethanolamine-
N-lissamine rhodamine B sulfonyl, triethylammonium salt) in the bilayers of
Transfersomes prepared from soya phosphatidylcholine and sodium cholate. The
suspensions were applied nonocclusively on mice skin, and after 4 to 12 hours,
the skin was examined ex vivo using CLSM. The investigators reported the pres-
ence of transport routes in the SC, the inter-cluster pathway between groups of
cells, which should be a preferred route of transport between corneocytes that
only partly overlap. However, the skin surface is not flat but contains many wrin-
kles. In recent experiments from our own group, we found also ‘‘clefts’’ with a
bright fluorescent appearance. However, in our studies these clefts may corre-
spond to wrinkles in the skin [116]. Intra-cluster pathways were also observed
by Schätzlein and by Cevc [107,108], because regions are observed with high
fluorescence intensity across the lipid bilayer regions. The authors interpret these
regions as being virtual pores between the corneocytes. In all interpretations, one
should realize that CLSM is a technique that cannot be used to visualize the
transport of vesicles as intact entities—it can only be used to visualize the trans-
port of the label, which is not necessarily still associated with the vesicle. In
addition, it was reported that by using in vitro time-resolved infrared ATR (atten-
uated total reflection) spectroscopy, Transfersomes resulted in a faster skin pene-
tration than liposomes. However, whether intact vesicles or liposomal fragments
penetrate is not clear from these experiments either, because in this case only
the lipids are detected and not the structure that is formed by the lipids [117].
Recently, estradiol penetration across human skin after application in Trans-
fersomes was studied in vitro [118]. In this excellent study, the ratio between
the lipids and surfactants was varied systematically in order to vary the elasticity
of the bilayers. A clear correlation was found between the molar ratio of the
bilayer and surfactant-forming lipids and the penetration rate of estradiol across
the skin, suggesting that indeed the Transfersomes increased the transport across
the skin more than the traditional liposomes or micelles.
Very recently the fate of vesicles prepared from single and double chain
surfactants has been studied. These vesicles have elastic bilayers but are entirely
prepared from surfactants. The vesicles that were most intensively studied were
prepared from a sucrose ester surfactant (double chain surfactant), polyoxy-
ethylene laurate ester and cholesterol sulfate. These vesicles were studied after
application onto human skin in vitro nonocclusively [119]. Studies were carried
out using RuO4 fixation in combination with thin sectioning and transmission
electron microscopy (TEM). Furthermore, the penetration pathway of a label in-
tercalated in the bilayers was visualized by two-photon excitation fluorescent
microscopy. The TEM results showed three types of interactions after nonocclu-
sive application of the elastic vesicles on human skin in vitro.
1. The presence of spherical lipid structures containing or surrounded by
electron dense spots, indicative of the presence of vesicle material,
both on the surface of the skin and in between the upper 3–4 cell layers.
2. Oligolamellar vesicles were observed between the 2–3 upper corneo-
cytes.
3. Large areas containing lipids, surfactants, and electron-dense spots
were observed deeper down into the SC.
Furthermore, after treatment with vesicles containing PEG-8-L and a saturated
C12-chain surfactant, small stacks of bilayers were found in the intercellular
spaces of the SC. Treatment with conventional vesicles affected the most apical
corneocytes only to some extent, whereas no lamellar stacks, oligolamellar vesi-
cles, or vesicular material were observed deeper down in the SC.
In addition, none of the vesicle formulations affected the viable epidermis
or dermis. Although not that frequently observed in vitro, in one donor treated
with elastic vesicles a very peculiar phenomenon was observed. Namely, large
areas of lamellar stacks were visualized that differed in appearance from the SC
lipid bilayers and were present throughout the entire stratum corneum. In some
regions, these lamellar stacks disorganized the intercellular skin lipid bilayers
(Fig. 9,a,b) by pushing them apart. The bilayers in these stacks were occasionally
oriented perpendicular to the bilayers of the SC (Fig. 9c) or were accumulated
and oriented randomly (Fig. 9d).
This phenomenon was observed very frequently in SC of hairless mouse
skin [120] when applied in vivo (nonocclusively). In various regions, isolated
areas of stacks had a different appearance than the bilayers observed in SC (see
Fig. 10).
It was speculated that under the influence of the hydration force, elastic
vesicles partition into the stratum corneum, after which (due to the elasticity and
the reduced water content in the stratum corneum) the vesicles might easily flatten
by releasing water from the interior of the vesicles. When these flattened vesicles
fuse together, the bilayer stacks are formed. Because these stacks contain mainly
liquid-state bilayers, the stacks remain phase-separated from the crystalline lipid
60 Bouwstra
Figure 9 TEM micrographs of human skin incubated nonocclusively with PEG-8-L:

L-595 vesicles (70:30) for 16 hours. (a) Overview of stratum corneum with disorganized
intercellular lipids (dicl). Scale bar represents 200 nm. (b) A detailed micrograph of disor-
ganized intercellular lipid bilayers. Bilayers appear to be detached from each other in units
of 3 bilayers (arrowheads). Scale bar represents 100 nm. (c) Frequently, stacks of bilayers
which resemble stacked flattened vesicles were observed with their bilayers oriented per-
pendicular to skin lipid bilayers and cell membranes (arrows); arrowhead ⫽ unit of 3 skin
lipid bilayers. Scale bar represents 100 nm. (d) Detailed micrographs of intercellular spaces
filled with round and oval stacks of bilayers (arrows) oriented at random. Scale bar repre-
sents 100 nm.
Figure 9 Continued
lamellae from the stratum corneum. A schematic overview of how such a lamellar
stack may be assembled is illustrated in Figure 11. Possibly, the vesicles flatten
in the direction in which the water will be removed most easily from the vesicles,
which is most probably water diffusion along the head groups. This speculation
might justify the perpendicular orientation of the lamellar stacks compared to the
skin bilayers. Once the skin lipid bilayers are disrupted, the lamellar stacks are
oriented randomly.
In addition to these extraordinary features, two-photon excitation micros-
copy revealed that the fluorescent label intercalated in the bilayers of conven-
tional vesicles resulted in a homogeneous distribution of the label in the intercel-
lular lipid domains. However, when the same label was intercalated in the bilayers
of the elastic vesicles, an inhomogeneous label distribution was observed (see
Fig. 12). It seems that thread-like channels are formed that serve as penetration
pathways for the dyes. These results certainly demonstrate that elastic vesicles
exert another interaction with the SC than the conventional vesicles. It would be
62 Bouwstra
Figure 10 Transmission electron micrographs of hairless mouse skin treated with

liquid-state PEG-8-L:L-595 :CS (70:30 :5) vesicles, non-occlusively. Detailed micro-
graphs of skin treated for 6 hours. Lamellar stacks are present in the intercellular spaces.
The lamellar stacks are often oriented perpendicular to the lipid bilayers (arrows) and
seem to ‘push’ the lipid bilayers apart. These lamellar stacks were observed after 1, 3 and
6 hours of application. Arrows ⫽ lamellar stack; * ⫽ lipid bilayer; C ⫽ corneocyte. Bar
represents 100 nm.
of great interest to gain more information on the fate of these vesicles in vivo
in humans.
E. Conclusions
Considering all the studies performed, we can generally conclude that drug trans-
port can be adjusted on demand by association of the drug with vesicles. One
of the central parameters is the thermodynamic state of the bilayers, which affects
quite dramatically drug permeation across the SC and, in addition, the interactions
with the SC. It seems that the size and the lamellarity of vesicles affect drug
Figure 11 Schematic presentation of the possible working mechanism of elastic vesicles

in SC.
Figure 12 TPE images of skin treated with PEG-8-L:L-595:CS (70 :30 :5) liquid-state
vesicles. Threadlike channels were formed in the entire stratum corneum after application
with elastic vesicles non-occlusively (a). In contrast, application of rigid vesicles non-
occlusively (b) resulted in a homogenous distribution of the fluorescent dye in the lipid
regions.
transport only slightly. In general, it can be concluded that using ‘‘traditional’’

liposomes, intact vesicle transport across SC does not occur. This is concluded
from visualization and permeation studies as well as from biophysical measure-
ments. Drug transport increases when single-chain surfactants are intercalated in
the vesicles. These single-chain surfactants can act as penetration enhancers, such
as in gel-state vesicles, or might result in a decrease in the interfacial tension and
make the vesicles more deformable. Compared to traditional liquid-state vesicles,
these deformable vesicles, often referred to as Transfersomes, have been shown
to increase drug transport across the skin even further. However, questions arise
about the mechanism involved in this increased drug transport. A first step has been
taken in studies of van den Bergh [119,120]. However, it would be of high interest
to determine the fate of the liposomes in human skin in vivo. Only then can more
clear indications be made about the working mechanisms of these vesicles.
VI. APPENDIX
Using the x-ray diffraction technique, the scattered intensities are measured as
a function of θ/2, the scattering angle (see Fig. 13). The intensity of the scattered
x-rays as a function of θ is directly related to the electron density differences in
the sample. If the electron density differences have a repeating pattern, the dif-
fraction pattern is characterized by a series of peaks (intensity maxima of scat-
tered x-rays) (see Figs. 14 and 15).
Figure 13 A schematic presentation of the x-ray diffraction technique.
Figure 14 The relationship between a lamellar phase periodicity (d) and its diffraction
pattern. In the diffraction curve the intensity is plotted as function of Q. Q is a measure
for the scattering angle. n is the order of the diffraction peak denoted by 1, 2, 3 etc. (long
periodicity) or I and II (short periodicity). An increase in d results in a smaller inter-peak
distance in the diffraction pattern.
Figure 15 The position of the alkyl chains in a liquid, hexagonal, and an orthorhombic
lattice (direction perpendicular to the chains) and the related diffraction pattern.
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3
Computer Modeling of Skin
Barrier Lipid Layers
by Molecular Dynamics
Monika Höltje
Institute of Pharmaceutical Chemistry, Heinrich-Heine University,
I. INTRODUCTION
A molecular modeling investigation of stratum corneum skin lipids is described

in this chapter. For all the readers who are not familiar with the details of compu-
tational chemistry, I want to give a brief introduction to the techniques we have
used.
What is molecular modeling? Molecular modeling is a general term that
covers a wide range of computer graphics and computer programs used to build,
display, manipulate, simulate, and analyze ‘‘realistic’’ molecule structures and
to calculate physicochemical properties of these structures. The main purpose of
molecular modeling is to provide three-dimensional model pictures that fit the
known experimental facts and can be used to rationalize the behavior of the mole-
cules or to help in the design of further experiments.
What is molecular dynamics? Molecular dynamics (MD) is a modeling
technique that can be used to simulate the thermal motion of a structure as a
function of time, using the forces acting on the atoms to drive the motion. The
masses of the atoms are known, so Newton’s second law of motion may be used
to compute the accelerations and thus the velocities of the atoms. The accelera-
tions and velocities can be used to calculate new positions for the atoms over a
short time (normally 1–2 femtoseconds), thus moving each atom to a new posi-
tion in space. This process can be done many thousands of times, generating a
75
76 Höltje
series of conformations of the structure. The velocities of the atoms are related
directly to the temperature at which the simulation is performed. A simulation
run at 310 K provides information on the structural fluctuations that occur around
the starting conformation at body temperature, perhaps to illustrate which parts
of a molecule are most flexible or to examine the number of conformational
transitions [more detailed introductions to the principles and applications of mo-
lecular modeling and molecular dynamics can be found in Refs. 1 through 4].
MD simulations can provide a detailed atomic-level understanding of the
structural and dynamic aspects of the investigated molecular assemblies. They
have been used very successfully during the past years to study phospholipid
membrane systems in molecular detail [for reviews on this field, see Refs. 5–7].
We wanted to benefit from these studies, trying to transfer the approved methods
to stratum corneum (SC) lipid model systems. The goal of our present study was
to receive a molecular picture of SC lipid structures that may assist the interpreta-
tion of experimental results.
In order to understand the complex nature of the SC lipid lamellae as well
as the relationship between lipid composition and functionality, there have been
many experimental investigations using small- and wide-angle x-ray diffraction,
electron microscopy, infrared spectroscopy (IR), and nuclear magnetic resonance
techniques (NMR). The results of these techniques, however, although used very
successfully to provide detailed atomic insights into protein structures, are often
difficult to interpret in the case of lipid layers. This is because of the heterogeneity
and semifluid character of lipid layers under physiological conditions. Usually,
lipid bilayers have two distinct phases in the physiological temperature range.
The lower-temperature phase is a highly ordered gel state in which the hydrocar-
bon chains are extended and closely packed, with little mobility. The higher-
temperature phase is the more disordered liquid crystalline phase. In addition,
skin lipids can arrange in hexagonal phases, even at physiological temperatures.
Thus, SC lipids are characterized by manifold chain-melting transitions at differ-
ent temperatures, and complex polymorphism seems to be common [8]. The pref-
erence of a lipid for a given phase is governed by the interaction forces that are
the combined results of volume, polarity, headgroup interactions, and van der
Waals attractions between the hydrocarbon chains under a certain condition of
concentration, temperature, pressure, water content, and pH. These interaction
forces appear to be a determinant of the aggregation form of the lipids. Among
the well-known macroscopic properties of a lipid system are analytical values
that are difficult to obtain by experiment. MD simulations offer an approach to
a detailed description of the packing parameters and other structural properties
of lipid assemblies.
Skin lipids are complex systems, composed of very diverse molecular struc-
tures. MD simulations are complicated too; a certain number of issues need to
Modeling of Skin Barrier Lipid Layers by MD 77
be resolved before a reasonable simulation can be performed. Thus, one has to

decide what is the appropriate choice of input (size of the system, number of
molecules, starting conformation, solvent type) and what is the appropriate choice
of technical parameters (time, force field, electrostatics, pressure, temperature,
etc.). Moreover, MD has a number of limitations. The treatment of the interaction
forces is a very simplified form compared to the ‘‘real’’ function. Another limita-
tion is the time and size problem. Current computational power allows simula-
tions of system sizes of roughly 5–10 nm on a time scale up to a few nanoseconds
(ns). Processes such as phase transitions at body temperature or phase separations
in lipid mixtures are out of reach in normal MD simulations.
To not get lost among all the various skin data and MD parameters, exten-
sive testing of the parameter sets on simple model systems, which can be com-
pared to experimental data, is necessary. We decided to build our skin lipid model
step by step and have chosen simple models as starting points. These simplified
skin barrier models have been used successfully in numerous experiments testing
skin permeability, toxicity, and barrier-perturbing effects of drugs and cosmetic
formulations [9].
Skin lipid compositions vary significantly, depending on sample origin and
sample preparation. It appeared to us that an equimolar mixture of fatty acids,
cholesterol, and ceramides might be a reasonable model. The fatty acids chosen
are palmitic acid and stearic acid. This choice is based on similar skin lipid mod-
els widely utilized in experiments, which we wanted to use for the experimental
validation of our simulation results [10]. A certain amount of the fatty acid chains
in stratum corneum is certainly longer than in our model. Long-chain saturated
fatty acids ought to form more or less rigid crystalline domains in SC at body
temperature, thus being not so interesting from a ‘‘molecular dynamic’’ point of
view. They may therefore be excluded from our models at this stage.
Our study consists of three parts. First, the simulation behavior of palmitic
and stearic acid is tested; this is followed by a study on the influence of cholesterol
on the fatty acids; and finally, the effect of ceramides is investigated. We started
our calculations with a fully hydrated free fatty acid bilayer (model A). In the
next step, this model was enlarged by adding an appropriate amount of cholesterol
(model B). In a further step, the components of model B were mixed with cera-
mide 2 (model C).
Model A was chosen to prove the simulation setup and to investigate the
dynamic behavior of free fatty acids. Subsequently, we compared the simulations
of model B and model C to determine the influence of cholesterol and ceramide
2 on a number of bilayer properties: conformational and orientational order pa-
rameters, areas per headgroup, and atom densities.
Simulation analysis data were compared to experimental data taken from
literature and to data of thermal analysis and FTIR experiments, which were
78 Höltje
performed by Förster et al. [11]. We would like to point out that the aim of our
investigations is an overall qualitative description of the model systems—not a
detailed quantitative evaluation. The reason for this is the lack of accurate experi-
mental data on analogous lipid mixtures on which our simulation results could
be fitted. We have focused mainly on hydrocarbon chain dynamics, with details
of headgroup and water interactions being omitted in the present study.
II. METHODS
A. Initial Structures
Starting from the crystal coordinates of stearic acid [12], we used the space group
operations and the lattice transformations of the stearic acid crystal to generate
a monolayer of 141 fatty acid molecules. The molecules in the x-ray crystal
structure are tilted and exhibit strong hydrogen bonds among the headgroups.
We adjusted the coordinates so that all hydrocarbon chains were perpendicular
to the layer plane and the crystal headgroup packing was disrupted in order to
save computational time. Two monolayers were used to construct a bilayer con-
sisting of 282 lipid molecules; 136 randomly chosen stearic acids (68 in each
monolayer) were changed to palmitic acids by removing the last two carbon
atoms in the chain. The fatty acid bilayer (model A) was transformed into model
B by exchanging 112 (⫽ about 50 weight %) of the free fatty acids randomly
for cholesterol.
Model C was composed of 132 palmitic acid molecules, 85 cholesterol
molecules, and 44 ceramide 2 molecules. In this model, only palmitic acid was
used, because model A and model B simulations indicated nearly no difference
in the overall behavior of stearic and palmitic acid.
In human skin, a pH gradient is found, reaching from pH 7 in the innermost
SC layers to a pH of about 5 on the SC surface. Thus, moving outwards, across
the SC, the degree of ionization will drop from 90% to less than 10% at pH 5
[13]. Because we are interested in the SC surface, we have used neutral fatty
acids and no corresponding soaps in the present study.
The models were put in rectangular boxes, with the z plane defining the
direction of the bilayer normal. The boxes were then enlarged on both tops to
receive water caps. The water content of SC is reported to be about 10 weight
% [14]. Simulations with a number of water molecules according to this value
gave unstable runs, because the very small hydration level of about 2.5 water
molecules per lipid led to insufficient solvation of the headgroups in the boundary
region. Thus we increased the water content to 26 weight % in model A (1515
H2O molecules) and model B (1770 H2O molecules). Model C received 2163
H2O molecules (29%) because the ceramides needed more water molecules per
headgroup. The chemical formulas of the lipid compounds are shown in Figure 1.
Figure 1 The chemical structures of the molecules used in the simulations.
Figure 2 is a schematic diagram of one bilayer surface of model B, illustrat-

ing the positions of the cholesterol molecules among the fatty acids. It should
be pointed out that our choice of a random cholesterol distribution among the
lipids is only one of several possibilities. Chong et al. [15] have suggested a
maximum separation of steroid molecules in phosphatidylcholine bilayers.
Smondyrev et al. [16] have compared regular cholesterol arrays and cholesterol-
rich stripes in their MD studies on diphosphatidylcholine/cholesterol mixtures
and found differences in equilibration time and stability of the bilayer models.
However, we do not have any experimental data concerning an ideal distribution
of cholesterol molecules in skin lipid models. So we took a random initial distri-
bution because we did not want to introduce an artificial order that would obey
particular rules, thus making the results more complex. For the construction of
model C, ceramide 2 was taken as a representative of the ceramides family and
again a random distribution was applied.
80 Höltje
Figure 2 Schematic diagram of the surface of model B showing the placing of choles-
terol among the fatty acids: # cholesterol, ■ palmitic acid, ★ stearic acid.
B. Simulation Conditions
The initial molecular geometry of the lipid layers together with the water caps
was first optimized with a conjugate gradient method to reduce any unfavorable
steric interactions among the molecules. All simulations were performed under
NPT conditions, which means that the number of particles N, the pressure P, and
the temperature T were kept fixed, allowing the volume to find its size according
to system behavior.
Periodic boundary conditions were applied in all three dimensions. Periodic
boundary is a term used to describe a method for dealing with the surface condi-
tions in molecular dynamics simulations. Computer simulations can track only
a very small number of particles (compared to experimentally used samples). As
a result, most of the molecules are near the edge of the sample—that is, near its
surface and the surrounding vacuum. The system size would have to be extremely
large to ensure that the surface has only a small influence on the bulk properties,
but such a system would be too large to simulate. To avoid artificial surface
effects (e.g., to prevent molecules from migrating in the vacuum) one can use a
maneuver, the periodic boundary conditions. In periodic boundary conditions,
the simulation box is replicated throughout space to form an infinite lattice. By
mirroring the contents of the central box, a periodic system is generated. When
a molecule diffuses out of one side of the box, it reenters on the other. Thus, a
constant density (number of particles N) can be maintained. Further details on
the force field and the MD parameters have been published elsewhere [11].
It is well known that membrane simulations starting with lipids in the well-
ordered and closely packed crystal lattice can require very long equilibration
times and resemblance to the primary ordering can still be seen in the final struc-
tures even with simulations up to several hundred of picoseconds (ps) at physio-
logical temperatures, a finding that agrees well with our own simulation experi-
ence. Thus, we have used a simulated annealing procedure to disrupt the crystal
packing of model A during a high temperature phase followed by a cooling down
to skin temperature, thus allowing the system to adjust its volume and shape and
to find its adequate size.
First, a 200 ps MD run was performed at 350 K, a temperature that is
above the melting temperature of palmitic acid (63°C ⫽ 336 K) and stearic acid
(69.6°C ⫽ 343 K). Then, the temperature was gradually lowered to 303 K. After
this temperature was reached, simulations were carried out at constant tempera-
ture for several nanoseconds.
The initial structure of model B was constructed from an ensemble taken
from the simulation of model A at 350 K. Model C was generated from the
starting structure of model B by inserting ceramide 2 molecules into the lipid
layers. Molecule building was performed with the aid of the program SYBYL6.4
[Tripos Inc., St. Louis, USA]. All simulations were done with GROMACS [17]
on a SGI indigo2 or a SGI Origin 2000 computer [Silicon Graphics, Mountain
View, CA, USA].
III. RESULTS AND DISCUSSION OF THE

MOLECULAR SIMULATION
A. Model A
We started our model A simulations from lipids in a solid crystalline phase with
the alkyl chains in the all-trans conformation and with a close alignment to each
other. When the system was heated to a temperature of 350 K, the highly ordered
crystal arrangement started to melt. The occurrence of gauche conformations cre-
ated kinks in the alkyl chains, which reduced the interaction between the chains.
The lipid packing became considerably looser because chain-chain interactions
got lost, due to the presence of gauche isomerizations. This evolution can be seen
very clearly from Figure 3a, which shows the development of the average alkyl
chain trans fraction during the heating/cooling cycle. Figure 3b shows the aver-
age surface area occupied by one fatty acid within the simulation box as a function
of time (calculated by dividing the xy surface area of the simulation box by the
number of lipid molecules in one layer). The number of trans bonds decreased
from 100% to 80% during heating to the high temperature of 350 K. Connected
with the conformational motions, the area per lipid increased from 20 Å2 to 24 Å2.
82 Höltje
Figure 3 Diagrams showing the time developments of (a) the fraction of trans bonds
in the hydrocarbon chains of the fatty acids and (b) the surface area per molecule during
the melting and recrystallization simulation of model A.
When the system was cooled down to skin temperature (303 K), the lipids
started to rearrange themselves in an ordered crystalline ensemble (Fig. 3a, b).
The area per lipid moved continuously to smaller values and the trans fraction
increased again. This process had not finished after 2600 ps, but because the
tendency could be seen clearly, we stopped the simulation at the point where the
trans fraction achieved 0.95 again and the area per lipid obtained a value of
22 Å2. The structural changes of model A during the simulation procedure can
be seen nicely from Figure 4, which shows a cross-section through the bilayer
from three different simulation steps (0 ps, 200 ps, and 2.6 ns) and an assembly
of stearic acids obtained from x-ray crystallographic coordinates [12].
Figure 4 Snapshots of the fatty acid bilayer after melting and recrystallization. (a) The
initial conformation of model A, composed of 136 palmitic acid molecules and 146 stearic
acid molecules. (b) Resulting molecular assembly at 350 K (liquid crystalline state).
(c) Final structure of model A at 303 K (gel state). (d) Molecular diagram of a unit cell
of stearic acid as derived from crystal analyses [12]. Note the similar collective tilts of
the fatty acid chains observed in the simulation and in the crystal structure. Hydrogen
atoms and water molecules are omitted for clarity. Polar heads are plotted as balls.
84 Höltje
Starting from fully extended solid crystalline hydrocarbon chains, which

were arranged perpendicular (Fig. 4a), the bilayer reached an unordered, liquid
crystalline–like phase during the high-temperature time steps (Fig. 4b). Cooling
down resulted in ordered chains again, which exhibit now a strong tilt in the
bilayer plane (Fig. 4c), a formation that looks similar to the Lβ′ gel phase in which
the polar headgroups are disordered but the mostly all-trans chains are packed
regularly in a tilted manner [18]. This tilt is also observed in solid crystals, as
can be seen from Figure 4d.
The behavior of the fatty acids in model A is in good agreement with experi-
mental data. Neubert et al. [19] have carried out FT-Raman analyses on the melt-
ing of stearic acid. They found that in a double-layered subcell the highly ordered
all-trans structure of the alkyl chains was present up to about 5°C below the
melting point. Between 65°C and the melting point, gauche bonds appeared
among trans sequences. On melting, the lamellae arrangement disappeared and
the resulting structure was a random mixture of gauche and trans bonds. Bearing
these results in mind, we interpret our simulation data as follows: within the
200 ps run at 350 K the lipids reached the premelting phase, the area per lipid
and the number of gauche bonds increased by 20%. Cooling down the tempera-
ture after 200 ps to skin conditions stopped the melting. The lipids slowly went
back to a high-order arrangement and reached a gel phase after 2.6 ns.
B. Model B
The starting configuration of model B was derived from premelting fatty acids
in which the cholesterol molecules were inserted, so no high-temperature run
was necessary. The total simulation was performed at 303 K for 2 ns. The re-
sulting molecular structure of model B is presented in Figure 5. It is seen that
the hydrocarbon chains stayed remarkably disordered. A large number of the
chains have a substantial gradient away from the bilayer normal, but in contrast
to the final structure of model A, no collective tilt can be found.
Figure 6a shows the corresponding trans fraction of the fatty acid alkyl
chains. From the start, the trans fraction oscillates around 0.8 and converges to
a value of 0.81 for the last 500 ps. No upward tendency can be seen, a result
that is quite in contrast to model A. Thus, the data suggest that when the fatty
acids are mixed with cholesterol in the premelted state, they reach a stable confor-
mational state immediately during the simulation time. To characterize that state,
we want to compare our trans fraction values with data from investigations on
dipalmitoylphosphatidylcholine (DPPC), one of the most studied lipids. Experi-
mental results for the liquid crystalline Lα phase of DPPC demonstrate trans
fractions of 0.76–0.6, depending on the method used [20–22]. For the Lβ′ gel
phase, a trans fraction of above 0.9 has been derived from Raman measurements
as well as from MD simulations [22,23]. The trans fraction in our model B simu-
Figure 5 Model B at the end of the MD simulation. The full system, which consists
of 87 stearic acids, 76 palmitic acids, 112 cholesterols, and 1770 water molecules, is shown
on the left side. Cholesterol molecules have been removed in the right plot to demonstrate
the conformations of the fatty acids. Water molecules are displayed as balls.
lation lies between the values of a gel and a liquid crystalline phase. The well-
ordered gel phase arrangement of the pure fatty acids is shifted to less rigid
conformations when cholesterol is added. Thus, cholesterol influences the fluidity
of the fatty acid chains. This fluidizing effect of cholesterol, which can be recog-
nized from our data, is experimentally well known [13,24]. But we should note
that the chains are not fully liquid crystalline, because the resulting trans fraction
of 0.8 is too high to indicate a complete Lα phase. Experimental investigations
show similar results. Several authors find in SC lipids at skin temperature ortho-
rhombic phases with alkyl chains in the predominantly all-trans conformation
when no cholesterol is present and hexagonal phases as well as gauche alkyl
conformations when cholesterol is added [8,13,25]. Förster and coworkers re-
ceived from FTIR and DSC analysis data that fit well to the simulation results.
The addition of cholesterol to an appropriate fatty acid mixture led to a slight
increase in conformational disorder, seen by a small positive shift of the CH2-
stretching frequency from 2848.0 cm⫺1 to 2848.3 cm⫺1 in the FTIR spectrum and
to a reduction in the melting enthalpy, which could be seen from thermal analysis
[11].
Now we turn to the surface area per molecule in model B. The time evolu-
tion of this parameter converged very rapidly, as can be seen from Figure 6b.
During the first simulation steps, the surface area was decreasing because the
placement of the cholesterol molecules among the fatty acids led to a somewhat
loose starting arrangement. After approximately 50 ps, the surface area had
dropped to a value of about 29 Å2 per molecule and stayed stable for the re-
maining run. We have analyzed the volume requirements of the cholesterol mole-
86 Höltje
Figure 6 (a) Time evolution of the fraction of trans bonds in the hydrocarbon chains
and (b) time evolution of the surface area per molecule during the simulation of model
B at 303 K.
cules in our simulations. The average surface area for a cholesterol molecule
has been determined experimentally by different authors and ranges from 26 to
39 Å2 [15,26–29]. Recently performed studies on MD simulations of mixtures
of phosphatidylcholine with cholesterol obtained values of 32.4 Å2, 38 Å2, and
39 Å2 [16,23,30,31].
In model A we have obtained an area per fatty acid molecule of approxi-
mately 24 Å2 when the trans fraction has reached 80%. Assuming that the area
per fatty acid has not changed in model B, because the trans fraction is likewise
80%, we get an estimate for the area per cholesterol molecule by subtracting
from the total area per monolayer the total average area occupied by the fatty acid
molecules (141 ⫻ 24) and dividing the difference by the number of cholesterol
molecules per monolayer. In this manner, we calculate an average surface area
of 35 Å2 for one cholesterol molecule in model B. This value is 4 Å2 smaller
than the value obtained by Hyslop et al. [28] in a pure cholesterol monolayer
and 2.5 Å2 larger than the values used by Tu et al. [23] and by Smondyrev et
al. [16] in their simulations on DPPC/cholesterol mixtures.
Molecular dynamics calculations on a pure cholesterol bilayer, which we
have performed, resulted in an area per cholesterol of 36 Å2. We interpret the
divergence in the overall data as follows: In pure cholesterol ensembles, the rigid
molecules exhibit highly hindered motions, which do not allow very close con-
tacts. When single cholesterol molecules are surrounded by flexible and pliant
hydrocarbon chains, a much closer arrangement is possible, reducing the surface
area to smaller values (e.g., down to 32 Å2, depending on the concentration).
Thus, a value of approximately 35 Å2 for our model B cholesterols seems to
be reasonable, because not all molecules are isolated and cholesterol-cholesterol
contacts are found in the assembly (see Fig. 2).
C. Deuterium Order Parameters

Order parameters characterize the orientational order of the hydrocarbon chains
and can be measured using the NMR technique. In molecular dynamics simula-
tions, the deuterium order parameter (SCD) can be calculated for each carbon in
a chain, using the following expression [32]:
SCD ⫽ (2/3 cos 2 Θ ⫺ 1/2), (1)
where Θ is the angle between the ith molecular axis and the bilayer normal (z
axis).
Calculated SCD values can vary between ⫺0.5 (full order along the bilayer
normal) and zero (in the case of full disorientation). Figure 7 shows a comparison
of the calculated SCD values of the palmitic acids in models A and B. The curves
are plotted as a function of the carbon position along the chain (the carbon atom
next to the carbonyl group is denoted as number 1; the terminal methyl group
is not calculated).
Let us first examine the order parameter profile of model A at the end of
the 303 K run. The high order within the alkyl chains, which occurred when the
temperature was reduced to skin values, can be clearly seen from the profile.
All carbon atoms exhibit very similar order parameters. In spite of the strong
conformational order within the chains, the average SCD value is relatively small
88 Höltje
Figure 7 Calculated deuterium order parameters SCD of the palmitic acid chains in model
A and model B at 303 K, averaged over the last 100 ps. Values are plotted as a function
of carbon atom position along the chain. Carbon number 1 corresponds to the first atom
of the hydrocarbon tail; the terminal carbon has not been calculated.
(⫺0.25). This reflects the fact that the hydrocarbon chains are now tilted and
their overall orientation is no longer parallel to the bilayer normal.
Experimental studies available for comparable fatty acids offer average SCD
values of soaps, ranging from ⫺0.19 to ⫺0.14 at room temperature [33]. Soaps,
due to their strong headgroup repulsion, need larger areas per lipid than neutral
fatty acids. This strongly influences the conformational behavior of the hydrocar-
bons (as can be seen from the low values). Therefore, we cannot compare our
calculated order parameters of model A directly with experimental order profiles.
The second profile in Figure 7 demonstrates the effect of cholesterol on
the order of the fatty acid alkyl chains. As can be seen, the influence is not
uniform along the chain. There is little effect on the order parameters of the first
two carbon atoms; these values are only slightly higher in model B than in model
A. Subsequently, the profile shows a strong rise with a small plateau region ex-
tending over carbon atoms 3–6, after which the values drop significantly toward
the end of the chain. It is apparent from the data that cholesterol induces a pro-
nounced decrease in conformational order at the tail end of the lipids, thus produc-
ing an order profile with a general feature as observed for lipid bilayers in the
liquid crystalline phase: a plateau region near the carbonyls, followed by a de-
crease in order to near zero at the terminal methyl groups. The average SCD values
do not differ so much (⫺0.25 for model A and ⫺0.26 for model B), whereas the
appearances of the profiles are strongly different. The experimentally known ef-
fect of cholesterol to disorder lipid chains in gel phase bilayers can be clearly
Figure 8 Example of a typical cholesterol–fatty acid ensemble. Cholesterol is drawn

in black; the hydrocarbon chains of palmitic acid (left) and stearic acid (right) are plotted
in gray.
seen from the order parameters. Adding 50 weight % cholesterol to the fatty acids
generates a phase that resembles the order of liquid crystalline lipids, although no
transition to a liquid crystalline phase has occurred, as already mentioned.
For a closer look at the influence of cholesterol on the alkyl chain order,
we present a representative set of molecules extracted from our model B simula-
tions (Fig. 8). It is clear from the picture why cholesterol has that profound effect
on the conformation of the alkyl chains at the tail end. For lipids neighboring
cholesterol, the upper half of the chains is in contact with the rigid steroid ring,
which reduces the conformational freedom, whereas the lower part is mainly in
contact with the skinnier and more flexible cholesterol tail, which allows kinks
in that part of the chains.
D. Model C
The introduction of ceramide into our model raised questions concerning its inte-
gration into the other lipids. The major reason for this is the difference in chain
length between ceramide 2 and the fatty acids and/or cholesterol and the differ-
ence in chain length within the ceramide itself. To date, the detailed organization
of the lipid classes that make up the matrix of the SC has not been elucidated.
A model for the molecular arrangement of ceramides among fatty acids and cho-
lesterol has been proposed recently by Bouwstra et al. [34]. From this model,
90 Höltje
we adopted the idea of an interdigitation of two opposite ceramides (see Fig. 11).
Thus, 22 interdigitated ceramide couples were randomly distributed in the bilayer.
A dynamics run of 3.8 ns was executed under conditions identical to those of
the model B simulation. A snapshot from the end of the simulation of model C
is shown in Figure 9.
On a first view, the bilayer formation of model C seems not so different
from model B. However, one can see from the picture that the tails of the cera-
mide chains occupy space in the bilayer center and that they are fairly disordered.
The time evolution of the trans fraction of the ceramides and the fatty acids
is shown in Figure 10. In the case of the palmitic acids, the trans fraction rises
from the initial value of about 0.8 to a value of about 0.89, whereas the value
for the ceramides settled into oscillations around 0.80 during the simulation. The
palmitic acid chains exhibit a higher conformational order compared with the
chains of the ceramides.
A closer look at the conformational changes that happened to the ceramide
molecules is given in Figure 11. We show two examples of ceramide pairs in
Figure 9 Model C at the end of the simulation at 303 K. The bilayer consists of 132
palmitic acids, 85 cholesterols, 44 ceramide-2 molecules, and 2163 water molecules. Wa-
ter is displayed as balls; palmitic acids and cholesterol molecules are drawn in gray; cera-
mides are shown in black.
Figure 10 Time development of the fraction of trans bonds in the hydrocarbon chains
of palmitic acid and ceramide-2 during the simulation of model C at 303 K.
Figure 11 Snapshots of ceramide molecules from the simulation. A and B, left part:
Interdigitated starting structures of two opposite ceramides. A and B, right part: Conforma-
tional arrangement at the end of the simulation. Note that the molecules in (A) stayed in
an interdigitated position, whereas in (B) they have separated.
92 Höltje
the interdigitated starting structure and their conformational arrangement at the

end of the simulation. Some of the ceramides stayed in the interlocked position
(example A), whereas in other couples the chains have turned away from each
other (example B). Nearly all ceramides in the assembly present well-ordered
upper chains and kinks in the end parts. The higher value for the palmitic acid
trans fraction may be accounted for by neighboring ceramide chain parts in trans
conformations.
The behavior of the ceramide molecules is somewhat in contrast to experi-
mental data, which propose highly ordered all-trans ceramide conformations at
body temperature [35,36]. We interpret the results as follows: In our model, the
distribution of more or less isolated ceramide pairs among the other lipids forces
the ceramides to resize to the shorter molecules in the neighborhood. If the cera-
mide chain length would be better compatible with that of the surrounding, one
might speculate that the molecules would stay much more conformationally or-
dered. Such a view is compatible with the proposal of separated crystalline cera-
mide domains in the SC matrix [37]. Recently, Forslind has proposed the domain
mosaic model of lipid organization: ceramides aggregate into the crystalline
phase, providing large areas that constitute the watertight barrier [38]. However,
at the border of these crystalline areas, lipids in a liquid crystalline phase can be
found. These ‘‘grain borders’’ allow water to pass through the barrier.
The systems studied here are different from experimentally used SC mix-
tures in that only very small ‘‘pieces’’ with no particular domains could be inves-
tigated. However, it seems that the mixture in our model C offers a picture of a
border situation, where long-chain ceramides meet short-chain molecules, with
the consequence that the ceramides become partly disordered and adopt a more
fluid phase.
Further support that our model C mimics well essential features of a ‘‘real’’
system comes from 2H NMR data. Fenske et al. [39] performed a study on SC
lipid models consisting of equimolar mixtures of bovine-brain ceramides, choles-
terol, and palmitic acid. From the spectra, they obtained a SCD profile for the
palmitic acids, which we have compared with the calculated order parameters of
our simulation. As can be seen from Figure 12, the comparison results in good
agreement between the two profiles. The experimental data show somewhat lower
SCD values in the plateau region (carbon 3–8), which may be due to the higher
temperature used in the measurement (the spectra were acquired at 50°C).
To establish the locations of the different molecule types in the bilayer, we
show in Figure 13 the atom densities (along the z axis of the simulation box) of
the oxygens of the ceramide OH-groups, together with those from the palmitic
acids and the cholesterols. It is clear from the figure that the cholesterols and the
palmitic acids are more likely to have their oxygens mainly below the ceramide
OH-groups. Thus, they prefer to sit deeper in the bilayer and allow the more
polar headgroups of the ceramides to reach for the water layer. Similar observa-
Figure 12 Calculated deuterium order parameters SCD of the palmitic acid chains of the
model C simulation in comparison to experimentally derived values. (From Ref. 39.)
tions have been reported for bilayers composed of phospholipids and cholesterol
[24]. A detailed analysis of the interactions among the headgroups of the lipids
and the water molecules at the interfacial region of the bilayer will be published
elsewhere [40].
Figure 13 Oxygen atom density profiles for the OH-groups of model C lipids along
the bilayer normal (Z-coordinate of the simulation box), averaged over the last 100 ps.
94 Höltje
Finally, we compared our model C simulation to available lamellar spacing

data recently published. Bouwstra and coworkers identified a short periodicity
phase in mixtures of ceramides (all had the same chain length as ceramide 2)
and cholesterol. They calculated from the electron density profiles a distance
between the two headgroup regions of about 4.75 nm [34]. This value is in good
agreement with our bilayer thickness: the average distance between the head-
groups in model C is 4.65 nm.
IV. CONCLUSIONS
We have carried out molecular dynamics simulations of three different simple

stratum corneum lipid models: a pure fatty acid bilayer (stearic acid, palmitic
acid), a fatty acid/cholesterol mixture at a 1 :1 ratio, and a palmitic acid/
cholesterol/ceramide 2 (1 :1 : 1) mixture. Biophysical aspects of the model struc-
tures have been investigated and compared with experimental results. At the
atomic level the behavior of the different compounds showed the following pic-
ture:
1. Pure free fatty acid layers can adopt a well ordered Lβ′ gel phase at
skin temperature.
2. Cholesterol fluidizes the rigid gel phases by decreasing the conforma-
tional order of the adjacent hydrocarbon tails.
3. Ceramides consolidate the lipid assembly and seem to play an impor-
tant role in the coherence of the bilayer because the tails of their long
hydrocarbon chains occupy the inner space between both monolayers.
The computed properties, such as trans fractions, order parameters, or bilayer

thickness, show reasonable agreement with experimental data. As can be seen
from the simulations, computer modeling methods can offer useful information
for validating or refining the interpretation of experimental data because they
provide a very detailed picture of molecular interactions.
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40. Manuscript in preparation
4
Role of Lipids in Skin
Barrier Function
Mitsuhiro Denda
Shiseido Life Science Research Center, Yokohama, Japan
I. INTRODUCTION
For terrestrial animals, the skin’s most important role is to protect the water-rich
internal organs from the dry environment. This cutaneous barrier function resides
in the stratum corneum. The water impermeability of this thin (10–20 µm) layer
is 1000 times higher than that of other membranes of living organisms [1]. This
is the same level as that of a plastic membrane with the same thickness [2]. The
stratum corneum is composed of two components: protein-rich nonviable cells
and intercellular lipid domains (Fig. 1). The lipid molecules in the intercellular
domain form a bilayer structure. Because of this specific ‘‘brick and mortar’’
structure, the stratum corneum shows high water impermeability [1,3].
When the barrier function is damaged by tape stripping or treatment with
an organic solvent or detergent, a series of homeostatic processes in the barrier
function is immediately accelerated, and the barrier recovers to its original level
[3]. This homeostatic repair process is blocked by occlusion with a water-
impermeable membrane such as plastic membrane or latex membrane [4]. The
occlusion with a water-permeable membrane such as Gortex does not perturb the
repair process [4]. The skin barrier function also has an ability to adapt to the
environment. Under a low-humidity environment, the barrier function is en-
hanced [5]. The thickness of the stratum corneum increases in a dry environment.
The content of the intercellular lipid in the stratum corneum increases and, conse-
quently, the transepidermal water loss decreases—i.e., the water impermeability
increases [5]. These results suggest that the skin barrier function senses the envi-
ronmental change and reorganizes its function to adapt to the new environment
97
98 Denda
Figure 1 Human skin section stained with fluorescent probe Nile Red. Intense white
membrane structure (neutral lipid: arrow) is seen in the uppermost layer of the epidermal
granular layer.
(Table 1). Thus, skin barrier homeostasis is a self-referential and self-organizing

system.
On the other hand, the skin barrier homeostatic system is under the influ-
ence of the central nervous system. Psychological stress delays barrier recovery,
and sedative drugs can prevent the delay [6,7]. Glucocorticoid in the serum medi-
ates the relationship between the stress and skin barrier homeostasis [7]. Odorants
that have sedative effects also improve barrier homeostasis [8]. Various environ-
mental factors that affect our emotions could influence the barrier function. More-
over, the barrier recovery rate shows a circadian rhythm [9]. The physiological
stage of the whole body is related to the barrier homeostasis (Table 1).
Table 1 Environmental and Physiological Factors That Affect Skin

Barrier Homeostasis
Environmental Barrier Physiological Barrier
factors recovery (ref.) factors recovery (ref.)
Low temperature Delayed (95) Aging Delayed (69)
Low humidity Accelerated (5) Circadian rhythm Altered (9)
High humidity Delayed (5) Increase of serum Delayed (7)
Psychological stress Delayed (6,7) glucocorticoid
Role of Lipids in Skin Barrier Function 99
In a healthy state, the stratum corneum barrier function is able to recover

from damage. After acute disruption of the stratum corneum barrier function by
tape stripping or acetone treatment, epidermal DNA synthesis [10] or mRNA
level of inflammatory cytokines [11] such as interleukin-1 (IL-1) or tumor necro-
sis factor (TNF), increase and then recover to the original level. However, even
when the level of damage is relatively small, it may have a significant influence
on the whole skin if it is repeated [12] or if it occurs in a dry environment [13].
Thus, improvement of the skin barrier is important not only for skin surface
condition but also for whole skin pathology.
Lipids in the stratum corneum play a crucial role in the barrier function.
The water impermeability and the water repellency of the lipids can protect our
bodies from environmental dryness and the invasion of harmful environmental
factors. Moreover, studies in the past few decades showed a biological activity
of the lipid molecules in skin barrier homeostasis. This chapter mainly focuses
on this water impermeable barrier function and the role of lipids in barrier homeo-
stasis.
II. DEFINITION OF LIPIDS IN THE STRATUM CORNEUM
The lipids in the stratum corneum have two origins: one is the keratinocytes in
the epidermis during its differentiation and another is the sebaceous gland. The
epidermis is in a constant state of self-replacement. At the bottom layer, keratino-
cyte stem cells divide into daughter cells, which are displaced outward and which
differentiate through successive overlying layers to enter the stratum corneum
(Fig. 2). Then, the keratinocytes die, and their cellular organelles and cytoplasm
disappear during the final process of differentiation. Intercellular lipids are pri-
marily generated from exocytosis of lipid-containing granules called lamellar
bodies, during the terminal differentiation. The secreted lipids spread over the
intercellular domains and form a bilayer structure [14] (Fig. 3).
Sebaceous glands are usually associated with hair follicles and are holo-
crine in structure [15]. Sebum is formed when the lipid-rich cells die and disinte-
grate. Sebaceous glands open onto the skin surface. They are surrounded by con-
nective tissue; on the peripheral basement membrane, there are germinative cells.
The lipid-producing cells differentiate, form lipid globules in the cytosol, and at
the final stage of differentiation, the nucleus disappears. Then the cellular struc-
tures are degraded, and the lipid is secreted through the sebaceous duct to the
skin surface. In human skin, the sebaceous glands are concentrated in the face,
forehead, and scalp and are absent on the palms and soles [15].
Thus, on the surface of human and other mammalian skin, there is a mixture
of lipids that have different origins (see also Chapter 1). Sheu et al. [16] described
in detail the structure of human skin surface lipids, an amorphous sheet of variable
100 Denda
Figure 2 A: Electron micrograph of the intercellular lipid bilayer structure (arrows) in

the human stratum corneum. B: Secreted lipids are stacked between the stratum corneum
and the stratum granulosum. C: Lamellar bodies (arrowhead) and exyocytosis of lamellar
bodies (arrow) in the human stratum granulosum.
thickness on the skin surface. The thickness was especially great on sebum-rich
regions such as face areas. Even between the desquamating corneocytes in the
uppermost several layers, a deranged lipid structure was found. On the other
hand, the investigators reported intercellular lipid lamellar and lipid envelope in
the desquamating cells. These findings suggested that the sebum from the seba-
ceous glands spread over the skin surface was mixed with lipids derived from
epidermal lamellar bodies and formed a film on the surface of skin. The physico-
chemical studies of the lipid film might be important for further understanding
of the protective function of the stratum corneum.
Figure 3 Process of the epidermal lipid synthesis and formation of the intercellular lipid
bilayer structure. The intercellular lipids are primarily generated from exocytosis of lipid-
containing granules called lamellar bodies during the terminal differentiation of the epider-
mal keratinocytes.
III. COMPOSITION OF LIPIDS IN THE

STRATUM CORNEUM
The main components of the lipids in the stratum corneum originating from epi-
dermal lamellar bodies are ceramides, cholesterol, and free fatty acid [14]. A
small amount of cholesterol sulfate has also been reported as the intercellular
lipids [14]. As described above, these lipids first appear in the lamellar body in
the epidermal granular layer. The lamellar body lipids are phospholipids, sphin-
gomyeline, cholesterol sulfate, glucosylceramide, and acylglucosylceramides. At
the final stage of keratinocyte differentiation, the lamellar body lipids are secreted
into the stratum granulosum–stratum corneum interface. During this process, the
lipids are also processed to three types of lipids in the stratum corneum. When
the barrier function is disrupted, the lipid synthesis, the lamellar body secretion,
and the lipid processing are accelerated to repair the recovery. Inhibition of lipid
synthesis [17,18], lipid processing [19,20], and migration of the lamellar body
[21] induces barrier abnormalities. There are six to seven types of ceramides,
and we previously demonstrated that the relative ratio of the species was altered
in experimentally induced dry skin or with aging [22]. Bouwstra et al. [23] dem-
102 Denda
onstrated that the difference in the ceramide species influences the lamellar
phases of the cholesterol and creamed mixture in vitro. The reason why such a
difference in ceramide species occurs in intact skin remains to be investigated.
Components of human sebum are squalene, wax esters, triglycerides, and
free fatty acids [15,24]. The free fatty acids are formed from the triglycerides
through the action of lipases. Cholesterol esters are also found in the skin surface
lipids, but they might be processed from cholesterol derived from epidermal kera-
tinocytes in the stratum corneum. The composition of sebum varies among mam-
mals [24]. Sebaceous activity and fatty acid composition vary with age and gen-
der because sebaceous gland activity is under the influence of sex hormones [15].
Tsuchiya et al. [25] demonstrated that the activity of the sebaceous glands was
also influenced by psychological stress. Various environmental factors and sys-
temic physiologic factors [15] might influence the sebum concentration on the
skin surface.
IV. BIOCHEMISTRY OF STRATUM CORNEUM

INTERCELLULAR LIPIDS
A. Lipid Synthesis
An important relationship between lipid synthesis and skin barrier function was
first demonstrated by Grubauer et al. [26]. They presented an approximately
threefold increase in the synthesis of cholesterol, fatty acid, and non-saponified
lipids in the epidermis 1–4 hr after disruption of the skin barrier by acetone
treatment. Importantly, those increases were perfectly blocked by occlusion with
water-impermeable plastic membrane. Then, Proksch et al. [27] demonstrated a
strong relationship between the rate-limiting enzyme in cholesterogenesis, HMG
CoA (hydroxymethylglutaryl coenzyme A) reductase, and skin barrier function.
The barrier disruption increased the enzyme activity within 15 min and the activ-
ity reached a maximum after 2.5 hr. Occlusion with a water-impermeable mem-
brane reduced the increase. Application of an HMG CoA reductase inhibitor,
lovastatin, inhibited the barrier recovery, and co-application of free cholesterol
reversed the inhibition [18]. Disruption of the barrier function by acetone treat-
ment or tape stripping increased the protein level and mRNA of HMG CoA [28].
The barrier disruption also increased the protein and mRNA levels of LDL (low-
density lipoprotein) receptor [28]. The changes induced by barrier disruption were
blocked by occlusion with a water-impermeable membrane [28]. Not only HMG
CoA reductase but also other key enzymes for cholesterol synthesis are related
to skin barrier function. Harris et al. [29] demonstrated that the barrier disruption
increased the mRNA levels of HMG CoA synthase and squalene synthase in
mouse epidermis and that the increase was prevented by occlusion with latex
membrane. These results suggest that an acute barrier disruption induces lipid
synthesis and lipid transport to repair the damage.
Fatty acid synthesizing enzymes are also associated with the barrier func-
tion. Ottey et al. [30] demonstrated that barrier disruption increased the activities
of both acetyl CoA carboxylase and fatty acid synthase, and that the increase
was prevented by occlusion with a water-impermeable membrane. The mRNA
levels of these enzymes in the epidermis also increased after barrier disruption,
and the increase was blocked by occlusion [29]. Yamaguchi et al. [31] suggested
a role of fatty acid–binding protein (C-FABP) in the epidermis. This protein
might transport intracellular fatty acids and induce fatty acid synthesis. They
demonstrated that C-FABP expression was prevented by occlusion with a water-
impermeable membrane after skin barrier disruption.
Ceramide synthesis is related to barrier homeostasis. Serine-palmitoyl
transferase catalyzes formation of 3-ketosphinganin (i.e., the first step of sphin-
golipid synthesis). Topical application of β-chloro-l-alanin, an inhibitor of
serine-palmitoyl transferase, inhibited the barrier recovery [17]. And mRNA of
this enzyme in the epidermis increases barrier disruption, and the increase is
prevented by occlusion with a water-impermeable membrane. Chunjor et al.
[32] demonstrated the importance of glucosylceramide syntase activity on the
barrier function. The activity of the enzyme was not altered by barrier disrup-
tion. However, the activity of this enzyme was higher in the outer epidermis
and inhibition of the enzyme by topical application of d, 1-threo-1-phenyl-2-
hexadecanoylamino-3-pyrrolidino-1-propanol delayed barrier repair. These re-
sults suggest that glucosylceramide synthase is also required for barrier homeo-
stasis.
Man et al. [33] demonstrated that inhibition of the synthesis of both choles-
terol and sphingolipid by fluvastatin (cholesterol synthesis inhibitor) and β-
chloro-l-alanine did not cause further worsening of the skin barrier function 5–
6 hr after barrier disruption. And 18–24 hr after treatment, the recovery rate of
mice skin, in which both cholesterol and sphingolipid synthesis was inhibited,
was better than in the animals in which only sphingolipid synthesis was inhibited.
This suggests the importance of the relation of both sphingolipid (ceramide in
the stratum corneum) and cholesterol.
Jensen et al. suggested an important role of sphingomyelinase [34]. Tumor
necrosis factor (TNF) induces activation of sphingomyelinase via p55 receptor
(TNF-R55). They demonstrated that TNF-R55–deficient mice showed delay of
barrier repair compared with the wild type. The barrier disruption increased the
sphingomyelinase activity in wild type and TNF-R75 (another type of TNF recep-
tor)–deficient mice but not in TNF-R55–deficient mice. TNF-R55 signaling plays
an important role in barrier homeostasis through the regulation of sphingomyeli-
nase activity.
104 Denda
B. Lipid Processing
During terminal differentiation and stratum corneum formation, the lipids in the
lamellar bodies are processed. This is also crucial for skin barrier homeostasis.
Man et al. [20] reported that processing of phospholipids, precursors of free fatty
acids, is necessary for barrier homeostasis. Topical application of phospholipase
A2 after the barrier disruption delayed the recovery [20]. Co-application of pal-
mitic acid with the inhibitor prevents the delay. Repeated application of these
inhibitors induces barrier abnormalities. In this case, a significant decrease of free
fatty acid content in the stratum corneum was observed. Again, co-application of
palmitic acid normalized the barrier function.
Hydrolysis of glucosylceramide by β-glucocerebrosidase is also important
for healthy barrier function [19]. This process produces free ceramide in the stra-
tum corneum. Inhibition of β-glucocerebrosidase by topical application of an
epoxide induced barrier abnormalities. In this case, the content of glycoceramide
in the stratum corneum was 6 times higher than that in normal skin, whereas free
ceramides in the stratum corneum did not show any significant difference. Elec-
tron microscopic studies showed an immature lipid bilayer structure in the stra-
tum corneum of the mouse, which was treated by the inhibitor. Doering et al.
[35] suggested an important role of sphingolipid activator protein, Pro-saposin,
on skin barrier homeostasis. This protein stimulates enzymatic hydrolysis of
sphingolipids such as glucosylceramide. They demonstrated that the pro-saposin
knockout mouse showed an accumulation of glucosylceramide and abnormal
structure of the intercellular lipid domain in the stratum corneum.
Abnormality of cholesterol sulfate processing also induces serious skin ab-
normalities [36]. In healthy epidermis, 5% of total lipids consists of cholesterol
sulfate, which decreases in the stratum corneum to about 1%. Steroid sulfatase
catalyzes the desulfation of cholesterol sulfate to cholesterol. In recessive X-
linked ichthyosis, which is associated with a large amount of abnormal scales,
the cholesterol sulfate in the stratum corneum was 10-fold higher than normal
because of the absence of steroid sulfatase. Sato et al. [37] demonstrated that
cholesterol sulfate inhibited both trypsin-type and chymotrypsin-type proteases,
resulting in the reduced degradation of desmosomes, which play a crucial role
in the adhesion of corneocytes and consequently the induction of abnormal scales.
Moreover, Nemes et al. [38] reported another potential negative role of choles-
terol sulfate in the stratum corneum. Involucrin cross-linking and involucrin
esterification with ω-hydroxyceramides are crucial for cornified envelope forma-
tion. They demonstrated that both reactions were inhibited by cholesterol sulfate.
The role of cholesterol sulfate in the normal epidermis should be studied.
Figure 4 shows a scheme of the synthesis and processing of the intercellular
lipids.
Figure 4 Diagram of synthesis and processing of the intercellular lipids in the stratum
corneum.
V. ROLE OF LIPIDS IN THE STRATUM CORNEUM
The intercellular lipids in the stratum corneum play a crucial role in skin barrier
function. The water impermeability is the result of the conformation of the lipid
molecules and also the ordering of the corneocytes [3]. The cornified envelope,
which is formed on the surface of the corneocytes, plays an important role in the
structure of the barrier [39] (Fig. 5). Another role of the stratum corneum is the
buffer function of water molecules in the corneocytes (Fig. 5). Decrease of free
amino acids in the corneocytes is commonly observed in various kinds of derma-
titis characterized by dry, scaly skin [40–43]. Decline of these functions leads
to deterioration of skin pathology.
Previous studies have suggested that the lipid structure itself can absorb a
huge amount of water [44]. However, this was later denied. Cornwell et al. [45]
demonstrated the effect of hydration on the intercellular lipid structure of human
stratum corneum using wide-angle x-ray diffraction. They monitored the packing
106 Denda
Figure 5 Structure of the corneocyte, cornified envelope, and intercellular lipid domain.
The cross-linked protein envelope and covalently attached lipid envelope on the protein
structure are formed around the corneocyte. Free amino acids and other water-soluble
small molecules in the corneocyte play a crucial role in holding water molecules.
arrangement of the lipid bilayers on the stratum corneum—which were hydrated

0, 20–40, 40–60, 60–80, and 300%—and observed no effects of hydration on
the lipid structure. The lipid bilayer structure contains some water molecules, but
the water content is relatively small in comparison with the amount of water
in the cornified cells. Moreover, in dry skin induced by detergent or tape strip-
ping, the total amount of stratum corneum ceramide did not change, though the
skin surface conductance, which is a measure of skin moisture, and barrier func-
tion decreased and the amino acid content decreased [42].
Tanaka et al. [43] reported that the amino acid content was reduced in the
stratum corneum in atopic respiratory disease and the transepidermal water loss
did not change. They suggested that the free amino acid content is a crucial factor
in the dry, scaly features of not only experimentally induced dry skin but also
atopic dermatitis. The ultrastructure of the intercellular lipids in the stratum cor-
neum contributes to the barrier function of healthy skin, but the decline of the
barrier function in dermatoses might be caused by various other factors. We pre-
viously evaluated the intercellular lipid alkyl chain conformation by attenuated

total reflectance infrared spectroscopy on healthy skin and surfactant-induced
scaly skin of human subjects [46]. In normal healthy skin, there was a correlation
between the lipid conformation and the transepidermal water loss. However, no
difference was observed in the surfactant-induced scaly skin. Disorders of the
corneocytes or phase separation of the lipid domain might cause barrier dysfunc-
tion. Reichelt et al. [47] demonstrated a significant alteration of lipid composition
in the stratum corneum of keratin 10–deficient mice. The mutual interaction of
proteins and lipids in the epidermis should be investigated for further understand-
ing the cause of abnormalities of the stratum corneum.
For the stabilization of the intercellular lipid bilayer structure, the hy-
drophobic envelope formed on the surface of the corneocytes plays an important
role [39]. During the terminal differentiation of the keratinocyte, the protein enve-
lope is formed on the keratinocyte. The cross-linked protein structure is mainly
composed of involucrin, loricrin, and filaggrin. Then, ω-hydroxyceramide mole-
cules covalently attach on the protein envelope. Any abnormality of the formation
of this protein-lipid envelope on the surface of the corneocytes induces barrier
abnormalities even when other lipid synthesis and processing systems are normal.
Behne et al. [48] demonstrated that inhibition of ω-hydroxyceramide inhibited
barrier repair after tape stripping. From their electron microscopic studies they
suggested that it was due to the disruption of the cornified lipid envelope and
lamellar membrane formation. Segre et al. [49] reported that a transcription fac-
tor, Klf4, is required for skin barrier formation. Klf4-deficient mice showed the
absence of the barrier and an abnormal cornified envelope, whereas mutant mice
showed a normal lipid profile. The process of the cornified envelope formation
has been studied by Steinert and his coworkers, who demonstrated that glutamine-
glutamate rich regions ordinarily come from involucrin as a major substrate for
the attachment of ω-hydroxyceramide [50]. Then, they demonstrated by their
series of in vitro studies that transglutaminase 1 played an important role for both
involucrin cross-linking [51] and attachment of ω-hydroxyceramide to involucrin
by ester bond formation [52]. However, Elias et al. [53] reported the existence
of a cornified lipid envelope in the scales of lamellar ichthyosis patients with
absence of transglutaminase 1. In the transglutaminase-deficient epidermis, other
enzymes might play a role in lipid envelope formation.
The role of sebum on the skin remains unknown. Abrams et al. [54] denied
the contribution of sebum to the water-impermeable barrier function of the stra-
tum corneum. They demonstrated that extraction of sebum by acetone did not
affect the barrier function, whereas extraction of ceramides, cholesterol, and fatty
acids by a chloroform and methanol mixture lowered the barrier function signifi-
cantly. Sebum might play a water-repellent role in human skin because it contains
hydrophobic lipids such as squalene [24]. Of interest, other mammals such as
mice, dogs, cats, and monkeys do not secrete squalene. Humans, and some water-
108 Denda
side mammals such as the otter and beaver, secrete squalene. Hairless humans
might need squalene to keep their bodies waterproof.
Although squalene in the sebum has been reported to be an oxygen-
scavenging agent [55], Chiba et al. [56] demonstrated that squalene-monohy-
droxperoxide induced skin roughness and wrinkle formation on hairless mice.
The biochemical role of squalene in human intact skin remains to be investi-
gated. On the other hand, Thiele et al. [57] reported that the uppermost layer of
sebum-rich facial stratum corneum showed significantly higher levels of the anti-
oxidant α-tocopherol than the stratum corneum on the arm. They also demon-
strated that sebaceous gland secretion was a major route of the α-tocopherol to
the skin surface.
Another report by Metze et al. [58] suggested that the sebaceous glands
secrete immunoglobulin A, which plays an important role in inactivation of in-
vading viruses. Recently, Man et al. [59] demonstrated that the dry scaly skin
of asebia mice, which have deficient sebaceous glands, could be improved by
application of glycerol, which is normally metabolized from triglycerides. People
in the cosmetic industry tend to focus on reduction of sebum secretion because
they believe it could prevent acne and also prevent makeup from coming off.
But such a reduction might cause a skin problem. The positive role of sebum
and the sebaceous gland should be investigated.
VI. TOPICAL APPLICATION OF LIPIDS
Effects of topical application of SC lipids were evaluated by researchers at the

University of California, San Francisco. They focused on the effects of lipids on
the barrier repair process [60–62]. First, they demonstrated that the application
of a single lipid among the main components of the intercellular lipids (i.e., cera-
mide, cholesterol, and free fatty acid) delayed barrier repair [60]. Application of
a mixture with two of them also delayed the barrier recovery. Also, an equimolar
mixture of ceramide, cholesterol, and free fatty acid did not delay barrier repair.
Finally, they found the optimal molar ratio of the lipid mixture that could acceler-
ate barrier recovery [61]. The molar ratios were ceramide :cholesterol :palmitic
acid : linoleic acid ⫽ 1 :1 : 1 :3 or 1 : 1 :3 : 1. Stearic acid, in place of palmitic acid,
also showed the same effect. Acylceramide alone did not accelerate barrier repair,
but a mixture of acylceramide and cholesterol accelerated barrier recovery. How-
ever, addition of a free fatty acid, such as linoleic acid, palmitic acid, or stearic
acid, did not further accelerate barrier recovery. The investigators also compared
the ‘‘physiologic lipids’’ (i.e., a mixture of the intercellular lipids) with petrola-
tum on the barrier repair process [21]. Petrolatum repaired the barrier more
quickly than the physiologic lipids, but 2 or 4 hr later, the application of a physio-
logic lipid resulted in a better recovery than petrolatum. An histochemical study
showed that the applied petrolatum stayed in the stratum corneum, whereas the
physiologic lipids were incorporated into the nucleated layers of the epidermis.
The applied physiologic lipids penetrated into the epidermis, followed by cellular
uptake. Then they entered the lamellar bodies, were secreted into the stratum
granulosum–stratum corneum interface, and reorganized the intercellular lipid
structures.
The effect of the application of the physiologic lipids varied depending on
the method of barrier disruption [62]. When the barrier was disrupted by tape
stripping or treatment with an organic solvent, the topical application of physio-
logic lipids was effective. However, when the barrier was disrupted by treatment
with a detergent such as sodium dodecyl sulfate or ammonium lauryl sulphosucci-
nate, the physiologic lipids did not accelerate barrier repair. When other deter-
gents, such as N-laurosarcosine free acid or dodecylbenzensulfuric acid were
used to disrupt barrier function, the lipid mixture could accelerate barrier repair.
A detergent may cause not only barrier disruption but also more extensive damage
in the nucleated layer of the epidermis.
Abnormalities of barrier function of recessive X-linked ichthyosis could
be improved by topical application of cholesterol [36]. Patients displayed a 10-
fold increase in cholesterol sulfate and a 50% decrease of free cholesterol in the
stratum corneum. They also showed lower barrier function and delayed barrier
repair. Studies have shown that abnormal cholesterol sulfate accumulation may
cause these abnormalities [36,37]. In healthy young people, topical application
of cholesterol alone delayed barrier repair as described above [60]. But in the
case of recessive X-linked ichthyosis, cholesterol accelerated barrier repair and
normalized the intercellular lipid ultrastructure [36].
Application of cholesterol is also effective for the abnormalities of aged
skin. Details will be given in the following section.
VII. AGING AND LIPIDS
Previous studies demonstrated that sebum secretion tends to decrease with age.
Saint Leger reported [63] an approximately 60% decrease in triglycerides on the
lateral mid-calf of the subjects (45 female and 5 male, aged 20–76). They also
showed an increase of skin dryness with aging. Nazzaro-Porro reported [64] that
the accumulation of upper chest skin surface lipids over 24 hr reached highest
values during ages 15–45 in both males and females and then started to decrease.
The decrease was more obvious in female subjects. Wilhelm et al. [65] demon-
strated the age-dependent surface sebum concentration on the skin at different
anatomic sites. A significant decrease of sebum was observed on the ankle. Alter-
ation of wax ester concentration on the skin surface with aging has been reported
by several investigators. Jacobsen et al. [66] demonstrated the wax ester secretion
110 Denda
rates on the forehead in male and female aged 15–97: rates were highest in those
15–35 years of age and then started to decrease with age. The rate of decrease
in male subjects was 23% per decade and 32% in female subjects. Yamamoto
et al. [67] also reported an alteration of sebaceous gland activity with aging by
the ratio of wax ester/[cholesterol ⫹ cholesterol ester] and showed similar results.
They also demonstrated a variation in the fatty acid composition of the wax ester
in the subjects. C16 iso-branched saturated fatty acid, C14, C15, C16, C18:1
straight, and C16:1 iso-branched mono-unsaturated fatty acids showed a signifi-
cant correlation with aging from infancy to the twenties. C15, C16:1 straight,
and C16:1 iso-branched mono-unsaturated fatty acids also showed a significant
correlation with aging after maturation.
Stratum corneum intercellular lipids also decrease with aging, but the de-
crease is relatively smaller than that of sebum. Hara et al. [68] demonstrated the
stratum corneum lipid contents of subjects with senile xerosis and of young con-
trols. The triglyceride concentration was 65% lower in the subjects with senile
xerosis and ceramide concentration was 28% lower. The xerosis skin showed a
significant decrease of water content in the stratum corneum, but the transepider-
mal water loss was not significantly different. An electron microscopic observa-
tion showed the decrease of keratohyaline granules in the granular layer of the
skin of patients with senile xerosis. These results suggest that the decrease of
water in the skin surface of the patients was the result of reduced skin surface
lipids and amino acid content in the stratum corneum.
We demonstrated the alteration of ceramide composition with aging [22].
A significant difference in ceramide composition was observed only in female
subjects. There was a significant increase in ceramide 1 and 2 with a correspond-
ing decrease in ceramide 3 and 6 from prepubertal age to adulthood. Thereafter,
the portion of ceramide 2 decreased with age, whereas ceramide 3 increased with
age. The alteration of the ceramide composition with aging is opposite to the
changes of ceramide composition in dry, scaly skin induced by tape stripping or
detergent treatment. These results suggest that ceramide composition is influ-
enced by epidermal proliferate activity and also by sex hormonal changes.
The transepidermal water loss in the elderly is the same or slightly lower
than that in young individuals, suggesting that the barrier function in the elderly
is not lower. However, Ghadially et al. [69] reported that the barrier function in
elderly subjects was destroyed more easily than that in young individuals, and
that the recovery rate of the barrier function after the disruption of the barrier in
the elderly subjects was lower than that in the young subjects. They compared
15 subjects aged 20–30 years and 6 subjects older than 80. The basal transepider-
mal water loss of the volar arm of the elderly subjects was not lower than that
in the young subjects. But barrier function was perturbed by 18 ⫾ 2 tape strip-
pings in the elderly subjects, whereas 31 ⫾ 5 strippings were needed in the
younger subjects. Moreover, barrier recovery 24 hours after barrier disruption
was only 15% for the elderly subjects, whereas the young subjects showed 50–
60% recovery at that time. The investigators observed the same tendency on aged
hairless mice skin. An electron microscopic study showed a similar number of
lamellar bodies in both young and aged epidermis, but a paucity of secreted
lamellar body content in the aged epidermis both from humans and mice.
Although the total lipid content in the stratum corneum decreased 30%
more in the aged mice than in the young mice, the composition of the main key
lipids (i.e., ceramide, cholesterol, and free fatty acid) did not differ between
young and aged mice. However, among the main stratum corneum intercellular
lipids (i.e., ceramide, cholesterol, and free fatty acids), synthesis of cholesterol
is reduced more than of the other two lipids [70]. Topical application of choles-
terol also accelerated skin barrier repair after barrier disruption. The physiologic
lipid mixture also improved barrier function and, moreover, a cholesterol :cera-
mide :palmitic acid :linoleic acid ⫽ 3 :1 : 1 :1 mixture with cholesterol as the dom-
inant lipid further accelerated barrier recovery in chronologically aged human
skin and hairless mouse skin. Electron microscopic observations showed that the
acceleration of barrier repair in chronologically aged skin was associated with
acceleration of replenishment of the interstices in the intercellular lipid domain
with lamellar structures [70].
Haratake et al. [71] demonstrated that topical application of mevalonic acid,
which is an intermediate of cholesterol biosynthesis, stimulates cholesterol syn-
thesis in the epidermis of aged mice. They also reported improvement of barrier
repair in aged mice by the treatment. The deterioration of the skin barrier function
with aging could be improved by the regulation of cholesterol in the epidermis.
VIII. PERSPECTIVE
As described above, lipids play various roles in human skin. Regulation of the
lipids on the skin surface can not only improve the superficial condition but also
cure whole skin pathology. Topical application of suitable lipids is one method
of lipid regulation. On the other hand, studies have suggested another way to
improve the condition of the stratum corneum. Skin barrier repair can be acceler-
ated not only by the topical application of the physiologic lipids but also by
regulation of nonlipid factors such as enzymes and ions (Tables 2 and 3). As
described above, repeated barrier disruption induces epidermal hyperplasia and
inflammation. The acceleration of barrier repair will improve those skin condi-
tions. Thus, biochemical and biophysical studies of epidermal barrier homeostasis
are important for clinical dermatology.
Lipid metabolism is regulated by a series of enzymes in the epidermis [72],
and each of them has its optimal pH [73] and other conditions such as ion balance
[74]. For example, the pH value of the healthy stratum corneum is kept acid
112 Denda
Table 2 Substances That Affect Skin Barrier Recovery
Barrier recovery Barrier recovery

Lipids (ref.) Ions (ref.)
Single lipid Delayed (60) Calcium Delayed (75)
Two-lipid mixture Delayed (60) Potassium Delayed (75)
Equimolar mixture Normal (60) Sodium Normal (75)
of three lipids Magnesium Accelerated (74)
Optimized mixture Accelerated (61) Magnesium Accelerated (74)
of three lipids ⫹ calcium
Nuclear hormone Acidic pH Normal (73)
receptor acti- Neutral or ba- Delayed (73)
vator sic pH
PPARα activator Accelerated (92)
because the lipid-processing enzymes have a low optimal pH. Mauro et al. [73]
demonstrated that topical application of basic buffer after the barrier disruption
delayed the repair process because the basic condition perturbs lipid processing.
Other ions such as calcium and magnesium [72,75] also play important
roles in the lipid metabolism of the epidermis. We demonstrated the heteroge-
neous distribution of calcium, magnesium, and potassium in human epidermis
[76]. Both calcium and magnesium are localized in the granular layer, and potas-
sium is localized in the spinous layer. Immediately after disruption of barrier
function, this distribution disappeared. Calcium plays various roles in stratum
corneum barrier formation [77]. For example, it induces terminal differentiation
[78], formation of the cornified envelope, and also epidermal lipid synthesis [79].
Menon et al. demonstrated that alteration of the calcium gradient affects the exo-
cytosis of the lamellar body at the interface between the stratum corneum and
the epidermal granular layer [80]. Vicanova demonstrated [81] the improvement
in barrier function of reconstructed human epidermis by the normalization of
epidermal calcium distribution. The heterogeneous field that is formed by calcium
and other ions with consumption of ATP might be crucial for terminal differentia-
tion and barrier formation of the epidermis. Magnesium is required for the activity
of Rab-geranylgeranyl transferase, which modifies Rab, a low-molecular-weight
GTP-binding protein [82]. After the modification, Rab plays an important role
on exocytosis and endocytosis [83]. For barrier formation, exocytosis of the la-
mellar body is an important process. Previous studies have indicated that Rab is
modified by Rab-geranylgeranyl transferase during the terminal differentiation
of the epidermis [84]. The topical application of calcium or potassium impaired
barrier repair, whereas magnesium or a mixture of calcium and magnesium salts
accelerated the repair process [74].
Table 3 Substances That Affect Skin Barrier Recovery
Histamine receptor
Barrier agonist and Barrier
Protease inhibitors recovery (ref.) antagonists recovery (ref.)
Trypsin-like serine Accelerated (72) H1 Receptor antag- Accelerated (94)
protease inhibitor onist
Other protease in- Normal (72) H2 Receptor antag- Accelerated (94)
hibitors onist
Plasminogen activa- Accelerated (72) H3 Receptor antag- Normal (94)
tor inhibitor onist
H2 Receptor agonist Delayed (94)
H3 Receptor agonist Normal (94)
Histamine Delayed (94)
Histamine releaser Delayed (94)
Recently, an important role of retinoid X receptors for the stratum corneum

has been suggested by several workers. Topical application of retinoic acid
decreased the skin barrier function. Imakado et al. [85] demonstrated that a
dominant-negative retinoic acid receptor α targeting mutant in the epidermis of
mice showed a severe decline of the barrier function. The transgenic mice showed
thin and loosely packed stratum corneum and, of note, there was no lipid bilayer
structure in the stratum corneum of the mutant mice.
Feingold and his coworkers have demonstrated an important role of nuclear
hormone receptors on epidermal differentiation and stratum corneum barrier for-
mation. First, Hanley et al. [86–88] demonstrated that activation of the nuclear
hormone receptors PPARα (peroxysome-proliferator-activated receptor α) and
FXR (farnesoid X–activated receptor) with oleic acid, linoleic acid, and clofibrate
accelerated the development of the epidermis and barrier formation in the fetal
skin organ culture system. Of note, activities of β-glucocerebrosidase and steroid
sulfatase, which play an important role in barrier lipid processing, were increased
by the activation of PPARα and FXR. Activation of PPARα by farnesol also
stimulated the differentiation of epidermal keratinocyte [89–91]. The cornified
envelope formation, involucrin and transglutaminase protein, and mRNA levels
were also increased by the activation of PPARα [92]. Of interest, DNA synthesis
was inhibited by the treatment [91]. Activation of PPARα in knockout mice that
showed focal hyperkeratosis did not increase the epidermal differentiation [93].
These results suggest that the nuclear hormone receptor plays a crucial role in
the development and differentiation of epidermis and stratum corneum barrier
homeostasis. They also showed that topical application of PPARα activators ac-
celerated barrier recovery after tape stripping or acetone treatment and prevented
114 Denda
epidermal hyperplasia induced by repeated barrier disruption [92]. Regulation of

the nuclear hormone receptor would open a new possibility for improvement of
cutaneous barrier function.
Recently, Ashida et al. [94] reported the relationship between the histamine
receptor and skin barrier function [94] (Table 3). The topical application of hista-
mine H1 and H2 receptor antagonists accelerated the barrier repair. Histamine
itself, H2 receptor agonist, and histamine releaser delayed the barrier repair. Nei-
ther a histamine H3 receptor antagonist nor agonist affected the barrier recovery
rate. Topical application of H1 and H2 receptor antagonists prevented the epider-
mal hyperplasia induced by barrier disruption in a dry environment. The mecha-
nism of the relationship between the histamine receptors and the barrier repair
process has not been clarified. However, these findings provide another perspec-
tive for future skin care systems.
The regulation of epidermal lipid metabolism by regulation with other fac-
tors might be effective to improve skin pathology, because it can improve the
endogenous homeostatic process. Occlusion or moisturization with artificial ma-
terial could improve skin condition. However, these treatments potentially perturb
the homeostasis of the skin. On the other hand, recovery of the original, endoge-
nous skin function by acceleration of its homeostatic process results in natural
healthy skin without side effects. A better understanding of skin homeostasis is
required to develop an ideal skin care system.
IX. CONCLUSIONS
Stratum corneum lipids play a crucial role in skin barrier function. Synthesis and
processing of lipids are associated with the barrier function. Although the epider-
mal barrier function is a self-referential and self-organizing system, it is also
related to the physiological condition of the whole body. Abnormalities of the
barrier function induced by various environmental or intrinsic factors may cause
whole skin problems. Topical application of physiologic lipids or suitable regula-
tion of the epidermal lipid metabolism could improve the skin barrier function
and the condition of the whole skin.
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5
Investigating Human Skin Barrier
Lipids with In Vitro Skin Models
Annie Black and Odile Damour
Hôpital Edouard Herriot, Lyon, France
Kordula Schlotmann
I. INTRODUCTION
Advances in technology and a movement toward reduced animal testing have

spurred the development of alternative methods for determining skin irritation,
sensitization, and efficacy of cosmetic products. The first generation of tissue-
engineered epidermal equivalents are simple cultures that are easy to produce
and permit efficient screening of the irritation potential of large quantities of
molecules. However, it was recently demonstrated that the response of skin-
equivalent systems to topically applied consumer products is influenced not only
by epithelium but also by epithelial-mesenchymal interactions [1].
Thus, skin-equivalent models, comprising a reconstructed epithelium to-
gether with dermal equivalent, have been designed to meet the research and test-
ing needs of the cosmetics, pharmaceutical, and chemical industries as well as
for mechanistic studies of skin physiology and clinical applications for acute or
chronic wounds. Unfortunately, the incomplete barrier function and short life
span of these constructs are considered major limitations preventing their exten-
sive use. The successful application of tissue-engineered skin equivalents requires
the correct organization and function of the reconstructed tissue.
This chapter gives a brief overview of keratinocyte and fibroblast cell cul-
ture techniques. The different epidermis and skin-equivalent models are discussed
121
122 Black et al.
as well as the characterization of a skin-equivalent model; finally, skin barrier

lipid analysis of these different epidermis and skin models are discussed.
II. KERATINOCYTE AND FIBROBLAST

MONOLAYER CULTURES
As a result of the work of Rheinwald and Green, serial passage of keratinocytes

has become accessible and permits the production of large quantities of cells [2].
Keratinocytes can be isolated form skin biopsies obtained from breast or abdomen
skin as well as foreskin by different enzymatic digestion techniques with trypsin,
dispase, a combination of the two [3], or a thermolysin-trypsin combination [4].
Epidermal cell suspensions then are seeded on a feeder layer of lethally irradiated
3T3 mouse fibroblasts or human fibroblasts that produce both extracellular matrix
and growth factors. These fibroblasts support keratinocyte attachment, stimulate
proliferation [5], and inhibit the growth of contaminating fibroblasts.
For culturing keratinocytes, various culture media are used, the most com-
mon being a mixture of Dulbecco’s Modified Eagle’s Medium (DMEM) and
Ham’s F12 medium (3 :1), supplemented with 10% bovine serum, hydrocorti-
sone, insulin, transferrin, cholera toxin, 1,25-dihydroxyvitamin D3, ascorbic acid,
and epidermal growth factor (EGF). EGF stimulates multiplication and increases
the life span of keratinocytes [6]. Medium and culture conditions have also
evolved and permit the growth of the cells without a feeder layer and in the
absence of serum [7,8].
Cultures of dermal fibroblasts can be generated from separated dermis of
foreskin, abdomen, or breast or any other type of skin sample. The tissue can be
digested by a collagenase treatment, after which the cell suspension can be seeded
in a mixture of DMEM with 10% serum. Fibroblasts can also be obtained from
explant cultures.
A single skin specimen can generate keratinocytes and fibroblasts and also
melanocytes [9] endothelial cells [10], and dendritic cells such as Langerhans
cells [11,12] and dermal dendrocytes [13,14] (Fig. 1).
Conventional monolayer cell cultures present many advantages for toxicity
and efficacy testing. They provide a large supply of material, in simple culture
conditions and in a relatively short time, which permits large-scale screening.
However, they have a limited capacity to organize into a physiological structure
and exhibit in vivo characteristics. Moreover, testing material is limited to water-
soluble compounds, and the lack of epidermal differentiation and stratum cor-
neum can result in an overestimation of toxicity of the tested compound.
Despite the fact that the use of two-dimensional cultures has resulted in
considerable progress in the understanding of keratinocyte biology, tissue-
engineered epidermal and skin equivalents have been developed in order to im-
Skin-Equivalent Models 123
Figure 1 Schematic representation of the extractions of dermal and epithelial cells from
fresh skin biopsies. First, epidermis and dermis can be separated by enzymatic digestion
by different enzymes. From the resulting cell suspension, melanocytes and Langerhans
cells can be isolated by selective medium, magnetic beads, or cell sorting. Dermal cell
suspensions (mainly fibroblasts) can be obtained after incubation with collagenase or by
explants. Endothelial cells can be obtained by selective medium or panning technique.
prove our understanding of cell-cell, cell-matrix, and dermal-epidermal interac-

tions.
III. TISSUE-ENGINEERED EPIDERMIS AND SKIN MODELS
Epidermis and skin models are three-dimensional systems produced by seeding

single cell suspensions of keratinocytes on an appropriate support. The keratino-
cytes attach to the substrate and proliferate. The culture is kept submerged for
a few days to ensure coverage of the substrate. Subsequently, the support covered
by a layer of keratinocytes is elevated at the air-liquid interface to induce terminal
124 Black et al.
differentiation [15–17]. Growth and differentiation of keratinocytes is also af-

fected by calcium and epidermal growth factor (EGF) concentration. These fac-
tors and a retinoic acid gradient created by the air-liquid interface is crucial for
the appearance of a multilayered differentiated tissue [17–21].
Various types of substrates can be used to support keratinocyte growth and
differentiation into reconstructed epidermis. They can be synthetic or biological,
which can be either cellular or acellular.
A. Epidermis Models
Keratinocytes can be seeded either on a culture insert made of polycarbonate
[22] or cellulose acetate [23] or on a layer of collagen type I and III overlayed
by collagen type IV [24].
Epidermalization can also be achieved on human de-epidermalized dermis
(DED) obtained from cadaver skin. The epidermis is removed and the dermal
cells are killed by multiple freeze-thaw cycles. Only the dermal extracellular
matrix and basement membrane components remain [25–27], which facilitates
the adhesion of keratinocytes and the reconstruction of the dermal-epidermal
junction.
These epidermal equivalents provide a local environment similar to that of
in vivo tissues in regard to the effect of compounds in contact with the epidermis.
The response of reconstructed tissues to these compounds may be normalized
compared to monolayer cultures. Moreover, the effect of keratinocytes on the
physiological organization and function of melanocytes and Langerhans cells can
be studied [28–30].
B. Skin-Equivalent Models
Skin-equivalent models consist of a living dermal equivalent associated with
an overlaying epidermis. Besides fibroblast-populated collagen gels, three-
dimensional dermal equivalents can be generated by synthesis of extracellular
matrix by fibroblasts inside a scaffold or on inert filters before keratinocyte seed-
ing (Fig. 2).
Three-dimensional dermal equivalents have been also generated using com-
binations of fibroblasts and endothelial cells either in a collagen gel [31] or in a
collagen sponge where the endothelial cells reorganize themselves into capillary-
like structures [32,33] (Fig. 3).
The inclusion of melanocytes [34–37], melanocytes in combination with
Langerhans cells [30], and melanocytes with endothelial cells compose the many
variations that have been developed (Fig. 4). These cells not only share the envi-
ronment of the keratinocytes and fibroblasts but interact with them in a manner
that can influence their activities.
Figure 2 Human skin equivalent culture. Fibroblasts are seeded onto a dermal substrate
and cultured for 14 days to obtain a dermal equivalent. The dermal equivalent is then
seeded with keratinocytes and cultured for 7 days immersed in culture medium and 14
days at the air-culture medium interface for a total of 35 days.
126 Black et al.
Figure 3 Tissue-engineered endothelialized skin equivalents. Biopolymers were seeded

with HUVEC and fibroblasts and keratinocytes and cultured for 35 days. Sections were
stained with Masson’s trichrome. White arrows show the capillary-like structures with a
lumen (L). Scale: (A) 1 cm ⫽ 16 µm; (B) 1 cm ⫽ 9 µm. Frozen sections were immuno-
stained for human vWF (C) and laminin (D). Note the typical granular staining of vWF
in the cells implicated in tubular structures (arrow) (C). Nuclei are stained with Hoechst
33258 (C). Basement membrane constituent, laminin (D), is observed surrounding tubular
structures (arrowheads). Deposition of laminin was also detected at the dermal-epidermal
junction (arrow) (D). Scale: (C) 1 cm ⫽ 27 µm; (D) 1 cm ⫽ 53 µm. Transmission electron
microscopy of a portion of a capillary-like structure observed. An internal lumen (L),
intercellular junctions (arrow), and Weibel-Palade bodies were seen (open arrows) (E, F).
Scale: (E) 1 cm ⫽ 0,8 µm; (F) 1 cm ⫽ 10 µm.
1. Collagen-based Dermal Analogues

With the knowledge that collagen is the essential compound of connective tissue,
Yannas was the first to use it to reconstitute an in vitro dermal analogue [38].
This acellular Dermal Substrate (DS) is obtained by lyophilization of a composite
matrix made by coprecipitating bovine collagen type I and III and chondroitin
sulfate. The cross-linking of collagen by glutaraldehyde is the most common
procedure [39–44]. However, glutaraldehyde is toxic and therefore requires a
fastidious elimination protocol. In addition, it can induce calcification of the
sponges, which can have harmful consequences [45,46]. This is why other meth-
ods of cross-linking have been developed, such as periodate [47], acyl azide [46],
or a dehydrothermic physical treatment [48]. This treatment consists of dehydrat-
ing the sponge to draw the constituent molecules closer together and thus permit-
ting the creation of amide links. Last, in order to avoid the use of chemical prod-
Figure 4 Melanocyte and endothelial cells are shown on serial frozen sections. Melano-
cytes are stained with MEL-5 (white arrow) and a capillary-like structure is stained with
EN4 (arrowheads) in a pigmented endothelialized skin equivalent. The dotted line shows
the basement membrane zone. Magnification: 40⫻.
ucts, a collagen sponge, made from bovine collagen and chondroitin sulfate, has
been insolubilized by chitosan [49]. Chitosan, obtained by deacetylation of chitin,
creates ionic bonds with carboxyl groups of collagen and sulfate groups of chon-
droitin sulfate. After lyophilization, these collagen-glycosaminoglycan-chitosan
(C-GAG-C) polymers form an alveolar structure between 50 and 150 µm. The
ionic bonds formed are sufficiently strong to give this sponge good mechanical
properties [50,51].
2. Noncollagenous Dermal Analogues

Many synthetic biocompatible polymers, biodegradable or not, can be used as
supports for fibroblast culture in the production of dermal equivalents. They differ
by their structure—either porous, mesh, or layer—or by their composition—
nylon, polyglycolic acid [52–54], poly-l-lactid, polyethylene oxide, or polybuty-
lene terephthalate [55,56]. When these dermal analogue fibroblasts are seeded,
they multiply, synthesize, and deposit new ECM.
3. Collagen Gel
Another way to obtain a dermal equivalent is by using a collagen gel [57,58];
this was proposed by Karasek and Charlton [59] and developed by Bell [60].
The resistance and insolubility of collagen is obtained by retraction of the gel
by fibroblasts. This living DE has a final size proportional to the number of cells
it contains and inversely proportional to the collagen concentration. In this model,
128 Black et al.
cell proliferation and collagen synthesis are inhibited, probably due to biochemi-
cal confinement, the fibroblasts being restricted in an environment of retracted
collagen.
The collagen gel model was also completed by the addition of hypodermis
composed of pre-adipocytes and mature adipocytes cultured in the inferior part
of a gel [61]. In addition to these cell populations, this model can also support
the growth of hair follicles [62,63].
4. Self-Assembly Approach
The self-assembly approach comprises the multiplication of fibroblasts and the
synthesis of extracellular matrix by the cells to obtain a three-dimensional tissue
without the support of any artificial scaffold [64]. The dermal equivalent is com-
posed of stacked fibroblast sheets where keratinocytes can be seeded. Complete
pilosebaceous units were also integrated [64].
IV. CHARACTERIZATION OF A TISSUE-ENGINEERED

COLLAGEN-GLYCOSAMINOGLYCAN-CHITOSAN
SKIN EQUIVALENT
Previous studies with a skin equivalent based on a collagen-glycosaminoglycan-

chitosan dermal substrate have demonstrated the importance of (1) fibroblasts
in the epithelial morphogenesis [65], (2) fibroblast newly synthetized ECM in
keratinocyte adhesion and the formation of a complex dermal-epidermal junction
[66], (3) fibrillar collagens in the re-expression of collagen types XII and XIV
[67], and (4) keratinocytes in the maturation and organization of elastin [68].
In all of these studies, the culture conditions favored fibroblast and keratino-
cyte proliferation and extracellular matrix synthesis but hindered keratinocyte
differentiation. To improve keratinocyte differentiation, which is necessary for
optimal pharmacotoxicological studies, it is necessary to control the proliferation-
differentiation balance.
Despite the similarities in tissue architecture, the reconstructed epidermis
in serum-containing media still exhibits some deviations from normal epidermis.
It lacks a stratum granulosum, and the stratum corneum contains a high number of
nuclear remnants. Many factors seem to be responsible for modulating epithelial
differentiation [69–73]. The development of optimal culture conditions, eliminat-
ing serum and ill-defined supplements from medium, should improve reproduc-
ibility and keratinocyte differentiation.
After 14 days of culture at the air-liquid interface in serum-free medium,
the epidermis of the skin equivalent is morphologically similar to normal human
skin [74] (Fig. 5).
Figure 5 Histological analysis of the skin equivalent. Keratinocytes seeded on the der-
mal equivalent multiply to form a stratified, differentiated epidermis with stratum basal
(SB), stratum spinosum (SS), stratum granulosum (SG), and stratum corneum (SC). The
fibroblasts (F) are numerous and have filled the pores of the dermal substrate (DS) with
newly synthesized extracellular matrix (ECM). Magnification: 40⫻.
The epidermis is stratified, well-organized, and uniform. A layer of cuboi-

dal basal keratinocytes is firmly attached to the dermal equivalent underlying the
stratum spinosum. The stratum granulosum is well developed, with large numbers
of keratohyalin granules and a stratum corneum.
Hemidesmosome structures can be found in the basal surface of basal kera-
tinocytes of the epidermis in contact with the dermal equivalent (Fig. 6).
Keratinocytes, joined by large numbers of desmosomes throughout the epi-
dermis, contain abundant cytoplasmic keratin filaments and synthetic organelles
(Fig. 7).
In the stratum granulosum, many keratohyalin granules are present (Fig.
7). The stratum corneum is six to seven layers thick, interspaced with desmosomal
remnants (Fig. 7). The borders of the cornified cells overlap, interdigitate, and
insert into adjacent cells (Fig. 7), and keratin filaments become more randomly
oriented (Fig. 7).
Lamellar granules (LG) were found in the cytoplasm of spinous keratino-
cytes. LG were partially filled with stacks of lamellae (Fig. 8). This fully devel-
oped skin equivalent expresses a number of protein products typically found in
130 Black et al.
Figure 6 Ultrastructural analysis of the basement membrane. The basement membrane

zone contains many hemidesmosomes (H) linked to keratin filaments (K) and characteris-
tic normal human skin structures such as lamina lucida (LL) containing anchoring fibrils
(AF). Underneath the lamina densa (LD) are anchoring fibers (AFb). These anchoring
fibers are linked to collagen fibers (C). Left: Bar indicates 200 nm. Right: Bar indicates
100 nm.
normal human skin. Keratin 14 is present in the basal layer and gradually disap-
pears in the suprabasal layers, whereas keratin 10 is found exclusively in su-
prabasal keratinocytes (Fig. 9).
The absence of serum-containing media for culture at the air-liquid inter-
face improved keratinocyte differentiation. This could be explained by the ab-
sence of retinoids, which are contained in serum and impede terminal differen-
tiation in vitro [75–77]. Another explanation of the differences in terminal
differentiation obtained in previous studies with this model is the presence of
epidermal growth factor. Chih-Shan et al. have demonstrated that in the continu-
ing presence of 10–20 ng/ml of epidermal growth factor, the epidermis is less
organized, thinner, and less proliferative [78]. EGF also depressed several indica-
tors of differentiation, such as keratohyalin granules, membrane-coating granules,
and filaggrin expression, and frequent nuclear retention was noted in the stratum
corneum [78,71]
The presence of basement membrane proteins and their correct structural
arrangement are critical elements for the stability of the dermal-epidermal junc-
tion. Contrary to findings in a collagen gel model cultured in defined conditions
[72], the absence of serum does seem to affect the synthesis of basement mem-
brane components in the equivalent grown on the collagen-glycosaminoglycan-
Figure 7 Ultrastructural analysis of suprabasal epidermal cell layers. The stratum spino-
sum shows numerous desmosomes (D), and the stratum granulosum contains keratohyalin
granules (KH). The stratum corneum is composed of six to seven layers interspaced with
desmosomal remnants (large white arrow). The borders of the cornified cells overlap,
interdigitate, and insert into adjacent cells (clear arrow) and keratin filaments become more
randomly oriented (K). Top left: Bar indicates 100 nm. Top right: Bar indicates 200 nm.
Bottom: Bar indicates 200 nm.
132 Black et al.
Figure 8 Lamellar granule ultrastructure. Lamellar granules are present in the spinous
layer of the epidermis but they are not completely filled with lamellae. Left: Bar indicates
200 nm. Right: Bar indicates 100 nm.
Figure 9 Immunohistochemical analysis of keratins. A layer of organized and adhering

basal cells expressing keratin 14 and suprabasal keratinocytes showing differentiation-
associated keratin 10 characterizes the epidermis of the skin equivalent. Similar staining
patterns are seen in normal human skin (NHS).
chitosan dermal substrate [74]. Immunohistochemistry has demonstrated the pres-

ence of major proteins of the dermal-epidermal junction such as collagen type
VII, laminin, and hemidesmosome-associated integrin α6. The structural integrity
of the basement membrane zone ensured by series of linked extracellular struc-
tures including anchoring filaments and anchoring fibrils is also observed as dem-
onstrated before in serum-containing conditions [66]. These results suggest that
basement membrane stability is independent of serum [74].
Fibroblasts seeded in the dermal substrate proliferate in the pores of the
sponge and synthesize their own extracellular matrix in which collagen and pro-
tein synthesis is abundant even in reduced serum conditions. The histological
and immunohistochemical results show that fibroblasts express some of their
morphogenic potential: reorganization of the matrix with synthesis de novo of
matrix constituents. The composition of this neosynthesized extracellular matrix
is close to that of normal human dermis; type I, III, and V collagens and fibronec-
tin (Fig. 10) as well as the reconstruction of elastic tissue has been demonstrated
(Fig. 11). Fibrillin-1 is detected in the dermis, with short fibers appearing perpen-
dicular to the basement membrane; deeper in the dermis, fibers are parallel. Elas-
tin is located close to the basement membrane zone in a parallel fashion.
Transmission electron microscopy has revealed a structured organization
of the neosynthesized extracellular matrix in which the collagen quarter-staggered
fibrils are regrouped into a network of bundles indicating complex dermal recon-
struction, and in between these collagen fibrils is an abundant microfibrillar mate-
rial (Fig. 12).
The absence of serum did not seem to affect the expression or stability of
these extracellular matrix proteins. Duplan-Perrat et al. demonstrated that ke-
ratinocytes influence fibroblast migration, proliferation, and extracellular matrix
synthesis [68]. Thus, keratinocytes could sustain this complex extracellular ma-
trix organization in the absence of serum.
Thirty-five days are required to obtain a mature skin equivalent in these
conditions. The equivalents were cultured for 14 additional days for a total of
49 days. This was an attempt to determine if the skin equivalents could be cul-
tured longer with an optimal differentiation. In these conditions, both dermal and
epidermal cells maintained their histotypical morphology. Basal cells are still
proliferating and the epidermis still shows the histotypical morphology of normal
human skin. Differentiation markers filaggrin and transglutaminase are still ex-
pressed in their respective positions, keratin 10 is expressed in the suprabasal
layers, and Ki67 demonstrates proliferating cells in the basal layer of the epider-
mis (Fig. 13), showing optimal differentiation after 4 weeks at the air-liquid inter-
face.
The complexity of the neosynthesized extracellular matrix provides a good
support for long-term keratinocyte culture survival. The long-term survival of
this collagen-glycosaminoglycan-chitosan–based skin-equivalent culture could
134 Black et al.
Figure 10 Immunohistochemical analysis of the newly synthesized extracellular matrix.

Frozen sections were immunostained for human type I collagen, type III collagen, type
V collagen, and fibronectin (F). Note that all these dermal extracellular matrix proteins
are synthesized by fibroblasts in the skin equivalent (SE) as seen in normal human skin
(NHS).
Figure 11 Elastic tissue reconstruction. Elastin and fibrillin-1 constitute the two major
components of the elastic system in normal human skin (NHS). In the skin equivalent (SE),
fibrillin-1 is detected in the dermis and shows an organization into microfibrils appearing
perpendicularly to the BMZ, and deeper in the dermis, fibers are parallel. Elastin is depos-
ited onto this microfibrillar network. Elastin staining seems to be more intense in the lower
part of the reconstructed dermis.
Figure 12 Ultrastructural analysis of neosynthetized extracellular matrix. Quarter-stag-

gered collagen fibrils are organized into mature collagen fibers, regrouped in cross and
longitudinal sections. Abundant microfibrillar material is also observed. Bars indicate 100
nm.
136 Black et al.
Figure 13 Long-term culture of the skin equivalent. Differentiation markers are still
expressed in their respective positions and Ki67 demonstrates proliferating cells in the
basal layer of the epidermis.
be explained by two reasons. First, the keratinocyte extraction and culture tech-
niques permit the transfer of stem cells into the skin equivalent [74]. Second, the
human extracellular matrix synthesized by the fibroblasts in conjunction with
soluble factors secreted by these cells could help maintain the keratinocytes in
their proper differentiated state by maintaining the balance between proliferation
and differentiation. The maintenance of the in vivo characteristics will permit a
more thorough investigation of the mechanisms involved in skin homeostasis.
An increase in life span will allow the investigation of mechanisms that require
longer exposure to active molecules or simply favor a more flexible management
of pharmacotoxicology tests.
V. SKIN BARRIER LIPID COMPOSITION OF

IN VITRO MODELS
The stratum corneum consists of protein-enriched corneocytes embedded in a

lipid-enriched, intercellular matrix [79,80]. These extracellular lipids are orga-
nized in bilayers originating from lamellar bodies. The lipid and proteolytic en-
zyme content is discharged and reorganized into broad lamellar bilayers com-
posed mainly of cholesterol, ceramides, and free fatty acids [81]. The composition
and the organization of epidermal lipids are thought to contribute substantially

to the permeability barrier of the stratum corneum.
Regarding the use of reconstructed human skin equivalents for fundamental
and applied research, for efficacy testing and toxicity screening, and as models
for drug transport and metabolism studies, the barrier function should resemble
normal human skin as closely as possible. Thus, the ordered extrusion of lamellar
bodies, the correct organization of the lipids in the lamellar bilayers as well as
a physiological lipid composition, has to be achieved. Different techniques can
be used to examine these phenomena—e.g., electron microscopy visualization of
intercorneocyte lipid bilayers, using ruthenium tetroxide as an additional fixative.
Various spectroscopy techniques such as small angle x-ray scattering and ATR-
FTIR spectroscopy can help to determine the molecular structure of the lipids
present in reconstructed skin models [82,83]. The lipid content and profile can
be evaluated by the extraction of lipids from total epidermis or stratum corneum
and analysis by high-performance thin-layer chromatography (HPTLC) [84–87],
whereas the functionality of reconstructed skin equivalents can also be examined
by techniques such as transepidermal water loss (TEWL) and percutaneous ab-
sorption.
Thirteen years ago, Ponec et al. [21] and Boddé et al. [20] investigated the
intercellular lipid structures and the lipid content of keratinocytes grown at the
air-liquid interface on de-epidermized dermis (DED). They found that the epider-
mal architecture was close to the in vivo situation, including the formation of
lamellar bodies and intercellular lipid lamella. However, unusual lipid structures
were observed locally between the corneocytes, and lamellar body structures were
abnormal. Although all lipid species that are present in native skin can be pro-
duced, the lipid composition, analyzed by thin-layer chromatography, differed
from that of human skin: Cultures contained significantly less linoleic acid
(18 :2) and significantly more oleic acid (18 :1) and palmitoleic acid (16:1), and
the triglyceride content was higher, whereas the content of glycosylceramides
and ceramides was lower compared with normal human skin [88]. These devia-
tions in lipid composition may induce the observed local imperfections and may
contribute to an impaired barrier function. The suggestion was that an improve-
ment of the lipid composition and a resulting improvement of the stratum cor-
neum barrier may be achieved by changing the culture conditions. This hypothe-
sis could be confirmed by different researchers. Mak et al. demonstrated that the
water permeability of reconstructed skin could be lowered by reduction of the
relative humidity in the environment, which possibly leads to a modulation in
lipid biosynthesis in the stratum corneum [88].
Ponec and her group examined whether the triglyceride accumulation in
the air-exposed cultures may be a result of an excessive supplementation of cells
with glucose. Lowering of the glucose content in the medium resulted in a de-
138 Black et al.
crease in lactate production and triglyceride synthesis, but the triglyceride content
remained still higher than in vivo, and the stratum corneum barrier function still
remained impaired [89]. Later, it could be shown that the high triglyceride content
is a consequence of EGF in the medium [71].
A clear improvement of lipid composition and an improved structural orga-
nization of the stratum corneum lipids could be obtained by using a fully defined
serum- and EGF-free medium and culturing the epidermis models on DED at
33°C [70]. Under these conditions, not only was the balance between cell prolifer-
ation and differentiation improved, resulting in an extension of the life span of
the cultures, but also the triglyceride content was low and similar to human skin,
and the amounts of ceramides and free fatty acids (FFA) were increased. This
may lead to a better solubilization of cholesterol and a reduction in the formation
of crystalline cholesterol in the intercellular spaces. Additionally, as seen by
small-angle x-ray scattering (SAXS), the structural organization of stratum
corneum lipids was markedly improved. Similar results with medium without
serum and no epidermal growth factor were seen using ATR-FTIR spectroscopy
[83].
Although the described attempts led to an improvement of the lipid profile,
the content of glycosylceramides still remained low, and the proportions of cera-
mide 4 to 7 were reduced, the largest reduction occuring in ceramides 6 and 7.
Starting from the point that the presence of ascorbate as a cofactor may be re-
quired for the hydroxylation of sphingoid bases and fatty acids, and antioxidants
may also be required to prevent lipid peroxidation during the enzymatic hydroxyl-
ation steps, supplementation of the medium with vitamin C and vitamin E was
performed [90]. As observed in the normalization of the lipid profile by high-
performance thin-layer chromatography (HPTLC), vitamin C plays a crucial role
in lipogenesis. Both glucosphingolipids (GSL) and the ceramide profiles were
normalized. The different GSL fractions (including acylglycosylceramides) and
ceramides 6 and 7 were synthesized in significant amounts in vitro. Vitamin E
alone did not show this effect. Adding vitamin C to the medium, the dermal
substrate used for the reconstruction of the epidermis was also not important
regarding the lipid composition: Whether using DED, inert filter fibroblast-
populated collagen matrix, or DED populated with fibroblasts, the overall lipid
profiles and the relative amount of ceramides were similar and close to those in
native epidermis [90].
Vitamin C improved additionally the epidermal morphology and the ultra-
structure of the stratum corneum as well as the stratum corneum lipid organization
(SAXS analysis). As in native epidermis, numerous lamellar bodies were present
in the stratum granulosum and excreted at the stratum granulosum/stratum cor-
neum interface. Lipid lamellae appeared with multiple alternating electron-dense
and electron-lucent bands. The number of intracellulary located lipid droplets
within the corneocytes was very low. Although great similarities in structure
between reconstructed and native skin was observed by electron microscopy,

there were still some differences in the SAXS pattern that were difficult to ex-
plain: only the long-range lipid lamellar phase was present; the short lamellar
phase, usually present in native skin, was missing. It was suggested that the des-
quamation process is involved in the regulation of stratum corneum lipid organi-
zation. Because this process is still impaired in reconstructed human skin, this
may lead to the deviations observed in SAXS analysis [90].
Up to now, the information concerning lipids in reconstructed skin is ob-
tained mainly from ‘‘in-house’’ models of reconstructed skin from the group of
Maria Ponec; the question is, therefore, whether the barrier function of other
Figure 14 Analysis of lipid profiles of normal human epidermis (HE) and Skinethic
epidermis model (with kind permission from Skinethic, Nice, France).
140 Black et al.
epidermis models is also close to the in vivo situation. Lipid content and profile
as well as the ultrastructure of the epidermis models EpiDerm, SkinEthic,
and Episkin were compared in a recently published study [87].
Lipid analysis revealed that the major skin barrier lipids are synthesized
in vitro but not in the same proportions as found in native skin (Fig. 14). The
content of free fatty acids, one of the major lipid fractions in the skin, was mostly
lower in reconstructed skin than in native skin. Lanosterol and cholesterol ester
were also found in lower amounts in reconstructed tissues, whereas the triglycer-
ide content was variable. The profile of glycosphingolipids and ceramides was
incomplete. The content of ceramides 5 and 6 was markedly reduced and the
most polar ceramide 7 was missing (Table 1). This may be the result of a lack
of ascorbic acid in the medium. Regarding the ultrastructure examined by electron
microscopy using ruthenium tetroxide as an additional fixative, all culture models
showed the unique organization of the characteristic alternating electron-dense
and electron-lucent lipid lamellae. However, this pattern did not exist throughout
the whole intercellular space. The stratum corneum in some Skinethic and in
most Episkin cultures was very compact, and multiple lipid droplets were seen
in the corneocytes, which were found only occasionally in Epiderm cultures
[87].
In conclusion, knowledge of the barrier function of reconstructed skin and
of lipids in the stratum corneum of these models has improved markedly during
the past years. Modulation of the culture conditions (lowering of temperature and
humidity) and of the medium conditions (no serum in the air-liquid interphase,
lowering of EGF and glucose, addition of vitamin C) has led to a nearly physio-
logical lipid profile. Although some deviations still exist in comparison to normal
Table 1 Ceramide Profile in Different Skin Models

Epidermis models
Native epidermis
% of total EpiDerm SkinEthic Episkin
ceramides (n ⫽ 5) (n ⫽ 4) (n ⫽ 3) (n ⫽ 6)
1 10.5 ⫾ 3.6 15.4 ⫾ 3.2 9.8 ⫾ 2.9 9.2 ⫾ 1.9

2 45.9 ⫾ 2.8 53.7 ⫾ 5.5 42.6 ⫾ 3.6 24.7 ⫾ 5.7
2a 12.6 ⫾ 3.9 2.4 ⫾ 2.4 16.7 ⫾ 4.2 2.7 ⫾2.3
3 15.1 ⫾ 2.6 18.8 ⫾ 3.7 23.8 ⫾ 2.6 21.7 ⫾ 0.5
4 4.5 ⫾ 0.6 3.5 ⫾ 1.6 3.0 ⫾ 1.4 4.8 ⫾ 1.1
5 8.9 ⫾ 1.8 4.7 ⫾ 1.3 3.4 ⫾ 1.8 20.9 ⫾ 0.3
6 2.4 ⫾ 0.6 1.4 ⫾ 0.5 0.6 ⫾ 0.4 5.7 ⫾ 0.5
7 0.0 ⫾ 0.0 0.0 ⫾ 0.0 0.0 ⫾ 0.0 10.3 ⫾ 0.8
Source: From Ref. 87.
human skin, reconstructed skin models are of excellent use in applied and fun-
damental research—e.g., as a model system for the study of the modulation of
lipid metabolism [91] as well as for pharmatoxicology and efficacy testing in
cosmetics.
VI. CONCLUSION
Tissue-engineered skin equivalents as alternatives to animal experimentation of-

fer not only a way to meet the demands of regulatory agencies, animal welfare
organizations, consumers, and scientists but also to provide a means to improve
and extend our knowledge of biological processes in the skin. This is particularly
important when the purpose of these studies is to extrapolate the results to hu-
mans. Progress in three-dimensional cell culture techniques has provided cocul-
ture models for growing keratinocytes, fibroblasts, melanocytes, endothelial cells,
and Langerhans cells. At this time, no validated and accepted model can accu-
rately replace animal experimentation, but alternative methods have evolved very
rapidly in the past few years, being a high scientific priority. In this respect,
human tissue engineered skin equivalents form promising alternatives, because
cells are of human origin and the equivalents closely resemble the tissue of origin.
Especially in regard to the stratum corneum, the lipid content and profile, and
the barrier function, the goal to achieve skin models that closely resemble human
skin has been nearly achieved by optimization of the culture medium and culture
conditions. Nevertheless, it has to be kept in mind that the lipid profile and the
organization of lipids in the stratum corneum of skin equivalents deviate in some
ways from human skin.
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88. Mak VHW, Cumpstone MB, Kennedy AH, Harmon CS, Guy RH, Potts RO. Barrier
function of human keratinocyte cultures grown at the air-liquid interface. J Invest
Dermatol 1991; 96:323–327.
89. Ponec M, Kempenaar J, Weerheim A, de Lannoy L, Kalkman I, Jansen H. Triglycer-
ide metabolism in human keratinocytes cultured at the air-liquid interface. Arch Der-
matol Res 1995; 287:723–730.
90. Ponec M, Weerheim A, Kempenaar J, Mulder A, Gooris GS, Bouwstra J, Mommaas
M. The formation of competent barrier lipids in reconstructed human epidermis re-
quires the presence of vitamin C. J Invest Dermatol 1997; 109:348–355.
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activated receptor-α enhances lipid metabolism in a skin equivalent model. J Invest
Dermatol 2000; 114:681–687.
6
Analytical Techniques for
Skin Lipids
Kristien De Paepe and Vera Rogiers
Vrije Universiteit Brussel, Brussels, Belgium
I. INTRODUCTION
The lipid lamellae of the intercellular spaces of the stratum corneum (SC) are
essential components of an adequate barrier function [1–3]. In combination with
the hydrolipidic layer—a water and oil mixture thought to cover part of the body
surface—the barrier lipids (i.e., ceramides, cholesterol, and free fatty acids
[FFAs]) prevent excessive transepidermal water loss (TEWL) and skin penetra-
tion of irritants and potentially harmful xenobiotics [4–6]. Because aged skin
displays an increased susceptibility to irritants and the water retention capacity
of surfactant-induced scaly skin is decreased, it has been hypothesized that
changes in barrier lipid composition or their physical structure may account for
these observations [7–11]. Furthermore, several skin disorders, such as atopic
dermatitis [12–14], lamellar ichthyosis [15–17], severe xerosis [18,19], and pso-
riasis [20–23], most likely can be attributed to abnormalities of the intercellular
lipids in the SC, which could be responsible for the functional disorders.
However, it still remains questionable whether the observed barrier func-
tion impairment is directly linked with changes in barrier lipid composition. A
general problem with reports in this field is the lack of background information
with respect to the many variables that could play a crucial role in the regulation
and modulation of the barrier lipid composition. Also, one should critically ana-
lyze the techniques used, because these often are complex, are not standardized,
and only provide semiquantitative results. In addition, skin sampling is not well
standardized, meaning that a variety of methods is used, including blister tech-
149
150 De Paepe and Rogiers
niques, skin strippings, surgical skin removal and in vivo lipid extractions. Fac-
tors affecting the barrier composition of the SC are given below.
II. FACTORS AFFECTING THE BARRIER COMPOSITION

OF THE SC
A. Age and Sex
Individual factors have been reported to play a role in barrier lipid composition,
such as age [9,11,24,25] and sex [9]. Although Denda et al. [9] showed sex differ-
ences in sphingolipid composition are a function of aging, it is now generally
acknowledged that there are no sex-related differences in barrier integrity or bar-
rier recovery [26,27].
With respect to age, conflicting data have been reported. These may result
from differences in sampling of SC lipids or from an incomplete assessment of
the lipid profile. Differences above the age of 50 [12,18,28] or 80 years have
been described [11]. Arguments for age-related differences are found in the obser-
vation that aged skin displays an altered drug permeability and an increased sus-
ceptibility to irritant contact dermatitis (ICD), suggesting an impaired epidermal
barrier function with an increased TEWL [11]. After solvent treatment or tape
stripping, the barrier recovered more slowly in aged than in young volunteers.
Also, xerosis is very common among the elderly. Its appearance changes ac-
cording to the season (winter xerosis), and it is more severe in a low-humidity
environment [25].
In various reports, decreases as a function of aging of the total SC lipid
content and, more specifically, of the ceramides, have been described [9–12,
19,24,25]. In one report, no correlation could be found between the SC lipid con-
tent and age or sex of the subjects [27]. Questionable, however, is that none of
these parameters was specified for the volunteers involved.
B. Anatomical Site
The measurement site on the body also is important because it has been shown
that regional anatomic variations in skin permeability are directly related to
SC lipid concentrations [19,25,29]. The differences in lipid weight found at four
sites (abdomen, leg, face and sole, see Table 1) were inversely proportional to
the permeability; also, a relationship with TEWL measurements was observed
[29,30]. In this respect, palms had the highest TEWL and the lowest lipid content,
whereas face samples revealed the opposite.
Analytical Techniques for Skin Lipids 151
Table 1 Regional Variation in Lipid Weight Percentage (wt %) of Human SC

Samples (Results expressed as mean values ⫾ SEM)
Site Abdomen Leg Face Plantar
Lipids (wt %) 6.5 ⫾ 0.5 4.3 ⫾ 0.8 7.2 ⫾ 0.4 2.0 ⫾ 0.6
SEM: standard error of the mean.
Source: Ref. 29.
C. Racial Factors
Skin type [26] and race [31,32] also seem to be reflected in the barrier lipid
concentrations. In a report published in 1959 [31], higher amounts of barrier
lipids in black than in white people were found, but these results were never
confirmed. Till today, data in the literature about race and phenotype were very
confusing and sometimes even conflicting. It is generally thought that racial dif-
ferences do exist at the level of the epidermal structure and function, but clear
evidence is hardly given. It is suggested that darkly pigmented skin displays a
more resistant barrier, which also recovers faster after mechanical perturbation
(tape stripping) [26,32]. However, when combining these observations with non-
invasive bioengineering measurements, such as TEWL, this type of conclusion
becomes problematic [33].
D. Dietary and Hormonal Factors

Except for essential fatty acid deficiencies (EFAD) [34,35], no hard data have
been found with respect to dietary influences or hormonal effects. Denda et al.
[9] suggested hormonal effects on epidermal lipid synthesis because the age-
related differences observed in SC lipid content were limited to women. Other
groups could not find any effect of the menstrual cycle on barrier integrity [26].
However, both Agner et al. [36] and Elsner et al. [37] reported about the changes
in skin sensitivity to irritation in relation to the menstrual status of women.
E. Medical Therapy
In some reports, skin effects by systemic treatment with hypocholesterolemic
drugs are discussed. Although local application of an inhibitor (e.g., lovastatin) of
hydroxymethylglutaryl CoA-reductase—the rate-limiting enzyme in cholesterol
synthesis—has been shown to delay barrier repair on murine skin [38], no effect
on the water permeability barrier of human skin was seen when statins were taken
orally [39,40].
Table 2 Summary of Weight Percentages of the Different SC Lipids of Healthy Human Skin
as Found by Different Research Groups (The numbering of the ceramide subgroups is according
to Wertz et al. [47]. If not indicated otherwise, values are expressed as a percentage of the total
lipids [mean ⫾ SD].)
Wertz
Wertz et Melnik et Lavrijsen and Wertz Yamamoto
al. 1985 al. 1989 et al. 1997 Downing 1996 Brod 1991 et al. 1991 Lampe et al. 1983
Author [47] [48] [49] 1991 [50] [3] [51] [13] [29]; Elias 1983 [52]
Forearm
skin
Forearm Plantar
Lipids skin skin a b NI NI NId Forearms Abdominald Legd Faced Plantard
Sphingolipids 30 ⫾ 3.5 18.2 ⫾ 2.8 25.9 ⫾ 1.3 26.5 ⫾ 0.9 34.8 ⫾ 2.1
Glycosylceramides 0.15 0 0.0 Traces 2.6 3.4 6.7 6.4
Ceramides 35.0 ⫾ 3.2 18.0 38.6 30 ⫾ 3.0 16.8 ⫾ 3.7 15.5 22.6 19.9 28.4
Cer 1 7.0 ⫾ 3.2 11.8 7.9 3.2 4.4 9.9 ⫾ 3.5
Cer 2 21.0 ⫾ 4.9 22.4 28.7 8.9 18.0 12.2 ⫾ 4.3
Cer 3 13.4 ⫾ 4.3 21.4 18.3 4.9 7.4 20.5 ⫾ 4.3
Cer 4 22.2 ⫾ 4.5 7.19 6.4 6.1 4.7 8.9 ⫾ 7.9
Cer 5 19.6 20.3 5.7 4.9 26.3 ⫾ 9.9
Cer 6I 9.8 ⫾ 1.1 6.4 5.9 12.3 8.2 21.9 ⫾ 4.0
Cer 6II 13.6 ⫾ 4.5 10.9 12.5
Phospholipids 5.0 3.2 ⫾ 1.1 1.95 0 ND 2.0 ⫾ 0.5 5.0 ⫾ 1.4 4.9 ⫾1.6 5.2 ⫾ 1.1 3.3 ⫾ 0.3 3.2 ⫾ 0.9
Cholesterol sulfate 3.2 1.8 ⫾ 0.7 1.4 1.1 1.9 1.5 ⫾ 0.4 3.2 ⫾ 0.6 1.5 ⫾ 0.2 6.0 ⫾ 0.9 2.7 ⫾ 0.3 3.4 ⫾ 1.2
Neutral lipids 35.1 66.0 ⫾ 2.8 77.7 ⫾ 5.6 65.7 ⫾ 1.8 66.4 ⫾ 1.4 60.4 ⫾ 0.9
Free sterols/
CHOL 14.9 28.9 ⫾ 3.6 10.9 16.8 26.9 28.0 32 ⫾ 2.5
14.9 ⫾ 2.8 14.0 ⫾ 1.1 20.1 ⫾ 2.0 17.3 ⫾ 0.5 32.8 ⫾ 1.6
FFA 8.0 19.2 ⫾ 3.5 7.1 13.0 9.1 14.1 20 ⫾ 2.0
8.0 ⫾ 4.9 19.3 ⫾ 3.7 13.9 ⫾ 1.8 19.7 ⫾ 0.6 9.0 ⫾ 1.7
DG/TG 9.1 3.5 ⫾ 1.4 50.4 13.4 0.0 2 ⫾ 0.5
9.1 ⫾ 2.1 25.2 ⫾ 4.6 20.1 ⫾ 1.0 13.5 ⫾ 1.0 5.9 ⫾ 0.6
Cholesterol esters 3.1 2.7 4 10.0 10 ⫾ 1.0
3.1 ⫾ 0.5
Sterol/wax esters 6.5 ⫾ 1.5 11.0 ⫾ 3.0 6.1 ⫾ 0.6 4.6 6.2 ⫾ 0.7 7.1 ⫾ 0.7
Squalene 0.2 ⫾ 0.1 2 ⫾ 0.5 21.3 ⫾ 6.2 6.5 ⫾ 2.0 3.6 6.9 ⫾ 0.3 2.9 ⫾ 1.8
n-Alkanes 1.7 ⫾ 1.3 3.3 7.0 3.7 ⫾ 0.5 3.0 2.8 ⫾ 0.3 2.9 ⫾ 1.0
Others 11.1 7.6
F. Environmental Factors
Environmental variables, including seasonal variations [25,41], exposure to UV
light [42], and the presence of sebaceous lipids [3,43] (see Sec. III.B.4), could
also affect the composition of the SC barrier lipids.
Winter xerosis is characterized by a scaly, rough, dry, and often itching
skin. In dermatology, the term is used for those conditions in which skin dryness
is more severe than commonly observed. Xerosis is especially frequent on the
lower legs. Only small changes in total SC lipid concentrations have been re-
ported, and no correlation has been found between cholesterol sulfate nor cera-
mides and the degree of non-eczematous dry skin [18,24,44]. However, in more
recent reports, a reduction in ceramides, and more precisely in ceramide 1 esteri-
fied with linoleate, was demonstrated in the winter months compared with the
summer period [25,41]. These results suggest that the SC is functionally inferior
Table 2 (Continued)
Imokawa Fulmer
et al. Lavrijsen Wertz Jass and Bonté et and Zellmer and Bonté et
1991 Paige et al. et al. 1992 Elias 1991 al. 1997 Kramer Lasch 1997 al. 1995
[12] 1994 [16] 1994 [53] [54] [30] [55] Long et al. 1985 [56] 1986 [57] [27] [58]
Forearm
skin Forearm skin
Forearm Lower
Arms Lower legse skin Leg skin Abdominal f g Intact SC Squamated legsh Plantar skin j k
24.4 ⫾ 3.8
0–1.3 0 traces ND ND ND ND
20.0 22.3 ⫾ 2.80 5.3–36.4 38 24.4 ⫾ 3.8 18.8 31.7 41.8 ⫾ 3.5 20.25 ⫾ 0.67 19.5 17.9
1.7 2.67 ⫹ 1.13 6.2 ⫾ 2.8 5.3 ⫾ 1.7 5.0 ⫾ 0.6
4.20 8.24 ⫾ 2.03 18.5 ⫾ 4.3 19.7 ⫾ 6.2 8.2 ⫾ 0.7
3.96 5.99 ⫾ 1.44 11.8 ⫾ 3.8 8.2 ⫾ 1.4 8.0 ⫾ 0.8
5.24 7.14 ⫾ 1.65 19.5 ⫾ 4.0 25.6 ⫾ 7.6 10.9 ⫾ 0.9
9.2 ⫾ 0.9
4.88 7.84 ⫾ 2.22 8.6 ⫾ 1.0 14.2 ⫾ 2.5
23.8 ⫾ 5.4 23.6 ⫾ 3.1
0–6.6 0 6.6 ⫾ 2.2 7.3 12.2 Traces 12.6 7.0
0.3–2.9 0 2.0 ⫾ 0.3 1.5 2.4 12.0 ⫾ 4.0 3.5 ⫾ 1.5 2.06 ⫾ 0.13 1.2 1.7
66.9 ⫾ 4.8
4.8–23.6 21.6 18.9 ⫾ 1.5 7.3 12.2 23.7 ⫾ 1.4 43.53 ⫾ 3.04 13.5 5.9
2.4–12.3 23 26.0 ⫾ 5.0 18.8 31.7 25.3 ⫾ 2.3 20.16 ⫾ 1.12 16.1 6.8
10.5–75.9 8.1 variable 11.6 NI 8.9 ⫾ 1.5 4.56 ⫾ 0.54
1.9–11.9 9.3 5.8 9.8 10.2 ⫾ 0.9 9.44 ⫾ 0.67 8.1 6.5
7.3 ⫾ 1.2 21.7 NI 11.0 47.3
0–0.2 6.5 ⫾ 2.7 7.3 NI 18.0 6.9
1.3–5.1 8.2 ⫾ 3.5
CHOL: cholesterol.
FFA: free fatty acids.
DG/TG: di-/triglycerides.
NI: not indicated.
ND: not detected.
a
Integral lipid extraction of SC with CHCl3 /MeOH (1 :2) (median values).
b
Topical lipid extraction with acetone/diethyl ether (1 :1).
c
Together they account for ⫾10% of the total lipid amount.
d
Mean values ⫾ SEM.
e
µg Ceramide/mg SC ⫾ SD.
f
% Total lipids with sebum.
g
% Total lipids without sebum.
h
ng Lipid/µg protein ⫾ SEM.
i
Detected but not quantified.
j
Mammary SC.
k
In vivo extraction of forearm skin.
during the winter season. This type of xerosis is not always correlated with a
significant decrease in the SC water content. It is thus better to talk about ‘‘rough
skin’’ instead of ‘‘dry skin,’’ especially since it is known that a decrease of the
sebum function occurs [18,35]. Moreover, Saint-Léger et al. [44] found that a
decreased amount of neutral lipids (sterol esters and triglycerides) together with
higher amounts of FFA (increased esterase activity) was associated with the se-
verity of rough skin.
G. UV Irradiation
As long as UV irradiation occurred at suberythemal doses, increases in the
amount of SC lipids and improvement of barrier function were observed [42].
This explains the beneficial effects of phototherapy on atopic skin. Lamellar body
content extrusion was improved, as was their conversion into lipid lamellae in
the SC [45]. However, high UV doses above the suberythemal level caused bar-
rier damage characterized by inflammation and scaliness of the skin with a con-
comitant increase in TEWL [42].
H. Expression of Results Obtained from Lipid Analysis

Table 2 gives an overview of the different SC lipids of healthy human skin as
found by various research groups. As already mentioned, the large variation
found between the different lipid components is most likely due to differences
in extraction procedure and efficiency, lipid analysis protocols, and sampling
location. Not all authors give a complete concentration profile of the main SC
lipid components (Table 2). The lack of total percentage of sphingolipids or neu-
tral lipids makes comparison between different publications even more difficult.
It is also important to notice that the quantitative expression of the results
is not uniform. Individual concentrations of skin lipids may be expressed as a
percentage of the total lipids or skin proteins. Expression as a percentage of the
epidermal or SC weight (dry versus wet weight) also is an option. In the case
of in vivo extractions, the total amount of lipids yielded after evaporation of the
extraction solvents may even be expressed versus the skin surface (in square
centimeters) involved [46].
III. ANALYTICAL TECHNIQUES TO DETERMINE SKIN

BARRIER LIPIDS
A. Sources of Skin Samples
Most skin sampling techniques are invasive. Apart from in vivo skin extractions
(see Sec. III.B.2) [46,47,53,58], skin samples can be obtained from biopsies after
surgery [21,22,29,57,59,60], tape stripping [14,19,53,61], or induced skin blisters

[62–66]. Also, SC sample collection by repeated scraping of the skin with a
single-edged razor blade [27,53] and a standardized shaving technique [48,57,67]
have been described.
When human skin samples are collected, the investigator has the responsi-
bility to ask the local ethics committee or other authorized instances for approval
of the protocols involved. Guidelines such as those developed for skin irritation
and contact allergy testing should be followed [68]. It is also important that all
volunteers provide signed informed consent. When healthy human skin is studied,
only volunteers with no skin pathologies, as diagnosed by a dermatologist super-
vising the experiments, should enter the study. Exclusion criteria should be stated,
and variables, including age, sex, medical history, and every parameter of poten-
tial importance for the study under consideration, should be noted. In several
cases, it is advisable to work with a homogeneous test population.
1. Ex Vivo Biopsies
When obtained during cosmetic or general surgery (e.g., breast, abdominal or
facial skin), full-thickness skin samples (ex vivo) should be transported as soon
as possible to the analyzing laboratory. This can be done in sterile medium (T-
medium) containing 10 µg gentamycin/ml PBS (phosphate buffered saline) solu-
tion [69]. When extraction is done directly, dry transportation is also possible.
In the latter case, skin samples should be properly spread out in appropriate recipi-
ents (e.g., Petri dish) to avoid contamination of the upper skin layers by lipids
from the adipose tissue.
Attention should be paid that, before handling, appropriate safety tests with
respect to bacterial and viral infections have been carried out. When not otherwise
specified in the protocol, skin samples should be obtained from areas free from
diseases or infections. It is also important that no scars or abrasions are present
and that the samples are relatively hairless [29].
2. Tape Stripping
Tape stripping techniques have gained popularity during the past few years.
Current protocols can be divided into two groups. The first one makes use of
lipid-free glass slide strips with one or two droplets of cyanoacrylate resin (e.g.
LocTite Superglue-5, Kreglinger-Loctite NV, Antwerp, Belgium or Bison
Super-colle, Perfecta Chemie, Goes, The Netherlands) [12,14,70].
In the second group, a number of adhesive tapes (Tesafilm-Leukoflex,
Beiersdorf, Germany; Scotch tape 3M or D-Squame, CuDerm Corporation,
Dallas, TX, USA) are consecutively applied to and removed from the skin
[19,41,53,55,71]. For both techniques, it seems important that a constant, repro-
ducible pressure is used when the strips are applied on the skin.
In the case of cyanoacrylate resin, a single strip (applied for 45 to 60 sec)

should be sufficient to remove the complete SC (⫾ 10 µm); for adhesive tapes,
15 to 20 strippings are needed (see also Sec. III.B.3) [53]. Imokawa and cowork-
ers [12] showed by histological biopsies that only 5 to 10 SC layers were stripped
when cyanoacrylate resin was used. Although under appropriate conditions both
techniques can remove the same amount of SC layers and lipid material, the
cyanoacrylate resin protocol seems to be less acceptable to the volunteers.
The amount of SC removed by stripping is not linearly proportional to the
number of strips removed [58,72]. This lack of correlation is even more pro-
nounced when inter- and intra-individual differences in anatomical regions are
studied.
Because tape stripping methods lead to significant increases in water loss
through the upper layers of the skin, transepidermal water loss (TEWL) measure-
ments can be used for the assessment of the degree of barrier perturbation [33].
TEWL, however, does not give any idea about the amount of SC that has been
removed. Barrier disruption is followed by a cascade of metabolic responses in
the viable epidermis, including the secretion of newly formed lamellar bodies.
Within 1 hr to 6 days, the physiological barrier repair process is completed
[73,74].
To quantify the stripped material, weighing of each single strip is com-
monly performed [55] (see also Sec. III.B.3) but it is rather labor intensive and
time-consuming. Some commercially available tapes are hygroscopic, making
proper weighing procedures even more complex. Therefore, Marttin and cowork-
ers [72] proposed an easier and faster method using spectrophotometric examina-
tion (at 278 nm) of the proteins present on the tape. Although less reliable (larger
variability), this technique revealed that light absorption correlated to the weight
of the SC material (see also Sec. III.C.4). An advantage of the latter method is
that the homogeneity of the individual strips can be examined.
3. Skin Blisters
An alternative to tape stripping, especially when the whole epidermis (⫾ 100
µm thick) needs to be collected, is the blister technique. Originally, the blister
method was developed to separate epidermis from dermis by mechanical force
only, avoiding chemical and thermal damage [62,63].
A negative pressure gradient is applied, provoking a multidirectional exten-
sion leading to a separation of the two skin compartments at the dermo-epidermal
junction. This basal membrane zone is attached with hemidesmosomes to the
epidermis and with a network of fibers to the dermis, resulting in a tight junction
responsible for several interactions between both skin layers (reviewed in [75]).
By electron microscopy, three structured layers are visible between epidermis
and dermis: the lamina lucida, the lamina densa, and finally the sublamina densa.
In vivo blistering can also be induced by exposing the skin to liquid nitrogen for
20 to 25 sec. This method is useful when small samples are required—for in-
stance, from the dorsal side of the hands or fingers [76].
An example of a commercially available device with a special dome-shaped
cap, made of Plexiglass, is Dermovac (Instrumentarium Corp., Helsinki, Fin-
land.) In a typical in vivo blister experiment, a suction of about 200 mmHg
(0.263 Pa) below the atmospheric pressure is applied consistently. The diameter
of the blister depends on the holes in the cap that is attached to the skin. The
applied pressure induces a suction power that increases the tension on the cell
junctions, which eventually will—in normal individuals—tear off the epidermis
at the level of the lamina lucida. The basal cell layer of the epidermis is still
intact, allowing self-regeneration of the epidermis. Normally, it takes 2 to 3 hr
to induce blister formation. Around 50 to 150 µl suction blister fluid is present,
and the SC as well as the underlying viable epidermis can be harvested. Clear
blister fluid roughly corresponds to interstitial fluid. Suction blister fluid is free
of white cells for the first 5 hr. Thereafter, few polymorphonuclear leukocytes
appear. The protein content of suction blisters is 60–70% of the corresponding
serum value. In diseased skin, blisters cannot be raised properly and, as seen in
some skin pathologies, externally applied suction may induce basal cell cytolysis
[65]. Consequently, secretion of fluid into the capsule with and without bursting
of the blister roof is observed. Standardization of the blister technique in diseased
skin has, as far as we know, not been established.
In Table 3, a chronological overview of the mechanical blister techniques
performed on human skin is described. The blister technique is based on an old
methodology, and therefore the basic literature goes back to the early 1960s. More
recent publications still use those basic principles and describe the applicability of
the blister technique in various biochemical and grafting studies [64,80]. Also,
the epidermal blister roof, which is not contaminated by fibroblasts and other
dermal cells, provides cell material for epidermal cell cultures [62].
Epidermal recovery follows blister formation. This occurs without the use
of external applied products; however, the latter could improve faster skin re-
pairment [82]. After removal of the blister roof, the existing disruption needs to
heal and partial epithelization is reported after 4 or 5 days [81]. The healing
period is very person-dependent, but usually epithelization is completed within
2 to 3 weeks [80,81]. Although blister techniques are mainly described as being
painless and without permanent scar formation [80,81], skin pigmentation distur-
bances may occur and remain visible for 2 to 12 months [64,80,83]. This is one
of the reasons why volunteers need to be properly informed before they give
their written consent. Individuals with a known medical history of bad wound
healing may not be included in this type of experiment.
Kiistala [63] investigated a number of parameters that could be important
for the induction of blisters. He reported that the induction time—for the same
158
Table 3 Overview of Variables Occurring During In Vivo Blister Induction in Humans (Suction blister time indicates the period
between the application of the pressure gradient and the appearance of the first vesicles.)
Anatomical φ
Authors site (mm) mmHg Time Apparatus Recovery Advantages Disadvantages
Kiistala & Mustakallio 1964 [77] Chest 20 200 ⬍2 h Angiosterrometer NI NI NI

Kiistala 1968 [62] Chest, Abdomen 5–70 150–200 ⬍3 h Dermovac NI NI NI
Kiistala 1972 [63] Ventral forearm
*Kariniemi et al. 1980 [78] Abdomen 5 200 2h NI NI NI NI
Fernandes et al. 1985 [79] Ventral forearm 8 400 105 min Gelman vacuum pump NI NI Intradermal bleedings
Suvanprakorn et al. 1985 [80] Different body sites NI 200–500 1–2 h NI Re-pigmentation Painless, no scars Hyper-pigmentation,
(Hand, foot, neck) (Site depended) After 7–14 days,
completed after
28–95 days
Michiyuki 1988 [64] Abdomen, tights 20 200 3–4 h Oil rotary Normalization of No scars Risk of loss of
Vacuum pump pigmentation after pigmentation, or
6 months hyper-pigmentation
Willsteed et al. 1990 [76] Ventral forearm 5 200 90–120 min NI NI NI NI
Taylor et al. 1993 [65] Ventral forearm 6 200 ⫾90 min Eschmann VP50 NI NI NI
†Kallioinen et al. 1995 [81] Abdomen 20 200 ⬍2 h Angiosterrometer Partial epithelization after NI NI
4–5 days, completed
after 9 days
Grönneberg et al. 1996 [82] Ventral forearm 9 300 2–3 h Negative pressure NI NI NI
De Paepe and Rogiers

at 39°C Suction system
*Haapasaari et al. 1997 [66] Abdomen 5–70 150–200 ⬍3 h Dermovac NI NI NI
Shukuwa et al. 1997 [83] Ventral forearm 8 1520 11/2 –2 h Hand vacuum pump NI No scars, painless Hyper-pigmentation
(Meward Enterprise)
NI ⫽ not indicated
* according to Kiistala 1968 [62]
† according to Kiistala and Mustakallio 1964 [77]
pressure applied—was significantly decreased above the age of 30 years. The

latter probably was due to the age-dependent decrease in cohesion between epi-
dermis and dermis. From that age on, no sex-related differences were observed.
However, in younger volunteers, females showed more resistance on mechanical
epidermal rupture than males did. This was explained as women having a more
elastic skin compared to age-matched male subjects. Nowadays, this explanation
is doubtful, and clear evidence is still lacking, especially because the elastic prop-
erties of the skin are mainly provided by the underlying dermis and not by the
epidermis nor SC (reviewed in [75]). Kiistala [63] also reported differences in
blister induction as a function of anatomical body site (chest, abdomen, ventral
forearm). Abdominal skin was shown to exhibit the lowest blister time.
4. In vitro Models
Lipid extracts can also be obtained from cultures of human epidermal keratino-
cytes [84,85]. Cultured skin equivalents are being used not only for transplanta-
tion and treatment of severe skin ulcers but also for toxicity studies and research
of potential skin irritants [86].
Conventional monolayer cultures of human skin cells (keratinocytes, fi-
broblasts) have their origin in the late 1970s [87,88]. Keratinocytes were plated
on plastic or on collagen-coated dishes. Disadvantages were an incomplete differ-
entiation and the absence of SC [89]. In the past two decades, successful attempts
have been made to develop keratinocyte cultures that are morphologically equiva-
lent to the native epidermis. These skin equivalents are three-dimensional struc-
tures based on the recombination of cultured cells to approach the skin tissue
more closely. Skin equivalents are generated by seeding normal human keratino-
cytes on an appropriate dermal substrate and culturing them at the air-liquid inter-
face [90]. Dermal substrates may consist of different materials of biological or
artificial origin and can be either cell-free or populated with fibroblasts. Under
the air-exposed culture conditions, the keratinocytes undergo complete terminal
differentiation that also results in the formation of a corneous layer. Only air-
lifted skin cultures have been proposed as having a functional permeability barrier
[90,91].
Commercially available three-dimensional human skin models comprising
a reconstructed epidermis with a functional SC are SkinEthic (SkinEthic Labo-
ratories, Nice, France) and EpiDerm (MatTek Corporation, Ashland, MA,
USA). Both models are lacking the dermis and consist of keratinocytes cultured
on an inert filter (e.g., cellulose acetate). The type of reconstructed skin experi-
mentally used depends on the requirements of the protocol under investigation.
Also EpiSkin (owned by L’Oréal, Paris, France) is an epidermis model recon-
structed on a collagen matrix. In addition to keratinocytes, the main cell types in
the epidermis, melanocytes [92] and Langerhans cells [93], can be incorporated.
An actual problem of these laboratory-made skin models, which do not contain

any blood vessels, is their short life span. Most of the time they can not be kept
alive for longer than one month [86,90].
In these so-called air-exposed keratinocyte cultures, all typical in vivo dif-
ferentiation markers can be observed at the ultrastructural level, including desmo-
somes, keratohyalin granules, lamellar bodies, and the intercellular lipid struc-
tures [91,94].
Some abnormalities in the expression of several specific protein markers
and disturbances at the level of the lipid composition still reflect deficiencies in
the quality and barrier properties of various in vitro skin equivalents (reviewed in
[89,94]). Lower contents of certain sphingolipids and the free fatty acids (FFAs),
linoleic and arachidonic acid, were reported [95]. Also, normal desquamation did
not take place, revealing the occurrence of impaired cell shedding [91,96,97].
B. Lipid Extraction
Various extraction protocols have been reported and there is not yet a clear agree-
ment which technique should be preferably used. Out of our own experience
there is, however, no doubt that the composition of the solvent mixtures, the
number of extraction steps, the polarity of the solvents, and many other factors
will have a tremendous effect on the quantitative outcome of the lipid analysis.
1. Ex vivo Biopsies and in vitro Skin Models

When lipids are extracted from biological samples (biopsies or blistered skin) or
from reconstructed skin, the classic approach is the use of a mixture of chloroform
(CHCl3) and methanol (MeOH) according to a modified Folch et al. [98] or Bligh-
Dyer [95] method [16,27,29,48,53,54,57,59,60,84,100,101]. In Figure 1, the ex-
traction procedure used in our laboratory and partially based on the method pub-
lished by Ponec and Weerheim [95], is given [102].
Other solvent mixtures used for the extraction of skin lipids from tissue
samples are n-hexane/MeOH 2:3 (v/v) [44,58].
It is important that all solvents used for extraction are of chromatographic
grade (e.g., pro analysis (pa) solvents). The recipients used to collect the extracted
lipids should be made of glass with Teflon inlays for the screw caps. The superna-
tants need to be transferred with glass pipettes to avoid any possible contamina-
tion with components extracted from various plastic materials.
After evaporation of the solvent mixture, the total amount of the extracted
lipids can be weighed on a micro balance (e.g., Type M5 SA, MT5, AT20 (2–
20 µg), Mettler Instrument AG, Zürich, Switzerland). To allow inter-person com-
parisons, the mass of each lipid fraction, as determined after lipid separation, can
Figure 1 Flow diagram for sequential extraction of human skin lipids.

a
For the extraction of the total epidermal lipids this preparative step is not carried out.
b
Addition of KCl is done to ensure extraction of the polar cholesterol sulfate into the organic phase.
c
Filtered through Whatman n°43.
be normalized to the total lipid amount of either the epidermis or the SC. The
pellet is used for the determination of the protein concentration [103].
2. In vivo Extractions
Due to their toxicological profile and skin aggression, CHCl3 and MeOH cannot
be used for the in vivo collection of SC lipids [104]. Even by using light micros-
copy, it could be shown that CHCl3 /MeOH induces cell damage in the living
epidermal cell layers [53].
Also n-hexane/MeOH 2 : 3 (v/v), as used by Saint-Léger et al. [44], was
not an option because exhaustive lipid extractions went together with severe skin
irritation. Cyclohexane/ethanol 2 :8 (v/v) was alternatively used [58].
To overcome this problem, various in vivo sampling extraction procedures
have been developed, including the use of pure acetone [31], ethanol 95%
[13,47,56], n-hexane/isopropanol 3 : 2 (v/v) [105,106], ethanol/diethyl ether 3 :1
(v/v) [42,67], and a mixture of acetone/diethyl ether 1 :1 (v/v) [12,46,53]. The
latter solvent mixture was used during two consecutive extraction steps of 5 and
25 minutes, respectively. Proper validation showed that it was a suitable extrac-
tion protocol to study SC lipid profiles, even in various skin disorders [53].
To bring extraction solvents in contact with the skin, a precleaned glass or
stainless metal cylinder [46,47,53] is applied and held properly in position to
prevent lateral leakage. The extraction can be split up in two consecutive steps,
having the advantage that with the first short step, the exogenous lipids as well
as the lipids of the hydrolipidic mixture can be largely removed. The second step
then collects the barrier lipids [53]. Sebaceous lipid contamination can also be
avoided by washing the skin with a cotton swab drenched in cyclohexane [106]
or by removal of the upper two horny cell layers by tape stripping [42].
Sequential application of either acetone or petroleum ether, utilizing pre-
cleaned (delipidized) cotton swabs followed by an extraction of the pooled swabs
by a Bligh-Dyer method, has been described only for murine skin [1]. Extraction
of human skin lipids by pure acetone [31] dissolves the hydrolipidic mixture and,
being a nonpolar solvent, selectively removes only a limited amount of some
superficial skin lipids [46]. After acetone treatment of the skin, no irregularities
have been reported at the level of the lamellar bodies, and physiological barrier
repair occurred without delay [107].
3. Extraction of Tape Strippings

CHCl3 /MeOH mixtures cannot be used for tape stripping extraction because of
contamination by the adhesive material. For cyanoacrylate resin, a smear of the
lipid bands occurs during chromatographic separation, making identification and
quantitative determination of the samples impossible [55,70].
Extraction with n-hexane/ethanol 95:5 (v/v) under ultrasonication, fol-
lowed by filtration through a solvent-resistant filter (e.g., Millex-SR, Millipore
0.2–0.5 µm, Molsheim, France or Whatman filters n°1 or 43, Whatman Ltd,
UK), has been reported by Imokawa et al. [7,12] and Di Nardo et al. [14] for
cyanoacrylate strippings. After solvent evaporation under N2, the samples were
redissolved in CHCl3 /MeOH 2 :1 (v/v) and kept stored at ⫺20°C before use.
When extracted lipids (µg) are expressed per milligram of SC, the residue
on the glass slide, composed of SC and cyanoacrylate resin, can be ultrasonicated

with dimethyl formamide (DMF) [12,14]. Consequently, the cyanoacrylate resin
is solubilized, while the dispersed SC can be separated from the DMF solution
by filtration. Finally, the residue on the filter is washed (DMF / MeOH), dried
under vacuum, and weighed.
Other research groups have used different extraction protocols, which can
be summarized as follows:
A pre-extraction step with MeOH (sonication), followed by a conventional
CHCl3 /MeOH extraction [19,41]
A two-step extraction with cyclohexane/ethanol 2 :8 and 5 :5 (v/v) [55,58]
A one-hour extraction in ethyl acetate/MeOH 60: 40 (v/v) [61].
4. Factors Affecting SC Lipid Profiles During Extraction

As already emphasized, the collection method of the lipid samples can have a
tremendous effect on the outcome of the lipid concentrations measured, making
comparison of reported data difficult. Indeed, in some methods whole epidermis
is collected (blisters, ex vivo biopsies); in other methods, only surface lipids or
superficial SC lipids are harvested. Also, the SC is not uniform across its entire
thickness, which can be at the origin of the collection of a non–properly defined
part of the SC in the case of tape stripping.
From results shown in Table 4 it is clear that, depending on the location
in the epidermis, a different lipid profile in weight percentage (wt%) is found as
a function of epidermal differentiation and cornification [52,59]. Also, Bonté et
al. [55] showed that the lipid gradient observed in the upper SC could be linked
with the number of tape strippings. For the assessment of the main barrier lipids
(i.e., ceramides, cholesterol, FFAs), collection of the SC layers is sufficient, im-
plying a tape stripping procedure of 15 to 25 strips or a trypsinization treatment
of epidermal samples (biopsies, skin blisters) [53,55].
Apart from the origin of the lipid samples, one cannot avoid that some
contamination occurs by exogenous lipids [108] and lipids originating from the
sebaceous glands [3]. A counter argument for the latter was reported by Lampe
et al. [29], who showed measurable quantities of squalene and wax esters in
plantar SC (Table 2). The sole is depleted of sebaceous glands, so these nonpolar
lipids could not be of sebaceous origin. A consecutive study of Lampe et al. [59]
showed that squalene and n-alkanes are evenly distributed in the viable epidermal
layers (Table 4), suggesting that they are not simply of sebaceous or environmen-
tal origin. Also, Williams and Elias [109] excluded all possible sources of con-
taminations and still found representative levels of n-alkanes. High quantities of
squalene, however, could reflect a high level of cholesterol metabolism in the
epidermis. So, one still has to be very critical when analyzing the lipid profiles
obtained.
Table 4 Variations in Lipid Composition During Epidermal Differentiation

and Cornification (Samples obtained from abdominal skin.)
Stratum basale/ Stratum Stratum
spinosum granulosum corneum
Lipids (wt %)a (wt %)a (wt %)a
Sphingolipids 7.3 ⫾ 1.0 11.7 ⫾ 2.7 18.2 ⫾ 2.8
Glycosylceramides 3.5 ⫾ 0.3 5.8 ⫾ 0.2 Traces
Ceramides 3.8 ⫾ 0.2 8.8 ⫾ 0.2 18.1 ⫾ 0.4
Phospholipids 44.5 ⫾ 3.4 25.3 ⫾ 2.6 4.9 ⫾ 1.6
Cholesterol sulfate 2.6 ⫾ 3.4 5.5 ⫾ 1.3 1.5 ⫾ 0.2
Neutral lipids 51.0 ⫾ 4.5 56.5 ⫾ 2.8 77.7 ⫾ 5.6
Free sterols/CHOL 11.2 ⫾ 1.7 11.5 ⫾ 1.1 14.0 ⫾ 1.1
FFA 7.0 ⫾ 2.1 9.2 ⫾ 1.5 19.3 ⫾ 3.7
DG/TG 12.4 ⫾ 2.9 24.7 ⫾ 4.0 25.2 ⫾ 4.6
Sterol/wax estersb 5.3 ⫾ 1.3 4.7 ⫾ 0.7 6.1 ⫾ 0.6
Squalene 4.9 ⫾ 1.1 4.6 ⫾ 1.0 6.5 ⫾ 2.0
n-Alkanes 3.9 ⫾ 0.3 3.8 ⫾ 0.8 3.7 ⫾ 0.5
TOTAL 99.1 101.1 99.3
a
Weight percentage (wt%) mean ⫾ SEM.
b
Sterol/wax esters present in approximately equal quantities as determined by acid hydrolysis (12%
borontrichloride in MeOH for 30 min at 90°C).
Source: Refs 52, 59.
An overall finding was that the total amount of lipids, extracted by using
topical in vivo extraction procedures, was lower than that found by integral ex-
traction of the SC [53] (see also Table 2). Questions to be answered included:
‘‘To what depth does in vivo extraction with mainly acetone/diethyl ether remove
lipids? What proportion of the SC lipids is extracted? Do the extracted lipid
classes reflect the overall SC lipid profile?’’ These questions were tackled by
Lavrijsen and coworkers [53], and they showed indeed that in vivo extraction
procedures did not remove significant amounts of lipids from the lower layers
of the SC or the epidermis, but that it was possible to collect a representative
ceramide profile. Thus, although the total lipid profile was not completely recov-
ered, the assessment of the main barrier lipids was satisfactory.
Although studies were sometimes based on only a few samples, several
authors have shown a great inter-individual variation in the overall lipid composi-
tion of the skin barrier [71,86]. The latter was irrespective of the extraction proto-
col used. However, ceramide profiles from different skin samples taken from the
same subject were similar. This profile uniformity was also found between differ-
ent subjects [53]. In addition, Norlén et al. [106] showed that the long-chain
FFAs of the SC were a stable, uniform lipid group, with a low inter-individual
variation, dominated by saturated lignoceric (C24 :0) and hexacosanoic acid
(C26 :0).
To control the inter-individual variations, it is of utmost importance to stan-
dardize the site and area of extraction in a homogeneous population (age, sex,
phototype, lifestyle). In case of tape stripping, time and applied pressure should
also be controlled (see Sec. III.A.2) [86].
In extraction studies, TEWL measurements have often been included to
assess the amount of water loss through the upper skin layers [21]. A direct
relationship between the efficiency of the barrier to water loss and the total lipid
weight percentage has been shown [1]. Consequently TEWL can be used as a
parameter to reflect the degree of barrier impairment after solvent extraction [46]
or tape stripping [53].
C. Lipid Analysis
In order to study epidermal barrier physiology, skin disorders, and barrier recov-
ery, a rapid and accurate analysis technique of the epidermal lipids is necessary.
The latter can be derived either from human biopsies, in vivo extractions, and
tissue culture specimens [48]. The lipid amounts in SC—especially in damaged
skin—are low, so sensitive techniques must be developed.
The most commonly used techniques are chromatographic methods such
as thin-layer chromatography for total lipid determination and ceramide profiles
(C.1) followed by gas chromatography, more specific for the quantification of
FFA, combined with mass spectrometry (C.2). Recently, Norlén and coworkers
were able to develop a high-performance liquid-chromatography (HPLC)/light
scattering detection (LSD)–based analysis method for the quantitative determina-
tion of skin lipids (C.3) [71,106]. Also spectrophotometric techniques (C.4) can
be used for individual lipid components and overall skin barrier characterization.
An overview of the various analytical techniques for qualitative and quanti-
tative lipid determination is available in a number of comprehensive books [110–
112]. This chapter does not have the intention to repeat this work, but for some
of the techniques (TLC, HPLC, GLC/MS), attention will be focused on their
relevance for extracted skin lipids. Apart from a short summary of the required
methodology, emphasis will be put on some pitfalls, and practical hints will be
given for experimental protocols and study designs.
1. Thin-Layer Adsorption Chromatography (TLC)

For a complete introduction to TLC and a full description of the analytical tech-
nique, the standard works of Jork and coworkers [113,114] are recommended.
One-dimensional high-performance thin-layer chromatography (HPTLC) is fre-
quently used. It is a suitable and easy-handling method for the separation of

individual epidermal lipid classes, based on their differences in mobility in a
system of two phases [34,47,48,95]. Besides a rapid screening, this technique
also enables an accurate quantitative determination of the different lipid classes.
Two-dimensional HPTLC has the advantages of exhibiting a higher resolu-
tion and allowing a faster identification of a great variety of individual lipid frac-
tions. For quantitative purposes, however, it is not very practical [95].
Standard lipids. Pure lipid standards, all of the highest purity available
are needed (e.g., Sigma, St. Louis, MO, USA). They usually include Cer type
III, Cer type IV, cerebrosides, trioleine representative for the triglycerides (TG),
oleic or stearic acid as FFA, cholesterol (CHOL), cholesterol oleate as cholesterol
ester (CE), and cholesterol sulfate (CSO4). Pentacosane, as a marker for n-alkanes
(ALK), and squalene (SQ) are often incorporated.
These lipids are dissolved in CHCl3 /MeOH 2 : 1 (v/v) and are used to pro-
duce calibration curves necessary to identify and quantify unknown skin samples.
Lipid standard mixtures mostly contain 100 ng to 2 µg of each lipid fraction.
However, for preparative HPTLC development, much higher individual amounts
are applied, ranging from 5 to 15 µg [115].
Because large differences exist in the mass of individual epidermal frac-
tions and peak areas are not always a linear function of lipid weight, several
increasing quantities of the standard mixture are applied [19,27,95].
Thin-layer Plates. The most commonly used TLC plates are precoated
silicagel 60 HPTLC plates without concentration zone (size 10 ⫻ 10 cm, 20 ⫻
10 cm, 20 ⫻ 20 cm; e.g., Merck, Darmstadt, Germany). The advantages of
HPTLC plates is that much lesser amounts of total lipid extracts (10–20 µg) are
required compared to ordinary TLC plates (2–3 mg), still allowing proper separa-
tion of the different lipid fractions [48].
In order to remove impurities that may interfere with lipid separation, the
plates are first washed in CHCl3 /MeOH/H2O/glacial acetic acid 120: 70 :9 : 1 (v/v/
v/v) [21] or in MeOH/ethyl acetate 60 :40 (v/v) [95], sometimes followed by a
second wash with CHCl3 /ethyl acetate/diethyl ether 30 : 20: 50 (v/v/v). After evapo-
ration of all solvents, the HPTLC plates are activated for 10 min at 130°C. Heating
can be done on commercially available heating plates (e.g., TLC Plate Heater III,
Camag, Muttenz, Switzerland or Heat Plate, Desaga, Wiesloch, Germany).
Application of Samples and Lipid Standards. Starting at a height of ap-
proximately 5 mm above the bottom edge of the plate, increasing volumes of
the lipid extracts are applied as narrow bands (3 mm or broader) at a constant
distance of about 5 mm from each other. For this purpose, automatic appliers
can be used (e.g., Linomat IV or Automatic TLC Sampler 4 (ATS4), Camag,
Muttenz, Switzerland or TLC-Applicator AS 30, Desaga, Wiesloch, Germany)
or appropriate manual syringes. The advantages of those appliers are easy-

handling and an accurate dot- or line-application, according to the spray-on
technique. For calibration reasons, it is essential to apply the standard lipids
on the same plate as the one used for the samples [13].
Lipid Separation. After application of both lipid extracts and standard
lipids, the plate is placed in a developing chamber containing the eluting solvent.
Horizontal developing chambers, in which the silica gel side of the plate is facing
down (e.g., Desaga, Wiesloch, Germany or Camag, Muttenz, Switzerland), are
preferred. For proper use, the chambers must be precisely horizontally leveled
and covered by a glass plate in order to avoid interference from the environment.
By capillary action the solvent moves up the plate, taking the various lipid compo-
nents with it at different rates, depending on their adsorption. TLC analyses are
typically performed at room temperature, and temperature fluctuations must be
avoided.
Skin lipids contain a variety of individual lipids differing in chemical struc-
ture and polarity [52]. This is the reason why it is virtually impossible to separate
all lipid classes by TLC using one solvent or even one solvent mixture. To allow
optimal separation of all barrier lipids on one plate, a multistep HPTLC technique
was developed [95]. According to this technique, HPTLC plates are sequentially
developed with series of different solvent mixtures (e.g., pro analysis). These
mixtures vary in polarity, allowing migration of only a limited number of lipids
during each development step; others remain adsorbed by the silica gel layer.
Different solvent mixtures for the development of total lipid extracts or,
more specific, for the determination of the ceramides profile, have been reported.
A brief overview of how lipids can be fractionated by using different development
systems is given in Table 5. After each development step, the plate needs to be
dried on a plate heater at 40°C for 3 min.
Development systems more complex than those shown in Table 5 have
been reported. Bonté and coworkers [58] described a method for the major SC
lipids by using an automated multiple development system (e.g., AMD Camag,
Muttenz, Switzerland or TLC-MAT, Desaga, Wiesloch, Germany). The tech-
nique consisted of a single isocratic step with toluene to remove and separate
the sebum lipids, followed by a 25-step gradient with a decreasing polarity range
from MeOH/H2O 97 : 3 (v/v) to n-hexane. The drying procedures between each
step were performed automatically. Two years later, this method was improved
by Zellmer and Lasch [27], resulting in a better separation between FFA and
triglycerides.
Staining and Charring. After the development is completed, the plate is
removed from the chamber and dried at 40°C. Subsequently, the plate is heated
at 100°C for 3 minutes, mainly in order to evaporate the ethyl- or hexyl acetate.
Finally, visualization of the separated lipid fractions is done. To detect certain
Table 5 Sequential Development Systems for the Separation of Individual Lipid

Fractions by HPTLC
Lipid extracts obtained from:
↓ ↓
Skin samples (biopsies/blisters) Tape stripping
or in vivo extraction (cyanoacrylate resin or adhesive tapes)
1) petroleum ether/diethyl ether/acetic 1) CHCl3 /MeOH/H2O (40:10 :1) → 100

acid (35 :15 :0.5) → 50 mm mm
2) toluene/n-hexane (40 :10) → 100 mm 2) CHCl3 /MeOH/glacial acetic acid
3) heptane → 100 mm (190 :9 :1) → 160 mm
❘r for separation of non-polar lipids 3) n-hexane/diethyl ether/acetic acid
1) CHCl3 /MeOH/H2O (40 :10 :1) → 65 (70 :30 :1) → 200 mm
mm [14]b
2) CHCl3 /MeOH/H2O/acetic acid
(40 :10:1 :1) → 35 mm 1) CH2Cl2 /ethyl acetate/aceton/
3) petroleum ether/diethyl ether/acetic 2-propanol (80 :16 :4 :1) → 30 mm
acid (15 :35 :0.5) → 100 mm 2) CHCl3 /acetone/MeOH (76 :8 :16) →
❘r for separation of polar lipids 20 mm
[57]b 3) n-hexane/CHCl3 /hexyl acetate/
acetone/MeOH (6 :80:0.10 :4) → 95
1) MeOH/CHCl3 /H2O (20 :95 :1) → 55 mm
mm [95]s
2) petroleum benzine/diethyl ether/acetic
acid (80 :20 :10) → 90 mm 1) MeOH/CHCl3 /H2O (20:95 :1) → 60
❘r for separation of ceramides mm
[42]s 2) n-hexane/diethyl ether/acetic acid
(80 :20 :10) → 85 mm
3) petroleum benzine → 100 mm
[70]b
b
distance from the bottom of the plate
s
distance from the spot line
types of lipids or functional groups, spraying with a specific chemical reagent can
be carried out; suitable nondestructive dyes—allowing preparative HPTLC—
include aqueous (0.25%) 8-anilino-1-naphthalene sulfonic acid (lipophilic fluo-
rochrome) for glycosphingolipids and neutral lipids [21,29,59,115] and 2′,7′-
dichlorofluorescein [56], both visualized under UV light. Alternatively, the plates
can be sprayed with a phosphoric or sulfuric acid solution combined with CuSO4
after which the lipids are charred by heating the plates at 160°C for 10 min
[14,48,61,95]. Before increasing the temperature of the heat block to 160°C, the
plates are preheated at 60°C until the staining mixture is evaporated. The sepa-
rated lipids become visible as discrete bands of black carbon spots.
To improve the quantification of various lipid fractions, a first identification

can be performed when the lipids are charred at 80°C during 10 min. At that
temperature, the sterol-containing components, as well as the most polar cera-
mides, appear as blue/violet bands [61]. Subsequently, the temperature can be
further increased to 160°C.
Determination of Lipid Profiles. Photodensitometric scanning of the

bands allows quantification. For this purpose a Camag TLC Scanner 3 (Muttenz,
Switzerland) equipped with a computerized image analyzer [22] or a BioRad
Scanning Videodensitometer (GS 710 or 800, BioRad, Hercules, CA, USA) [14]
can be used. Desaga (Wiesloch, Germany) and Shimadzu (Kyoto, Japan) have,
respectively, the Densitometer CD 60 and the Photodensitometer CS-9301PC,
on the market.
Examples of commercially available software for densitometric evaluation
are winCATS (Camag, Muttenz, Switzerland), ProQuant (Desaga, Wiesloch,
Germany), or BioRad Quantity One (BioRad, Hercules, CA, USA).
After choosing the appropriate conditions (slit width and height ⫽ beam
dimensions, measuring wavelength and light source, absorption/reflection mode,
etc.), these methods are suitable for automatic measurements, integration of sam-
ples, and evaluation of standards. After video integration, individual peak lists
are reported containing the name of the component, Y-position, peak height, and
area.
Photodensitometric scanning also allows recording of spectra. This tech-
nique is useful for a quick identification of unknown substances and is indispens-
able for determining the optimum wavelength for which increased sensitivity and
small peaks identification are characteristic. Background spectra are used for the
correction of the substances spectra. Current densitometers for direct photometric
evaluation cover a wavelength range from 190 to 800 nm.
Research groups do not always provide all technical details about their
methodology. We know of scannings at 420 nm, 450 nm, or 550 nm in the
absorbance/reflectance mode after degrative charring, by the reports of Rawlings
et al. [19], Bonté et al. [58], and Zellmer and Lasch [27], respectively. A wave-
length of 632.8 nm was used by Melnik et al. [48]. However, this technique was
questioned by Röpke et al. [70], and they repeated the same protocol followed
by individual recording of the spectra of the different lipid components. They
found an absorption maximum at 325 nm. This was exactly the same wavelength
as found by our group when lipid extracts were separated according to the proto-
col described in Figure 2. [102]. As an example, the separation of an epidermal
(abdomen) skin sample is shown.
The ratio to the front (Rf) of each lipid fraction can be calculated by divid-
ing the distance of the migrated lipid component by the total distance of the
solvent front. Compared to the individual Rf values of the co-migrated lipid stan-
Figure 2 HPTLC lipid profile of a human epidermal skin sample obtained after the
extraction protocol given in Figure 1. Lane 1: Sample, human abdominal epidermis. Lane
2: Blank solvent (for background subtraction). Lanes 3–6: Lipid standards in increasing
amounts. Cer type III and Cer type IV (Sigma, St. Louis, MO, USA) were used as standards
for cer 1 and cer 2, and for cer 3 to 7, respectively. Lipid separation was done according
to the sequential ceramide development system. (modified from Refs. 17,95).
1. 40 mm n-hexane/CHCl3 /acetone (8 :90 :2)
2. 10 mm CHCl3 /acetone/MeOH (76:8 :16)
3. 70 mm n-hexane/CHCl3 /hexyl acetate/acetone/MeOH (6 :80 :0.1 :10:4)
4. 15 mm CHCl3 /acetone/MeOH (76:4 :20)
5. 75 mm n-hexane/CHCl3 /hexyl acetate/ethyl acetate/MeOH (8 :80:0.1 :6 :6)
6. 95 mm n-hexane/diethyl ether/ethyl acetate (78 :18 :4)
The plate was sprayed with acetic acid/H2SO4 /H3PO4 /H2O 5 :1 :1:95 (v/v/v/v) and 0.5%
CuSO4 after which the lipids were charred by heating the plates at 160°C for 10 min.
Cholesterol esters (CE), Rf 0.87; triglycerides (TG), Rf 0.75; cholesterol (CHOL),
Rf 0.64; free fatty acids (FFAs), Rf 0.55 and 0.58; ceramides (cer), Rf 0.27, 0.29, 0.32,
0.34, 0.36, 0.40, 0.42 (numbering according to Ref. 116); acylglucosphingolipids (AGC),
Rf 0.18; glucosphingolipids (GSL), Rf 0.16; cholesterol sulfate (CSO4 ), Rf 0.11.
dards, qualitative determination of the unknown lipid fractions is allowed. From

the list of peak surfaces of the standards, calibration functions are calculated.
Consequently, because the weight of the applied standards (in µg) and the optical
density of both the standard lipids and the sample fractions are known, the sample
lipid weight—by linear, but mostly polynome regression—can be calculated.
As already emphasized, the degree of charring varies for different lipid
classes. This means that for each HPTLC plate, individual calibration curves are
required for every lipid class [27,95]. In addition, one should realize that most
of the standard lipids used are rather representative for—and not identical to—
the various skin lipid components recovered after extraction. Consequently, quan-
tification of unknown skin samples relatively depends on the charring behavior
of the selected standard lipids. The latter usually are different in the reports pub-
lished [16,29,48,95], making comparisons of results even more difficult.
Another possibility for quantifying samples is to include an internal stan-
dard in the standard lipid mixture. For this purpose, methyl oleate, an ester that
is not present in human skin, can be used (0.25 mg/ml solvent) [14].
In order to allow correct quantification, solvent blanks should be applied
along with the lipid samples and standards to bring the background profile and
possible solvent contamination into account [109]. The latter is of particular im-
portance when tape strips are analyzed, as tape-stripping contaminants co-migrate
in different chromatographic solvent systems.
Nowadays, chromatogram evaluation by video scanning technology, image
acquisition, and quantitative image analysis (intensities of the image pixels) is
gaining field. Although the principles of planar chromatography remain un-
changed, it is probably only a matter of some years before video technology—
which is faster, is more flexible, and allows electronical storage of chromato-
grams—will take over the classic densitometry (e.g., Video-Technology ProVi-
Doc with ProResult program, Desaga, Wiesloch, Germany or Video Imaging
System, Shimadzu, Kyoto, Japan).
2. Gas-Liquid Chromatography/Mass Spectrometric

Techniques (GLC/MS)
Gas-liquid chromatography (GLC) with flame ionization detection (e.g., GC-
17A, Shimadzu, Kyoto, Japan) is very suitable for the determination of the methyl
esters (FAME) of FFA or of FA liberated after chemical hydrolysis [29,55,117].
This method is also useful to establish the structural analysis of individual cera-
mides and the composition of their FAs and long chain bases [25,41].
After preparative HPTLC (i.e., sprayed with an aqueous 8-anilino-1-naph-
thalene solution), the neutral and polar lipid bands are excised followed by a re-
extraction of the lipid-containing silica gel by the extraction solvent (e.g., CHCl3 /
MeOH 2/1 (v/v)). The residue is then separated from the supernatant, and after
a second wash, the organic phase is dried under nitrogen and weighed. Dissolved
in MeOH/n-hexane 2 :0.5 (v/v), FAs can be converted to FAMEs by a complex
of (12%) borontrichloride (or -fluoride) in MeOH at 90–100°C for 1–11/2 hours
followed by extraction of methyl esters in n-hexane and fractionation in the sol-
vent system petroleum ether/diethyl ether/glacial acetic acid 80 :20 : 1 (v/v/v) to
recover purified FAMEs [29,59,105]. Besides ester preparation, it is important
that chromatographic parameters including resolution, peak asymmetry, and total
analysis time are optimized as well as the linearity of the flame ionization detec-
tion and the injection technique [106].
Glass capillary columns with polar polyester liquid stationary phases are
most suitable for FAME analysis as they allow a clear separation of the esters
of the same chain length, unsaturated components eluting after the related satu-
rated ones. A chromatogram is obtained in which the individual FAME peaks
are characterized by their retention time and area. Identification of the individual
FAMEs can be provided by direct comparison of their retention times with those
of known standards [13]. Tricosanoic acid (C23:0) is normally not present in the
human SC and is often used as an internal standard [106,118]. Determination of
the areas of the chromatographic peaks can be made by a computing integrator
(e.g., Shimadzu, Kyoto, Japan).
In the study of Lampe et al. [59], GLC combined with mass spectrometry
(MS) was used to identify cholesterol sulfate (CSO4), which was believed to be
present in trace amounts. By using both desorption and fast atom bombardment
(FAB) sources, and by identification of free sterols after solvolysis, it has been
shown that CSO4 was present in all viable epidermal layers, with the highest
concentration in the stratum granulosum (see also Table 4) [59,119]. From Table
4, it is clear that significantly lower concentrations of CSO4 are present in the
SC, providing the evidence that its desulfation by the enzyme steroid sulfatase is
required for the physiological desquamation of the SC [119,120]. Current HPTLC
separation and determination techniques have sufficiently been improved and re-
fined so that even small amounts of CSO4 can be determined with planar chroma-
tography, without the use of expensive equipment [61].
In the study of Norlén et al. [106], special attention was focused on the
FFA fraction because the unsaturated FFAs exert a key function in the regulation
of the skin barrier properties. They also showed that short-chain FFAs (less than
C20), including the unsaturated species, are mainly contaminants from sebaceous
glands and the environment.
3. Liquid Chromatography
Although planar chromatographic methods are easy-handling and offer quick
qualitative screenings of various lipid classes, relevant criticisms include the lim-
ited densitometric sensitivity and the influences of temperature and humidity as
well as the higher degree of variability in solvent mixtures [121]. Also, day-to-
day variability of Rf values and resolution cannot be ignored. To avoid those
problems, some research groups have tried to develop HPLC methods allow-
ing direct quantification of the major lipid classes using one or more detectors
[71,106,118,121].
Because GLC methods are not able to separate complex mixtures of neutral
lipids of varying polarity, Murphy and coworkers [121] standardized a HPLC
method for the separation of triacylglycerols, cholesterol and cholesterol esters.
In addition, Flamand et al. [122] focused on the concentration and distribution
of the free long-chain sphingoid bases (sphinganine, sphingosine and phytosphin-
gosine) in the SC, whereas Schäfer and Kragball [118] analyzed phospholipids.
Whenever a complete determination of all individual SC lipids is required
in conventional TLC, multiple development steps are necessary (see Sec. III.C.1).
Therefore, Norlén and his group developed a new HPLC-based method for the
quantitative analysis of the inner SC lipids, meaning the intact skin barrier, unper-
turbed by degradation processes [71,106]. They were able to separate and quan-
tify all main lipid classes by HPLC and light scattering detection (LSD), while
the FFA fractions were further analyzed by GLC. MS was used for peak identifi-
cation and flame ionization detection for quantification (see Sec. III.C.2). How-
ever, it must be noted that with the single-step HPLC method, a complete separa-
tion between different skin ceramide subtypes was not obtained [106].
For this type of analysis, more specialized laboratory equipment is needed
including a HPLC pump, column oven, injector (manual or automatic), gradient
system controller, detector (i.e., spectrofluorimeter or light scattering detection),
integrator, etc. (e.g., Shimadzu, Kyoto, Japan). All solvents used need to be of
HPLC grade. To ensure high accuracy during long-term experiments, calibration
curves for all lipid components need to be run daily to control the variations in
detector response [106]. Coefficients of correlation must be calculated for all
calibration curves, because only within the linear detectable range can reliable
concentration measurements be performed. Consequently, direct quantification
of several lipid classes is carried out by peak area analysis. In the case of tape
stripping, an appropriate blank can be obtained by making a chromatographic
analysis of the derivatized extract of an identical piece of adhesive tape.
4. Spectrophotometric Techniques
As described in Sec. III.A.2, spectrophotometric measurements of SC tape strips
are useful for the inspection of the homogeneity of single strips. They also allow
a rapid screening of the amount of SC material stripped. For this purpose, a
Shimadzu UV 190 double-beam spectrophotometer equipped with a SC-3 Gel
Scanning device was used (Shimadzu, Kyoto, Japan). Untouched, nonused tapes
served as blanks. A drawback of this method, however, is the light scattering of
the adhesive tapes used, which could overshadow the absorption of the proteins
present in the SC material [72].
For the various UV/VIS systems, software packages are offered by differ-
ent specialized companies (e.g., Shimadzu, Kyoto, Japan), allowing data pro-
cessing as well as good laboratory practice (GLP)-specific functions.
Whereas individual lipid fractions are commonly fractionated by quantita-
tive, sequential HPTLC techniques, various lipid classes can also be spectropho-
tometrically determined after the formation of a specific colored complex with
a known absorbance. After extraction and drying (see Sec. III.B.), the total lipid
content is redissolved in CHCl3 and can consequently be determined using the
sulfo-phosphovanillin-reaction. The colored complex obtained (pink) is then
measured at 530 nm [69]. Two of a number of colorimetric reactions that can
be carried out for some of the major SC lipid classes are as follows:
Phospholipids can be determined by the molybdate-vanadate reaction (yel-
low color) and measured at 405 nm.
Cholesterol dissolved in acetic acid can be determined after conversion by
H2SO4 into cholestadiene, which reacts with a second molecule to form
bischolestadiene. This dimer is sulfonated (catalyzed by Fe3⫹) to its
mono- or disulfonic acid derivative, which gives a maximum absorption
at 550 nm.
The assays described are simple and quick; due to a co-prepared standard series,
calibration curves can be calculated, allowing quantitative determinations. In col-
orimetric techniques, plain reagent solutions serve as blanks.
IV. CONCLUDING REMARKS
It is acknowledged that the composition and organization of the intercellular lip-

ids play an important role in the barrier function of human SC. Differences in
SC lipid profiles between healthy and diseased skin exist, but can only be charac-
terized by applying accurate methods for collection and quantification of epider-
mal and SC lipids. Therefore, the analytical techniques currently applied for the
determination of skin lipids need to be evaluated critically.
For the validation of both in vivo and in vitro experiments, it is important
to standardize the many variables that play a crucial role in the composition of
the SC lipid fractions. Person-linked factors such as age, sex, race, and anatomical
site have been reported to influence the lipid composition. Also, environmental
factors and UV irradiation may affect the outcome of the lipid concentrations
measured. These variables must be controlled in a reproducible and standardized
way in order to be able to show a clear and direct relationship between various
skin conditions, barrier function alterations, and barrier lipid composition.
Various sources for sampling epidermal or SC lipids (in vivo, ex vivo, in

vitro) are described, including skin biopsies after surgery, tape stripping, and skin
blisters. Both the tape stripping and blister techniques have the advantage that
skin samples can be obtained from different parts of the body, allowing compara-
tive studies. This is not always the case for skin samples coming from plastic
surgery, which are mostly restricted to breast, abdominal, or facial skin. A major
advantage of the stripping method is that the lipid composition can be studied
as a function of SC depth. However, these sampling techniques are invasive and
should be applied only under approved ethical conditions.
Although various extraction protocols can be compared, a clear agreement
on which technique should be preferably used is still doubtful. Attention needs
to be focused not only on conventional extraction protocols of biological samples
but also on human in vivo techniques. A prerequisite for direct in vivo sampling
of SC lipids is the application of noninvasive techniques. In this respect, the use
of a mixture of acetone/diethyl ether 1 :1 (v/v) is proposed. Many factors, such
as sample sources and contaminations, may affect the SC lipid profiles during
extraction and should therefore be controlled.
For chemical analysis of epidermal lipids, chromatographic methods are
most widely used. Quantitative analysis of the different lipid fractions after se-
quential separations is commonly performed by high-performance thin-layer
chromatography (HPTLC). Individual lipids are separated on HPTLC plates and
subsequently quantified by computerized densitometry. Although lipid separation
is quickly obtained, disadvantages still are the time-consuming quantification of
the different lipid fractions and the appropriate calibration procedure. However,
as an answer to the relevant criticisms of planar chromatographic methods, high-
performance liquid-chromatographic (HPLC) techniques are making their way
up.
V. ACKNOWLEDGMENTS
The authors thank Dr. Maria Ponec and Mr. Arij Weerheim from the Skin Re-
search Laboratory, Leiden University Medical Center (Leiden, The Netherlands)
for their kind advice and critical review of the manuscript.
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7
Biophysical Methods for Stratum
Corneum Characterization
Hans Lambers and Hans Pronk
Sara Lee Household and Body Care Research, The Hague, The Netherlands
I. INTRODUCTION
A. General Background
There is no doubt that the application of cosmetic lipids has many positive effects
on the structure and function of the skin. These effects are pleiotropic, caused
either by direct interaction with the epidermis, particularly the stratum corneum,
or indirectly, by influencing the physiologic, homeostatic condition of the skin.
Generally, the overall result may be a range of skin benefits such as:
Improved moisturization
Enhanced barrier function
Smoothing of the microrelief
Improved mechanical properties
Reduction in scaliness
Cosmetic lipids have also more general benefits, such as improvement in
skin pH, temperature, and color.
Special strategies with regard to penetration and targeting of cosmetic lipids may
be considered in order to enhance various skin properties; for instance, whether
to increase the superficial stratum corneum emolliency, to enforce the stratum
corneum lipid barrier, or even to realize trans-(epi)dermal transport all need dif-
ferent product formulation approaches. This will be covered in other chapters of
this book (see, for example, Chapter 9).
Many biophysical methods have been developed during the past 50 years,
all of which involve the application of physical principles and methods to study
185
186 Lambers and Pronk
and explain the structure and function of the skin and to assess the above-men-
tioned properties. These properties of the skin are somehow interlinked and re-
lated to each other, which make proper and accurate assessment of biophysical
parameters often a complex matter. For instance, a change in moisturization is
intimately linked to changes in mechanical properties such as elasticity, but there
also exists a relation to the degree of desquamation, barrier function, and so on.
Existing biophysical methods are maturing and improving all the time; also,
the development of new biophysical methods is a continuous challenge to the
cosmetic scientist. Although, in general, this will improve the possibilities to
characterize the structure and function of the skin, it must be realized that proper
standardization of measuring devices and protocols is often still lacking; this
may give rise to different results in different laboratories, making inter-laboratory
comparison sometimes a difficult task.
In order to perform biophysical evaluations, a number of general conditions
should be met for optimal results.
Important for almost all of the methods that are described in this chapter are the
following:
All examinations should be done in an air-conditioned laboratory that guar-

antees constant room temperature (preferably between 20 and 23°C) and
humidity (preferably between 40% and 60% relative humidity) [1].
The volunteers should sit in this air-conditioned laboratory at least 30 min-
utes before the assessment and throughout the test procedure. Short-term
conditions affecting the assessment (e.g., journey to the test institute by
bicycle or car) are equalized in this way. Standardized conditions are
essential for physiological examinations of the skin. However, this proce-
dure does not compensate for climatic conditions.
Subjects should be in a relaxed physiological and psychological state and
be equilibrated fully to the room conditions.
A suitable body test site for measuring influences of topical treatments
should have an even surface and few hair follicles. The volar aspect of
the forearm meets most of the requirements.
Preferably, the assessor should be skilled in the art and possess a large
amount of experience.
B. Scope of the Chapter

This chapter focuses on the description of the most popular, easy-to-handle, and
frequently used noninvasive biophysical methods—c.q., devices to characterize
in vivo human skin, in particular the stratum corneum. In some cases tape-strip-
ping of the skin may be used for characterization [2]. Also, ex vivo and in vitro
(epi)dermal tissue may be used, but these require mostly special conditions and
Biophysical Methods for SC Characterization 187
will not be further considered here in detail. A practical approach is chosen,

aiming at increasing the general knowledge and understanding of the relatively
inexperienced cosmetic scientist. Various examples are given, which may be used
for claim substantiation related, for example, to moisturization, barrier function,
microrelief, mechanical properties, scaliness, and the like. Methods to study and
quantify sebum surface lipids are also covered because these lipids form an inter-
face between stratum corneum and the external environment and are, although
somewhat indirectly, related to the biophysical properties of stratum corneum.
Moreover, this method may also be used to quantify the amounts of externally
applied cosmetic lipids. Special attention is paid to the relationship between the
assessment of the effects of cosmetic lipids and stratum corneum structure and
function.
The chapter will be concluded by a brief description of other less frequently
used biophysical methodologies to measure stratum corneum parameters such as
skin pH, temperature, and color. A list of supplier addresses of most of these
biophysical devices is provided at the end of this chapter.
Techniques that are directed more toward getting structural information,
such as basic histological techniques or the more sophisticated techniques (e.g.,
confocal [fluorescence] laser scanning microscopy, magnetic resonance imaging
[MRI] and electron spin resonance [ESR]), and other biophysical techniques that
are relatively unknown and not (yet) used very often, such as brillanometry/
reflection and frictiometry, are not or only briefly described at the end of this
chapter. For more advanced and detailed description of the methodologies men-
tioned here, the reader is referred to general books such as the ones edited by
Marks [3], Serup [4], and Elsner [5]
II. SKIN MOISTURE ASSESSMENT

A. General
Skin moisturization is one of the most relevant parameters characterizing the
condition of the stratum corneum [6]. Water acts as plasticizer for the skin and
is also an essential part of the highly organized (liquid crystalline or gel phase)
lipid barrier of the stratum corneum. As water is evaporating continuously from
the surface of the skin—depending among others on the relative humidity and
temperature—skin may become dry, brittle, and flaky and even can show fissures.
So nature and the cosmetic industry have taken measures to prevent drying out
of the skin:
The human body is an almost infinite source of water, which compensates

for this continuous loss of water. This compensation does not result in
an equilibrium but in a steady state.
This steady state is governed by the water-binding and water-retarding

properties of the stratum corneum.
The stratum corneum gets its water-binding properties from the natural
moisturizing factor (NMF) present in the stratum corneum and also from
humectants supplied by cosmetics.
The water-retarding properties are governed by barrier properties of the
stratum corneum. These properties are strongly related to the structure
of the lipid region of the stratum corneum. This structure can be affected
by washing (surfactants) but also ameliorated by the lipids and emollients
supplied by creams or lotions [see also under Sec. III].
The moisturization can further be improved by (semi-)occlusive layers (se-
bum, lipids, emollients) at the surface of the skin.
B. Techniques
Accurate assessment of the moisture content of the stratum corneum is difficult
for several reasons:
The moisture content of the stratum corneum varies from relatively low
(about 15%) in the outer layers to relatively high (about 40%) in the
deepest layers [7]. Assessment of the moisture level will result in an
average value. In most cases it is not known what the exact contribution
is of the outer layers to this average value nor the contribution of the
deeper layers.
The moisture content is not evenly distributed in each layer: the moisture
content of the corneocytes (horny cells) differs from the moisture content
of the lipid regions.
Three types of water are generally recognized in literature: tightly bound
water, bound water, and free water [8].
Most assessments are based on an indirect measurement of skin moisture
(e.g., the electric properties of the stratum corneum). We cannot be sure
that the outcome of these assessments is indeed proportional to the mois-
ture content.
Although the absolute skin moisture is hard to measure, any increase or decrease
can easily be detected: currently a couple of devices are on the market that are
capable of measuring skin moisture within seconds. These devices are commonly
accepted and can be used, for example, for claim substantiation (moisturization,
repair of barrier function of the outer layers of the stratum corneum) and for the
assessment of skin compatibility of cleansing agents.
Some of the most frequently used commercial devices are the Corneome-
ter CM820 and the Corneometer CM825, supplied by Courage ⫹ Khazaka.
Others are the DPM 9003 (NOVA) and the Skicon-200 (IBS, Hamamatsu).
All these instruments measure the electric properties of the skin. They work at
different frequencies, using various sizes of probes that are applied with distinct
pressure on the skin. All of them give hydration values (expressed in arbitrary
units) that are not linearly correlated with the hydration state of the skin [8].
Readings are sometimes influenced by salts and humectants (such as glycerol)
present on the skin.
The Corneometer CM820 and the Corneometer CM825 (new version)
measure capacitance and operate at low frequency (40–75 Hz). They are sensitive
to the relative dielectric constant of the measured materials. And as water has a
high dielectric constant, the device is very sensitive to water. It estimates the
water content in the epidermis to an approximate depth of 60 to 100 µm [9,10].
Yet it is very likely that the (outer) layers of the stratum corneum are overpropor-
tionally contributing to the readings because the device is very sensitive to appli-
cation of moisturizing creams whereas the deeper layers of the skin will have a
fairly constant water level. This sensitivity might be due to a direct measurement
of the increased moisture content of the stratum corneum or to an indirect effect,
namely the deeper penetration of the electric field due to moisturization of the
stratum corneum [11].
The DPM 9003 uses measurements of phase angle. Phase angle is one
of the two coordinates of impedance at each particular frequency of stimulation.
The device uses frequencies up to 1 MHz. It measures the outer stratum corneum
layers. The device is not discriminative for dry skin: if the skin is very dry, the
outcome of the skin measurement will be zero. Yet it is very useful for assessing
the moisturizing effects of moisturizing creams.
The Skicon-200 measures the conductance at high frequency (3.5 MHz).
Like the DPM 9003, it measures the outer stratum corneum layers.
Other, less frequently used techniques to measure skin hydration are infra-
red spectrography [12], nuclear magnetic resonance [13], and magnetic resonance
imaging [14]. Also, the desquamation and skin elasticity measurements [15] give
information about the degree of skin moisturization.
C. Example
As the natural moisturizing factor present in the skin is water-soluble, even wash-
ing with water will (partly) remove it, resulting in a slight dehydrating effect.
This dehydrating effect can be more pronounced after washing with cleansing
products because the surfactants from these cleansing products can remove skin
lipids and furthermore are able to disturb the lipid ordering in the stratum cor-
neum. These dehydrating effects are shown in Figure 1 (corneometer readings
taken 12–16 hours after last washing). This figure also shows that these dehydrat-
ing effects can be (over)compensated by application of a moisturizing product.
Figure 1 The corneometer CM825 demonstrates the drying-out effect of a shower gel
during the first 2 weeks of the test period and the combined restoration and protection
effect by a lipid-containing cream during the last 2 weeks (baseline corneometer value
38 arbitrary units).
1. Some Practical Advice

The conditions during the measurements are crucial for a useful assessment of
skin moisture [16,17]. For example, perspiration has to be prevented for obvious
reasons. Furthermore, the contact between probe and skin should be very close:
hairs and product residues (including waxes, oils, and inorganic UV-filters) will
influence the readings. So, before any assessment one should clean the skin (e.g.,
by paper tissues) if there is any doubt about product residues at the skin’s surface.
However, the assessor should realize that removed product remnants cannot con-
tribute anymore to skin hydration.
In order to substantiate moisturizing claims for moisturizing products, it is
advised to apply the product(s) at the volar side of the forearms. As the assess-
ments are not very accurate (yet also not very time-consuming), one should take
at least three—but preferably ten—readings from each spot. To prevent occlusive
effects caused by the probe, waiting periods of at least 5 seconds should be ob-
served between measurements at identical skin sites. Furthermore, an untreated
control site should be included in order to take environmental variables into ac-
count.
Figure 2 Schematic representation of water distribution in the stratum corneum for nor-
mal skin and for skin with improved barrier properties for the outer layers.
For the right interpretation of the data we have to realize that the assessment
indicates the average skin moisturization. And as the effect of lipids on moisturi-
zation is different from that of humectants, we have to take this into account.
Also, differences in stratum corneum thickness may lead to misinterpretations.
2. Theoretical Effect of Skin Strengthening

In general, the deepest layers of the stratum corneum will have the best barrier
properties. Treatment of the skin with barrier-improving lipids will have the big-
gest impact at the more superficial layers, as these layers are easiest to strengthen.
Beyond these strengthened layers a new steady state will be established. This is
represented in Figure 2, which depicts this relation schematically.
It is clear from this graph that the outer layers have not benefited much by
this treatment, although the deeper layers clearly have. Such beneficial effect can
easily be assessed by the corneometer, but only with difficulty by devices such
as the DPM 9003 and the Skicon-200, because these devices preferentially mea-
sure the moisture content of the outer layers.
3. Theoretical Effect of Humectants

In general, use is also made of humectants, which enhance the moisture content
of the whole stratum corneum (Fig. 3).
mal skin and for skin with applied humectants.
mal skin and for thin skin.
Such effects are easily detected by the Corneometer CM825 as well as

Skicon-200 and DPM 9003. Note: Application of occlusive products results in
similar skin moisture effects; assessment of the skin moisture increase, however,
requires the removal of the occlusive layer.
4. Theoretical Effect of Stratum Corneum Thickness

The stratum corneum forms the main barrier for water; thus, the ‘‘water level to
depth’’ relation will be steeper for thin skin. This is represented in Figure 4.
Assessment of skin hydration will produce in this case the highest value
for thin stratum corneum, although in this example in both cases the hydration
of the surface is the same. Even if the surface hydration is lowest for thin stratum
corneum, the hydration assessment might result in the highest value. This phe-
nomenon has to be taken into account in comparing young to (relatively thin)
old skin, male to (thin) female skin, and also UV-exposed (thick) to nonexposed
skin.
III. BARRIER ASSESSMENT

A. General
The barrier function of the skin prevents, on the one hand, the excessive diffusion
of water through the epidermis and, on the other hand, the penetration into the
skin of external compounds that come in contact with the surface of the skin.
This barrier is determined largely by the integrity of the stratum corneum, which
is formed by stacked corneocytes embedded in a lipid continuum, mainly con-
sisting of ceramides, cholesterol, and free fatty acids. This lipid continuum is
composed of highly ordered lipid bilayers, which form the actual barrier, and is
located at the deeper layers of the stratum corneum with thin layers of bound
and/or free water in between. A healthy skin in good condition has a proper
barrier function, which is characterized by low values of transepidermal water
loss (TEWL) [18,19].
In chemically and/or physically damaged skin and in certain pathological
skin conditions, the barrier function is impaired, resulting in increased values of
TEWL. The barrier function can be assessed by measuring the amount of water
that passes through the stratum corneum barrier and leaves the skin as water
vapor; it provides information on the integrity of the epidermis and the effects
that topical (pharmaceutical or cosmetic) products have on the epidermal barrier
[20,21].
Indeed, it is a big challenge and opportunity to develop products that con-
tain cosmetic lipids that will enhance the stratum corneum lipid barrier function
of the skin. This will require highly specialized formulation strategies to target
cosmetic lipids to become an integral part of the lipid barrier system.
Figure 5 Schematic diagram showing the relation between TEWL and hydration state
in skin.
As mentioned in Section II, the strengthening of the barrier is one way of

increasing the overall hydration state of the skin, but TEWL and moisturization
are not necessarily linked directly to each other. High TEWL and low hydration
may coexist, and are in fact a typical phenomenon for dry, xerotic skin [22]. On
the other hand, damaging the stratum corneum barrier (e.g., by stripping) results
in a skin condition in which high TEWL and high hydration state coexist. Fig-
ure 5 shows the relation that in general is expected to exist between TEWL and
hydration. The lowest TEWL-value will reflect healthy skin with optimal barrier
properties.
B. Techniques
The measurement of TEWL is now generally recognized as one of the most
popular and commonly used methods to assess barrier function [23].
The following devices are often used and seem to be the most popular: the
Evaporimeter (Servo Med), TEWA-meter (Courage ⫹ Khazaka) and Der-
maLab (Cortex).
The measuring principles of these three devices are basically the same
[24,25]. All devices have the advantage that the measurements can be performed
non-invasively and relatively fast and accurately. The results obtained are ex-
pressed in g/m 2h. The evaporimeter seems to have a somewhat lower sensitivity
and a higher susceptibility to air circulation and relative humidity [26].
Under steady state conditions, the human skin surface is surrounded by a
water vapor boundary layer, in which an inner-outer gradient exists. This vapor
gradient is correlated with the stratum corneum water gradient, which in turn is
a function of the barrier (quality). The water vapor gradient is measured by a

probe that is placed perpendicular on the skin. The probe consists of an open
cylinder containing two hygrosensors coupled with two thermistors placed at
different distances from the skin surface. At both points the local relative humid-
ity and temperature are measured, and the corresponding vapor pressure is calcu-
lated. The difference between the vapor pressure at both points along the gradient
is directly related to the rate of the water loss from that particular skin site [27].
Many factors influence proper TEWL measurements with the TEWL devices;
the most important ones will be mentioned here and should be given special
attention [23,25,28]:
The temperature of the measuring probe. This is an essential variable. For
instance, an increase of the probe temperature from 22°C (⬃room tem-
perature) to 30°C (⬃temperature of the skin) may result in an increase
of TEWL of more than 100% [26].
Sweating. Physical, thermal, and emotional sweating need to be controlled
because these will have profound influence on TEWL measurements.
The temperature and relative humidity of the ambient air. Under constant
relative humidity, there is an almost linear increase of TEWL as a func-
tion of ambient temperature.
The circulation of the ambient air. Only major changes in air circulation
significantly affect the measurements, but care should be taken.
Condition of the skin. Diseased skin and any damage of the barrier function
of chemical and mechanical origin may result in increased TEWL values.
Other techniques used to assess the barrier function of the skin are usually more
elaborate and less straightforward. Two of these techniques are only briefly men-
tioned here:
A gravimetric method in which the weight increase of hygroscopic salt,
attached to the skin, is determined in an unventilated chamber as a mea-
sure of water loss. Not so popular anymore [19].
The measurement of other, indirect biophysical parameters such as skin
redness, caused by the penetration of biologically active compounds,
such as methyl nicotinate; this is an (indirect) indication of the quality
of the stratum corneum barrier [29].
C. Example
Some general examples in which TEWL measurements may be used are as
follows:
The assessment of the damaging effect on the stratum corneum barrier func-
tion caused by surfactant-containing rinse-off products.
The assessment of the restoration of a damaged stratum corneum barrier

by certain lipid-containing creams.
The assessment of the prevention of damage caused by chemical or physical
treatment (e.g., stripping) by certain lipid-containing creams.
The results of a test in which these principles play a role are shown in Fig-
ure 6. The volar forearms were washed twice daily with a moderately aggressive
shower gel; the surfactants caused a slight barrier damage and consequently
TEWL values increased from ⬃6 g/m 2h to ⬃10 g/m 2h. Using this moderately
aggressive washing regime, a ‘‘damaged steady state’’ was reached after about
2 weeks, as demonstrated by the leveling off to an (elevated) TEWL plateau.
When a lipid-containing cream is applied on the forearm in between the washings
with the shower gel, a normalization of the TEWL values can be realized.
In this case, the TEWL normalization is caused by a combination of lipid
barrier repair and an increased protection against further barrier deterioration by
the shower gel. These findings are in line with the results of the moisturizing
test (see Sec. II, Fig. 1), demonstrating that increased TEWL values often result
in a drying out effect of the skin (see also Fig. 5).
Figure 6 The TEWA-meter TM210 demonstrates the damaging effect of a shower gel
during the first 2 weeks of the test period and the combined restoration and protection
effect of a lipid-containing cream during the last 2 weeks (baseline TEWL 6.2 g/m2h).
IV. ASSESSMENT OF THE MICRORELIEF OF THE SKIN

A. General
The skin surface contains wrinkles and lines, which can be classified according
to their depth [30]:
Clearly visible wrinkles, grooves, thin folds, and furrows (100 µm to sev-
eral millimeters)
Primary lines, criss-crossing the skin to form squares, parallelograms, and
rectangles (20–100 µm)
Secondary lines, branching off from the primary lines (5–40 µm)
Tertiary lines, forming the borders of the corneocytes (about 0.5 µm)
Quaternary lines, corresponding to the corneocyte relief (about 0.05 µm).
The wrinkles and the primary lines reflect the contours of the dermis; neverthe-
less, the condition of the stratum corneum (scaling, thickness, and degree of
swelling) has a huge impact on the microrelief. For example, swelling (due to
increased moisturization and/or uptake of lipids) of the stratum corneum from,
say, 20 µm to 25 µm may result in a decrease of the depth of the primary lines,
much more than the 5 µm thickness increase of the stratum corneum. This phe-
nomenon is due to squeezing of the lines.
The skin texture reflects the subject’s age, the weather, and the environmen-
tal conditions and also the effect of topical applications. So, objective measure-
ments of the microrelief and morphological structure of the human skin is impor-
tant in developing effective cosmetics.
Several parameters are used to describe skin roughness [31]. Commonly
accepted are the depth of roughness (Rt) for surfaces dominated by wrinkles and
the mean depth of roughness (Rz) for surfaces dominated by primary and second-
ary lines. These variables explore the variations of the skin profile in the vertical
direction.
Rt is the maximum peak to valley depth for a given scan length L. The
value for L (usually 5–15 mm) is the length of a chosen line across the (replica)
surface. Rz represents the arithmetic average of the different segment depths of
roughness calculated from 5 equal sections of L.
Both parameters originate from the metallurgical industry for scanning me-
tallic surfaces and are somewhat outdated but still widely used.
B. Techniques
Two main techniques [32–34] can be distinguished to measure the skin surface:
The skin replica technique: replicas are taken from the skin and analyzed
afterward.
The living skin technique: the skin is analyzed directly.
1. Skin Replica Techniques

Skin replicas can be made of polymerizing silicone. Within about 5 minutes, a
rather faithful negative reproduction of the skin is obtained. Such replicas can
be analyzed by several techniques:
The oldest technique is the contact stylus method [35]. Replicas are scanned
by a mechanical profilometer such as the Hommel Tester (Hommel-
werke): a microprobe consisting of a diamond stylus moves at constant
speed along straight lines over the replica. The vertical displacement of
the stylus is converted into electrical signals proportional to the deflec-
tions. This technique is still used although analyzing the replicas is very
time-consuming. It is advised to scan at least ten sweeps, resulting in an
analyzing time of about 10 minutes for each replica.
A similar technique (acoustic profilometry) makes use of a touchless acous-
tic pickup. Scanning is performed by the Nanoswing, also supplied by
Hommelwerke.
A modern technique is optical shadowing profilometry [36]. Under grazing
illumination of the replica, the shadows behind the crests (i.e., grooves
of the skin) are captured by a video camera and used for image analysis.
This method has some obvious limitations yet is useful and fast. Further-
more, it can be used to calculate the ratio between the true and the appar-
ent skin surface area, which represents an advantageous profilometric
parameter.
Dynamically focusing laser profilometry is another new method [37] that
has resulted in several commercially available devices. The replica is
scanned by a laser beam autofocusing at a preselected number of spots.
Drawbacks of this method are the high investment required and the time-
consuming procedure of scanning (up to hours per replica). This method,
however, makes it possible to describe skin roughness with three-dimen-
sional parameters [38].
Another optical profilometric technique is based on the triangulation
method [37,39,40]. In this method, the image of the replica is pro-
jected—dot by dot—on a detector. The main advantage is the high scan-
ning speed and the possibility to obtain three-dimensional information
of the surface.
The light transmission technique or transparency profilometry makes use
of thin dyed silicone replicas. The replicas are analyzed by the Skin
Visiometer SV500 supplied by Courage ⫹ Khazaka. Light is absorbed
according to the thickness of the replica according to Lambert-Beer’s
law. It is a fast method, recently validated [41]. The technique is simple,
rather accurate, and not very expensive. A limitation of the method is
that—because of the thickness of the replica itself—grooves with a

depth more than about 400 µm cannot be measured accurately.
2. Living Skin Techniques

These touch-free ‘‘living skin’’ techniques are still not fully developed but are
promising because time-consuming replica taking is no longer needed. Further-
more, elimination of the replica taking step reduces the chances of obtaining
erroneous results. Measurement of living skin, however, makes great demands
on the measurement times. Effects of skin movements due to trembling and mov-
ing of the subjects, their breathing, and the pulsation of minor arteries have to
be excluded.
Two techniques are commercially available:
In vivo topometry of human skin by projected fringe technique [42–44].
FOITS (fast optical in vivo topometry of human skin) developed by
Breuckmann and PRIMOS (phaseshift rapid in vivo measurement of
skin) developed by GFMesstechnik allow three-dimensional information
to be gathered from the surface of the skin in an extremely short time.
However, a shortcoming of this technique is that dealing with hairy sur-
faces seems to be problematic.
Surface evaluation of living skin by a graphic depiction technique [45,46].
The Visioscan VC98 device (Courage ⫹ Khazaka) is a video camera
that monitors the skin surface illuminated under an UV-A light source.
Interpretation of the image by the supplied software gives information
about skin roughness. A serious drawback of this new technique is that
quantitative assessment of the depth of lines and grooves is not yet possi-
ble. Also, dark and white spots and hairs seem to influence the outcome
of the measurement. A similar device is the Direct Skin Analyzer [47].
An alternative for the skin replica and the living skin techniques is the visual
assessment of the skin relief [48,49]. Especially for assessment of the degree of
facial wrinkling, using a photo scale, this technique is valid.
The scanning electron micrography (SEM) technique is used to obtain a
high magnification of skin replicas. It can also be used to study ex vivo human
skin, skin biopsies, and skin surface strippings [50,51]. This sophisticated but
expensive technique is a suitable method for fundamental research on the intra-
and extracellular structure of the stratum corneum surface.
C. Examples
The scanning direction is an important factor for the evaluation of (the replica
of) the skin because the texture of the skin is highly anisotropic, at least in elderly
people. For wrinkles, it is advised to measure perpendicular to the major grooves

and to use Rt as a parameter.
Surfaces without wrinkles are better measured in a circular manner because
the major direction of the primary lines is not always easily recognized. Rz is in
this case the right choice for skin smoothness. However, it has to be realized that
a drawback of this choice is that one or more of the five sections for measuring
Rz just covers a plateau of the skin and not the primary lines. This is a more
serious problem if old subjects are measured than in the case of young subjects
because the distance between primary lines increases with age [41]. This effect
is illustrated in Figure 7 by the relation between length of L (sum of the five
sections) and Rz.
This anisotropy of the skin is gradually developed and is far more marked
on the skin of elderly people than on that of children, where the distribution is
almost isotropic. Figure 8a shows the forearm pattern of a 3-year-old boy and
Figure 8b that of a 76-year-old man. Both pictures are reproduced by the Visio-
meter SV500, using silicon replicas from the skin.
Some practical advice:
The correct calculation of roughness parameters from the original data is
only possible after elimination of superimposed elements of form and waviness
Figure 7 Relation between Rz and scan length L given for a 19-year-old and a 64-year-
old man, measured by Visiometer SV500. For each replica analysis, 180 circular arranged
lines were used.
Figure 8 Replicas of the skin reproduced by the Visiometer SV500: (a) replica of the
skin of a 3-year-old boy, (b) replica of the skin of a 76-year-old man. For both replicas,
the same magnification was used.
of the original skin profiles by mathematical procedures. This elimination (filter-

ing) will in most cases be performed by the software. However, it may be a
source of erroneous corrections. Ideally, the software should show what the effect
is of these corrections.
Special attention has to be given to the next items:
If the skin surface is covered by a product (e.g., cream), the replica will
not yield a faithful image of the skin surface.
Stretching of the skin influences the depth of the lines and wrinkles, so
measurements have to be performed under standardized conditions and
positions; for example, for measurements of the forearm, the angle be-
tween forearm and upper arm has to be fixed (e.g., to 90°).
V. ASSESSMENT OF BIOMECHANICAL PROPERTIES

A. General
Assessment of the biomechanical properties of the skin, and in particular of the
stratum corneum, is a difficult task. One of the main reasons is that the skin is a
very complex organ and its final biomechanical properties are a result of complex
interactions of different layers of the skin (e.g., epidermis, dermis, and hypoder-
mis). This is reflected by the fact that skin has a combination of elastic, viscous,
and plastic properties, which as yet cannot be adequately described in an overall
mathematical model. Skin mechanics are described mostly by stress (⬃force)/
strain (⬃deformation) relationships and the course of deformations in time; inter-
pretation is often complicated and factors such as age, skin type, skin thickness,
body site, pretreatment, environmental conditions, and so forth should be taken

into account and may all have profound effects on these parameters. A more
detailed description of the attempts to describe human skin biomechanics is be-
yond the scope of this chapter, and the reader is referred to Rodrigues [52] and
Serup [53].
It is generally accepted that the stratum corneum contributes to the overall
biomechanical properties of the skin, albeit less than the viable epidermis, the
papillary plus the reticular dermis and the hypodermis.
The main descriptors for skin biomechanics are extensibility (⬃flexibility)
and elasticity, which in turn may be translated into more qualitative benefits such
as suppleness, firmness, softness, and resilience. It must be emphasized that inter-
pretation of the relation between extensibility and elasticity is not uniform and
definitively not standardized and therefore is often subject to much confusion
and discussion. Figure 9 shows a schematic diagram, giving some subjective
descriptions of skin biomechanical perception in relation to elasticity and extensi-
bility; by no means is it meant to be an accurate account of these perceptions.
Figure 9 Schematic diagram indicating some qualitative biomechanical perceptions in

relation to elasticity and extensibility. (Slightly adapted from Rodrigues [52].)
The topical application of cosmetic lipids may have profound effects on

the biomechanical properties, with special reference to the stratum corneum. Inte-
gration of these lipids (e.g., emollients) will generally improve the moisturization
and emolliency status of the skin, which in turn will result in improved skin
properties such as flexibility and softness.
B. Techniques
There is a wide variety of different techniques that are designed to assess the
biomechanical properties of the skin. Mostly, all these techniques are based on
variations on the way a force (⬃stress) is applied onto the skin and subsequently
to look in time if and how the skin retakes its normal position. The forces can
be applied either vertically or parallel to the skin surface, which can be further
nuanced into different forces such as extension, torsion, indentation, suction, pull-
ing, bouncing, and frictional forces [52,54].
A typical measurement, showing stress-induced skin deformation (usually
referred to as strain) and the recovery in time is shown in Figure 10. Various
ratios of the deformation parameters are also used to describe the biomechanical
status of the skin. For instance, the ratio Ur /Uf (i.e., ratio between immediate
Figure 10 A graphical representation of a typical strain-time curve measured by cuto-

meter SEM575, including the most commonly used parameters.
recovery and maximal extensibility of the skin) is considered a biologically im-

portant factor for the characterization of elastic recovery [55].
In this chapter, we describe the three most commonly used devices, each
of which is based on different stress/strain methods.
The Cutometer SEM575 (Courage ⫹ Khazaka) is a suction device,
whereby a variable vacuum (ranging from 50 to 500 mbar) is applied to the skin
surface. Using a hand-held probe, the skin is pulled by this vacuum into the
aperture of the probe. The skin adjacent to the opening of the probe is maintained
in position by a guard ring. Usually, the strain course under constant vacuum is
shown as a function of time and allows the calculation of a series of mechanical
parameters related to elasticity, viscosity, and plasticity (Fig. 10).
Special attention should be paid to the following specific variables:
1. The three possible measuring modes—probe diameter aperture, on-set
and off-set time, and vacuum strength—will profoundly influence the
measurements and should always be indicated. For instance, a smaller
aperture will monitor the (visco) elastic properties of more superficial
layers of the skin.
2. Pressure application on the skin. Although the probe has a spring sys-
tem, one should pay extra attention to ensure that constant pressure on
the skin surface is ensured, because this will strongly influence the
measurements.
3. Repeated suction. Repeated cycles will cause hysteresis and as such
may even provide extra information.
The cutometer may measure both the mechanical properties of the superficial
skin as well as the deeper layers (e.g., dermis and subdermis) to an unknown
extent [56,57].
With the Dermal Torquemeter (Dia-Stron Ltd), a force parallel to the
surface is applied. A disc glued to the skin is set into motion by a torque motor
and the torque plus the amount of rotation induced are recorded. The torquemeter
will measure the mechanical properties of the more superficial layers (e.g., epider-
mis). The elongation of the skin can be controlled by a guard ring. It has been
claimed that the use of a guard ring and a low torque increases the importance
of the stratum corneum contribution of the measured mechanical functions. Usu-
ally, like with the cutometer, the strain course under constant torque is shown
as a function of time. Reproducibility and accuracy may cause a problem and
strict standardization is needed [53]. A variant of this device is called the Twisto-
meter [58].
The GBE, the gas-bearing electrodynamometer (not commercially avail-
able) is, contrary to the methods mentioned before, especially designed to mea-
sure predominantly the viscoelastic properties of the stratum corneum. As men-
tioned before, the tissue underneath the stratum corneum has a relative large
impact on the measurement of mechanical skin properties. The GBE device is

designed in such a way that the probe (attached to the skin using sticky tape)
picks up sensitive deformation of the stratum corneum as a result of a sinusoidal
low stress onto the skin. As with the torquemeter, a stress parallel to the skin is
applied, and the results of stress and displacement measurements are typically
displayed as a hysteresis loop, yielding information about elastic and viscous
properties of the skin. For a more detailed description, the reader is referred to
Hargens [59]. Recently, a new design, called the linear skin rheometer, has been
described, which is said to yield more reproducible results [60].
The GBE is relatively sensitive to changes in, for example, thickness of
the stratum corneum; also, positioning adjustment and the imperceptible move-
ments of volunteers are a source of major variability in measurements [61–63].
Various other devices have been described; here, we limit ourselves by
mentioning a few of them:
the Dermaflex [64], like the cutometer, based on suction-force
the Extensometer [65], based on stretch-force
the Indentometer [66,67], based on compressing force
the Ballistometer [68], based on drop impact force
Recently, a new device was introduced by Courage ⫹ Khazaka called the Revis-
cometer RVM600, based on acoustical shock waves, without the application
of external forces.
Certainly, the fact that so many devices exist demonstrates that there is no
unique, generally accepted technique that has emerged as a ‘‘standard’’ method,
although the cutometer as well as the torquemeter seems to be quite popular at
the moment.
C. Example
The relationship between the biomechanical parameters (see Fig. 10) and its phys-
iological significance are often complex and not straightforward. For instance,
the extensibility of the skin (Uf) may be increased after treatment with a cosmetic
product, but, on the other hand, aging skin shows also a gradual increase in Uf.
In studying the aging of the skin, the Ur /Uf ratio (i.e., the elastic recovery) seems
to be a particular useful biomechanical parameter, in which typically the more
visco-elastic properties of the skin are expressed. Indeed, aging skin shows a
continuous decrease in Ur /Uf, which may amount to more than 50% after seven
decades (Fig. 11). This considerable decrease is especially manifest on the dorsal
forearm, because here the effects are a combination of both intrinsic aging (i.e.,
biological or chronological aging) as well as extrinsic aging (i.e., photoagaing).
On the volar forearm the decrease is much less pronounced, indicating that UV-
exposure during one’s lifetime has a great impact on the elastic properties of
Figure 11 A plot of the elastic recovery (Ur /Uf) of the dorsal forearm versus age for
32 subjects, measured by the Cutometer SEM575. R ⫽ 0.82; aperture diameter: 2 mm;
pressure: 500 mbar; pressure-on time: 1 sec; pressure-off time: 1 sec repetition: 3; pre-
time: 0 sec.
the skin. Numerous studies have indeed shown that UV radiation causes photo-
elastosis, in which, among other factors, massive accumulation of unstructured
elastin causes a loss of skin’s elasticity [69]. It seems that the cutometer is more
appropriate for measuring this phenomenon than the torquemeter, which is in
line with the fact that the torquemeter registers the more superficial, rather than
the deeper, dermal biomechanical changes of the skin [70].
VI. ASSESSMENT OF DESQUAMATION

A. General
The loss of stratum corneum at the skin surface (desquamation) is an integral
and essential part of epidermal physiology, which takes place in a controlled
manner by the loss of single corneocytes (fine flakes). The term desquamation
is, however, also used to describe the shedding of scales (or squames), defined
as flat plates or coarse flakes of stratum corneum, which actually are conglomer-
ates of corneocytes.
Using the first definition, the rate of desquamation is expressed as the num-
ber of corneocytes released per square centimeter per hour. This rate is related
to the stratum corneum turnover time. Stimulating the epidermal cell renewal
can shorten this turnover time and increases the rate of desquamation (and thus
gives the skin a ‘‘younger’’ appearance).
Using the second definition, the degree of desquamation is related to the
extent of scaliness. And as scaly skin is generally associated with dry skin, a
high degree of desquamation is also associated with dry skin. So, depending on
the definition used, rather contradictory phenomena can be described, giving rise
to confusion.
The mechanical strength of the stratum corneum is based on the coherent
lipid layers and on the intercellular junctions (desmosomes). The breakdown of
the desmosomes in the outer layers of the stratum corneum is essential for the
desquamation process (loss of single corneocytes) and requires the action of pro-
teases such as stratum corneum chymotryptic enzyme (SCCE). Desmosomal de-
gradation must occur to ensure that desquamation proceeds in an orderly fashion.
One of the most important factors for these enzymatic reactions is an optimal
water and lipid environment, which in turn will lead to optimal desquamation
[71,72]. In case of insufficient breakdown, dry, scaly skin will arise. Such skin
is characterized by groups of elevated corneocytes and flakes, which give the
skin a rough, cracked, gray appearance (xerosis).
Large scales are clearly visible to the naked eye because of the occurrence
of air between the scales and the surface of the skin (due to the large differences
in refractive indices). Application of a lipid-rich cosmetic product generally will
result in replacement of the air by lipid, making the scales less visible. The scales
will become clearly visible again after absorption of the lipid or after washing
of the skin. Daily application of a well-formulated cosmetic product will result
in an improved skin condition and might eventually result in a skin without scales.
This latter process will take about one week.
B. Techniques
There are three possible approaches to characterize the process of desquamation:
the assessment of the stratum corneum turnover, the measurement of the intracor-
neal cohesion, and the quantification of scaling.
1. Assessment of the Rate of Desquamation and Stratum

Corneum Turnover
Measurement of the rate of desquamation can be direct [73], by counting the
number of corneocytes released at the surface with a passive chamber technique
(expressed as number of corneocytes released per square centimeter per hour) or

with a forced desquamation technique such as the detergent scrub method [74].
An indirect measurement of the rate of desquamation estimates the clear-
ance rate of loss of a stain on the stratum corneum. Staining methods aim to
apply a substantive dye, such as the fluorescent dye dansyl chloride, to the stratum
corneum. [75]. After penetration, the entire thickness of the stratum corneum
should be labeled. When the stained stratum corneum has been shed completely,
the stain will have disappeared, and the time taken is the stratum corneum turn-
over time (usually about 20 days). An alternative for staining is artificial tanning
[76] of the skin induced by dihydroxyacetone (DHA). Fading of pigmentation
occurs during shedding of the stratum corneum. The evaluation of the intensity
of browning of the skin is assessed colorimetrically (see also Sec. VIII).
2. Measurement of the Intracorneal Cohesion

The release of the intracorneal cohesion (ICC) allows desquamation to occur.
This binding force can be measured using a cohesograph. This device employs
a piston that is stuck to the skin surface with a cyanoacrylate adhesive and the
force required to distract a segment of stratum corneum from the surface is mea-
sured [77]. One of the drawbacks of this method is its complexity.
3. Quantification of Scaling
Scaly skin can be assessed clinically or instrumentally. The clinical assessment
can be performed either by the subject himself or herself or by an expert evaluator
[78]. Very helpful for the clinical assessment could be the use of a microscope
(in vivo microscopy) or the use of the Visioscan VC98 device (Courage ⫹
Khazaka). This video camera monitors the skin surface illuminated under a UVA
light source. The spectrum of the light is optimized in order to exclude reflections
from the deeper layers of the skin. This results in sharp images from the scaly
skin. These images can be analyzed afterward by a graphic depiction technique
[45] or by visual scoring of the degree of scaling.
Visual examination of tape strippings of the stratum corneum can reveal
differences in the extent of dryness not noticeable by visual inspection of the
skin [79]. New image analysis techniques were developed, following this simple
method, to objectively analyze the desquamation of the stratum corneum. Skin
surface sampling discs, such as the commercially available D-Squames (Cu-
Derm) and Corneofix (Courage ⫹ Khazaka), can be used to sample loose cells
and scales from the superficial stratum corneum. The contact time is usually 5
to 30 seconds. After placement of the disc or tape on a black background, an
experienced observer can grade the extent of scaliness. It is a convenient method
for evaluating the effectiveness of cosmetic products and also for classifying
cleansing products for their irritation/compatibility potential. One option is also

to take video images of these discs and to process them afterward with the aid
of an image analysis program to calculate the degree of desquamation [80].
When appropriately stained, scales harvested by the adhesive discs develop
an intense color. This property is used in the squamometry method to improve
the sensitivity [81–83]. The rinsing process, which is needed for the removal of
excess of stain, is critical, however: too intense rinsing will remove the scales;
mild rinsing will not remove excessive stain completely. Corneosurfametry [84]
deals with staining of cyanoacrylate skin surface strippings after contact with
surfactant solutions. Both methods (squamometry and corneosurfametry) can be
used for comparison of the human skin compatibility of personal care cleansing
products.
C. Examples
Figure 12a shows scales sampled from untreated forearm skin by a Corneofix
skin surface sampling disc (image taken by Visiometer SV500). Figure 12b shows
the scales sampled from the opposite arm washed with an alkaline soap during
one week. From these pictures it is clear that aggressive cleansing products can
induce formation of large scales.
Techniques to quantify scaling can be used to select mild cleansing prod-
ucts but can also be used to prove that leave-on products improve the condition
of the skin. Figure 13a shows the scaly (untreated) skin of the forearm; Figure
13b the opposite arm after one week of product application. The last picture is
taken 18 hours after the last product application.
Figure 12 Images taken by Visiometer SV500 from sampled scales: (a) untreated fore-
arm skin, (b) opposite forearm, washed during one week with an alkaline soap.
Figure 13 Pictures of forearm skin, taken by the Visioscan VC98: (a) untreated, scaly
forearm skin, (b) opposite forearm, after 1-week application of a moisturizing product.
VII. ASSESSMENT OF SURFACE LIPIDS

A. General
The skin is covered by a thin layer of lipids that are derived mainly from sebum
excreted from the sebaceous glands via the hair follicle. Although no evident
role can be attributed to sebum (e.g., it is not essential for proper moisturization
of the skin), interaction with the stratum corneum may be responsible for certain
biophysical effects. Indeed, Blanc et al. [85] have demonstrated a substantial
capacity of the stratum corneum to absorb sebum. Sebum lipids, which consist
mainly of squalene, wax- and cholesterol-esters, and triglycerides, are often called
skin surface lipids (SSL). Analytical methods, including contamination problems
with epidermal (⬃stratum corneum) lipids, will not be described in this chapter
(see Chapter 6).
Sebum lipids are not an integral part of the stratum corneum epidermal
lipids and as such do not play an essential role in the skin’s barrier function.
Sebum quantities present on the skin surface may be as high as 50 up to 500
µg/cm2, much higher than the amount of epidermal lipids, which varies from 5
to 50 µg/cm2 [86]. Under normal conditions, sebum is present in an emulsified
form with water and/or sweat, constituting the so-called hydrolipidic film [87].
Cosmetic products, especially the lipid fraction (i.e. its emollients and emulsifi-
ers) will interact with this hydrolipidic film [88]; this may result in altered absorp-
tion kinetics and biophysical effects of the products, a phenomenon that is often
overlooked by cosmetic scientists.
Several skin disorders, such as acne and seborrheic dermatitis, are associ-
ated with aberrant sebum secretion levels, and strategies to reduce sebum secre-
tion are an increasing area of interest [89–91].
B. Techniques
Two parameters are of importance in the assessment of surface lipids: the homeo-
static, casual level of sebum present on the skin and the sebum excretion rate
(SER), which can be determined after proper degreasing of the skin and looking
at the refatting kinetics. Alcohol seems to be the best cleansing agent [88].
Amounts of SSL vary greatly depending on number and activity of sebaceous
glands, which in turn depend on body site; for example, scalp, face (i.e., the so-
called T-zone) and upper side of trunk have a high density of sebaceous glands
(ca. 500 per cm2 vs. ⬍50 per cm2 on other sites [92,93]).
Various techniques for the collection and quantification of SSL have been
described [94]. The two most popular sebumetric methods will be described here.
The Sebutape (CuDerm Corporation) is a tape containing a polymeric
film that can be directly attached to the skin [95]. On places where SSL lipids
are absorbed, the color of the film will be changed. Thus, not only a ‘‘fingerprint’’
of the number of follicular openings but also the activity of its sebaceous glands
is obtained [96,97]. The technique can be used to determine a variety of parame-
ters such as:
SER
total produced quantity
number of excreting follicles
quantity per follicle
Quantification of these parameters can be realized in different ways: (1) visual

assessment, (2) color measurements using reflectance chromametry, (3) densito-
metric measurement, or (4) image analysis [89]. Moreover, quantitative and quali-
tative lipid analysis is possible after extraction of the lipids from the tape.
Whatever the parameter under investigation, strictly controlled experimen-
tal procedures are required for proper assessment of SSL quantities. Control of
temperature, relative humidity, and proper acclimatization period of volunteers
are of critical importance.
Some conditions that may influence the SER and SSL quantities are:
History of application of oil/lipid-containing topical products, which may

influence SER
Body site: scalp, face, upper chest, and shoulders have highest levels of
SSL [92,93]
Age and sex of volunteers: generally, sebum production is low among chil-
dren and is higher in male adults than in female adults, and a gradual
decrease is seen with increasing age. This is mainly due to the fact that
sebum secretion is under hormonal (androgenic) control.
The Sebumeter SM810 (Courage and Khazaka) is a photometric device and is

based on the measurement of increased transparency of a frosted plastic film,
caused by lipid absorption. The film is pressed on the skin and lipids are trans-
ferred from the skin onto the film; its rough surface is smoothed, because the
spreading of the lipids fills up the cavities. Incident light is less scattered and
more light can pass through the coated surface. A cartridge contains a continuous
plastic film that is sufficient for approximately 300 measurements. The cartridge
is placed in a measuring device that measures the transmission of light, emitted
from a photocell, through the film. The difference in transparency before and
after lipid sampling relates to the amount of SSL, and proper calibration converts
the data into µg SSL per cm2. Unlike the Sebutape method, the sebumeter does
not measure the number of excreting follicles and quantity of sebum per follicle.
It should be mentioned here that the sebumetric techniques may also be
used to measure the absorption rates of lipophilic fractions of cosmetic prod-
ucts—i.e., the emollients and emulsifiers per se. Of course, proper removal of
SSL prior to product application is important.
Various other methods and devices have been described in the literature,
such as cigarette paper and bentonite clay methods and the Lipometre (not com-
mercially available) [98]. Another interesting method is the combination of Sebu-
fix (Courage ⫹ Khazaka) and the Visiometer (see Sec. IV), which visualizes
the sebaceous secretion in time (not published). An overview of the various meth-
odologies is given by Piérard [99].
With reference to the presence or absence of SSL, four different skin types
are in general recognized (see Fig. 14) [100]. Relatively high SSL levels are
found in people with oily and mixed skin.
C. Examples
Figure 15 shows a typical course of the reappearance of SSL on the forehead,
after it has been removed by a facial cleanser. From these data, a person’s typical
SER can be calculated. Generally, 3 to 4 hours are necessary to normalize the
sebum levels for a normal skin type. For oily skin, this takes much less time.
It may be noted that the starting value in this examples is relatively low
(180 vs. 300 µg/cm2); this is not the subject’s casual level of SSL, but it is the
result of the fact that the volunteer had washed his face at home in the morning
and the test took place quite early in the morning before normalization had oc-
curred. This illustrates once more that the assessor should be alert at all times!
Especially on body sites that have only low endogenous SSL levels (e.g.,
the volar forearm), the sebumeter can be used to quantify the amount of lipids
from a cosmetic product, deposited on the skin and subsequently absorbed.
This is demonstrated in Figure 16, where the absorption of the lipid phase
of a cosmetic product in time is shown. The 14% lipid phase consisted of 5%
Figure 14 Schematic categorization of different skin types in relation to presence of

SSL and hydration state.
Figure 15 Course of sebum (SSL) levels on the forehead versus time, after two times
washing with a facial cleanser; measured by the Sebumeter SM810.
Figure 16 Absorption kinetics on the volar forearm of emollients from a cosmetic prod-
uct, as measured by the Sebumeter SM810.
cetearyl glucoside/cetearyl alcohol (emulsifier) and 9% of a mixture of isohexa-

decane, caprylic/capric triglyceride, and ethylhexylpalmitate (emollients). A cal-
culated amount of 270 µg/cm2 lipids was applied on the whole volar forearm.
Within 40 minutes approximately 80% is absorbed; Notably, after a second appli-
cation of the same amount of lipids, the absorption is much lower, i.e. ⬍50%
after 40 minutes. This clearly demonstrates that the skin becomes lipid-saturated
at high application levels.
VIII. MISCELLANEOUS TECHNIQUES
In this section, some less frequently used in vivo, noninvasive techniques are
briefly described. Other techniques are described elsewhere in this book (see
Chapters 6 and 8).
A. High-Resolution Ultrasound
High-frequency (20 MHz and 50 MHz) ultrasound measurements can be used
to examine the lipid and water content of living epidermis and the intrinsic (bio-
logical) and extrinsic (photoaging) of the skin [101,102]. This technique gener-
ates two-dimensional pictures representing the skin structure. It can also be used
for the in vivo estimation of the thickness of the dermis [103] but is not appro-
priate to measure the thickness of the stratum corneum.
B. Optical Coherence Tomography

Optical coherence tomography is a new diagnostic in vivo method for tissue
characterization. Using this technique, structures of the stratum corneum, the liv-
ing epidermis and the papillary dermis can be distinguished [104].
C. Magnetic Resonance Imaging

Magnetic resonance imaging is a sophisticated technique allowing deep explora-
tion of the skin, including the hypodermis [105]. It offers possibilities to assess
the hydration level of human stratum corneum by measuring proton density and
proton relaxation times [14,106].
D. Confocal Laser Scanning Microscopy

A very promising in vivo technique is confocal (laser scanning) microscopy. It
produces spatial 3-dimensional information on the skin: epidermal cells can be
individually observed [107]. It is also able to measure the thickness of the stratum
corneum.
E. Skin Color
Skin color measurements can be performed by scanning reflectance spectropho-
tometry (e.g., Minolta Chromameter CR-200), using the L*a*b*-classification
system as the preferred system to characterize the color [108]. The parameter L*
represents the brightness, a* the green-red, and b* the yellow-blue axis. This
means that white skin will show high values for L*, erythemic skin high values
for a* [109], and tanned skin high values for b*.
Skin color measurements can also be performed by narrow-band reflectance
spectrometry [110]: Erythema/Melanin Meter (Dia-Stron), Mexameter
MX18 (Courage ⫹ Khazaka), and Dermaspectometer (Cortex). The aim of this
technology is to explore the presence of melanin and hemoglobin. The data are
expressed as erythema and melanin indices.
It has to be taken into account that skin color is influenced by a variety of
factors, including local blood flow, skin surface lipids, and scaling. And as blood
flow is also influenced by temperature, pressure exerted by the probe, and position
of the measured skin site relative to the heart, these factors might also affect skin
color.
Figure 17 Effect of washing with soap and washing with tap water on skin pH, mea-
sured by the Skin-pH-Meter (baseline pH 5.1).
F. pH
Standard pH meters with a flat surface electrode can be used to measure the pH
of the skin [111]. Figure 17 shows the effect of washing the skin with an alkaline
soap: the pH of the skin increases for several hours. Also washing with tap water
increases the pH to some extent, as tap water usually is slightly alkaline.
G. Skin Temperature
Skin temperature may be measured by readily available skin surface temperature
measuring devices [112]. To avoid direct contact between skin and probe, infra-
red thermography is the preferred technique for measuring the temperature of
the skin. This technique is also able to visualize the temperature profile of rela-
tively large surfaces such as the face or the forearm [113].
One of the applications of skin temperature assessments is measuring ery-
thema [114].
H. Friction
The frictionmeter measures the power necessary to move an object on the skin
surface. The measured parameters are adhesional and glide friction [115]. High
friction values are an indication of a rough skin. Nevertheless, most moisturizing

creams increase friction after application [116,117]. Interpretation of the obtained
data is difficult.
SUPPLIERS
Breuckmann GmbH
Torenstrasse 14, 88709 Meersburg, Germany
Telephone: ⫹⫹49 7532 1563
Fax: ⫹⫹49 7532 9377
E-mail: [email protected]
Internet site: http://www.breuckman.com/
Cortex Technology
Smedevaenget 10, 9560 Hadsund, Denmark
Telephone: ⫹⫹45 9857 4100
Fax: ⫹⫹45 9857 2223
Internet site: http://www.cortex.dk/
Courage ⴙ Khazaka electronic GmbH

Mathias-Brüggen-Str. 91, 50829 Cologne, Germany
Telephone: ⫹⫹49-221-956499-0
Fax: ⫹⫹49-221-956499-1
Internet site: http:/ /www.courage-khazaka.de/
CuDerm Corporation
17430 Campbell Rd., Suite 106, Dallas, TX 75252, USA
Telephone: ⫹⫹1-800 690 1933
Fax: ⫹⫹1-972 248 1094
Internet site: http://www.cuderm.com
Dia-Stron
Unit 9, Focus 303, Business Centre South Way Andover Hampshire,
SP10 5NY, United Kingdom
Telephone: ⫹⫹44 1264-334700

Fax: ⫹⫹44 1264-334686
GFMesstechnik GmbH
Warthstrasse 21, D- 14513 Teltow/Berlin, Germany

Telephone: ⫹⫹49 3328 305185
Fax: ⫹⫹49 3328 305188
Internet site: http://www.gf-messtechnik.de
Hommelwerke GmbH
Alte Tuttlinger Str. 20, 78056 Villingen-Schwennigen, Germany

Telephone: ⫹⫹49 77 20 60 20
Fax: ⫹⫹49 77 20 60 21 23
Internet site: http://www.tipcoeurope.com
MINOLTA
Internet site: http://www.minolta.com
NOVA Technology Corporation
75 Congress Street, Portsmouth, NH 03801-4006, USA

Telephone: ⫹⫹1-603-422-9595
Fax: ⫹⫹1-603-446-34066445522-7330
Internet site: http://www.novatechcorp.com/
Servo Med AB
P. O. Box 47, S-432 21 Varberg, Sweden

Telephone: ⫹⫹46-340664455
Fax: ⫹⫹46-34017320
Internet site: http://www.servomed.se
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8
Detection of Cosmetic Changes
in Skin Surface Lipids by Infrared
and Raman Spectroscopy
Thomas Prasch and Thomas Förster

I. INTRODUCTION
Human skin consists essentially of three layers: the deep subcutaneous fatty layer,
the dermis, and the epidermis. The outermost layer of the epidermis is the horny
layer, or stratum corneum (SC). The barrier function of the skin resides almost
entirely in the outermost portion in the SC [1]. It presents a system that prevents
dehydration of the underlying tissues and excludes the entry of noxious sub-
stances from the environment [2,3]. The stratum corneum consists of 10–15 lay-
ers of flattened, anucleate, keratinized cells embedded in a lipidic matrix. Typi-
cally, the dry SC is approximately 10 µm thick.
The barrier function is mainly the result of the unique structure of proteins
and lipids in the skin. The lipids in the stratum corneum are arranged into lamellar
structures that are covalently linked to proteins of cornified envelopes. In that
way, a water-impermeable layer of lipids is formed in the SC. The number of
disulfide cross-links in the SC is significantly lower than in nail or in hair. In
the SC, a noteworthy amount of sidechain mobility is found. This is due to the
loose packing of keratin filaments in the SC.
The main constituents of the SC are protein, 75–80%; lipids, 5–15%; and
unidentified materials, 5–10% on a dry weight basis [4,5]. The protein fraction
within the cells consists mainly of α-keratin (approx. 70%) with a smaller amount
of β-keratin (approx. 10%) and cell wall envelopes (approx. 5%). In the SC,
227
228 Prasch and Förster
several types of lipids are found: neutral lipids, sphingolipids (ceramides), polar
lipids, and cholesterol sulfates.
The stratum corneum is not a static but instead a dynamic barrier that is
continually being formed by the dermis by differentiation of keratinocytes to
corneocytes while on average one layer of corneocytes is lost from the upper
surface per day. Small-angle x-ray scattering (SAXS) experiments have shown
that human skin lipid layers are arranged in two types of parallel layers, which
have interlayer distances of 6.4 nm and 13.4 nm [6,7]. In contrast to normal cell
membranes, these lipid multilayers are not liquid-crystalline at skin temperature
but exhibit a complex polymorphism of mainly solid phases in which the lipid
alkyl chains are tightly packed and immobile [8,9].
Infrared [10,11] and Raman [12] spectroscopy are two techniques that have
proved especially suited for the investigation of the stratum corneum and the
interaction of cosmetic products with the stratum corneum [13]. By using the IR-
spectra of the facial skin, an investigation panel is classified into different skin
types according to the sebum content. A comparison with the position of the CH2
stretching vibrations of synthetic lipid mixtures with a known degree of order
allows quantification of the degree of order of the skin lipids in vivo. The effect
of a mild facial cleansing is investigated using a cleansing milk as an example
and compared with the use of a surfactant-based shower gel. Oils and lipids,
the chief constituents of skincare cosmetic creams, show completely different
interactions with the skin lipids; this can be utilized positively as the basis for
the development of biomimetic lamellar creams [13].
In vitro skin cultures are another research area that has contributed tremen-
dously to a deeper understanding of skin function in the past years. Today, not
only are epidermal skin cultures commercially available and used routinely but
also the much more complex full-skin models have been successfully cultured
in some laboratories [14]. Due to their similarity to normal human skin on one
hand and their inherently low biological variability on the other hand, in vitro
skin cultures are especially useful for basic cosmetic research. The analysis of
IR and Raman spectra helps to obtain a fundamental understanding of the similar-
ities and differences in the stratum corneum barrier between normal human skin
and in vitro skin models.
II. TEST METHODS

A. Biophysical Techniques Applied to the Study of SC
and Skin Lipids
Several biophysical techniques such as differential scanning calorimetry (DSC)
[15,16], x-ray diffraction [7], nuclear magnetic resonance (NMR) [17], and elec-
tron spin resonance (ESR) [18] have been applied to study and characterize the
Detection of Changes in Skin Lipids by IR and Raman Spectroscopy 229
SC. One important approach is the use of vibrational spectroscopy to probe the
molecular nature of the skin and especially the SC. The early work concentrated
on the use of Fourier transform infrared (FT-IR)-spectroscopy [19]. The water
concentration in the tissue has been determined by means of IR-spectroscopy
[20]. It has been used successfully to probe the tissue in vivo using attenuated
total reflection methods [21,22]. For the exact characterization of the lipid layer
structure in the stratum corneum, IR spectroscopy has proved itself in practice.
The exact spectral position of the symmetrical CH2 stretching vibrations in the
IR spectrum can provide information about the average degree of order of the
lipid alkyl chain conformation [23]. An alternative vibrational spectroscopic tech-
nique, which has gained considerable interest, is Raman spectroscopy.
B. Description of the Basics of Vibrational Spectroscopy

Molecules consist of atoms that have a certain mass and that are connected by
elastic bonds: As a result, they can perform periodic motions. They have vibra-
tional degrees of freedom. Nonlinear polyatomic molecules with n atoms possess
3n-6 normal vibrations that define their vibrational spectra. Linear molecules pos-
sess only 3n-5 vibrational degrees of freedom.
Molecular aggregates such as complexes or biomembranes behave like
‘‘super-molecules’’ in which the vibrations of the individual components are cou-
pled. The two most important methods of vibrational spectroscopy are IR and
Raman spectroscopy. They provide complementary images of molecular vibra-
tions, because in these spectroscopic techniques the mechanisms of the interac-
tion of light quanta with molecules are quite different. Further theory and back-
ground of vibrational spectroscopy can be found in the literature [24–26].
C. Description of IR Spectroscopy
Infrared spectra are usually recorded by measuring the transmittance of light
quanta with a continuous distribution of the sample. The frequencies of the ab-
sorption bands are proportional to the energy difference between the vibrational
ground and excited states. The absorption bands due to the vibrational transitions
are found in the wavelength region of λ ⫽ 2.5 µm up to 1000 µm, which corre-
sponds to a wavenumber range of ν̃ ⫽ 4000 cm ⫺1 ⫺ 10 cm ⫺1.
Interaction of infrared radiation with a vibrating molecule is possible only
if the electric vector of the radiation field oscillates with the same frequency as
the molecular dipole moment does. The consequence is that vibration is only
infrared active if the molecular dipole moment is modulated by the normal vibra-
tion. The following condition needs to be fulfilled to observe an IR-band
∂µ
≠0 (1)
∂q
In this expression, µ is the molecular dipole and q stands for the normal coordi-
nate describing the motion of the atoms during a normal vibration.
D. Description of the Attenuated Total

Reflectance Technique
One special IR technique, that is important for the investigation of the skin barrier
is the attenuated total reflectance technique. It belongs to the class of reflectance
techniques that are often applied when normal transmittance methods cannot be
successfully applied. The sample is brought into optical contact with the surface
of a special crystal. The IR-beam, propagating within the crystal by means of
several total reflections, senses the material on the surface by penetrating into
the layer over a distance, which is calculated below. The measuring beam is
directed through the crystal to be reflected at the interface to the sample; for
this reason the technique is also referred to as internal reflection. For detailed
information on the ATR technique, the books of Harrick [27,28] and Mirabella
[29] are recommended.
1. Theory of the ATR Technique

An explanation of the basic theory of the ATR method follows: Radiation is
totally reflected at the boundary between a medium with a refractive index n1
and a medium with lower refractive index n2 if it hits this boundary with an
incident angle greater than the critical angle θ c ⫽ arcsin (n2 /n 1). The reflected
radiation energy penetrates the boundary as a so-called evanescent wave. The
penetration depth d p is the thickness in which the intensity decreases to 1/e of
the intensity at the boundary. The penetration depth d p depends on the refractive
indices n 1 and n 2, the incident angle θ, and the wavelength λ (in vacuum):
λ n2
dp ⫽ with n 21 ⫽ (2)
√
n1
2πn 1 sin θ ⫺ n
2 2
21
The penetration depth for skin is usually on the order of 0.3–3 µm, depending
mainly on the wavelength of interest, the material of the ATR crystal, and the
hydration level of the sample.
The sample absorbs the evanescent field so that the totally reflected wave
is attenuated accordingly. The consequence is that the reflectance resembles
closely the corresponding transmission spectrum. The resultant attenuated radia-
tion is measured as a function of wavelength by the spectrometer and gives rise
to the absorption spectral characteristics of the sample.
Some sensitivity is lost with angles of reflection well above the critical
one. But it can be regained by multiple internal reflections. The signal/noise ratio
Figure 1 Schematic representation of the ATR-technique.
of the spectrum obtained by means of the ATR-technique can be adjusted by the

number of reflections used. It depends on the size of the sample-coated area of
the slab: whether both surfaces of the crystal, only one, or only a fraction of it
is exploited for the measurement.
2. Practical Aspects of the ATR Technique

The crystals (also called internal reflection elements, IRE) used in ATR cells are
made from materials that have a proper refractive index to allow internal reflec-
tion. Moreover, they should offer a low solubility in water, and the material
must show transparent regions in the infrared. Commonly used materials are zinc
selenide (ZnSe, refractive index 2.4), germanium (Ge, refractive index 4.0), and
thalliumiodide/thalliumbromide (KRS-5, refractive index 4.0). The shapes of the
commonly used crystals are trapezoid or parallelepiped.
The basic experimental setup of an ATR experiment is illustrated in Figure
1.
E. Description of Raman Spectroscopy

1. Theoretical Background
The second important type of vibrational spectroscopy is Raman spectroscopy.
If a sample is irradiated with an intense beam of monochromatic radiation (e.g.,
from a laser) of a frequency ν, most of the radiation is transmitted by the sample.
Only a very small fraction of the exciting radiation (approx. 1 photon in 10 4) is
elastically scattered. This fraction of the radiation is called Rayleigh scattering.
The wavenumber of the Rayleigh scattering is equal to that of the incident radia-
tion. An even smaller portion (approx. 1 photon of 10 8) scatters inelastically with
wavenumbers different from the incident radiation (ν ⫾ ν i, where ν i represents
a vibrational frequency of the molecule). This inelastically scattered radiation is
designated as Raman scattering.
The Raman scattering derives from the excitation of vibrational and rota-
tional levels of the electronic ground state of the molecules. This causes an energy
loss of the incident radiation and a band shift to longer wavelengths as compared
to the Rayleigh line, which is known as Stokes shift. Anti-Stokes lines can be
observed when the molecules under consideration are in excited vibrational levels
before the interaction with the laser source. At room temperature, these anti-
Stokes lines are weaker than the Stokes lines.
When a molecule is exposed to an electric field, electrons and nuclei are
forced to move in opposite directions. A dipole moment is induced which is
proportional to the electric field strength and to the molecular polarizability α.
A molecular vibration can be observed in the Raman spectrum only if there is
a modulation of the molecular polarizability by the vibration. The condition
冢冣
∂α
∂q
≠0 (3)
needs to be fulfilled for a vibration to be observed in the Raman spectrum.
2. Complementarity of IR and Raman Spectroscopy

Raman and infrared spectroscopy are complementary techniques that differ in
their interactions with the incident radiation. For a vibrational mode to be infrared
active, the dipole moment of a bond must change, whereas for a mode to be
Raman active the polarizability of a bond must alter. The differing selection rules
for activity in these two techniques are the reasons for the complementary infor-
mation content of IR and Raman spectra.
For a CC O moiety with an existing dipole, a change in the dipole moment
can easily be induced and consequently the mode is strongly infrared active. But
such a dipole-distorted bond cannot easily have its polarizability altered and so
only a weak Raman effect results. Homopolar bonds such as C CC moieties can
easily have their electron clouds distorted and so are polarizable and Raman ac-
tive, whereas they possess no dipole moments and hence are infrared inactive.
The basic principles of IR and Raman spectroscopy are compared in Fig-
ure 2.
3. Advantages and Disadvantages of Raman versus

IR Spectroscopy
One practical consequence of the different selection rules for Raman and IR-
spectroscopy is that water is a very weak Raman scatterer but strongly absorbs
infrared radiation. This is a clear advantage for Raman spectroscopy as a tool in
the analysis of the molecular structure of biological materials. Moreover, the
wavenumber range that is accessible to Raman spectroscopy is greater than that
of infrared. But Raman spectroscopy is rather insensitive because it examines
Figure 2 Mechanisms of infrared absorption and Raman scattering.
very weak scattered radiation. Therefore, Raman spectroscopy is not such a versa-
tile tool in the analysis of minor compounds.
4. The Main Components of IR and Raman Spectrometers

Today there are two main types of IR and Raman spectrometers. They use either
the dispersive or the Fourier transform technique. Both comprise four main instru-
mental components: a radiation source, optics to illuminate the sample and to
collect and focus the radiation to be analyzed, a monochromator (for dispersive
spectrometers) or an interferometer (for FT-instruments), and a detector.
Radiation Sources Used in IR Spectroscopy. For the generation of the
infrared radiation in middle infrared (MIR), usually a thermal radiation source
is used. Today the most popular radiation source for MIR spectrometers is the
so-called globar (glow bar). It is a rod or a tube with a diameter of 6–8 mm
consisting of SiC. It is heated by a high current at low voltage. Its emission is
about 75% of that of a black body at about 1400 K.
Radiation Sources for Raman Spectroscopy. The excitation of Raman
scattering is (at least theoretically) not restricted to a specific region of the electro-
magnetic spectrum. Usually an ultraviolet, visible, infrared, or near-infrared exci-
tation source is used. Raman scattering is much weaker than Rayleigh scattering.
Therefore, a very strong excitation source is required. The advent of lasers has
revolutionized Raman spectroscopy. Lasers provide strong, coherent monochro-
matic light in a wide range of wavelengths. The selection of the most appropriate
laser radiation source depends on sample color, stability, and molecular features
that may result in fluorescence. Fluorescence is often much more intense than
the Raman effect. Especially, biological samples such as skin tend to have a
pronounced fluorescence effect. Fluorescence usually gets weaker as the laser
moves toward the infrared region of the electromagnetic spectrum. For this rea-
son, manufacturers have developed near-infrared Fourier transform Raman spec-
trometers. The Nd:YAG (neodymium-doped yttrium aluminum garnet) with a
wavelength of 1.064 µm is the most widespread excitation source for NIR-
Raman-spectrometers, but Raman spectra can also be obtained by means of laser
excitation in the ultraviolet, visible or infrared region.
Dispersive and Fourier Transform Spectrometers. Today there are two

main types of IR and Raman spectrometers. They utilize either the dispersive or
the Fourier transform technique. In dispersive spectrometers, a grating monochro-
mator is used. The essential problem with the dispersive spectrometer lies in its
monochromator. This contains narrow slits at the entrance and exit that limit the
wavenumber range of the radiation reaching the detector to one resolution width.
These limitations can be overcome through use of Fourier transform infrared
spectrometers. In Fourier transform spectrometers, the basic optical component
is a Michelson interferometer. The essential experiment to obtain an FTIR spec-
trum is to produce interferograms, both with and without sample in the beam, and
then transform these interferograms into spectra by means of the mathematical
operation of a Fourier transformation, which transfers frequency domain data
into time domain data and vice versa. The ratio of the source with sample absorp-
tions and without them corresponds to the IR-spectrum of the sample. The FT
can be calculated rapidly on-line with modern microcomputers connected to the
spectrometer. FT instruments simultaneously measure the signal of multiple data
points by analysis of a single signal from a detector providing the full spectral
region from only one scan. The data accumulation is superimposable, so that FT
spectrometers allow accurate coaddition of scans.
FTIR spectrometers offer many significant advantages over dispersive
spectrometers. The Fellgett (or multiplex) advantage is the result of an improve-
ment in the S/N ratio per unit time, which is proportional to the square root of
the number of resolution elements being monitored. It results from the large num-
ber of resolution elements being monitored simultaneously.
The Jacquinot (or throughput) advantage derives from the fact that no re-
stricting device such as a slit is necessary in FTIR spectroscopy. Particularly at
low resolution, the total radiation source output can be passed through the sample
continuously. This results in a substantial gain in energy at the detector, which

leads to an improved S/N ratio.
Moreover, there is a speed advantage. It is possible to obtain FTIR spectra
on a millisecond time scale. FTIR spectroscopy also allows one to determine the
exact position of an IR band with extremely high precision, is much better than
that achieved with a dispersive spectrometer.
Detectors. For standard applications often a pyroelectric detector such as
deuterium triglycin sulfate (DTGS) is used. Liquid-nitrogen-cooled semiconduc-
tor quantum detectors, such as mercury cadmium telluride (MCT) detectors, are
frequently used for more demanding applications in IR and Raman spectrometers.
They offer a very high sensitivity and an advantageous low noise equivalent
power (NEP). For detection in the visible and ultraviolet region, photographic
plates, photomultipliers, and charge-coupled diode (CCD) array detectors are
commonly applied.
F. Comparison of IR and Raman Spectra of SC

The assignment of the bands of proteins and lipids in the stratum corneum has
been done for IR and for Raman spectra [5]. The number of visible modes in
the Raman is nearly twice as high as in the IR spectrum. By means of lipid
extraction of samples of human stratum corneum, the origin of bands could be
determined.
Several comparisons of human and animal tissues have been published
[30,31]. The molecular structure of snake skin is markedly different from that
of human stratum corneum. The ceramides, characteristic of the lipids of human
SC, are replaced in snake skin by phospholipids. Moreover, snake skin possesses
an outer β-keratin sheet layer. SC from pigs resembles more closely that of the
human SC. By means of a Fourier self-deconvolution technique, the main assign-
ments and peak positions in Table 1 were confirmed [32].
In the IR spectrum, there is a strong water feature around 3300 cm ⫺1 that
is largely absent in the Raman spectrum. The positions of the CH stretching
modes around 3100 cm ⫺1 to 2700 cm ⫺1 indicate the conformation of the intercel-
lular lipid chains. The fingerprint region of the spectra between approx. 1800
cm ⫺1 to 1000 cm ⫺1 show some characteristic differences. The Amide I band
(mainly CCO stretching vibration) is strong in the infrared, but it is compara-
tively weak in the Raman. However, the CH 2-scissoring modes of the lipid chains
are stronger in the Raman. However, most of the bands appear in both techniques.
The IR spectrum below 1000 cm ⫺1 tends to lose some definition, and peaks
are difficult to observe because of the strong IR-absorbance of water. Characteris-
tic for the Raman spectrum is a series of weak but important bands between 1200
cm ⫺1 and 1000 cm ⫺1. They can be assigned to the CE C stretching modes of
Table 1 FTIR and FT Raman Band Assignments Consistent with the Vibrational
Modes from Human Stratum Corneum
Raman frequency IR frequency
(cm ⫺1 ) (cm ⫺1 ) Assignment
424 δ(CCC) skeletal backbone
526 ν(SS)
600 ρ(CH) wagging
623 ν(CS)
644 ν(CS); amide IV
746 ρ(CH 2) in-phase
827 δ(CCH) aliphatic
850 δ(CCH) aromatic
883 ρ(CH 2)
931 ρ(CH 3) terminal; ν(CC) α-helix
956 ρ(CH 3); δ(CCH) olefinic
1002 ν(CC) aromatic ring
1031 ν(CC) skeletal cis conformation
1062 1076 ν(CC) skeletal trans conformation
1082 ν(CC) skeletal random conformation
1126 ν(CC) skeletal trans conformation
1155 ν(CC); δ(COH)
1172 ν(CC)
1207 not assigned
1244 1247 δ(CH 2) wagging; ν(CN) Amide III disordered
1274 ν(CN) and δ(NH) Amide III α-helix
1296 1298 δ(CH 2)
1336 not assigned
1366 δ[C(CH 3) 2] symmetric
1385 1389 δ(CH 3) symmetric
1401 δ[C(CH 3)]
1421 δ(CH 3)
1438 1440 δ(CH 2) scissoring
1451 δ(CH 3) antisymmetric
1460 δ(CH 2)
1515 not assigned
1552 1548 δ(NH) and ν(CN) amide II
1585 ν(CCC) olefinic
1602 not assigned
1652 1650 ν(CCO) amide I α-helix
1656 ν(C CO) amide I disordered
1743 1743 ν(CCO) amide I lipid
1768 ν(COO)
2723 ν(C ECH 3)
Table 1 Continued
Raman frequency IR frequency

(cm ⫺1 ) (cm ⫺1 ) Assignment
2852 2851 ν(CH 2) symmetric
2873 ν(CH 3) symmetric
2883 ν(CH 3) symmetric
2919 ν(CH 2) antisymmetric
2931 ν(CH 2) antisymmetric
2958 2957 ν(CH 3) antisymmetric
3000 not assigned
3060 ν(CH) olefinic
3070 1 st overtone, amide II at 1548 cm-1
3287 ν(OH) of H 2O
Abbreviations: δ ⫽ deformation; ν ⫽ stretch; ρ ⫽ rock.

Source: Ref. 5.
the lipid chains. The conformation of the CE C bonds is correlated with the
position and intensity of the Raman-bands in that region. The Raman spectrum
shows further spectral features such as the stretching modes of SE S bonds from
proteins down to around 400 cm ⫺1.
1. Determination of SC Moisture from the Amide Band Ratio

In the infrared spectrum, the ratio of the band heights for amide I (1580 cm ⫺1 –
1720 cm ⫺1) and amide II (1475 cm ⫺1 –1580 cm ⫺1) is a measure of the skin mois-
ture. The amide I band is underlaid by water so that the band height of this
absorption increases as the skin moisture increases. The larger it is, the greater
the skin moisture.
In the Raman spectrum, the amount of bound water is determined from the
ratio of the CH band height around 2940 cm ⫺1 and the OH stretching band height
around 3250 cm ⫺1 [33]. This band ratio increases with the skin moisture.
2. Determination of the Greasiness

The greasiness is determined from the IR spectrum by using the band height of
the ester absorption and the fatty acid absorption (1690 cm ⫺1 –1790 cm ⫺1). This
value is placed in relationship to the height of the amide I band.
3. Determination of the Fatty Acid/Ester Ratio

The determination of the fatty acid/ester ratio is similar to that for the determina-
tion of the amide band ratio. In this case, the band heights of the fatty acid absorp-
tion (1690 cm ⫺1 –1720 cm ⫺1) and the ester absorption (1720 cm ⫺1 –1790 cm ⫺1)
are determined and placed in relationship to each other.
4. Determination of Lipid Alkyl Chain Order

ATR-FTIR has been extensively used to study the phase behavior of lipid mem-
branes [34,35]. The disorder of the SC lipids can be studied by means of that
technique because it was shown that the degree of the alkyl chain disorder results
in a shift of the CE H stretching absorbances to higher wavenumber [36]. This
can be correlated to the introduction of gauche conformers in the alkyl chain
[37].
In Raman spectroscopy, the degree of alkyl chain order is given by the
lateral interaction parameter S lat [38]. From the ratio of the band heights for the
CE H stretching modes at 2890 cm ⫺1 and 2850 cm ⫺1, the order parameter for
the lateral interaction S lat is calculated:
Slat ⫽ (I 2890 /I 2850 ⫺ 0.7)/1.5 (4)
S lat indicates the packing order of the lipidic alkyl chains. It changes from 0 for
the liquid state to 1 for the crystalline state [38].
III. VIBRATIONAL SPECTROSCOPY

OF THE STRATUM CORNEUM
Some examples from the literature shall illustrate potential application areas of
IR and Raman spectroscopy for the investigation of the SC and for SC lipids.
They are characteristic but by no means comprehensive examples of scientific
work in that field and give an overview of the potential of vibrational spectros-
copy.
A. Studies on Model Skin Lipid Mixtures

FTIR was employed to investigate the thermotropic phase behavior of stratum
corneum lipid multilamellae [39]. It has been demonstrated that the lipids of the
stratum corneum provide the primary electrical and transport resistance in the
skin. These lipids are unusual in their composition, structure, and localization;
they contain only cholesterol, fatty acids, and ceramides and they form broad,
multilamellar sheets, which are located extracellulary. The FTIR results from
both the symmetric CH 2 stretching and the CH 2 scissoring vibrations suggest that
the SC lipids exhibit polymorphic phase behavior below the main phase transition
temperature. The multiple phases are most likely crystalline mixtures of different
alkylchain packings, along with solid-liquid phases. Similarities between the
FTIR results reported here for SC lipids and those obtained for cholesterol-
containing gel phase phospholipids suggest that the nonuniform distribution of
cholesterol occurs in each system.
The domain structure of the SC lipid multilamellae has been characterized
by FTIR spectroscopy in a three-component SC lipid model consisting of cera-
mide III, cholesterol, and perdeuterated palmitic acid [40]. At physiological tem-
perature, the CD 2 scissoring mode of the palmitic acid methylenes, and the CH 2
rocking mode of the ceramide methylenes, are each split into two components.
This indicates that both components exist in separate, conformationally ordered
phases, probably with orthorhombic perpendicular subcells. The magnitude of
the splitting indicates that the domains are at least 100 chains in size. The thermo-
tropic behavior of the CD 2 stretching vibrations demonstrates that conformational
disordering of the palmitic acid commences at 42°C with a transition midpoint
of 50°C. The CH 2 stretching frequency indicates the ceramide chains remain
ordered until 50°C, then they disorder with a midpoint of 67°C. The results pro-
vide a molecular characterization for the complex low temperature (10–40°C)
dynamic behavior suggested also by recent 2H NMR experiments [9].
The position of the CH 2 stretching vibrations alters with great sensitivity
with the fraction of trans and gauche conformers in the alkyl chains of the lipids.
Solid-liquid phase boundaries of well-defined model lipid mixtures with a simple
composition can therefore provide information about the maximum possible alter-
ation of the band position of the CH 2 stretching vibrations of the alkyl chains of
the stratum corneum lipids. If the temperature is increased from 25 to 60°C, the
solid gel phase of the investigated lipid/water mixtures melts completely to form
a liquid-crystalline phase that can be recognized in the DSC measurements as
melting transitions (Table 2).
Table 2 Melting Transitions of Model Lipid Mixtures

Lipid mixture A Lipid mixture B
Stearic acid 9.78 4.77
Palmitic acid 33.43 16.40
Oleic acid 30.75 16.11
Cholesterol 0.00 36.96
Water 26.04 25.76
Melting transition/°C 40–50 (peak at 48) 40–50 (peak at 47)
Melting enthalpy/J/g 63 28
CH 2sym /cm ⫺1 at 25°C 2848.0 2848.3
CH 2sym /cm ⫺1 at 37°C 2848.1 2848.4
CH 2sym /cm ⫺1 at 60°C 2852.9 2850.9
Source: Ref. 13.
The addition of cholesterol to the fatty acid mixture (Lipid mixture B) does
not broaden the melting range but it clearly reduces the melting enthalpy. The
symmetrical CH 2 stretching vibration shifts during the melting process from
2848.0 cm ⫺1 to up to 2852.9 cm ⫺1 for the fatty acid/water mixture and from
2848.3 cm ⫺1 to up to 2850.9 cm ⫺1 for the fatty acid/cholesterol/water mixture.
This means that the addition of cholesterol has different effects on the different
phases: at 25 and 37°C, the solid gel phase is present and cholesterol leads to a
positive shift of the wavenumber of the CH 2 stretching vibration, which indicates
a lower degree of order of the lipid alkyl chains. In contrast, at 60°C in the liquid-
crystalline phase, cholesterol increases the degree of order of the lipids in model
mixture B. This adjustment of the degree of order of the alkyl chains in the
lamellar gel and liquid-crystalline phases manifests itself in the smaller melting
enthalpy of model mixture B in the melting transition.
B. Analysis of Porcine Stratum Corneum Ex Vivo

The most informative lipid absorbances are those originating from the hydropho-
bic alkyl chain in the analysis of SC vibrational spectra. The antisymmetric (ap-
prox. 2850 cm ⫺1) and symmetric (approx. 2920 cm ⫺1) carbon-hydrogen stretching
mode are sensitive to the trans/gauche ratio of the alkyl chain. These two bands
are used in the analysis of the conformation of the hydrocarbon chains. The envi-
ronment within the interior of the bilayer can be analyzed by means of the anti-
symmetric (approx. 2956 cm ⫺1) and symmetric (approx. 2870 cm ⫺1) stretching
modes of the terminal methyl groups. The lateral packing within the lamellae
can be described by the methylene scissoring (1462–1474 cm ⫺1) and rocking
(720–730 cm ⫺1) vibrations [36]. Melting of hydrocarbon chains and phase transi-
tions are monitored by the analysis of the methylene stretching vibrations. The
temperature dependence of the symmetric methylene stretching frequency of por-
cine SC has been studied. One obtains a sigmoidal curve with an abrupt increase
in frequency between 60 and 80°C, which is typical for SC. From the absolute
frequencies together with the magnitude of the thermal shift, the degree of hydro-
carbon chain order can be deduced. This can be interpreted as the transition from
gel to liquid-crystalline phase. This transition is characterized by an increased
amount of gauche rotational conformers along the alkyl chains. A higher energy
is required to excite the corresponding vibrations for these gauche conformers
and thus they are occurring at higher IR frequencies. For stratum corneum lipids
obtained from pigs a shift in the position of the symmetrical CH 2 stretching vibra-
tions of the SC lipids from 2849.4 to 2853.6 cm ⫺1 (⫺10°–100°C) has been re-
ported [39]. In addition to this increase in vibrational energy, an increase in band-
width is observed on heating. The latter finding correlates with the increase in
the number of conformational states and in motional freedom of the alkyl chains.
The temperature dependence of the terminal methyl group conformation

has also been scrutinized for porcine SC [39]. In contrast to the methylene stretch-
ing frequency, the methyl stretching frequency increased progressively with in-
creasing temperature and no distinct phase transition was found. This can be
interpreted as a consequence of the less constrained environment toward the cen-
ter of the bilayer, compared to the methylene groups closer to the polar head-
groups.
C. Study of Human Stratum Corneum Lipids

According to the literature, human stratum corneum lipids obtained from skin
biopsies alter the spectral position of their symmetrical CH 2 stretching vibrations
in the temperature range from 25 to 60°C only from 2849.7 to 2850.8 cm ⫺1 [23].
In an in vivo study of humans, the position of the symmetrical CH 2 stretching
vibrations on the cheek was found between a minimum of 2849.4 cm ⫺1 for dry
and a maximum of 2850.8 cm ⫺1 for greasy, sebum-rich skin. On the lower arm,
the sebum content is lower and the symmetrical CH 2 stretching vibrations had
an average of 2849.1 cm ⫺1. The degree of lipid order in vivo is therefore less
than in the model lipid mixtures like A or B in Table 2 [13].
In Raman spectra, the positions of the CH stretching modes around 3100
cm ⫺1 to 2700 cm ⫺1 indicate the conformation of the intercellular lipid chains,
and they have been used to investigate the phase transitions in model lipid sys-
tems [38].
The separation between the CH 2 antisymmetric and symmetric stretching
mode was used as an indicator of lipid order. In this Raman spectroscopic study,
human SC was heated from 25°C to 100°C and three lipid transitions were ob-
served. This is in good accordance with the results from thermal analysis. The
analysis of the scissoring mode which is reflected in a Raman band at 1440 cm ⫺1
shows the three aforementioned lipid transitions at 37–40°C, 70–72°C, and 80°C.
Additionally a further transition can be observed at 55°C, which suggests that a
minor reorganization of the methylene groups of the lipid alkyl chains takes place.
It is also found that bands at 1126 cm ⫺1 and 1065 cm ⫺1 which are characteristic
for CE C bonds in the trans configuration decrease in intensity on heating. It
can be concluded that higher temperature gradually increases the amount of free
rotation around the C EC bond.
D. Penetration Enhancer Studies Using

Raman Spectroscopy
Signal overlap is a severe problem encountered in the study of molecular interac-
tions between penetration enhancers and lipids in the SC by means of vibrational
spectroscopy. There is significant interference of some vibrational modes of the

enhancer with those of the tissue. This is found especially for the C E H stretching
modes. Therefore, deuterated enhancers have been introduced, which shift the
C-D modes to lower wavenumbers [41]. Raman spectroscopy allows the linear
subtraction across the whole wavenumber range without the need for complex
calibration curves. Therefore, spectra can be generated with an enhancer present
and subsequently the signal of the enhancer can be removed by normalization
on a unique band. After this procedure, the spectrum of the enhancer modified
SC can be analyzed. This method has been used for tissue treated with dimethyl
sulphoxid (DMSO) and the terpene derivative 1,8-cineole, respectively [42,43].
The C EC stretching modes were disturbed by DMSO treatment [42]. The
observed effect is indicative of a transition of a trans gel to a trans-gauche liquid-
crystalline phase. The α-helical keratin in the SC was altered to a β-sheet confor-
mation. The effect could be semiquantified by curve fitting and intensity measure-
ments. The data from 1,8-cineole indicated a direct modification of the lipid
domain [43].
E. Comparison of in Vitro Skin Models with Normal

Human Skin
The infrared spectra of human skin in vivo and in vitro (epidermis model and
full-skin model) resemble each other in principle (example in Figs. 3 and 4).
Figure 3 Infrared and Raman spectra of normal human skin.

Figure 4 Infrared and Raman spectra of a full-skin model.
There are slight differences in the absolute wavenumbers of the amide vibrations
(Table 3). However, the calculation of moisture content from the ratio of amide
I to amide II band leads to nearly the same moisture content for the full-skin
model as for human dry skin, but to a higher value for the epidermis model. The
CE H stretching bands are much smaller for both skin models compared to hu-
man skin in vivo and therefore not detectable in the underlying noise of the
spectrum. As a consequence, an exact positioning of the C EH-stretching vibra-
tions is no longer possible.
Table 3 Infrared Data on Human Skin in vivo and in vitro

Skin sample Human dry skin Epidermis model Full-skin model
ν (C CO)/cm ⫺1 Amide I 1645.8 ⫾ 0.3 1640.4 ⫾ 0.5 1636.5

ν (CEN)/cm ⫺1 Amide II 1539.6 ⫾ 0.3 1536.2 ⫾ 0.5 1542.8
Moisture/arb. units 1.66 ⫾ 0.05 1.28 ⫾ 0.02 1.61
ν (CH 2) sym /cm ⫺1 Alkyl chain 2849.7 ⫾ 0.16 2849.3 ⫾ 0.4 not determined
order
ν (CH 2) asym /cm ⫺1 Alkyl chain 2915.9 ⫾ 0.13 2915.9 ⫾ 0.3 not determined
order
Mean values; n ⫽ 4, if SEM indicated, otherwise n ⫽ 2.

Source: Ref. 13.
The Raman spectra (examples in Figs. 3 and 4) provide complementary

information regarding the skin status. The absolute wavenumbers for the epider-
mis as well as the full-skin model differ slightly from the ones of normal human
skin ex vivo (Table 4). It is interesting to see that moisture content—as deter-
mined from the Raman spectra—differs considerably from moisture content as
determined from the amide I to II ratio from the infrared spectra. According to
the Raman results, moisture content is the same for the full-skin model and nor-
mal human skin ex vivo. However, the epidermis model seems to be less hy-
drated. A possible reason is faster drying out under the comparably long near-
infrared laser irradiation during the Raman measurement.
Information on the lipid packing order is easily obtained from the Raman
spectra, even in the case of the skin models. The evaluation of the lateral order
parameter S lat reveals a distinct reduction in lipid packing order for the epidermis
and the full-skin model compared to normal human skin. The intercellular lipids
are obviously less organized in the skin models, as has been found also in an
earlier ATR-FTIR study [2].
F. Determination of Skin Type from Infrared Spectra

IR-spectroscopy was used as a tool to classify an investigation panel of 35 female
test subjects into different skin types. Skin-type characterization by IR spectros-
copy is carried out on the basis of the spectra recorded 2 hours after the skin
had been cleansed. By clustering into four skin type subgroups (dry, normal,
greasy, mixed) based on the sebum content (greasiness), the standard devia-
tion of 0.80 obtained for the whole group from the band heights of the trigly-
ceride absorption measured on the forehead, which is a measure of the sebum
content of the skin, could be considerably reduced (Table 5). After this cluster-
ing, the following standard deviations for the individual groups were obtained:
0.39 for dry skin, 0.63 for normal skin, 0.79 for greasy skin, and 0.36 for mixed
skin.
If the corresponding standard deviations are now investigated when the
skin types are assigned according to the visual skin typing, then the following
values are obtained: 0.66 for dry skin, 0.78 for normal skin, 1.10 for greasy skin,
and 0.60 for mixed skin. In this case the standard deviations are clearly larger
than those obtained by clustering based on FTIR data. Assignment according to
IR spectroscopy and according to classical-visual skin typing therefore differ
from each other. Each sorts the skin types according to different criteria. De-
pending on the application range, one or other of these two systems is to be
preferred. For example, effects on the size of skin pores are best described by
visual skin typing. The IR method offers the advantage of better reproducibility
and quantification in the investigations of the effects of cosmetic products on the
stratum corneum.
Detection of Changes in Skin Lipids by IR and Raman Spectroscopy
Table 4 Raman Data on Human Skin ex vivo and in vitro
Human skin
Skin sample 36y 55y Epidermis model Full-skin model
ν (CC O)/cm ⫺1 Amide I 1666.5 ⫾ 0.3 1666.3 ⫾ 0.6 1653.8 ⫾ 0.5 1654.6 ⫾ 0.7
δ (NH) and ν(CEN)/cm ⫺1 Amide III 1271.5 ⫾ 0.1 1271.3 ⫾ 0.3 1271.1 ⫾ 0.7 1268.0
ν(CE C) in proteins/cm ⫺1 938.8 ⫾ 0.1 938.8 ⫾ 0.1 936.7 ⫾ 0.5 938.3 ⫾ 1.2
δ (OH) sym of water/cm ⫺1 3223.7 ⫾ 1.4 3225.2 ⫾ 2.5 3235.5 ⫾ 10.1 3230.5 ⫾ 1.5
δ (CH 2) asym in proteins/cm ⫺1 2942.5 ⫾ 0.2 2942.2 ⫾ 0.1 2932.6 ⫾ 0.3 2936.0 ⫾ 0.1
Moisture/arb. units 0.5 ⫾ 0.0 0.6 ⫾ 0.0 0.05 ⫾ 0.005 1.16 ⫾ 0.03
ν(CH 3) sym in lipids/cm ⫺1 2881.6 ⫾ 0.1 2881.6 ⫾ 0.3 2878.9 ⫾ 1.5 2882.0 ⫾ 0.9
ν(CH 2) sym in lipids/cm ⫺1 2848.4 ⫾ 0.2 2849.3 ⫾ 0.2 2848.5 ⫾ 0.1 2848.8 ⫾ 0.2
Alkyl chain order parameter S lat 1.02 ⫾ 0.03 0.93 ⫾ 0.02 0.68 ⫾ 0.02 0.75 ⫾ 0.03
δ (CH 2)(CH 3) in proteins and lipids/cm ⫺1 1451.2 ⫾ 0.2 1451.4 ⫾ 0.1 1448.7 ⫾ 0.5 1450.6 ⫾ 0.3
Mean values; SEM for n ⫽ 4.
245
Table 5 Skin type classification by FTIR on the cheek; SEM for n ⫽ 32
Skin type Dry skin Mixed skin Normal skin Greasy skin
Moisture 1.66 ⫾ 0.05 1.58 ⫾ 0.04 1.6 ⫾ 0.03 1.52 ⫾ 0.04
Greasiness 0.44 ⫾ 0.11 0.59 ⫾ 0.09 0.69 ⫾ 0.05 1.0 ⫾ 0.14
Free fatty 0.09 ⫾ 0.02 0.16 ⫾ 0.07 0.09 ⫾ 0.02 0.23 ⫾ 0.09
acids/esters
Position of the 2849.7 ⫾ 0.16 2849.8 ⫾ 0.25 2849.8 ⫾ 0.16 2850.8 ⫾ 0.23
symmetrical
CH 2 stretch-
ing
vibrations/
cm ⫺1
Position of the 2915.9 ⫾ 0.13 2915.7 ⫾ 0.11 2916.1 ⫾ 0.12 2916.3 ⫾ 0.16
antisymmetri-
cal CH 2
stretching
vibrations/
cm ⫺1
Source: Ref. 13.
The other skin parameters that can be derived from the IR spectrum are
skin moisture, fatty acid to ester ratio, and position of the CH 2 stretching vibra-
tions, which gives the degree of order of the lipid alkyl chains. The different skin
types differ slightly in their moisture. However, for classification the ‘‘moisture’’
parameter appears to be unsuitable; in the case of ‘‘dry’’ skin, it is even mis-
leading. The degree of order of the lipid alkyl chains in the stratum corneum,
given by the position of the antisymmetrical CH 2 stretching vibration, increases
as the sebum content decreases. The skin barrier properties differ significantly
between the greasy skin and dry skin subgroups.
IV. EFFECTS OF COSMETIC PRODUCTS

ON THE STRATUM CORNEUM
A. Introduction
Apart from other environmental influences, daily cleansing with soap or surfac-
tants can lead to an impairment of the skin barrier. The cleansing surfactants do
not just wash off dirt and excess sebum as required, but can also remove part of
the intercellular lipid mixture [44–47]. Even when the amount of lipid removed
is only small [48] the selective removal of free fatty acids and cholesterol esters
can lead to a significant alteration in the composition of the intercellular lipids

[49,50]. In addition, surfactants penetrate the stratum corneum, adsorb on the
keratin of the corneocytes [51], and mix themselves with the intercellular lipids
[52]. The result is an impairment of the skin barrier.
In the cosmetics industry, great efforts are made to avoid these undesirable
effects. Mild surfactants attack the intercellular lipids to a considerably lesser
extent than more aggressive surfactants with a similar cleansing performance.
The lipid film, or at least a part of it, can be restored by refatting oil additives
or creams applied after washing [53–55]. In this case, differentiation should be
made between physical effects on the stratum corneum and biological effects on
the metabolism of the living epidermis. On skin whose barrier has been damaged,
paraffin oil causes an immediate partial restoration of the skin barrier properties
of the stratum corneum, and physiological lipid mixtures slowly penetrate into the
epidermis and rebuild the barrier in a natural way by accelerated metabolization in
the lamellar bodies, playing a part in the recovery of squamous skin following
surfactant damage.
B. Effects of Rinse-Off Products

1. Cleansing with a Shower Gel
FTIR spectroscopy is an elegant method of following the skin cleansing process
quantitatively with respect to the sebum content (Fig. 5). The cleansing effect
has been quantified here on the cheek and lower arm by evaluation of the band
heights of the esters standardized against the amide I-absorption [13]. During
facial cleansing with a commercially available surfactant-based shower gel, the
fatty acid ester content of the cheek is reduced by 53% (from 0.84 units to 0.28
units). Within 2 hours, sebum secretion has increased it again to 84% of the initial
value.
On the forearm, the sebum content is lower by almost a factor of 10 and
the cleansing effect is correspondingly weaker. The ester content is reduced from
0.09 to 0.03 units.
2. Facial Cleansing with a Cleansing Milk

An important reason for the different preferences and expectations of consumers
is provided by individual skin differences, which are particularly evident in the
facial area. In addition, facial skin reacts particularly sensitively to external stimu-
lation, so that facial cleansing was selected for a differentiation between various
cleansing products.
During a mild facial cleansing process with a commercially available
cleansing milk, the sebum content sinks as expected (Fig. 6) [13]. In comparison
to a surfactant-based shower gel, the defatting effect of the cleansing emulsion
Figure 5 Defatting of the facial skin by a surfactant-based shower gel and endogenous
refatting, measured as the averaged band heights of the esters on the cheek and forearms
of 30 volunteers. (From Ref. 13.)
is somewhat less (⫺0.50 units instead of ⫺0.56 units on the cheek for the whole
group).
A comparison of the cleansing performance for the different skin types is
interesting. The defatting effect is considerably more noticeable on greasy skin
(⫺1.1 units) than on dry skin (⫺0.2 units). Alterations to the skin moisture con-
tent or the ester/fatty acid ratio are not observed. In the dry skin, the initial fat
content has already been reestablished 2 hours after cleansing by sebum secretion.
Endogenous refatting can also be demonstrated for greasy skin, but after 2 hours
this has not reached the original level. The cleansing milk is therefore ideally
suitable for removing dirt and sebum from facial skin in a manner suited to the
skin type without unwanted side effects.
C. Effects of a Leave-On Product

1. Strengthening the Skin Lipid Film by Creams
An important requirement for skin care creams is that the skin barrier is strength-
ened. Conventional creams, particularly of the water-in-oil (w/o) type, reduce
Figure 6 Defatting of the facial skin by a cleansing milk and endogenous refatting,
measured as the band height of the esters on the cheeks of 34 volunteers. (From Ref. 13.)
skin permeability by the so-called occlusive effect: the oil components of the
cream spread out on the skin surface and form a continuous film that inhibits
transepidermal water loss and thus causes an increase of moisture in the skin
[56]. The occlusive effect happens quickly but fades away after a short time when
the oil slowly penetrates the lipid layers of the stratum corneum and mixes with
the skin lipids.
A long-term strengthening of the skin barrier is to be expected when cream
components interact directly with the skin lipids and in this way increase the
degree of order and thus also the packing density of the lamellar lipid film in
the stratum corneum [44,57]. A cream with this effect would ideally contain lipids
that themselves build up lamellar gel structures and whose structure therefore
resembles the morphology of the lipid film in the stratum corneum.
The influence of a water-in-oil cream and a lamellar cream on the degree
of order of the skin lipid film and on skin moisture was investigated by FTIR
measurements on the lower arm before and after cream treatment [13]. Six hours
after cream application, the cream components had penetrated the stratum cor-
neum; this could be demonstrated by the lack of characteristic IR-bands of the
applied cream in the skin print. Whereas the W/O cream reduced the degree of
order of the lipids, the lamellar cream increased the degree of order (Fig. 7). This
Figure 7 Degree of order of the lipid alkyl chains after use of a w/o cream and a lamellar
cream on the forearm, measured as the band position of the antisymmetric CH 2 stretching
vibrations on 13 volunteers for the w/o cream and 14 volunteers for the lamellar cream.
(From Ref. 13.)
effect could be observed throughout the whole course of the daily cream treatment
over a period of 2 weeks and, in the positive case of the lamellar cream, could
still be recognized even after 12 hours with a statistical significance of 75%. This
means that the lipid-rich lamellar cream increases the conformational degree of
order of the alkyl chains of the lamellar lipid film in the stratum corneum, whereas
the liquid oil of the w/o cream actually reduces the degree of order. The lamellar
cream therefore strengthens the skin lipid film in a biomimetic manner.
The parallel IR spectroscopy measurement of the skin moisture via the
amide band ratio shows that both creams, which have the same moisture factor,
also increase the skin moisture in a similar way (Fig. 8). Comparative measure-
ments with the corneometer could not determine any significant effect on the
moisture after 6 or even 12 hours.
This shows how sensitive ATR-FTIR measurements can detect cosmetic
alterations to the skin moisture and morphology of the skin lipid film quantita-
tively in vivo.
Figure 8 Skin moisture after use of a w/o cream and a lamellar cream, measured by
the amide I/amide II band ratio on 16 and 17 volunteers, respectively. (From Ref. 13.)
V. CONCLUSIONS
FTIR and Raman spectroscopy provide valuable insights into the structure and
dynamic of the SC. Both methods are versatile tools to unravel the structural
heterogeneity of the SC. The central role of the intercellular lipid domains in SC
barrier function has been elucidated by means of FTIR and Raman spectroscopy.
The understanding of this complex membrane mechanisms and functions has
improved during the past years. The effects of cosmetic products on the skin
surface lipids can now be studied successfully and verified by vibrational spec-
troscopy.
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52. Friberg SE, Goldsmith L, Suhaimi H, Rhein LD. Surfactants and the stratum cor-
neum lipids. Colloids Surfaces 1988; 30:1–12.
of surfactant dry skin. Arch Dermatol Res 1989, 281:45–51.
54. Mao-Qiang M, Brown BE, Wu-Pong S, Feingold KR, Elias PM. Exogenous non-
physiologic vs physiologic lipids. Arch Dermatol 1995; 131:809–816.
55. Förster T, Guckenbiehl B, Ansmann A, Hensen H. Neuartige Körperpflegemittel auf
Basis von Mikroemulsionen mit Alkylpolyglykosiden. SÖFW 1996, 122:746–753.
56. Potts RO. Stratum corneum hydration: experimental techniques and interpretations
of results. J Soc Cosmet Chem 1986; 37:9–33.
57. Potts RO, Francoeur ML. Lipid biophysics of water loss through the skin. Proc Natl
Acad Sci 1990; 87:3871–3873.
9
Lipidic Ingredients in Skin Care
Formulations
Ghita Lanzendörfer
Beiersdorf AG, Hamburg, Germany
I. INTRODUCTION
The history of the use of lipids (waxes and oils) is closely connected with the
cultural development of mankind. Lipids served first as food, but their use was
extended to the preservation of other foodstuffs—for example, in the sealing of
amphorae with beeswax. Lipids were basic ingredients in pigment dispersions
and were used for wall or body painting, for greasing the skin, and for impregnat-
ing leatherware and wood. With the development of better isolation and refining
methods for lipids, purer fractions could be used for the extraction of fragrances
from plant leaves and their preservation or for medicinal treatment. In medieval
times, so-called witches were accused of using this kind of extraction method.
It was believed that they were boiling toads in fat and using the so-obtained
extract as a body salve to be able to fly.
Lipids also served as fuel for illuminating the nights with a steady burning
flame in oil lamps and candles. In different ancient cultures, various lipids were
used for those purposes depending on the kinds available (tallow, beeswax, olive
oil, etc.). In those days, no distinction was made between medicine, cosmetics
or body care, and religious purposes. Several recipes from ancient Egypt, India,
and Greece show that body hygiene and cosmetics were on comparably high
levels. But as good as ‘‘cosmetic formulations’’ were at those times, they were
based entirely either on lipids or on solutions in water—stable emulsions were
not known then. Ancient cosmetics consisted almost entirely of lipids.
Galen’s formula for cold cream is thought to be the first example of an
emulsion written down in the first London Pharmacopoeia in 1618. However,
255
256 Lanzendörfer
Table 1 Ceratum Refrigerans
Cera alba: 130 g

Oleum amygdalarum: 535 g
Aquae rosae: 330 g
Borax: 5 g
This formula shows an example of a cold
cream, Unguentum Leniens.
Source: Ref. 1.
the original formula did not contain borax, which was introduced in 1890 for the
manufacture of cold creams, as borax was discovered in the California desert in
1859.
As this cream mainly consists of a wax and a liquid triglyceride, the lipid
components still make up the major part of the formula. But with water contents
higher than 45%, it is possible to obtain O/W emulsions. For centuries, cold
cream remained ‘‘state of the art’’ when it came to incorporating water into oil.
In addition to beeswax, wool fat was known to be of cosmetic value since
ancient times (mentioned by Dioscorides about a.d. 60, de materia medica).
Wool fat can absorb up to 300% water, but its use was limited because of its
distinct smell and the odor of the products made from it. This changed substan-
tially after 1882, when Braun and Liebrich succeeded in the production of the
first purified wool lipids and named it lanolin [2]. With the development of the
industrial processes of washing and deodorizing wool lipids, an acceptable raw
material for the development of ointments was available. With refined wool lip-
ids, almost odorless products can be obtained.
Another lipid very much used in centuries past for application on skin was
sperm oil. In the golden age of whale hunting, abundant quantities of this material
were isolated. Sperm oil and wax were extracted from the hollows of the skulls
of sperm whale, where the oil was accumulated. Oil and wax were separated by
crystallization. Later, when whale hunting was banned, sperm oil was replaced
by jojoba oil of plant origin and the wax by cetylpalmitate of synthetic origin.
A result of the industrialization was the discovery of petrolatum in 1859
by Robert August Chesebrough. He discovered a paraffin-like residue on the oil
fields of Pennsylvania that was used by the oil workers to soothe cuts, burns,
and wounds. He perfected the extraction method as well as the refining process to
sell odorless, tasteless petroleum jelly (Brochure, Vaseline Worldwide Research,
Cairns & Associates, 1994). Paraffin oil, also a product of industrial oil produc-
tion and distillation, became a substitute for triglycerides. The use of paraffin
resulted in whiter and more stable preparations (not prone to oxidation).
Lipids in Skin Care Formulations 257
Also discovered in the 19th century, and industrially isolated from 1920
on, is lecithin, which was at first isolated from eggs and is now mainly obtained
from soya beans. It was soon found to be essential for the structural integrity
and function of living cells. Walker stated that lecithin also has marked action
on skin respiration [3]. Lecithin had its breakthrough in cosmetics applications
in the late 1980s; it was used to form liposomes.
Together with the evolution of lipid extraction, purification, and synthesis
and also with the change of attitude toward medicine and religion, the knowledge
of ‘‘cosmetics’’ did not remain in monasteries but became the know-how of phar-
macists. And in the past century, it also became industrial and scientific knowl-
edge.
Because the synthesis of new raw materials—emulsifiers, lipids, hydro-
philic and lipophilic thickeners, antioxidants, antimicrobials—and the optimized
refining processes for natural products in the past century, development of cos-
metic products grew exponentially. This progress supported the development of
a huge variety of cosmetics and today’s topical preparations used for daily skin
care. Nowadays, emulsions typically contain 60–80% water. Furthermore, even
emulsions containing up to 99% water have been made, although at the moment
they are more of academic interest.
High water contents improve the cosmetic properties (convenience and ef-
ficacy) of emulsions, make them easier to apply, and improve skin feel during
and after application. Today, lipids are no longer the only ingredient of cosmet-
ics—they even can be left out—but still contribute considerably to their charac-
teristics.
The following chapters will focus on the chemical characteristics and the
application of lipids for skin care formulations, concentrating on lipids that are
typically used in the oil phases of emulsions. The recent investigations and find-
ings covering the interaction of lipids with the skin are reviewed.
The characteristics of amphiphilic lipids are described thoroughly by Small
[4], Israelachvili [5], Lipowski and Sackmann [6], and Seddon and Templer [7].
II. CHARACTERISTICS OF LIPIDS
Lipids are one of the four major classes of biomolecules which are essential for
life. In contrast to the other three classes (proteins, carbohydrates, nucleic acids),
lipids cannot be defined by a common chemistry like for instance proteins (char-
acteristic building blocks are amino acids and the bondings are of peptide type).
The shared characteristic of lipids is their hydrophobicity, which is a result of
the presence of long chain hydrocarbon residues, which can be linear, branched
or even cyclic.
258 Lanzendörfer
Lipids are found in all living organisms and are a major source of cellular
energy. They are also essential for maintaining the integrity of all living matter,
because the amphiphilic molecules form a barrier separating the living cell from
the outside world.
Additionally, they have various roles in the microscopic and the macro-
scopic world and, because of their diversity, can function in many specific ways:
as antigens, for example, and as receptors, sensors, electrical insulators, and bio-
logical detergents. Many hormones are lipids—for example, steroid hormones
(cortisol, estrogens, progesterones, androgenes), prostaglandins, and leuko-
trienes.
Transportation of lipids to and from animal cells takes place in the form
of small aggregates called lipoproteins.
Lipids are essential for the cells of plants and animals: they are used as
building blocks for membranes during growth and repair. They also fulfill specific
functions—for example, some waxes in plants secreted on the leaves form films
on the surface, thus protecting the leaves from drying out or preventing them
from the attack of certain harmful insects. In seeds, triglycerides are accumulated
to protect the seeds, serve as energy deposit in growth, and solubilize antioxi-
dants.
Lipids are stored in large quantities in certain aquatic animals; they are
used as insulators and for buoyancy. Waxes coat the feathers of aquatic birds to
increase the feather-water surface tension and thus prevent immersion.
Lipids also play an important role in industry and modern technology. Pe-
troleum, for example, is still the world’s major source of energy. The food indus-
try uses lipids not only for their nutritional value but also as emulsifiers, stabiliz-
ers, and moisturizers, which are so important in processed food technology.
Lipids can be spread on water for wave damping in harbors and are used
to prevent excessive water evaporation from reservoirs. In modern technology,
lipidic components are used in liquid crystalline displays (LCD), where due to
their molecular arrangement, optical effects can be produced.
All these functions are related to the chemical structure of lipids and the
resulting possible amphiphilic interactions between lipid molecules or with other
media such as water.
Table 2 depicts a classification of lipids based on their polarity, solubility,
and saponifiability. All saponifiable lipids are either acids or have ester bonds
that can be subjected to alkaline saponification. In the group of the saponifiable
lipids, neutral and polar lipids are discerned; neutral lipids dissolve in acetone
and polar lipids do not. Complex lipids also contain ester groups, but the esterified
phosphate-groups, amines, or sugar residues render them more polar than lipids
that are esterified with aliphatic alcohols.
It is obvious that the physical behavior of such chemically divergent mole-
cules will be quite different. Indeed, one of the most interesting characteristics
of lipids is their tremendously varied behavior in aqueous systems, ranging from
almost total insolubility (paraffin oil, sterol esters) to nearly complete solubility
(soaps, detergents, bile salts, and gangliosides). These characteristics also can be
used to group lipids (Table 3).
A very similar grouping also can be achieved by analyzing the molecular
shape of lipids [5]. For that purpose, the relative sizes of the polar and the nonpo-
lar portion of the molecule are taken into account and a packing parameter is
defined. Large hydrophilic groups and relatively small lipophilic tails, for in-
stance, favor an assembly in the form of a spherical micelle. In molecules in
which the molecular dimensions of the polar and nonpolar part are relatively
similar, less curved arrangements are favored (i.e., lamellar layers).
The use of lipids in cosmetic formulations is not limited to the naturally
occurring compounds. Modern synthetic methods enable selection from a wide
variety of synthetic esters, polymers, silicones, or chemically modified natural
compounds. Often those compounds are preferred to the natural compounds be-
cause of their availability, stability, or price. The main chemical groups used for
cosmetic formulations are depicted in Table 4.
A. Waxes
In Table 4, wax esters are mentioned. These are not the only compounds that
count as waxes: the term ‘‘wax’’ does not describe a certain class of lipids but
classifies lipids according to their physical characteristics. These are kneadability,
melting behavior, and crystallinity. The following criteria have to be fulfilled for
a substance to be classified as a wax:
Kneadable at 20°C
Solid to brittle hard
Coarse to fine-crystalline
Transparent to opaque, but not glasslike
Melting above 40°C, without decomposition
Above melting point relatively low viscous
Strong temperature-dependent consistency and solubility
Polishable under low pressure
Taking these characteristics into account, substances of many different chemical

groups can be waxes: paraffins, high or low density polyethylenes (mol weight
from 2000 to 9000), esters of long-chain alcohols and acids, long-chain fatty
acids and their soaps. Also, stearic acid and cetyl alcohol belong to the group of
waxes because of their physical behavior.
260
Table 2 Classification Scheme for Lipids
Lipid class Structure (example)

Free (not esterified) fatty acids Neutral lipid
Acetone soluble
Simple lipids
Waxes (Waxesters, paraffins, R1ECOEOER2
fatty alcohols, fatty alde-
hydes)
Glycerides (fats) CH2EOECOER1


CHEOECOER2

CH2EOECOER3
Phosphatides H2CEOECOER1
Glycerolphosphatides  Polar lipids
HCEOECOER3 Acetone insoluble
 O Complex lipids

Saponifiable
H2CEOEPEOECholine

O⫺
Lanzendörfer
O

1
Sphingophosphatides R ECHECH2EOEPEOECholine Sphingolipids
 
NH O

COER2
Lipids in Skin Care Formulations
Glycolipids R1ECHECH2EOEGalactose Sphingolipids
Sphingoglycolipids 
NH

COER2
Glycerolglycolipids CH2EOECOER1

CHEOECOER2

CH2EOEGalactose
Aminolipids
Isoprenoids
Terpenes Neutral lipids
Acetone soluble
Unsaponifiable
Steroids
Source: Ref. 8.
261
262 Lanzendörfer
Table 3 Interaction of Lipids with Water
Interaction with water

Class in water on the surface Examples
Nonpolar lipids* crystals or oil do not spread Squalene, paraffins
Amphiphatic lipids*
Insoluble, nonswell- crystals or oil form stable film fatty acids, wax esters,
ing* cholesterol, fatty alco-
hols, vitamin A, D, E
and K
Insoluble, swellable liquid crys- form stable film monoglycerides, phos-
tals phatides, lecithins
Soluble lipids
Micelle-forming lip- micelles unstable films lysophosphatides, an-
ids with lyotropic ionic soaps, cationic
mesomorphic be- detergents, betaines
havior
Micelle-forming lip- micelles unstable films bile acids and their
ids without lyo- salts
tropic mesomor-
phic behavior
* Groups of lipids which are commonly used in skin care preparations as lipids.
Source: Ref. 9.
B. Polymers
Also defined by physical properties are the substances termed polymers. Poly-
meric compounds are macromolecules derived from the polymerization of mono-
mers having average molecular weights of above 10,000 Daltons. They are
mainly found in the classes of the hydrocarbons or silicones, but triglycerides
also can be polymerized.
C. Some Lipids in Detail

At this point, some important cosmetic lipids shall be discussed in more detail.
1. Vaseline
Vaseline is not the name of a chemically homogeneous substance. Vaseline is a
mixture of mostly saturated n-, iso-, and cyclo-paraffins of different molecular
weight, thus rendering a crystalline and a fluid phase. The relative amounts of
these compounds differ between natural vaselines and is determined (a) by the
Table 4 Overview of Lipids Important for Cosmetic Formulations
Chemical
class Examples
Hydrocarbons, Liquid Natural, distilled paraffins: min-
Paraffins eral oil, synthetic isoparaffins
Squalane (natural, modified)
Semisolid Petrolatum, polyisobutenes
Solid Microcrystalline wax, paraffin
wax, ceresin, ozokerite
Silicones Dimethicone, cyclomethicone, si-
licone copolymers, perfluori-
nated silicones
Triglycerides Synthetic triglycerides, natural
oils, hydrogenated tryglycer-
ides
Esters Derived from branched or un- Isopropyl palmitate, cetyl palmi-
branched long chain fatty tate
acids
Derived from acids with chain C12–15 Alkyl benzoate, myris-
lengths ⬍ C12 tyl lactate
Derived from branched alcohols Neopentyl dicaprate
or polyhydric alcohols
Wax esters Jojoba oil, beeswax, carnauba
wax
Lecithins Phospholipids (Phosphatidylco-
line, -ethanolamine, -inositol)
UV-Filters Octylmethoxycinnamate
Alcohols Aliphatic alcohols Fatty alcohols unbranched and
branched C-chains, Guerbet al-
cohols
Sterols Cholesterol, phytosterols, lanolin
alcohols
Tocopherols Tocopherol
Ethers Dicaprylyl ether, PPG-ethers, eth-
yleneoxide ethers, steareth-20
Other Lipids Ceramides Ceramides, sphingolipids
Fatty acids Stearic acid
264 Lanzendörfer
Table 5 Composition of Vaseline*
C-chain main C-chain

Composition c[%] distribution C-chain average
n-Alkanes: 16–19 C17–C51 C28 C29
iso-Alkanes: 11–15 C20–C48 C30 C32
‘‘Oilpeak’’: 66–73 C21–C37 C27 C27
Full vaseline C17–C51 C27–28 C28
* According to Häusler and Führer, who determined the qualitative and quantitative composition of
vaseline using gaschromatography.
Source: Ref. 10.
composition of the crude oil from which vaseline is isolated and (b) by the isola-
tion method, which accounts for the relations of n-, iso-, and cyclo-paraffins.
Vaseline is described as a colloidal system, in which the iso-paraffins form
a solid amorphous region that accounts for the oil-binding capacity of vaseline.
They build up ‘‘Fransenmicelles,’’ a structure that immobilizes the fluid paraffins.
2. Beeswax
Beeswax is derived from honeybees, which belong to the genus Apis. The bees
‘‘synthesize’’ the wax by enzymes from carbohydrates from their food and ex-
crete it from the wax glands. One thousand bees produce about 9 g of wax in
only 9 to 10 days of their life span, which lasts about 35 to 45 days.
Beeswax is a mixture of wax esters of long-chain fatty acids, free fatty
acids, and alcohols.
Table 6 Composition of Beeswax

Composition c[%]
Waxesters:
Myricyl palmitate, myricyl ceroate, myricyl hypogaeate, cetyl hydroxy- 71
palmitate, esters of dicarbonic acids, esters of polyhydric alcohols,
cholesterolester
Free Acids:
Lignoceric acid, cerotinic acid, montan acid, melissinic acid, physillinic 13–15
acid (C33H66O2)
Free alcohols 1
Hydrocarbons (C25–C31): 10–13
Pentacosan
Source: Ref. 11.
Like other esters, the esters of beeswax can be hydrolyzed or modified,

resulting in lipidic derivatives with different characteristics (i.e., higher polarity),
facilitating the incorporation in emulsions [12]. Beeswax is a long-known ingre-
dient for cosmetic formulations and is used, for instance, in lipsticks and cold
creams.
3. Lanolin
Lanolin is the unctuous secretion of the sebaceous glands of sheep; it is deposited
onto the wool fibers and is also referred to as wool wax. It serves to soften the
fleece and protect it from the elements. It is a complex mixture of esters, di-esters,
and hydroxy-esters, methyl-esters of high molecular weight lanolin alcohols (69
aliphatic alcohols, chain lengths from C12 to C36 and 6 sterols) and high-molecu-
lar-weight lanolin acids (approximately 138, chain lengths from C7 to C41) [13].
The distribution of the hydrocarbon chain lengths of the saponifiable frac-
tion of lanolin, the lanolin alcohols, ranges from C12 to C36, including ω-1 and
ω-2 methyl-substituted alcohols, and alkane-diols. Also, sterols (cholesterol, la-
nosterol, agnosterole, and others) are known as lanolin alcohols.
The lanolin acids are composed of unbranched, ω-1 and ω-2 methyl-substi-
tuted acids, α-hydroxy and ω-hydroxy acids, and combinations of methyl and
hydroxy substitution.
The composition of lanolin alcohols and lanolin acids is thoroughly re-
viewed by Motiuk [14,15].
Lanolin is an effective emollient, which—by subjective evaluation—ef-
fects a softening and improvement of rough skin caused by lack of sufficient
natural moisture retention. Idson reported that lanolin causes the water in the
skin to build up to its normal level of 10–30% by retarding without completely
inhibiting transepidermal waterloss (TEWL) [16]. Lanolin also accounts for the
enhancement of the adhesion of the formula to skin, thus rendering a long-lasting
water-impermeable film.
In past years, the allergy and sensitization potential of lanolin was discussed
thoroughly, resulting in different views of the matter. For some time, especially
the iso- and anteiso compounds of hydrogenated lanolin were described as sensi-
tizers or allergens [13], whereas today it is understood that many of the formerly
found allergies resulted from impurities in the lanolin [17–19]. The data pub-
lished on lanolin allergy, especially lanolin alcohols, were reviewed thoroughly
by Kligman, who showed that almost all of the so-called allergic responses to
lanolin and lanolin alcohols were false positives due to testing on persons with
diseased or damaged skin [20,21]
Lanolin can easily be fractionated or chemically modified, resulting in a
variety of compounds for different applications (i.e., emulsifiers, oils, or waxes).
Lanolin oil, a fraction of lanolin, is a preferred ingredient in lipsticks due
266 Lanzendörfer
to its good pigment-dispersing properties [22] and its skin care efficacy, measured
as reduction of the dryness of the lips [23].
4. Jojoba Oil
Jojoba oil is derived from the fruits of the jojoba bush, which grows in the semi-
desert areas of the southwestern United States and in the northwest of Mexico.
The oil, which is a fluid wax ester, is composed of the esters of the unsaturated
C20–C24 alcohols and unsaturated C20–C22 acids. The chain length distribution
is as follows:
C16:0: 1.1%
C18:1: 9.0%
C20:1: 71.5%
C22:1: 14.2%
C24:1: 1.6%
The main components are the esters of the C20 and C22 acids and alcohols. The
double bond in both molecule moieties renders the substance fluid. Its big success
in cosmetic formulations began when a substitute for sperm oil was looked for.
Jojoba oil can be partially or completely hydrogenated, giving solid products
with much more waxlike appearance.
5. Esters
Derived from the reaction of alcohols with acids, a tremendous diversity of esters
with very different characteristics can be obtained, making them the biggest group
of lipids. With variation of the chain length and grade of branching on either
side of the molecule, the physical properties (melting points, polarity, viscosity)
can be modulated (see Table 7). For example, esters are also used to wet pig-
ments, to dissolve chemical sunscreens, and to promote spreading of sunscreens
on skin.
From the reaction of saturated linear fatty acids and alcohols, solid products
such as cetyl palmitate can be obtained. These compounds are used as bodying
agents for emulsions because they increase viscosity and impart a dry skin feel.
Introducing an alkyl branch in either the alcohol portion or the acid portion, the
esters (compared to the unbranched compounds of similar molecular weight) are
liquid at room temperature and have good spreading properties.
Some examples of the diversity of the acids used are C12–C15 alkyl benzo-
ate when an aromatic acid is used or alkyl lactates by the use of the short chain
acid lactic acid. Using polyols as the alcoholic component, one can obtain com-
pounds such as triglycerides with glycerol. One prominent example is caprylic/
capric triglyceride, which certainly is the most important synthetic triglyceride.
Other polyoles, such as pentaerythritol, can be used, leading, for instance, to
Table 7 Examples of Esters and Their Physical Properties
Polarity [mN/m]
Alcoholic Melting interfacial tension
part Acidic part point Spreading against water
Butyl Stearate 22°C — —
Cetearyl Stearate 55°C — —
Myristyl Myristate 41°C — —
Isocetyl Stearate ⫺2°C Medium 17
Ethylhexyl Stearate 10°C Good 32
Isopropyl Palmitate 14°C Good 29
Isopropyl Stearate 19°C Good 22
Diisopropyl Adipate ⫺6°C Very good 14
Lauryl Lactate ⫺3°C N.D. N.D.
Myristyl Lactate 13°C N.D. N.D.
Ethylhexyl Hydroxystearate 15°C Poor N.D.
Pentaerythrityl Tetraisostearate ⬍ ⫺10°C Poor 10
Isodecyl Neopentanoate ⬍ ⫺30°C Medium–good 30
Butylene Caprylate/ ⫺10°C Good 21.5
Glycol Caprate
N.D. ⫽ not determined.
pentaerythrityl tetraisostearate. Also, use of polyhydric acids is possible, leading

to products such as Tri C12–13 alkyl citrate.
By partial esterification of polyhydric alcohols or acids, the hydrophobic
characteristics are reduced, leading to amphiphilic compounds that typically are
used as emulsifiers (e.g., glyceryl mono stearate).
6. Natural Triglycerides
Triglycerides form the group of lipids longest known for their use as food and
for skin care. This group of compounds also is referred to as fats. Fats that are
liquid at room temperature are commonly defined as oils. Chemically, they are
glycerol esterified with three fatty acids, which can vary in chain length and
saturation.
Triglycerides derived from animal fatty tissue normally are solid at room
temperature due to the high amounts of bound stearic acid. Fish oils are different
from other animal-derived triglycerides because they are rich in unsaturated long-
chain fatty acids with up to 22 C-atoms. Additionally, these acids contain—
calculated as a C20 acid—on average more than five double bonds. This unsatura-
tion renders them liquid but also makes them susceptible to oxidation, which is
responsible for the distinct fish-like smell.
268 Lanzendörfer
Vegetable triglycerides also contain considerable amounts of unsaturated

fatty acids, thus making them liquid and more susceptible to oxidation than satu-
rated animal-derived triglycerides. For the effective inhibition of oxidation, the
oils contain tocopherols. However, tocopherol quantities are not high enough to
preserve the lipids in cosmetics. Synthetic antioxidants have to be added.
Triglycerides are extractable from all kind of seeds or fruits, and modern
extraction methods make clear, almost odorless oils available. The natural triglyc-
erides differ in fatty acid composition, which is characteristic for the species the
oil is obtained from. Also, the positions of fatty acids in the glyceride in natural
oils are not random. The more unsaturated acids favor the 2-position and the
more saturated ones favor the 1- and 3-position of the glyceride [24].
Triglycerides with specific properties isolated by fractionated crystalliza-
tion are used as additives in the food industry—for example, to achieve a specific
mouthfeel in chocolates. Isolated by transesterfication, specific triglycerides are
also used in the medical field for the formulation of parenteral nutritionals [25].
Those fractions are of less importance for skin care formulations.
Vegetable oils are used in skin care formulations because of their specific
fatty acid profile. Olive oil contains high amounts of oleic acid, sunflower seed
oil contains linoleic acid, and evening primrose oil γ-linolenic acid. Linoleic and
γ-linolenic acids are so called essential fatty acids [26]. These acids are ω-6 unsat-
urated fatty acids, which are deficient in certain pathological skin conditions such
as atopic dermatitis, in which the enzyme ∆-6 desaturase is impaired [27,28].
Essential fatty acids achieved their popularity after it was shown that skin
condition could be improved after topical application of products containing these
acids [29,30]. Recently, seabuckthorn oil [31] and hemp oil [32] gained interest
as vegetable oils that also contain high amounts of α-linolenic acid. Meadowfoam
seed oil is interesting also because of its fatty acid profile, containing considerable
amounts of C20:1 and eicosanoic acid, which are rare in vegetable oils (Fig. 1)
[33].
7. Silicones
Silicone is a generic name for many classes of organo-silicone polymers with
repeating siloxane (Si-O) units. Silicone fluids are also called silicone oils be-
cause they are hydrophobic. Many families of silicones exist with a wide range
of possible molecular weights, including linear, cyclic, and cross-linked varieties.
The introduction of various functional groups, such as amino, phenyl, alkyl, or
polyether, changes the hydro- and lipophobic behavior of silicones. It is also
possible to introduce amphiphilicity along the chain allowing silicones to act as
emulsifiers.
Silicone oils are used because of the following characteristics:
Figure 1 Fatty acid profile of some vegetable oils with different acid profiles. Olive
oil contains high amounts of oleic acid. Sunflower seed oil and evening primrose oil both
contain high amounts of linoleic acid, but only evening primrose oil contains γ-linoleic
acid. Hemp oil and seabuckthorn oil contain considerable amounts of α-linoleic acid; in
seabuckthorn oil the ratio of oleic to linoleic to α-linoleic acid is almost 1 :1:1. Mead-
owfoam seed oil mainly contains unsaturated eicanoic acid.
1. They exhibit a very good resistance to high temperature for extended

periods of time and are resistant to oxidation.
2. Their viscosity changes less over a wider temperature range than non-
silicone fluid.
3. They are chemically inert and usually have high flash points. Due to
their low surface tension, they are easily spreadable and have high
surface activity. They are resistant to breakdown by mechanical shear-
ing and are noncorrosive [34].
These physicochemical properties of silicones lead to an impressive array of
properties and benefits in skin care formulations, including detackification (reduc-
tion of the greasy/oily feel of other ingredients); permeability (‘‘breathable
films’’); lubrication of the skin and characteristic smooth feel (aesthetics); barrier
effects (protection); substantivity (long-lasting); anti-adhesive effects; and easy
spreading of other materials such as pigments or actives (efficacy and advantages
in wetting surfaces).
A large variety of alkylmethylsiloxanes has been synthesized with different
physical properties (Fig. 2).
270 Lanzendörfer
Figure 2 Chemical structure and structural elements of polyorganosiloxanes. R ⫽ H

to C45H91, x ⫽ 0 to 1000, y ⫽ 0 to 1000, z ⫽ 0 to 1000.
1. Volatile fluids are typically materials with molecular weights in the

range of 300 to 600 and with hydrocarbon-to-silicone ratios ranging
from 0.25 to 1. Alkyl chain length is low.
2. Nonvolatile fluids may have molecular weights up to 100,000; how-
ever, the R-substituent is typically not longer than C18.
3. Silicone waxes may range in molecular weight from 500 to 100,000,
and the R substituent is typically C16 or longer. The softening points
of the waxes range from 25°C to 70°C.
8. Ceramides and Pseudoceramides

Because ceramides constitute a major portion of the skin lipids, extraction from
natural sources (animal and plant origin) as well as synthesis of natural and so-
called pseudoceramides for cosmetic purposes has been a field of high interest.
The structural element of ceramides is a sphingosine backbone amide-linked to
a long-chain fatty acid residue. Thus, ceramides are formed with a polar head to
which two aliphatic chains are attached (Figs. 3 and 4). The naturally occurring
ceramides are optically active and have a D-erythro configuration.
Chain length, saturation and hydroxylation vary in either the fatty acid resi-
due as well as in the sphingosine or phytosphingosine residue of natural cera-
mides (see also Chapter 1). Synthesis of ceramides with D-erythro configuration
can only be obtained by classical chemistry in multi-step synthesis [35]. Alterna-
tively, biosynthetically derived ceramides are available, but their availability is
restricted to the phytosphingosine derivatives so far.
Figure 3 General structure of a ceramide, R ⫽ H or OH, R′ ⫽ H or ester linked fatty

acid; the asterisks indicate chiral positions; the line marks the sphingosine- and fatty acid
residue. When R ⫽ OH, another chiral C-atom is present.
Figure 4 General structure of ceramides on basis of a phytosphingosine, R ⫽ H or OH.
The structural elements of pseudoceramides are similar to those of cera-

mides, but they lack chirality and often possess a different polar head group
arrangement. Examples are trihydroxypalmitamido-hydroxypropyl myristyl ether
(Fig. 5) or myristyl-propylene glycol hydroxyethyldecanamide.
Ceramides and many pseudoceramides are hard-to-brittle substances with
high melting points; they are insoluble in water and only partly soluble in cos-
metic lipids, thus making them difficult to formulate in high amounts into cos-
metic formulations.
III. FUNCTION OF LIPIDS IN COSMETICS
Of the variety of skin care formulations (Fig. 6), emulsions are by far the biggest
and most important group of formulas applied, followed by lipsticks and oils.
Therefore, in this chapter mainly the effect of lipids in emulsions will be dis-
cussed.
A. General Aspects
Cosmetic emulsions normally contain about 5–30% (w/w) of lipids, rendering
them the second major component in cosmetic emulsions after water. The choice
of lipids and of the emulsifying system determines the characteristics of the
product.
Figure 5 Structure of trihydroxypalmitamido-hydroxypropyl myristyl ether.

272 Lanzendörfer
Figure 6 Product forms (with friendly permission of Dr. Sven Gohla).
The influence lipids exert covers stability (important for water-in-oil

[W/O] emulsions), viscosity, skin feel, wettability of pigments and solubility of
active compounds, and skin care efficacy of the final formulation.
Lipids also account for the film-forming properties of the formulation on
the skin, thus rendering it waterproof, for example for sunscreen products, or
transfer-resistant for decorative products. Additionally, the film-forming proper-
ties are connected with skin care, as the film prevents the skin from drying out
[36].
In anhydrous systems such as lipsticks or ointments, lipids are important.
Additionally, waxes are included that build the matrix in which the more liquid
lipids are incorporated. The characteristics they exhibit depend on the system in
which they are incorporated.
B. Influence of Lipids on Emulsion Stability and Viscosity

The factors influencing the rheology of emulsions are volume fraction of the
disperse phase (inner phase), viscosity of the disperse droplets, droplet size distri-
bution and the viscosity of the outer phase, and the interfacial rheology of the
emulsifier film [38].
The most important factor influencing viscosity and stability of W/O emul-
sions is the fraction of the disperse phase (water), also called phase volume ratio.
For better understanding, a critical phase volume ratio is defined that corresponds
to close-packed spheres (for monodisperse distributed droplets, Φc ⫽ 0.74). At
this ratio, the water droplets get into contact with each other, and the rheological
behavior of the emulsion changes from a liquid particle-solution to that of a close-
packed solid network of water droplets [36]. For all practical purposes, that means
that the more oil incorporated in a W/O emulsion system, the lower the viscosity
becomes.
The viscosity of W/O emulsions also is regulated by the viscosity of the
oil phase (viscosity of the outer phase), meaning that the viscosity of the final
product is proportional to the viscosity of the oil phase [37,38].
Stable W/O emulsions are preferably formed with nonpolar lipids such as
paraffins. W/O emulsions formed with triglycerides exhibit higher viscosities
than those with mineral oil [39]. Nevertheless, the choice of emulsifier and the
amount of energy used for the dispersion of the water droplets significantly affect
the factor of stability and viscosity.
For oil-in-water (O/W) emulsions, there is no preferred class of lipids for
achieving stability because of the gel network established by the emulsifier sys-
tem, which acts independently of the lipids [40].
In O/W emulsions, viscosity normally is not regulated by lipid content but
by the choice of emulsifying system, the co-emulsifier (fatty alcohol or mono-
glyceride), incorporation of solid lipids, and hydrophilic thickener.
C. Influence of Lipids on the Sensory Properties of Skin

Care Products
Lipids in emulsions directly influence viscosity and skin feel of the formulation.
These are two main characteristics that are also perceived by consumers and
influence their choice of product. Therefore, these parameters should be adjusted
thoroughly (see also Chapter 11). For that reason, lipids have been studied thor-
oughly for the sensory characteristics they cause. Many efforts have been made
to find a sensory characterization matrix that covers all sensory patterns of lipids.
As parameters influencing the skin feel, spreading rate, surface tension, skin ab-
sorption (viscosity, solidification temperature), and the ‘‘quality’’ of the after-
feel can be evaluated and compared.
Therefore, not only were the lipids alone tested, but their characteristics in
emulsions can be evaluated as well [41,42]. However, in all studies conducted
so far, no general relationship between the sensory properties and the physical
constants of the lipids could be found. Nevertheless, some correlations are valid.
As a general rule, spreadability values decrease with increasing viscosity
of the oil. The spreadability of an oil itself correlates with the subjectively experi-
274 Lanzendörfer
enced absorption capability into the horny layer of the epidermis and the time
course of the fatty character [43]. And the higher the viscosity of the oil, the
higher the subjectively experienced ‘‘fatty feel’’ [44].
The correlation between viscosity and ‘‘skin absorption’’ also is valid for
triglycerides. In that group of lipids, synthetic medium-chain triglycerides show
a balanced pattern of spreading, absorption, and after-feel, whereas most of the
natural triglycerides have a pronounced fatty after-feel, which additionally can
be correlated with low spreading and absorption.
Synthetic esters normally show good spreading and absorption characteris-
tics and account for a dry after-feel.
By comparing lipids of the same viscosity, Zeidler additionally found some
rules that are valid for different lipid classes: Spreadability increases with de-
creasing surface tension; C12–15 alkyl benzoates (relatively high surface tension,
very poor spreadability) → decyl oleate → octyl stearate (relatively low surface
tension, medium spreadability).
Table 8 Examples of Lipids with Different Viscosities, Surface Tensions,

and Spreadability Values
International Nomenclature Viscosity Surface tension Spreadability
of Cosmetic Ingredients [mPas] [mN/m] [class]
Octyl octanoate 3.3 26.8 Good
Dicaprylyl ether 3.3 27.4 Good
Cyclopentasiloxane 3.8 18.3 Very good
Isopropyl myristate 4.6 28.4 Good
Hexyl laurate 5.1 28.7 Medium
Isopropyl palmitate 6.1 28.9 Good
Octyl laurate 6.3 28.8 Medium
Isopropyl stearate 7 29.2 Medium
Octyl palmitate 10.7 29.9 Medium
C12–15 Alkyl benzoate 11.8 31.6 Very poor
Octyl stearate 12.2 30.2 Medium
Dimethicone 13 19.8 Medium
Caproic triglyceride 13.2 29.2 Medium
Decyl oleate 13.5 31 Poor
Octyldodecyl neopentanoate 14.6 28.1 Medium
Cetearyl isononanoate 15.5 29.5 Medium
Isocetyl palmitate 22 30.1 Very poor
Caprylic/Capric triglycerides 23.7 29.4 Very poor
Paraffinum liquidum 25.4 29.7 Poor
Octyldodecanol 44.7 28.7 Very poor
Avocado oil 64.3 32.1 Very poor
Source: Ref. 36.
When the surface tension remains nearly constant, the spreadability de-
creases with increasing viscosity; isopropyl palmitate (low viscosity) → caproic
triglycerides → octyldodecanol (high viscosity).
If the viscosity remains unchanged, alcohols spread more quickly than hy-
drocarbons, which spread faster than esters. In all cases, it is found that some
branched-chain compounds spread better than unbranched ones [44].
Tackiness of a formulation normally is an unwanted sensory characteristic.
Lipids are responsible for this sensation, and it occurs when substances having
high surface tension and high viscosity are incorporated.
In that respect, silicone oils are favored ingredients for modification of the
sensory characteristics of emulsions because they promote spreadability of the
incorporated oils due to their low surface tension [36].
IV. FUNCTION OF LIPIDS ON SKIN

A. Behavior of Emulsions after Application to Skin
The dynamics of the structural change of emulsions due to water loss after appli-
cation to the skin are suspected to have a major impact on product performance.
Therefore, this behavior has been the subject of investigation by several groups,
and attempts were made to visualize emulsion behavior on skin [45]. Our own
results showed that the evaporation of water from O/W emulsions occurred
within the first 10 minutes after application and is complete after that time.
A valuable method is the microscopic observation of the structural changes
of emulsions applied to glass. Figure 7 shows microscopic pictures (magnification
625-fold) made under phase-contrast illumination [46]. The thickness of the
emulsion film applied is 30 µm.
Surprisingly, discrete droplets stay intact for several minutes, and very
abruptly (from minute 7 to 8) the surface flattens and the surroundings of the
droplets appear smeared. What is left looks like a continuous oil film.
The structural changes of an emulsion can also be studied under polarized
light, where the change of birefringence can be measured. By image analysis the
brightness of the discrete pictures can be calculated and plotted as a function of
time.
Wepf investigated the penetration behavior of the water and lipid phases
of emulsions applied to porcine skin with confocal laser microscopy in vitro.
These results suggested that the water contained in the emulsion does not pene-
trate the skin as a whole [47]. For this investigation, the water and lipid phase
of the emulsion were colored with different fluorescent dyes (Fig. 8). For the
water phase, a green color (Rhodol-green) was chosen, and for the lipidic phase,
the red color DID. Confocal laser microscopy was carried out 30 minutes after
application of the emulsion. Images of the skin surface and depth profiles of the
epidermis were obtained. On the surface, the red and green color are still persis-
276 Lanzendörfer
Figure 7 a: O/W emulsion after 2 min. b: O/W emulsion after 7 min. c: O/W emulsion
after 8 min. d: O/W emulsion after 20 min.
tent. However, the red color is also seen in the upper layers of the stratum cor-
neum, which suggests that lipids or lipophilic components may penetrate.
The ability of lipids to penetrate the upper layers of the stratum corneum
found in this study is in good agreement with results found by Ghadially [48]
and Brown [49]. Ghadially examined the fate of topically applied petrolatum,
which appears to reach all levels of the stratum corneum in both acetone-treated
and untreated stratum corneum. Brown studied the penetration of hydrocarbons
into intact skin and found a similar behavior for hydrocarbons.
A good example of an emulsion being able to penetrate the uppermost
layers of the SC was provided by Pfeiffer, who could detect residues of a W/O
emulsion by Cryo raster electron microscopy in the upper layers of the SC [50].
All these investigations show that an emulsion converts into a kind of a
lipid-emulsifier-gel after topical application, which itself accounts for the cover-
age of the skin, film formation, or occlusivity, as well as for the homogeneous
(a) (b)
Figure 8 Green channel (a); red channel (b). Confocal fluorescence image of a W/O
cream applied to porcine skin in vitro. The water and lipid phases are colored individually
with fluorescent colors, green and red respectively. Figure 8a shows the signal of the green
channel (representing the water phase), which is restricted to the surface of the skin. Figure
8b shows the signal of the red channel (representing the lipid phase), which clearly is
found in deeper layers of the SC than the green signal.
distribution of UV filters or the penetration of active ingredients. Lipids are the

major part of that ‘‘residue’’ and influence its characteristics.
B. Film Formation—Occlusivity
Film formation contributes to the efficacy of emollients and lipids in general. A
good film on the skin surface (homogeneous and of certain thickness), leading
to an optimal occlusivity, should promote endogenous moisturization due to re-
duction of transepidermal water loss (TEWL) of the skin.
Film formation on skin can only be measured indirectly. Therefore, some
of these indirect methods shall be discussed. Mostly, water vapor transmission
experiments are conducted in vitro and in vivo. Furthermore, water tightness or
SDS challenges of pretreated skin are valuable tools for estimating the protective
properties of such films on skin surface.
Wepierre et al. [51] and Choudhury et al. [52] discussed the optimal combi-
nation of lipid and emulsifier to obtain films of good quality. For that purpose,
they formed mixtures of water, oil, and emulsifier at different HLB values and
determined the area of the isotropic oil phase in the phase diagram. They could
establish a correlation between the occlusivity of the O/W emulsion and the area
of the isotropic phase. Furthermore, they noticed that the occlusivity of an O/W
emulsion with a given emulsifier system is directly influenced by the choice of
the lipid.
Occlusivity can be estimated in vivo by water permeability measurements
through a membrane either gravimetrically or by TEWL measurement. In vivo,
278 Lanzendörfer
Figure 9 Correlation of in vivo TEWL with in vitro water vapor transmission ◆ ⫽

Dibutyl sebacate, 䊉 ⫽ Cetyloctanoate, ■ ⫽ Caprylic/capric triglyceride, ⊗ ⫽ Dimethi-
cone, 䊐 ⫽ Mineral oil, 䉱 ⫽ Petrolatum.
the measurement of occlusivity can be estimated by measuring the reduction of

the TEWL after application of an emollient.
Frömder [53] systematically studied the occlusivity of certain lipids in vivo
and in vitro and established a correlation between the TEWL reduction in vivo
and the water permeation rate in vitro after application of single lipids (Fig. 9).
In general, however, occlusive properties measured with different methods
are not directly comparable because they are influenced by the membrane and
application techniques chosen [54–59].
Nevertheless, some trends can be seen. In all studies, it is found that hydro-
carbons and especially petrolatum are very occlusive components, synthetic
branched-chain esters are less effective [59], linear and cyclic silicone oils are
not occlusive in a wide range of viscosity and molar weight, and even silicones
with high molecular weights do not show substantial occlusivity [55,60].
Only silicones with long-chain alkyl residues show occlusive properties
[61]. Beeswax also has good occlusive properties [58].
C. The Role of Skin Barrier Lipids in Skin Condition

The stratum corneum (SC) constitutes the main barrier to the diffusion of sub-
stances into the skin. It consists of corneocytes and three intercellular lipid
classes, ceramides, sterols, and free fatty acids. Its integrity requires the organiza-
tion of the lipids into intercellular membranes subsequent to the secretion of
epidermal lamellar body contents at the stratum granulosum–SC interface [62].
Recently, Norlén [63] proposed a different barrier lipid composition by
including cholesterol esters that constitute a large portion of barrier lipids.
Table 9 Proposed Stratum Corneum Lipid Composition
Cholesteryl esters Free fatty acids Cholesterol Ceramides

Weight percentage 18 11 24 47
Molar percentage 15 16 32 37
Source: From Ref. 63.
It is interesting that he also discovered that inter-individual differences in

relative amounts of free fatty acids, cholesterol, and ceramides are rather high
(greater than 100%), but the variance in the ratios of cholesterol/ceramides is
only 10.1%.
Several pathological skin conditions with perturbed barrier function have
been demonstrated to have abnormal lipid composition, such as X-linked ichthyo-
sis [64] or lamellar ichthyosis [65]. A disrupted lipid organization has also been
demonstrated to result in a decreased barrier function in psoriasis and atopic
dermatitis [66]. In all these skin conditions, also a paucity of ceramide 1 occurred
[67–69]. The deficiency of ceramide 1 was compensated by a surplus of ceramide
5 [70].
Also, aging seems to have an effect on the composition of the SC lipids.
Sauermann and Schreiner showed that the sterole content of xerotic skin of el-
derly people is decreased [71]. In another study, Schreiner found an apparent
increase in free fatty acids and a compensatory decrease in ceramides in healthy
aged skin [72]. Nevertheless, he could not find any clues on morphological alter-
ations of the intercellular membranes, in contrast to Ghadially [73], who studied
volunteers of above 80 years of age.
1. Influences on Skin Condition

The interrelationship of season, individual parameters, and lipid content of the
skin on skin condition has been the subject of several investigations. It was found
that season is a major factor for the generation of dry skin condition, which itself
can also be characterized by dryness score, skin roughness, or increased TEWL
[74–77]. According to Yoshikawa, skin adapts to dry environmental conditions
by an increase in ceramide content of the barrier. This is not the case in skin
sites that typically show symptoms of dryness, such as the calf [74].
In contrast, prolonged exposure of hairless mice to a dry environment (rela-
tive humidity [RH] below 10% for 2 weeks) resulted in an increased SC thickness,
increased amount of SC lipids, and accelerated barrier recovery compared with
mice exposed to a humid environment (RH ⬎ 80%). Exposure to low humidity
produced histologic evidence of inflammation, epidermal hyperplasia, and other
280 Lanzendörfer
Figure 10 Influences on skin condition with respect to barrier function.
changes in skin. These could be prevented by an occlusive plastic membrane,

petrolatum, or glycerol (10%) [78,79].
Low ceramide content can be related to irritability of skin and is influenced
by season as well as by atopic disposition. Reduced ceramide content of the SC
lipids account for higher irritability of the skin [80,81].
Besides individual differences in irritability of the skin [82] there are inter-
and intraindividual differences in skin thickness and TEWL [83]. These findings
support the assumption that dry skin and barrier disorders are related.
Not only do lipid contents of the stratum corneum and the irritability of
the skin depend on seasonal changes but so does the biophysical appearance of
skin (e.g., dryness or roughness) (Figs. 10 and 11) [84,85].
2. Different Roles of Ceramides in Barrier Function of the SC

Ceramides have been shown to play a vital role in maintaining the barrier proper-
ties and the functionality of the stratum corneum. However, not much is known
about the importance of the ceramide subspecies 1–7 for barrier function.
Ceramide 1 has been shown to be essential for barrier integrity: as humans
who lack ceramide 1 have an elevated TEWL and dry skin [75]. The structural
impact of ceramide 1 on the stratum corneum lipid lamellar phase formation was
discovered by studying the lipid ordering in artificial lipids mixtures by x-ray
diffraction measurements [86]. It was detected that ceramide 1 is important for
the formation of the long periodicity phase. The long periodicity phase is also
formed by the stratum corneum lipids in situ (see also Chapter 2).
By investigating the relationship of SC lipid composition and membrane
organization in vivo, Schreiner could show that a lack of the long periodicity
Figure 11 Seasonal changes of skin microtopography as measured by changes of mean

RzDin of untreated skin of 120 healthy human volunteers (standard deviation given by width
of the curve). (From Ref. 85.)
phase coincides not only with a paucity of ceramide 1 but also with a reduced
ceramide 4/ total ceramide ratio and elevated ceramide 2 and ceramide 5 ratios
[72]. However, a diminished ceramide 1 content occurred more often in dry skin
types than in normal skin. This clearly demonstrates that the changes in barrier
function can be related to changes in ceramide ratios, which themselves might
be caused by alterations of the ceramide biosynthesis or glycosylceramide pro-
cessing.
D. Penetration Enhancement by ‘‘Normal’’

Cosmetic Lipids
Because the skin, especially the stratum corneum, is an effective barrier against
penetration of substances through the skin, the lipid composition of the SC is
thought to be of major importance. The integrity of the lipid barrier often is
assessed by the ability of certain substances to penetrate the skin. On the other
hand, certain classes of lipids are suspected to be absorbed by the SC lipids and
either to be incorporated into the structure or form separate domains, thus altering
the barrier properties of the SC or altering the penetration ability of other sub-
stances.
For the investigation of the effects of lipids on the stratum corneum lipids
and on penetration enhancement, several different approaches are used. Most
282 Lanzendörfer
often, in vitro penetration studies, either with porcine or mouse skin, are con-
ducted. Those skins, although not exactly comparable with human skin, neverthe-
less are valid in vitro systems for the investigation of the interaction with stratum
corneum lipids [87–89].
For in vivo investigations, TEWL is regarded as an indicator of the en-
hancement capacity of skin permeation enhancers using water vapor as a ‘‘model
drug’’; also it is used to monitor intrinsic skin barrier properties. It is used in in
vivo studies in addition to Laser Doppler Flowmetry or visual scoring, which
are used for assessing the irritation achieved with a compound.
1. Fatty Acids
It is well known that unsaturated fatty acids can act as effective penetration en-
hancers for certain substances. The underlying mechanism has been the subject
of investigation by several groups. The effect of oleic acid on stratum corneum
lipids was investigated by Differentially Scanning Calorimetry (DSC) [90,91]
and Fourier Transform Infrared Spectroscopy [92] in studies of the thermal phase
behavior of the SC lipids as well as the penetration enhancement of selected
drugs.
The mechanism attributed to the penetration-enhancing action is the distur-
bance of lamellar packing order of the SC lipids by the unsaturated (and therefore
bent) alkyl chain of the unsaturated fatty acid, leading to a fluidization of the
lipid mixture, which can be seen as a drop in the phase transition temperature.
The other possible mechanism is the formation of a separate phase, which was
found by Ongpipattanakul in 1991 to account for the penetration-enhancing ac-
tion of oleic acid [92]. These findings were confirmed using deuterated oleic acid
in in vivo experiments, although stratum corneum lipid fluidization could not be
ruled out completely [93].
Chain Length, Degree of Unsaturation, and Number of Double Bonds. After
oleic acid became known as a penetration enhancer, several fatty acids were
investigated in order to elucidate their structure-activity relationship. Therefore,
investigations with hydrophilic [94,95] as well as lipophilic model drugs [96–
98] in vitro and in vivo were conducted.
Shifting the position of the double bond toward the hydrophilic end obvi-
ously enhances the penetration-enhancing activity. Cis-omega-12-octadecenoic
acid (petroselinic acid) was found to be a better penetration enhancer than oleic
acid (cis-omega-9-octadecenoic acid) [94], and for gondonic acid (cis-11-eico-
senoic acid), maximum enhancement of skin permeation of indomethacin was
found [95].
On the other hand, Tanojo found monounsaturated cis-6-, 9-, 11-, 13-octa-
decenoic acids to enhance the permeation of p-amino benzoic acids to the same
extent. The polyunsaturated fatty acids—linoleic, α-linolenic, and arachidonic
acids enhance PABA permeation more strongly than monounsaturated acids, but
additional double bonds did not further increase the degree of enhancement [97].
For the saturated fatty acids with 6 to 12 carbons, using PABA as penetrant, he
found a parabolic correlation between enhancement effect and chain length, with
a maximum at nonanoic and decanoic acids.
Barrier-Perturbing Effects of Fatty Acids. By comparing in vitro penetra-
tion-enhancing effects with in vivo TEWL measurements, Tanojo found that bar-
rier disruption (measured as TEWL) does not necessarily correlate with penetra-
tion enhancement [98]. From the in vitro studies, the saturated fatty acids with
C-chains of 9 to 12 were revealed as excellent permeation enhancers with an
equal or even higher capability compared to unsaturated fatty acids. In the in
vivo study, however, unsaturated fatty acids increased both TEWL and irritation
effects as assessed by measurement of epicutaneous blood flow with laser doppler
velocimetry (LDV) to a higher extent than the saturated fatty acids. Thus, the
enhancement capability of saturated fatty acids as shown for some compounds
might not have a connection with the perturbation of skin lipids in vivo.
The mechanism of action for unsaturated fatty acids has been shown to be
exclusively the perturbation of intercellular lipid domains in the skin (SC), be-
cause they enhance TEWL but not the permeation of hexyl nicotinate. The lack
of correlation between the average TEWL values and the irritation potential
(LDV, visual scoring) after the application of unsaturated fatty acids suggests
that the degree of irritation does not necessarily correlate with the degree of
barrier modulation of fatty acids.
2. Other Compounds
Schmalfuss et al. [99,100] investigated the penetration enhancement of a hydro-
philic drug from a microemulsion system. They found that 10-methyl palmitic
acid caused a decrease in drug penetration, and cholesterol caused an increase.
They did not find the penetration-enhancing action of oleic acid in that system
higher than that of the investigated microemulsion alone.
Walters [101] could show different penetration-enhancing capacities of
fatty alcohol ethoxylates in hairless mouse skin for methyl nicotinate. Laureth-
10 was found to be the most effective enhancer for increasing permeation rate.
Also the subject of investigation were alkanols with chain lengths C2 to
C12; a maximum penetration enhancement was found for alkanols with a chain
length of C6 (in vitro measurements on hairless mouse skin). Further increase
in the chain length of the alkanol led to a decrease in penetration of the nicotin-
amide despite the higher skin uptake of alkanol. From these investigations it is
concluded that alkanols also have effects on the stratum corneum lipids [102].
Leopold and Maibach investigated the action of lipids on the stratum cor-
neum lipids of human skin using DSC measurements and an in vivo method
284 Lanzendörfer
using methyl nicotinate as the model drug, which was dissolved in the investi-
gated lipid. It was found that isopropyl myristate and light mineral oil acted as
penetration enhancers but the medium chain triglycerides and dimethicone did
not [103]. Leopold and Lippold investigated the mechanism in in vitro studies
with human stratum corneum by observation of the change in thermal phase tran-
sitions (enthalpies) of the SC lipids after pretreatment with the lipids by DSC
measurements. They showed that branched materials such as light mineral oil
and isopropyl myristate induced a reduction of the phase transition temperatures
and enthalpies [104].
All these studies show that cosmetic lipids can affect SC lipids when ap-
plied in the right medium. But penetration-enhancing experiments have to be
interpreted with care because many factors besides the choice of penetration en-
hancer influence the permeation of substances. The solubility of the substance
of choice in the medium has to be regarded as well as the release pattern of
the ‘‘formulation.’’ In the studies cited above, therefore, the investigations are
restricted to comparably simple systems such as dispersions in propylene glycol.
Cosmetic formulations are more complex systems because the emulsifier and the
lipids act differently on the solution of a ‘‘permeant,’’ so that emulsions often
have ‘‘bad’’ release characteristics.
E. Efficacy of Lipids Applied to Skin

For cosmetic purposes, lipids normally are not applied as pure compounds on
the skin but in the form of an emulsion, which is a far more convenient way of
application. The required cosmetic or dermatological results are (1) improvement
of skin barrier properties, (2) skin protection, and (3) skin care expressed as
reduction of skin roughness or scaliness and improvement of skin moisturization.
Because emulsions are complex systems, the efficacy of a product is not
solely the result of the lipid, but of the whole system as such. Comparison of
the efficacy of different lipids, therefore, often is difficult, because efficacy of
the emulsion itself can be high and the additional effect of lipids comparably
small. In addition, the test strategies applied for efficacy measurements vary con-
siderably. Only in the area of skin roughness and moisturization are test methods
somewhat standardized. For the assessment of barrier integrity and skin protec-
tion, a huge variety of test strategies exist, which makes an overall comparison
rather difficult. Here, some examples shall be discussed.
1. Recovery of Skin Barrier Function

The most obvious possibility for recovering the skin barrier function is by the
replacement of the intercellular lipids. The skin of hairless mice damaged with
acetone has provided a useful in vivo model to study the restoration of barrier
function and has been thoroughly investigated by the group of Elias [105–107].
These studies have demonstrated that after extraction of skin lipids with
acetone, the barrier function can be partially restored by the application of a
mixture of skin-type lipids. TEWL is used as an indicator of barrier integrity and
barrier recovery is measured as percentage recovery as a function of time com-
pared to untreated. It was found that for optimal barrier recovery, the lipid mix-
tures consisted of free cholesterol, ceramide (3 and 4), and fatty acids. The effect
was optimized at a cholesterol: ceramide: palmitic acid: linoleic acid molar ratio
of 4:2:1:1 [105].
Inspired by these results, the application of ceramides or pseudoceramides
alone or as a component of an emulsion has been in the focus for skin care as
well. Imokawa investigated the improvement of water-retention properties of the
skin [108]. He induced dryness by using a mixture of acetone/ether and measured
the improvement in skin condition following the application of pseudoceramides
and ceramides. Pseudoceramides are less effective in repairing the barrier than the
natural ceramides. However, these synthetic lipids were superior to the untreated
control.
Möller et al. used an in vitro model system using porcine skin and measured
the TEWL to rank pseudoceramides; they found alkyl-succinic acid derivatives
to be most effective [109]. Lintner studied the effect of a synthetic ceramide (N-
stearoyldihydrosphingosine) after barrier perturbation with SDS in vivo [110].
Incorporated in concentrations of 0.5 and 1% in an emulsion, the synthetic cera-
mide effectively reduced TEWL, whereas the emulsion itself showed no effect.
Despite the efficacy shown in the above-mentioned studies, ceramides and
pseudoceramides until today were not deployed in cosmetic formulations. This
may be explained in part by their poor solubility in common cosmetic ingredients
and their high melting point and the resultant difficulties in formulating stable
emulsions containing ceramides and pseudoceramides.
The restoration of the epicutaneous barrier is of major importance in patho-
logical skin conditions such as atopic dermatitis. Atopic skin, even if non-
lesional, shows elevated TEWL, signs of skin dryness, and a deficiency in barrier
lipids [67]. The efficacy of emulsions containing evening primrose oil on the
barrier restoration in atopic skin were demonstrated in several studies [111–113].
Jánossy demonstrated that the application of an evening primrose oil–containing
cream on atopic dry skin for 3 weeks significantly reduced the TEWL on the
treated skin sites [111]. Maas-Irslinger additionally found a stronger reduction
of skin roughness for an evening primrose oil–containing cream compared to
placebo [112]. Gehring et al. discovered that the effect on skin barrier function
might even depend on the vehicle applied. The TEWL-reducing effect of evening
primrose oil was significantly stronger if it was applied in an W/O emulsion
instead of an O/W emulsion [113]. Therefore, they concluded that the vehicle
is of crucial importance for the efficacy of the active ingredient.
In dry skin conditions induced by prolonged exposure towards water or
286 Lanzendörfer
water-soluble irritants (i.e., detergents), the epidermal barrier is perturbed, which

can result in severe irritation and skin problems. Therefore, the skin irritation
model with SDS often is used to investigate effects on barrier recovery after
irritation.
Using such a test design, Lodén showed the effectiveness of canola oil and
the sterol-enriched fraction of canola oil in skin barrier recovery [114]. Phytoster-
oles are thought to exert beneficial effects to the skin barrier because of their
structural relationship to cholesterol [115,116].
2. Skin Protection
Due to their hydrophobicity, lipids also act as a barrier towards water and water-
soluble irritants on the skin. For maximum protection, the lipids should com-
pletely cover the skin site and form a homogeneous and durable film. Unfortu-
nately, they do not form a barrier against lipophilic ingredients and often favor
their solubility and the persistence of those substances on the skin.
In order to measure the efficacy of lipids or barrier creams against the
irritating action of water soluble-substances, three main test strategies are applied:
Single application and single irritation (occlusive)
Repeated applications and repeated irritation (occlusive)
Application and open irritation, single or repeated (‘‘wasching test’’)
Sodium dodecyl sulfate (SDS), sodium hydroxide, and lactic acid are recom-
mended as model irritants. However, SDS is the irritant that is most frequently
used.
Petrolatum is thoroughly tested in many different approaches, and because
of its good performance it is known as the prototype skin protectant [117]. It
also has been tested in in vivo skin irritation models [118] as well as in in vitro
investigations [119]. Petrolatum obviously combines all the properties of a good
barrier lipid. It is nonpolar and semisolid and although it is known to penetrate
the SC, it forms a separate nonlamellar phase in the corneocyte interstices [73].
Accordingly, petrolatum exerts an immediate protective action on the skin surface
and a prolonged effect due to its incorporation in the SC.
Other lipidic ingredients also have been shown to be beneficial in terms of
skin protection. These are waxes such as beeswax or paraffinic waxes [120] as
well as silicones [60], perfluorhydrocarbons [121], paraffin, or natural oils [122].
3. Skin Care
The most important cosmetic property of lipids is their skin care efficacy. Skin
care comprises moisturization and smoothing of the skin as well as a visual reduc-
tion of the signs of dryness. The term emolliency often is used in order to express
the efficacy of lipids to influence the skin’s softness. The improvement of the
Figure 12 Reduction of scaliness after application of the lipstick for 14 days.
skin condition is also connected with the ability of the lipid to form an occlusive
film on the skin surface, where the lipids reduce TEWL and therefore account for
a better moisturization of the skin [123]. Petrolatum or lanolin oil are examples of
occlusive lipids (see also previous chapters). Additionally, not only the kind but
also the amount of lipid incorporated in an emulsion accounts for the occluding
properties of the final product [123]. Furthermore, the ability of lipids to form
liquid crystalline lamellar phases is thought to be an important factor for skin
care efficacy [115,124].
The use of lanolin oil in lipstick preparations has been shown to have bene-
ficial effects on the scaling of lips [23]. Three lipstick formulations were com-
pared (Fig. 12).
Table 10 Composition of Lipsticks
Formula code A B C
Paraffin 30% 30% 30%
Petrolatum 30% 20% 30%
Liquid petrolatum (350–360 cps) 30% 30% 20%
Polyethyleneglycol 400 distearate 10% 10% 10%
Liquid lanolin — — 10%
Wool fat, anhydrous — 10% —
Source: Ref. 23.
288 Lanzendörfer
Figure 13 Decrease of skin roughness measured microtopographically after application

of a W/O emulsion containing 0, 2, and 4% of Eucerit (containing lanosterol and choles-
terol). n ⫽ 24 healthy volunteers; area tested is volar forearms; application twice daily;
treatment was stopped about 14 hr before measurement. (From Ref. 71.)
By comparing the dryness of the lips before and after treatment and group-
ing the results in three classes, Silverman found the formula containing liquid
lanolin to be the most effective in reduction of scaliness.
Sterols are one of the three lipid classes in human stratum corneum. Sauer-
mann and Schreiner published the effect of sterols on skin roughness when ap-
plied in an emulsion system [71] (Fig. 13). They found a dose-response curve
for the effect of sterols on skin roughness reduction. This finding is in agreement
with the good skin care properties proposed for sterols and lanolin derivatives.
Fatty acids are the second class of barrier lipids. Consequently, topical
application of saturated fatty acids should also exert skin care benefits. An aug-
mentation in the content of cholesterol, free fatty acids, and tryglycerides in the
SC could be detected after application of an emulsion containing the same. The
enrichment of the lipids correlates with increased skin moisturization [72] (Fig.
14).
F. Discussion
The actions lipids can exhibit on skin are very diverse. They render a characteris-
tic skin feel, give a certain occlusivity to the product, and can penetrate into the
SC interstices to a certain extent.
The activity of emulsions is even more complex as emulsifiers and water
are combined with lipids. Furthermore, lipid and water-soluble active ingredients
Figure 14 Significant incorporation of skin-related lipids in the stratum corneum after

14 days of application of a lipid-enriched cream. (From Ref. 125.)
can be incorporated. Using such complex systems, the investigation of effects

caused by a single ingredient is very difficult. Measurement of the in vivo effects
such as skin moisturization or reduction of skin roughness are valid parameters
for the assessment of skin care products but do not give any information about
the mechanism underlying these effects.
In that respect, a quote from Peter Flesch is remarkable; he published an
article on the hydration of the skin surface by fats and emulsions and voiced
some thoughts about the effects of lipids and emulsions on the skin which in
general are still valid today [126]:
The question was raised in the beginning concerning the respective merits
of fats and oils versus emulsions in promoting hydration of the skin surface.
In the absence of adequate tests and satisfactory quantitative data, no final
statement can be made. The following represents a personal educated guess
rather than definite recommendations. Oils and fats can have only a single
effect on hydration. This could be occlusion of the surface or added hygro-
scopicity. Much too little is known about absorption to be considered here.
On the other hand, emulsions having several types of components may
have a variety of effects: they can occlude the surface, can add water directly
to the horny layer and may increase its hygroscopicity if they contain some
suitable hygroscopic compound.
290 Lanzendörfer
Some of these questions can be answered today, such as occlusive effects or film
forming characteristics. However, new questions arose and certainly will arise.
In the future, there will be systems available to investigate effects of lipids on
the structural arrangements of SC lipids selectively, and as a consequence they
will enable the cosmetic chemist to specifically choose substances that further
enhance barrier function of the skin.
On the other hand, knowledge of the interaction of different ingredients in
emulsions applied to skin will rise, thus making it possible to choose an even
better combination of ingredients for maximum activity.
Also, in terms of subjectively perceived skin care, progress will be made,
because the consumer acceptance still is and will continue to be the yardstick
for the quality of a skin care product. Consumer choice is influenced mainly by
sensorial factors such as the smell of the product and the feeling it leaves on the
skin. Furthermore, the subjectively experienced care effect of a product is not
necessarily identical with the objectively measured skin care efficiency of the
product. Because lipids are the main carriers for sensory effects (see also Chapter
11), the combination of lipids that have proven skin care benefits with those
transporting the sensory effect will garner more interest.
I think in the future we can expect many developments in that direction.
ACKNOWLEDGMENTS
I would like to express my thanks to my colleagues Volker Schreiner, Andreas

Bleckmann, Roger Wepf, and Rainer Kröpke, who supported this work with their
knowledge and many helpful suggestions. I am also very thankful to Ralph
Schimpf, Volker Skibbe, and especially Günther Schneider, who judiciously read
this chapter and with their comments helped to make it complete. Last but not
least, I am grateful to Thomas Förster, who gave me the opportunity to publish
what I wanted to write about lipids for quite a long time.
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10
Benefits of Lipidic Refatters
in Surfactant Products
Ulrich Issberner
Cognis Deutschland GmbH, Düsseldorf, Germany
I. INTRODUCTION
Soap and synthetic surfactants are commonly used in personal care products to
increase the cleansing performance and to create a pleasant foam. They act on
the skin surface by dispersing, emulsifying, and removing all types of surface
soil. This includes organic material from detached scales and intercellular mate-
rial (lipids, fatty acids, amines), body secretions, sebum residues, micro-organ-
isms, and a variety of externally applied substances, such as makeup and medical
ointments.
Soap, in use in ancient civilizations, helped to maintain the health of the
Phoenicians and Romans, and is still an item of daily use. Synthetic surfactants,
which became commercially available after World War II, enabled new types of
body cleansing products to be created.
However, surfactants can also damage the skin by removing skin lipids and
causing corneocytes to swell. Therefore, along with other environmental influ-
ences, everyday washing with soap or surfactants can impair the skin barrier,
resulting in an increase in transepidermal water loss, roughness, and scaling of
the skin.
Mild surfactants with cleansing properties similar to those of aggressive
surfactants do not remove lipids to the same extent, and they irritate skin only
when used at high concentrations under artificial conditions. The admixture of
lipids and lipid compounds to surfactant-based body cleansing products can coun-
teract the negative side effects. Although skin care ingredients have been a feature
of personal cleansing products for some time, selected newer formulations are
299
300 Issberner
making more substantial claims, which can be proved in controlled consumer

studies.
II. SURFACTANTS USED IN CLEANSING PRODUCTS
Surfactants are characterized by a hydrophilic head group and a hydrophobic tail.

Modern body wash products usually combine anionic, amphoteric, and nonionic
surfactant types to improve cleansing performance, foaming behavior, consis-
tency, and mildness.
A. Anionic Surfactants
1. Soap
Soap (ROO⫺M⫹ ) is the alkali salt of a fatty acid. It is generally produced by the
saponification of triglycerides, fatty acids, or fatty acid methyl esters. Soaps are
subdivided into water-soluble and water-insoluble types. The former are the salts
of fatty acids with ammonia, low-molecular-weight amines (especially alkanol-
amines), and alkali metals (especially sodium and potassium). Water-insoluble
fatty acid salts result from reaction with polyvalent metallic cations, such as zinc
and aluminum, alkaline earths such as calcium and magnesium, and long-chain
fatty amines. The water-soluble salts of fatty acids, derived from alkaline hydroly-
sis (saponification) of plant or animal fats and oils, are used widely as skin cleans-
ers and in laundry and other cleaning applications.
Because of soap’s poor foaming properties in hard water, its application
in body wash products is limited; but in cleansing bars, soaps are still widely
used.
2. Alkyl Sulfates
Alkyl sulfates (ROSO 3⫺M⫹ ) are produced by the sulfation of fatty alcohols. Solu-
bility decreases with increasing carbon chain length (⬎16), concomitant with an
increase in the sensitivity to water hardness: lauryl sulfate has been found to
yield the best foam and solubility characteristics, whereas longer chain deriva-
tives, such as cetyl/stearyl sulfate, are better tolerated by skin but are less water
soluble and foam less copiously [1,2].
3. Alkyl Ether Sulfates

Alkyl ether sulfates (ROE(CH 2 E CH 2 E O) n E SO 3 H) are made primarily by
adding ethylene oxide to fatty alcohols, followed by the sulfation of the ethoxy-
Benefits of Lipidic Refatters in Surfactant Products 301
lated fatty alcohols and subsequent neutralization with a suitable base (e.g., so-
dium hydroxide).
The solubility of the ether sulfates is influenced by the hydrophilic polygly-
col ether groups and is noticeably higher than that of the corresponding alkyl
sulfates. The solubility of calcium salts is very significant; thus, ether sulfates
are quite insensitive to water hardness. An increase in the degree of ethoxylation
reduces a product’s interfacial activity but improves its dermatological properties.
On the other hand, an increase in the alkyl chain length (⬎16) has a negative
influence on foaming power and also on cold-water solubility, but skin compati-
bility is improved. Ether sulfates exhibit synergistic effects in combination with
other surfactants—for example, with regard to foaming power, mildness (e.g.,
combination with betaines), and oil-dispersing ability [1].
4. Sulfosuccinate Esters
Two types of sulfosuccinate esters exist: the sulfosuccinate monoester
(ROOHCCH 2 CH(SO 3⫺M⫹ )COO⫺M⫹ ) is more frequently used in skin cleansers
than the diester (ROOHCCH 2 CH(SO 2 (SO 3⫺M⫹ )COOR). They are generally pro-
duced from maleic anhydride, but maleic acid or fumaric acid may also be used.
O O
储储
XOECCH2CHCEOY

SO3⫺M⫹
Regardless of substitution, the sulfonic acid group is always ionized, and M⫹

represents the counterion. In compounds in which X or Y represents an alkyl or
substituted alkyl group, the remaining carboxyl function is also present in salt
form (e.g., disodium deceth-6 sulfosuccinate). If both X and Y represent alkyl
or substituted alkyl groupings, the sulfosuccinate is a diester (e.g., dioctyl sodium
sulfosuccinate). Fairly complex multifunctional substituents can be present on
the carboxyl groups of this category. Alternately, the XO or the YO groups may
be replaced by a substituted N-atom, in which case the resulting sulfosuccinamate
is a monoamide (e.g., disodium stearyl sulfosuccinamate).
5. Acylglutamate
Acylglutamates are amides derived from L-glutamic acid and natural higher fatty
acids [3]. They have good foaming and detergency behavior, even with hard
water and exert a soft feeling to the skin during and after use. An example is
sodium lauroyl glutamate [4].
302 Issberner
HOOCCH2CH2CHCOONa

HNEC(CH2)10CH3
储
O
B. Amphoteric Surfactants
Amphoteric surfactants are characterized by a molecular structure containing two
different functional groups with anionic and cationic character, which change
their charge in response to pH.
1. Acyl Derivatives of Ethylene Diamine

These derivatives include monocarboxylates, dicarboxylates, and sulfonates; they
differ primarily in their fatty side chain.
This large group of amphoteric materials exhibits the above structure. They show
very good foam stability and hard-water resistance and are compatible with cat-
ionic, anionic, and nonionic agents in all preparations [2].
2. Betaines
The betaine group of cosmetic raw materials includes the quaternized alkyl or
substituted alkyl derivatives of N,N-dimethyl glycine. They have the following
structure,
CH3

REN⫹ECH2COO⫺

CH3
in which the nitrogen atom always carries a positive charge regardless of pH. At
the slightly acidic pH values normally encountered in cosmetics, this charge is
counterbalanced by a negative charge on the carboxyl group (zwitterion). Beta-
ines are not truly amphoteric compounds, because they do not exhibit exclusively
anionic characteristics at high pH. R represents an alkyl group (e.g., C 14H 29⫺
in myristyl betaine) or an amide-interrupted alkyl group (e.g.,
C 17 H 35 CONH(CH 2 ) 3⫺ ) in stearamidopropyl betaine. Related amphoteric com-
pounds are derived from amino propane sulfonic acids (see sulfonic Acids), e.g.,
lauryl sultaine. The betaines are zwitterionic, surface-active compounds that are
employed as emulsifiers, detergents, foam boosters, aqueous viscosity increasing
agents, and skin and hair conditioners. They are not affected by water hardness
and produce excellent foam with good stability. Exerting very low skin-irritation
potential, they have also been found to be effective in reducing the irritation poten-
tial of alkyl sulfates, alkyl ether sulfates, and soaps. Alkyl amido betaines are the
most common variants of the betaines. Their preparation is carried out in a two-
step process, starting with fatty acids or their esters, by condensation with dimethyl-
amino propyl amine and reaction with sodium chloroacetate.
C. Nonionic Surfactants
1. Alkyl Glucosides
Alkyl glucosides are produced by reacting corn starch glucose with fatty alcohol.
The resulting nonionic surfactant is used as a cosurfactant in skin cleansers, in
which it exerts performance synergy in combination with anionic surfactants.
In addition to the advantage of commercial availability from renewable, vegeta-

ble-sourced raw materials, alkyl glucosides display a very high degree of biode-
gradability.
III. SKIN–SURFACTANT INTERACTIONS
Along with other environmental influences, everyday washing with soap or sur-
factants can stress the skin and impair the skin barrier. Surfactants wash off not
only soil and excess sebum, as required, but also remove some of the skin’s
intercellular lipids [4–7]. As expected, the strongly cleansing surfactants also
have a strong defatting effect on the skin (Fig. 1). If standardized to the same
cleansing performance, mild surfactants such as the nonionic surfactant Polysor-
bate-20 shown in Figure 1 can be identified by their slight defatting action [5].
Even if the amount of removed lipids is only small [8], the selective dissolv-
ing out of free fatty acids, fatty acid glycerides, and cholesteryl esters leads to
a significant change in the profile of the intercellular lipids [4,9,10]. Moreover,
304 Issberner
Figure 1 Cleansing performance (‘‘washing number’’) and defatting by different sur-

factant solutions. (Adapted from Ref. 5.) (◆ ⫽ significant reduction in skin lipids com-
pared to untreated skin, ◊ ⫽ no significant changes in skin lipids).
surfactants penetrate into the stratum corneum, where they are adsorbed on the
keratin of the corneocytes [11–13] and mix with the intercellular lipids [14]. The
consequent impairment of the skin barrier can be demonstrated very sensitively
by measurements of the skin’s transepidermal water loss (TEWL). As long as the
degree of impairment is only slight, the rise in TEWL correlates with a decrease in
the lipids’ degree of order, thus clearly indicating the important role of the lipid
film’s morphology in the skin barrier [4].
The corneocytes of the stratum corneum are dead keratinocytes, consisting
mainly of the protein keratin, which is present in various forms. Solid keratin
microfibrils are embedded in amorphous keratin [9,10]. In addition, dry corneo-
cytes contain about 10% water, which is bound to polar side chains of the keratin
[15]. Ionic, polar, and nonpolar bonding forces between the side chains of the
keratin polymers are responsible for the mechanical strength of the corneocytes
[16].
During washing, water and surfactants penetrate into the corneocytes. Wa-
ter accumulates at the polar and, above all, the ionic side chains. Due to the high
dielectric constant of water, the salt bridges between oppositely charged keratin
side chains are weakened and the corneocytes swell [8–10].
Surfactants are adsorbed at nonpolar protein side chains as a result of hy-
drophobic interactions. Moreover, they can also bond to oppositely charged kera-
tin side chains by electrostatic interaction. At the pH of 6.5 that prevails in many
cleansing products, keratin has a slight excess of anionically charged side chains,
so anionic surfactants increase the negative charge of the keratin by bonding

hydrophobically to nonpolar side chains, thus increasing the degree of swelling
(Fig. 2) [11]. At this pH, cationic surfactants neutralize free anionic side chains
and reduce the swelling slightly [11]. Like anionic surfactants, nonionic surfac-
tants are adsorbed at nonpolar groups but only enhance the swelling to a small
extent.
After excessive exposure to surfactants, TEWL increases sharply and—
depending on the disposition and sensitivity of the individual—the skin becomes
dry and often scaly, which points to a disruption of the desquamation process
[4,8,17]. In this phase, the degree of order of the lipids no longer correlates with
the increase in TEWL. This is a further indication that in scaly and irritated skin,
other harmful biological mechanisms such as irritation processes are superim-
posed on the purely physical effects of the surfactants on the lipid film [4,18].
In the cosmetics sector, great efforts are being made to avoid these undesir-
able effects. Mild surfactants with similar cleansing properties to aggressive sur-
factants do not attack the intercellular lipids to the same extent [5,6]. The use of
refatting oil additives and the application of creams after washing can at least
partially restore the lipid film [7,17,19]. A distinction must be drawn at this point
between physical effects on the stratum corneum and biological effects on the
metabolism of the living epidermis. Petrolatum brings about an immediate partial
restoration of the previously impaired skin barrier properties of the stratum cor-
neum, whereas physiological lipid mixtures slowly penetrate into the epidermis
and, by naturally accelerating the process of metabolization in the lamellar bodies
Figure 2 Swelling behavior of human stratum corneum in various surfactant solutions.

Error bars indicate SEM. (Adapted from Ref. 11.)
306 Issberner
Figure 3 Skin compatibility (erythema) of different surfactant solutions: PAR ⫽ sodium

C12–15 pareth sulfate (5%; 120 mM); SLS ⫽ sodium lauryl sulfate (2%; 65 mM); ISE
⫽ sodium cocoyl isethionate (5%; 148 mM); SUL ⫽ disodium laureth sulfosuccinate
(10%; 181 mM); LAU ⫽ lauryl glucoside (10%; 238 mM); DEA ⫽ cocamide DEA (10%;
323 mM); AMP ⫽ sodium cocoamphoacetate (10%; 274 mM); BET ⫽ cocamidopropyl
betaine (10%; 286 mM). (Adapted from Ref. 18.)
[19], build up the skin barrier again and help surfactant-induced scaly skin to
recover [17].
An overview of the skin compatibility of different surfactants after a human
48-hour patch test was given by Barany et al. [18]. This work is remarkable
because of the test concentrations—which were adjusted to concentration and
molar weight (Fig. 3).
IV. LIPIDIC REFATTERS
The boundaries are merging between skin care and body care: Each skin care
ingredient can be used in body care products, in principle. Therefore, the lipids
that have been discussed in the preceding chapter (9) can be used as well in
personal cleansing products. However, the efficacy of the lipids as active ingredi-
ents is highly dependent on the technology of the formulation. In some cases,
the use of ready-made compounds can be helpful for the easy production of lipidic
surfactant skin cleansers [25].
With lipidic refatters, highly sophisticated claims are possible: by deliv-

ering proceramides to the upper skin layer, promotion of ceramide production has
been asserted, and with high amounts of moisturizers, long-lasting moisturizing is
claimed [20,21].
The development of these types of cleansing products can be likened to
playing a piano concerto in which many factors come into play: The amount and
polarity of the lipids, the combination of synergistically acting surfactants, and
the application of the product should be considered to influence the cleansing
performance, to balance the foam stability, and to fulfill the promotional claims.
A patent disclosure of Unilever comprises a stable cosmetic liquid cleansing com-
position containing high levels of emollients [22], an example of which is shown
in Table 1 [22].
Winder et al. [23] developed a personal cleansing system comprising a
diamond mesh bath sponge and a liquid cleanser with moisturizer, which are
packed together in a cleansing kit. The following example has been given (Table
2) [23].
Colgate-Palmolive [24] disclosed a skin cleanser comprising surfactants, a
silicone fluid, a hydrocarbon, a cationic polymer, a combination of hydroalkyl
cellulose and an acrylate copolymer, and water. An example is shown as follows
(Table 3) [24].
The above-mentioned examples are composed of at least one lipid ingredi-
ent that is claimed to improve not only the mildness of the products but also the
efficacy, (e.g., to moisturize the skin). These claims have to be proved in studies
using human volunteers. In combination with biophysical measurements which
are (explained in detail in Chapter 7), skin care benefits from rinse-off products
can be found.
Table 1 Skin Cleansing Lotion

Skin cleansing lotion Weight %
Sodium laureth sulfate 10.0

Sodium lauroamphoacetate 5.0
Sunflower seed oil 15.0
Lauric acid 2.5
Citric acid 0.8
Magnesium sulfate 1.5
Fragrance 1.0
Water Add to 100.0
Source: Ref. 22.
308 Issberner
Table 2 Moisturizing Liquid Cleanser
Moisturizing liquid cleanser Weight %

Sodium laureth-3 sulfate 12.0
Cocoamphoacetate/cocoamphodiacetate 6.0
Alkylpolysaccharide 2.0
Coconut monoethanol amide 2.8
Soybean oil 8.0
Maleated soybean oil 2.0
Polymer JR30 0.4
PEG(6) caprylic/caprylglycerate 4.0
Myristic acid 2.0
Glycerine 3.0
Titanium dioxide 0.1
Perfume 1.8
Preservative 0.2
Water 55.7
Source: Ref. 23.
V. ASSESSMENT OF SKIN BENEFITS

A. Single 24-hour Patch Test
The single 24-hour patch test is an epicutaneous plaster test method (COLIPA
standard [28]). Applying the test substances to the back under occlusive condi-
tions allows skin compatibility to be studied as a function of application time
under various exaggerated conditions. The treatment has been carried out on hu-
Table 3 Skin Cleanser with Improved Stability

Skin cleanser with improved stability Weight %
Sodium laureth sulfate 7.6
Cocoamidopropylbetaine 2.1
Decylpolyglucoside 0.6
Dimethicone 1.0
Petrolatum 2.0
Polyquaternium-7 0.2
Hydroxypropyl methylcellulose 0.5
Acrylates/C 10–30 alkyl acrylate crosspolymer 0.5
Water 83.5
Source: Ref. 24.
man volunteers by means of epicutaneous plaster for a period of 24 hours. The

skin reactions are evaluated at various intervals (6, 24, 48, and 72 hr) under
standardized conditions, and the observed reactions are rated in terms of redden-
ing, swelling, scaling, and fissures. For each of these parameters, the volunteers’
individual reaction ratings are added together to give a total irritation score.
The skin compatibility of test substances can be determined by direct com-
parison within the group and by comparison with a positive control (⫽ 100%).
The positive control has to exhibit slight to moderate skin irritation under the
test conditions.
Shower gel formulations used in the single 24-hour patch test caused no
immediate skin reactions when used in dilutions approximating the usual applica-
tion concentrations (below 5%—i.e., less than 1% surfactant active substance).
For this reason, Förster et al. [25] increased the overall concentrations to 30%
(i.e., 5% surfactant active substance). Under these conditions, even mild formula-
tions induce skin reactions, whose strength and frequency can be used to differen-
tiate between the products (Fig. 4). The shower gel without added refatting sub-
stances (a combination of sodium lauryl ether sulfate with alkyl glucoside and
Figure 4 Skin compatibility of surfactant mixtures: Irritation sum scores of shower gel
formulations in the 24-hour patch test. The differences between shower gel without lipids
and shower gel with hydrogenated castor oil were significant (P ⬍ 0.05). The differences
between shower gel without lipids and shower gel with cetyl palmitate particles and
shower gel with glyceryl oleate/APG liquid crystal were highly significant (P ⬍ 0.01).
(From Ref. 25, with kind permission.)
310 Issberner
Table 4 Surfactant Formulations Used in a Single 24-hr Patch Test
Cleansing shower gel compositions 1 2 3 4

Sodium laureth sulfate (70% AS) 16.0 16.0 16.0 16.0
Cocamidopropyl betaine (40% AS) 4.0 4.0 4.0 4.0
Coco glucoside (50% AS) 3.75 3.75 3.75 2.7
Coco Glucoside (35% AS) (and) glyceryl oleate 0.0 0.0 0.0 3.0
Hydrogenated castor oil 0.0 1.0 0.0 0.0
Cetyl Palmitate (and) beheneth-10 (and) hydro- 2.3 0.0 0.0 0.0
genated castor oil (and) glyceryl stearate
Phenoxyethanol (and) dibromo dicyanobutane 0.1 0.1 0.1 0.1
Water to 100 to 100 to 100 to 100
pH 5.5 5.5 5.5 5.5
Source: Ref. 25.
cocamidopropylbetaine, formula 1 in Table 4) exhibited a higher irritation poten-

tial under these conditions. The strength and frequency of the observed skin reac-
tions were comparable with the positive standard SDS 0.5%. Shower gels con-
taining refatting substance performed much better (formulas 2 to 4 in Table 4).
Shower gels with wax particles of hydrogenated castor oil or cetyl palmitate at
these concentrations evoked comparably few skin reactions, and the shower gel
with added glyceryl oleate and cocoglucoside caused the fewest skin reactions
[25].
B. Arm Flex Wash Test

The arm flex wash test is an open epicutaneous test method that is used to study
formulations by repeated application in association with mechanical factors (e.g.,
by rubbing on the skin). This test is suitable for use as a controlled application
test (COLIPA) to determine the skin compatibility of two different products by
comparing them under conditions of everyday use [26,27].
The inside surface of the elbow of one arm of each volunteer is washed
with the test solution. The test design provides for a total application period of
6 minutes. The product is applied, followed by 2 minutes scrubbing and then
intensive washing. This procedure is repeated once. After the third and final appli-
cation, the product is left on the skin for 2 minutes without scrubbing and then
washed off. The other arm is treated in exactly the same way with the second
test solution. The two test products are used randomly in pair comparisons (right/
left). The washing procedure is done twice daily over a total period of 10 washing
days. Before each wash and after the final application, skin irritation at the test
zones is assessed visually (erythema, scaling, sensory perceptions) on the basis

of a scoring system (0–4) and by TEWL measurements.
The arm flex wash test enables the skin compatibility of body cleansing
products to be assessed against objective and subjective criteria under near-
normal conditions (Fig. 5). In a study of Jackwerth et al. [27], 20 volunteers used
a cleansing product twice daily on the sensitive inside surface of the elbow over
a period of 2 weeks. Reactions were then assessed in terms of reddening (ery-
thema), scaling, edema (swelling), and fissures (small cracks in the skin). In addi-
tion, the degree of skin barrier damage was determined objectively by measuring
TEWL. Finally, the volunteers gave their subjective assessment of whether the
cleansing product evoked itching, tingling, burning, or a feeling of tautness.
The 10% solution of the anionic surfactant sodium lauryl ether sulfate
caused slight but measurable and tangible skin irritation [27]. In comparison, a
nonionic alkyl glucoside was considerably gentler to the skin. Erythema and skin
scaling were decreased by three-quarters and there was no subjective feeling of
skin irritation (see Fig. 5). In this test, too, a combination of the strongly foaming
sodium lauryl ether sulfate and the nonionic alkyl glucoside resulted in a clear
improvement in skin compatibility. This surfactant basis can thus be used to
produce cleansing formulations with tailor-made application properties such as
skin compatibility, cleansing performance, foaming properties, and viscosity.
Figure 5 Results of the arm flex wash test with 10% surfactant solutions of sodium
lauryl ether sulfate, alkyl glucoside (APG) and a 3 :1 mixture. (Adapted from Ref. 27.)
312 Issberner
C. Application Study with Lipid Analysis

For the purpose of eluting the refatter glyceryl oleate from the stratum corneum,
Förster et al. [25] wetted the inside surface of the lower arm of each of 20 volun-
teers with warm water (30–34°C); the product was then used for 15 seconds.
The skin zone was subsequently rinsed with warm water for 30 seconds, carefully
patted dry with paper towels, and allowed to dry for 2 minutes. The lipid film
absorbed was finally eluted with a medical cotton pad soaked in ethanol. For the
elution, a plastic ring with a defined internal diameter was placed on the treated
zone on the lower arm of the volunteer, and the skin within this test zone was
wiped three times with the moist cottonwool pad with a circular movement. The
pad was then kept in ethanol until analyzed. The refatter in the eluate was quanti-
tatively determined by a gas chromatography/mass spectroscopy method.
Applications of body wash products were made once or over a period of
days or weeks to measure short-term and cumulative skin refatting effects. A
mild body wash product without lipids was used in a 1-week preconditioning
phase and for the duration of the application phase. The use of creams and lotions
on the forearms was forbidden during the study.
With this technique, Förster et al. [25] could detect the refatter glyceryl
oleate in ethanolic eluates after a single application, after 1 week of use, and
after 2 weeks of use (Fig. 6). A statistically significant increase after 1 week in
comparison with a single application was detected without an ‘‘overfatting’’ of
Figure 6 Penetration of glyceryl oleate into the stratum corneum after treatment with
a shower gel containing a refatter. The differences after 1-day treatment are highly signifi-
cant compared to untreated (P ⬍ 0.01). The differences between 1-day treatment and 1-
week treatment are highly significant. (From Ref. 25, with kind permission.)
the skin but as a pleasant skin feel, as has been shown by the volunteers’ answers
to questions about their sensory perceptions.
D. Forearm Wash Test with Skin Roughness

Determination
To assess skin roughness, Förster et al. [25] combined a forearm wash study with
fast optical in vivo topometry of the skin (FOITS [29]). The comparative study
of shower products was carried out with a group of 30 women; the inside surfaces
of the lower arms were the test fields. An image of each test zone was prepared
with FOITS before and after 3 weeks of product use. The measuring system
consists of a projection unit and a charge coupled device (CCD) camera, fixed
at the so-called triangulation angle. This technique involves projecting a sequence
of grid lines on the skin. The recorded strip pattern enables the order, phase, and
strip quality of each point of the image of the examined zone to be measured.
Changes in the skin profile were quantified on the basis of the parameters
Ra and Rz. Ra is the arithmetic mean of the absolute values of all deviations of the
roughness profile from the center line within the total path. The rough structure of
the test zone is described by the parameter Rz. The product effects were statisti-
cally confirmed by ANOVA calculations.
The assessment was made by comparing the initial and final values. During
a 3-week study period, the volunteers used the product three times daily. This
was done by wetting the test zone and then applying 0.5 ml of product. After a
first washing phase of 30 seconds, the product was washed off with warm water
and the zone was washed again for 30 seconds. All of the studies were done in
a specially climatized laboratory with a constant room temperature of 22 ⫾ 1°C
and a relative humidity of 60 ⫾ 5%.
The FOITS results proved the positive effect of the skin-refatting compo-
nent. Whereas the test sample without refatting components tended to increase
the roughness of the skin, the glyceryl oleate–containing formulation resulted in
smoother skin after 3 weeks of use. Statistical analysis of the results showed
significant differences between the two formulations after all measurement inter-
vals. The skin surface profile was clearly improved by application of the refatting
formulation (Fig. 7).
E. Leg Wash Protocol

To assess the dry skin improvement of personal cleansing products, Ertl et al.
[30] developed a wash test on dry leg skin. Washes were conducted over a period
of days or weeks.
The volunteers had to shave their legs 3 days before the baseline treatment
evaluation. A mild cleansing bar was used instead of the usual shower or bath
314 Issberner
Figure 7 Skin roughness measurement values after a 3-week period of use of a shower
gel containing a refatter and a shower gel with no refatter. The differences between the
products are highly significant for both Ra and Rz, with P ⬍ 0.01. (From Ref. 25, with
kind permission.)
product for the duration of the study. The subjects were obliged not to use the
bar or its lather directly on their legs. Bath oil, cream, or lotion use on the legs
was not allowed, as were leg skin–affecting situations (excessive ultraviolet light
exposure, swimming in chlorinated pools).
Visual and instrumental evaluations were conducted on each site before
the start of the treatment (baseline). Visual dryness was measured using a grading
procedure [31]. Only volunteers with a visual dryness score between 2 and 4 on
each site at the baseline treatment evaluation continued into the treatment phase.
Stratum corneum hydration was assessed via skin capacitance measurements.
TEWL was measured with an evaporimeter.
Two regimens of the preconditioning phase were evaluated: Washing the
legs twice daily with a supplied commercial soap bar for one week or leaving
the legs untreated. In an evaluation study, the changes in clinical parameter values
on subjects legs after a 1-week preconditioning phase were compared [30]. The
subjects used a syndet bar for cleansing one leg and washed their other leg twice
daily in a controlled manner with the soap bar. Greater damage to the soap-
washed leg was demonstrated (Table 5) [30].
An analysis of variance (ANOVA) model was used to analyze the data,
with baseline skin condition being used as a covariant in the analysis. Data from
studies comparing the same clinical protocol were pooled using a meta-analysis
technique [32].
Table 5 Skin Properties after Washing with a Syndet or Soap Bar
Visual Visual Skin

dryness redness capacitance (pF) TEWL (g ∗ m⫺2 ∗ hr⫺1)
Soap bar—con- 0.96 0.37 ⫺1.34 0.71
trolled wash
Mild syndet bar— 0.64 0.45 ⫺0.61 0.09
ad lib wash
Comparison of clinical parameters after one week of preconditioning phase. Both instrumental end
points showed significantly (P ⬍ 0.008) greater damage to the soap-washed leg after this phase
(n ⫽ 24)
Source: Adapted from Ref. 30.
With this protocol, Ertel et al. [30] found that some cleansing products can
lead to moisturization of the dry skin, even for periods as long as 24 hours. In
a series of 11 leg wash studies, a body wash product yielded significant reduction
in visual dryness at all evaluation time points and a significant improvement in
stratum corneum hydration at three of the evaluation time points (Table 6).
VI. OUTLOOK
As the result of innovative lipid-surfactant product concepts—and also the devel-

opment of new kinds of applications (e.g., pore strips, wet wipes), cleansing is
one of the fastest growing categories within the body and skin care market. Stud-
Table 6 Changes in Visual Dryness and Skin Capacitance for a Body Wash Product
Relative to a No-Treatment Control
Dryness change Capacitance change
Evaluation visit (mean ⫾ SEM) (mean ⫾ SEM)
3 hours post first wash ⫺0.6 ⫾ 0.044* 1.2 ⫾ 0.267*

24 hours post first wash ⫺0.2 ⫾ 0.038* 0.4 ⫾ 0.282†
24 hours post fourth wash ⫺0.3 ⫾ 0.041* 1.6 ⫾ 0.317*
3 hours post fifth wash ⫺0.8 ⫾ 0.047* 2.5 ⫾ 0.355*
* P ⬍ 0.0001.
† P ⫽ 0.10.
Source: Adapted from Ref. 30.
316 Issberner
ies with surfactant-lipid mixtures demonstrate that boundaries are merging be-
tween skin care and body care.
The compatibility of surfactant mixtures can be increased by selecting mild
surfactants and by combining favorable properties. Lipid-containing compounds
are the focus of intensive research efforts. Improvement of the skin lipid structure
by lipid-containing surfactant products prevents dehydration and scaling of the
corneocytes and thus reduces skin roughness and increases skin hydration. In
addition to their primary cleansing effect, skin care products must meet consumer
expectations of skin-compatible body care ingredients and support other aspects
of modern body cleansing such as fun and wellness.
REFERENCES
1. Biermann M, Lange F, Piorr R, Ploog U, Rutzen H, Schindler J, Schmid R. Synthesis

of Surfactants. In: Falbe J, ed. Surfactants in Consumer Products. Berlin, Heidelberg:
Springer-Verlag, 1987:24–124.
2. Thau P. Surfactants for Skin Cleansers. In: Rieger MM, Rhein LD, eds. Surfactants
in Cosmetics. New York, NY: Marcel Dekker, 2nd Ed. 1997:285–306.
3. Acylglutamate Bulletin, Ajinomoto Co., Inc., 1991.
Dermatol Res 1994; 286:41–46.
5. Gloor M, Munsch K, Friederich HC. Über die Beeinflussung der Hautoberflächen-
lipide durch Körperreinigungsmittel I. Derm Mschr 1972; 158:576–581.
6. Gloor M, Tretow CW, Friederich HC. Über die Beeinflussung der Hautoberflächen-
lipide durch Körperreinigungsmittel II. Derm Mschr 1974; 160:291–296.
7. Gloor M. Influence of surface active agents, emollients, and cosmetic applications
on skin and hair lipids. Cosmet Toilet 1977; 92:54–62.
8. Froebe CL, Simion FA, Rhein LD, Cagan RH, Kligman A. Stratum corneum lipid
removal by surfactants: relation to in vivo irritation. Dermatologica 1990; 181:227–
283.
9. Fulmer AW, Kramer GJ. Stratum corneum lipid anormalities in surfactant-induced
10. Dykes P. Surfactants and the skin. Int J Cosmetic Sci 1998; 20:53–61.
11. Rhein LD, Robbins CR, Fernee K, Cantore R. Surfactant structure effects on swell-
ing of isolated human stratum corneum. J Soc Cosmet Chem 1986; 37:125–139.
12. Robbins CR, Fernee KM. Some observations on the swelling of human epidermal
membrane. J Soc Cosm Chem 1983; 34:21–34.
13. Rhein LD. Review of properties of surfactants that determine their interactions with
stratum corneum. J Soc Cosmet Chem 1997; 48:253–274.
14. Friberg SE, Goldsmith L, Suhaimi H, Rhein LD. Surfactants and the stratum cor-
neum lipids. Colloids Surfaces 1988; 30:1–12.
15. Potts RO. Stratum corneum hydration: experimental techniques and interpretations
of results. J Soc Cosmet Chem 1986; 37:9–33.
16. Speakman JB, Stott E. Trans Faraday Soc 1934; 30:539–548.
of surfactant dry skin. Arch Dermatol Res 1989; 281:45–51.
18. Barany E, Lindberg M, Loden M. Biophysical characterization of skin damage and
recovery after exposure to different surfactants. Contact Dermatitis 1999; 40:98–
103.
19. Mao-Qiang M, Brown BE, Wu-Pong S, Feingold KR, Elias PM. Exogenous non-
physiologic vs physiologic lipids. Arch Dermatol 1995; 131:809–816.
20. Unilever Plc. Patent No. WO9612469.
21. Procter & Gamble Patent No. GB2297762.
22. Unilever PLC, WO9904751.
23. Procter & Gamble, US5650384.
24. Colgate-Palmolive Co, WO9962493.
25. Förster Th, Issberner U, Hensen H. Lipid/surfactant compounds as a new tool to
optimize skin-care porperties of personal-cleansing products. J Surf Det 2000; 3:
345–352.
26. Strube DD, Koontz SW, Murahata RI, Theiler RF. The flex wash test: a method for
evaluating the mildness of personal washing products. J Soc Cosmet Chem 1989;
40:297–306.
27. Jackwerth B, Krächter H-U, Matthies W. Dermatological test methods for optimising
mild tenside preparations. Parfümerie Kosmetik 1993; 74:134–141.
28. Walker AP, Basketter DA, Baverl M, Diembeck W, Matthies W, Mougin D, Paye M,
Röthlisberger R, Dupuis J. Test guidelines for the assessment of skin compatibility of
cosmetic finished products in man. Food Chem Toxicol 1996; 34:651–660.
29. Rohr M, Schrader K. Fast Optical In Vivo Topometry of Human Skin (FOITS),
SÖFW-Journal 1998; 124:52–59.
30. Ertel KD, Neumann PB, Harwig PM, Rains GY, Keswick BH. Leg wash protocol
to assess the skin moisturization potential of personal cleansing products. Int J Cosm
Sci 1999; 21:383–397.
31. Ertel KD, Keswick BH, Bryant PB. A forearm controlled application technique for
estimating the relative mildness of personal cleansing products. J Soc Cosmet Chem
1995; 46:67–76.
32. Boisits EK, Nole GE, Cheney MC. The refined regression method. J Cut Aging
Cosmet Dermatol 1989; 3:155–163.
11
Sensory Assessment of Lipids in
Leave-On and Rinse-Off Products
Thomas Gassenmeier and Peter Busch*
I. SURVEY OF SENSORY MEASUREMENT TECHNIQUES

The sensory assessment of all kinds of consumer goods, foods, or objects of daily
life is doubtless as old as mankind itself. Standardization of testing procedures
was first introduced for the assessment of certain foods and drinks—for example,
wine, spirits, coffee, fish, and meat. At the start of the 20th century, the devel-
oping food industry required a scientific sensory assessment of its products. It is
not surprising, therefore, that the generally accepted basic principles of a modern,
formalized, and systematic methodology of sensory assessment were established
in the food industry.
The present chapter is designed to give a short overview of these generally
accepted basic principles. A detailed description of sensory techniques can be
found in Sensory Evaluation Techniques [1].
A. Measurable Properties in Sensory Assessment

Which properties can be measured by sensory assessment? In principle, every-
thing that we can perceive with our five senses—for example:
Appearance (e.g., color, luster, shape, size, transparency)
Taste, aroma
Odor, smell
Consistency, texture (e.g., viscosity, cohesiveness, softness, wetness, dry-
ness)
Sounds (e.g., pitch, loudness)
* Current affiliation: Cognis Deutschland GmbH, Düsseldorf, Germany.
319
320 Gassenmeier and Busch
Obviously, relevant quantities vary from product to product. Thus, taste plays a
role in all foods but is of no importance in cosmetics. Among cosmetic products
themselves, different parameters are likewise of interest for different categories:
the quantity and characteristics of the foam produced are of elementary impor-
tance for surfactant-based agents for washing the body and the hair but are not
significant for other skin care products.
B. Influences on the Assessment Procedure

The various sensory characteristics such as external appearance, smell, aroma,
flavor, consistency, and sounds are perceived primarily through the sense organs,
namely the eyes, skin, nose, tongue, and ears: chemical or physical stimuli are
registered and transmitted (Fig. 1). Both physiological and psychological factors
have an influence on the primary registration of these stimuli. The physiological
factors include the phenomena of adaptation or potentiation. For example, if,
when assessing the sweetness of a particular test material, the subject has been
given a sweet material immediately beforehand, the test material is perceived to
be significantly less sweet. The reason: the reduction in the sensitivity of the
sense of taste as a result of the repeated administration.
Psychological factors play a particular role in the registration and pro-
cessing of stimuli. These influences include a particular expectation, errors due
to adaptation, logical errors, so-called halo effects (i.e., where one perception
influences a succeeding one), the order in which samples are presented, influence
by third parties, or personal motivation at the time.
What is really decisive for the measurement of effects, in addition to the
actual registration of the stimuli by the sense organs, is their—practically simulta-
neous—interpretation by the mental process.
Both the sensory perception and the mental interpretation of the registered
stimuli depend on a large number of particular factors. Thus, the anatomic reali-
ties are different for every human being; moreover, they change during each
person’s lifetime. The psyche, which plays a role in mental interpretation, like-
wise differs from person to person, depending on the individual’s culture, mem-
bership in particular social groups, age, education, religion, and upbringing.
These differences, which can hardly be systematized in any way, are responsible
for the fact that the typical findings of a sensory assessment study show a general
tendency toward vagueness.
The world of individual experience is reflected particularly strongly in lan-
guage. Language, indeed, is what opens our door to experience: the greater our
language resources, the more we experience. The proof can be adduced by means
of ‘‘open interviews’’ [3]. If different panels are made up of subjects with differ-
ent personal experience histories or training levels, and they are asked to describe
Sensory Assessment of Lipids in Skin Care Products 321
Figure 1 Schematic survey of the major types of mammalian cutaneous sensory endings
and their afferent fibers. (From Ref. 2.)
Figure 2 Panel test for generation of words.
a face-care cream in words, the great differences in linguistic ability become

apparent (Fig. 2).
C. Measures to Reduce Extraneous Influences

in Sensory Assessment
1. Test Controls
If usable test results are to be obtained, the practical implementation of sensory
tests requires the choice of a careful test design that keeps the effect of the influ-
ences described above as small as possible. One basic precondition is that sensory
assessment be carried out under strictly controlled conditions. First of all, this
means that the test venue must be arranged in such a way that the panelists are
able to perform as well as possible. Some of the design requirements for a sensory
assessment laboratory are listed in a guideline issued by the American Society
for Testing Materials (ASTM) [4]. In addition, controlled conditions must also
be maintained with respect to the test products (manufacture, presentation) and
the panelists (training).
2. Test Setup
A skillfully setup test is a further precondition for keeping the effect of extraneous
influences as small as possible. Various techniques will be described below.
3. Tests for Sameness/Difference

Triangle test. In the triangle test, three samples are administered, of which
two are identical and one different. The subjects must identify the differ-
ent product.
Two-out-of-five test. This test is also designed to establish differences be-
tween two samples. Here, two or three (as the case may be) of the five
samples are identical. The advantage of this test lies in the fact that the
probability of a result that is correct by chance is small (1 in 10). The
disadvantage is that the numerous samples lead to adaptation and fatigue
effects, which make the test really only suitable for visual and tactile
applications.
Duo-trio test. In contrast to the triangle test, subjects in the duo-trio test
are required to compare two different samples with a reference sample
(one of the samples is the same as the reference, the other is not). The
disadvantage of this setup is the high probability of a chance correct
response (50%); the advantage is that it is easy to understand.
Simple difference test. This form of test requires subjects to compare two
different or—as a control—two identical test products.
Difference-from-control test. The difference-from-control test provides in-
formation about a possible difference between two samples and—unlike
the test setups mentioned hitherto—also about the degree of difference.
In actual practice, the subjects are given one or more test products and
a reference sample. What is measured is the degree of difference between
each test product and the reference.
Sequential tests. Sequential tests are carried out in order to save time and
costs by keeping down the number of tests needed. In the test procedures
described above, with a fixed number of judgments and resulting type I
error (α ⫽ probability of stating that a difference occurs when it does
not), the type II error (β ⫽ probability of stating that no difference occurs
when it does) is minimized. This means that the possibility of false posi-
tive results is accepted in order to avoid false negative results and to
make do with a fixed number of judgments. In sequential tests, by con-
trast, α and β are laid down in advance, and the required number of
judgments is calculated from test results as they are obtained. Depending
on the course taken by the test, more or fewer assessments are required
in order to ensure a particular degree of statistical certainty. Sequential
testing in practice often uses triangle or duo-trio tests.
4. Tests to Determine Differences in Particular Characteristics

Paired comparison and multisample difference tests. Distinctions between two
or more products in respect to a particular characteristic can be made in paired-
comparison or multisample-difference tests. Here, the subjects are given two or

more samples and required to assess whether the products are different. If more
than two products are assessed, the intensity of the relevant characteristic is also
assessed for the various test products. Depending on the number of samples,
different procedures are required for statistical evaluation (e.g., analysis of vari-
ance, Friedman analysis, or other specific statistical procedures).
5. Descriptive Analysis Technique

In descriptive analysis, the panelists must be able to perceive and describe the
sensory characteristics of a sample. This methodology thus includes a qualitative
aspect, defining the product, as well as the quantification of the respective qualita-
tively discovered parameters. A detailed description of the method can be found
in Sensory Evaluation Techniques [1].
An important precondition of descriptive analysis is for the judges to re-
ceive considerably more elaborate training. This is necessary in order to explain
to them the nomenclature of the sensory parameters used, and to make sure that
the words for the quantitative assessment of intensity differences are used in a
uniform way. In addition, defined reference patterns are used to exemplify the
terminology.
6. Panel Management
A further important measure to ensure good results by sensory analysis is the
selection and training of the test panel. General guidelines on this topic can be
found in the literature [5,6]. The first stage in the setting-up of a test panel is the
selection of suitable judges. This can be done by means of preliminary tests in
which, for example, potential panelists are required to determine the sameness
of, or the differences and the size of the differences between, various samples.
In the case of panels for descriptive testing, the greater demands make it highly
desirable to give particular care to the recruitment of suitable panelists. The usual
method is to draw up a short list by means of a questionnaire, and to make the
final selection by means of acuity and ranking tests using known samples. Once
selected, the judges have to be trained. For example, the panelists must be taught
about correct behavior before the test, about the use of the samples, about ways
of reducing adaptation, and about the product characteristics that are to be as-
sessed. Where descriptive analysis is concerned, the panelists must first of all
learn the necessary parameters for the product category in question, and the pre-
cise expressions used to assess them. This is followed by practical training with
exercises of increasing difficulty. The usual total training time required ranges
from 40 to 100 hours, depending on product category.
D. Test to Establish Product Acceptance

To establish product acceptance, it is usual practice to carry out consumer tests or
in-house panel tests. The advantage of consumer tests lies in their high degree of
realism; in other words, the panelists consist exclusively of ‘‘normal’’ consumers.
In practice, consumer tests are a commonly used instrument to assess the accep-
tance of newly introduced or modified market products or to assess possible market
potential. What all consumer tests have in common, however, is that they need a
large number of subjects (approx. 100–400) in order to achieve reliable results.
This is associated with high costs, and, at several weeks, a great deal of time.
II. SENSORY ASSESSMENT OF LIPIDS IN COSMETICS
Following the general explanation of sensory techniques, we shall now, with the
help of numerous examples, give an overview of the sensory assessment of lipid-
containing cosmetic preparations.
A. Measurement of Cosmetic Effects

There are two basic ways of obtaining information about the effects of cosmetic
products. On the one hand, there are the various biophysical or dermatological
measuring techniques, such as the measurement of transepidermal water loss,
sebumetry, corneometry, patch tests, and so forth. These procedures are described
in detail in other chapters of this book. The advantage of these objective test
methods is that they provide exact, comprehensible, and easy-to-communicate
(i.e., intersubjective) results. The disadvantage of many physical or physicochem-
ical procedures is that their practical relevance is not always certain. Transepider-
mal water loss (TEWL) measurements, for example, can give very precise infor-
mation on the barrier characteristics of the stratum corneum—but whether
consumers can really notice any significant measurable difference in the barrier
characteristics of their own stratum corneum following cosmetic treatment is
questionable, in view of the fact that there is no organ to provide direct informa-
tion about them.
Another possibility for obtaining information on the effects of cosmetic
preparations is to carry out subjective tests. The advantage of these methods is
that they are, without question, highly realistic. The disadvantage is that the re-
sults are usually imprecise. The reasons for the imprecision have already been
mentioned, and these include variations in skin status, variations in the functional
efficiency of the sense organs, and, of course, differences due to cultural, social,
or religious influences in the mental processing of identical stimuli. In sensory
Figure 3 Intersubjectivity box.
assessment, the assessment of products by trained professional teams leads to a

significant increase in intersubjectivity while maintaining a high degree of realism
(Fig. 3).
B. Sensory Assessment Practice in Cosmetics

For the subjective assessment of cosmetic effects, all the above-mentioned tech-
nologies and procedures could in principle be used. In actual practice, for the
sensory assessment of cosmetic preparations, it is primarily difference tests and
quantitative descriptive analysis that are suitable and described in the literature
[7–10].
The usual test methods all have in common this requirement: to reduce the
influence of extraneous factors that could vitiate the precision of the method, the
test conditions must be strictly controlled. Training the panelists—which, for a
descriptive analysis in cosmetic matters, takes at least 30 hours per person—is
also expensive and time-consuming.
C. Quantitative Testing
The requirements described above regarding enhancing the precision of sensory
assessment, in particular the extensive training of the panelists, are, as stated,
both expensive and time-consuming. For this reason, a simplified methodology
has been developed that builds on two basic principles: the use of precisely de-
fined sensory parameters and the carrying out of a comparative test using refer-
ence products [3].
1. Test Parameters
Table 1 sets out test parameters for skin care products and surfactant-based body-
cleansing preparations. These parameters have been established in preliminary
linguistic tests. Each of the given parameters is precisely defined (Figs. 4 and
5).
2. Reference Products
The use of reference products to facilitate assessment is a standard procedure,
being a component, for example, of the duo-trio and difference-from-control tests
outlined above. Normally, the reference products are selected from products on
the market. As the composition and characteristics of products on the market are
changing with increasing speed as a result of diminishing product-cycle times,
it is advisable to use one’s own standard products whose composition is known
and constant. In a recent article [3], the use of reference samples derived from
the cremor basalis of DAC (German Pharmaceutical Codex) is suggested for the
sensory assessment of skin care products (Figs. 6 and 7).
This aqueous hydrophilic cream can be varied easily in respect to its content
of different modules such as emulsifiers, lipids, or rheological modifiers [11].
For every sensory parameter to be assessed (Table 1), three reference composi-
tions are used, which respectively evince the relevant characteristic strongly,
weakly, or to an intermediate degree.
In practice, these reference samples are used as follows. The test product
(i.e., the one to be assessed) is first tested for the relevant sensory characteristic
against the intermediate reference sample. If judged identical, it is given a score
of 4 on a 7-point scale. If judged to be different, the test-product is tested against
Table 1 Sensory Parameters of Skin Care and

Surfactant-Based Products
Skin care products Surfactant-based products
Pick-up Distribution
Consistency Slipperiness
Peaking Flash foam
Cushion Amount of foam
Distribution Foam bubble size
Absorption Creaminess
Smoothness Foam stability
Stickiness Foam cushion
Oiliness (residues) Smoothness of the skin
Waxiness (residues) Skin dryness
Cushion/Body
150 mg of substance are placed on the fingertips of both index fingers. The index finger
and thumb are rubbed against each other. Evaluate the amount of product perceived be-
tween index finger and thumb during the rubbing procedure. The more product is per-
ceived, the higher the cushion effect.
Figure 4 Definition of Cushion/Body.
the reference sample that deviates in the same direction from the standard. At
this point at the latest, the final score on the 7-point scale can be given, whereby
scores 2, 4, and 6 represent identity with a standard product, 3 and 5 a position
between the reference samples, and 1 and 7 extreme values (Fig. 8).
3. Validation
In order to test the extent to which the method provides comparable results be-
tween different laboratories, a validation procedure was carried out for the sen-
sory assessment of cream products.
The experiment was set up in the following way: one test product was
assessed in five laboratory panels each with 12 judges, and the results then statisti-
cally evaluated. Those who carried out the test in the respective laboratories had
previously taken part in a one-off training session. The 12 panelists were familiar-
ized with the test procedure for each of the sensory parameters to be assessed,
Flash Foam
Both hands are immersed in warm water (38°C) before the test. Then 0.5 g of the product
to be tested is placed in the palm of the hand together with 2.5 g water. The panelist is
asked to start the washing procedure by using the second hand, which is moved with circle
movements with slight pressure and a frequency of two movements/sec. for 10 sec. over
the area where the product has been applied. After that, again 2.5 g of water are applied
and the procedure is repeated for another 10 sec. The speed of foam formation is evaluated
in comparison to the reference product.
Figure 5 Definition of Flash Foam.
Ingredient Amount [% (w/w)]

Glyceryl Stearate 4.0
Cetearyl Alcohol 6.0
Caprylic/Capric Triglyceride 7.5
Petrolatum 25.5
PEG-20 Glyceryl Stearate 7.0
Propylene Glycol 10.0
Aqua 40.0
100.0
Figure 6 Cremor Basalis DAC.
Figure 7 Strategy for generation of reference products.
and they were subsequently in a position to assess the test product immediately.
Ten sensory parameters were covered: pick-up, consistency, peaking, cushion,
distribution, absorption, smoothness, stickiness, oiliness, and waxiness. Each of
the parameters was precisely defined in a test protocol according to the kind and
quantity of the application of the test or reference product and the characteristic
to be assessed by the subject.
The mathematical-statistical evaluation of the ring experiment was per-
formed according to the following procedure [12]. First, the arithmetic mean,
Figure 8 Sensory profile sheet.

Sensory Assessment of Lipids in Skin Care Products
Table 2 Raw Data Ring-Test
mean DGK
Laboratory 1 Laboratory 2 Laboratory 3 Laboratory 4 Laboratory 5
mean of all
Parameter members a b N a b N a b N a b N a b N
Pick-up 5.15 3.91 1.76 11 5.08 1.56 12 5.57 1.28 14 6.08 0.67 12 4.92 2.07 12
Consistency 4.56 4.82 0.60 11 4.67 0.65 12 4.29 0.91 14 4.50 0.67 12 4.58 0.79 12
Peaking 3.18 3.36 1.50 11 3.25 1.21 12 2.93 0.62 14 2.50 0.67 12 3.92 1.38 12
Cushion 5.28 4.36 1.86 11 5.42 0.90 12 5.79 1.12 14 5.25 1.14 12 5.42 0.79 12
Distribution 4.38 3.73 1.56 11 4.42 1.56 12 4.29 0.99 14 5.00 0.43 12 4.42 0.90 12
Absorption 4.10 4.28 1.42 11 3.92 1.62 12 3.57 1.83 14 5.00 0.43 12 3.83 1.70 12
Smoothness 4.46 5.00 1.73 11 4.42 1.51 12 4.50 1.61 14 4.75 1.22 12 3.67 0.89 12
Stickiness 2.31 3.09 2.07 11 2.17 1.19 12 3.43 2.06 14 1.25 0.45 12 1.50 0.67 12
Oiliness 3.87 3.00 1.55 11 4.08 0.90 12 3.07 1.86 14 4.92 0.29 12 4.33 0.89 12
Waxiness 2.38 2.45 0.69 11 1.83 0.72 12 2.79 0.58 14 2.42 0.67 12 2.33 0.49 12
a ⫽ mean; b ⫽ standard deviation
331
Figure 9 Sensory profiles of a test cream (ring-test).
the standard deviation, and the total number of scores were established for each
laboratory and each parameter. The test to reject extreme scores, recommended
in the quoted literature at this point, was not employed in the current investiga-
tion, as we did not consider that the distribution of scores by the judges pointed
to any gross errors of measurement. The next steps in the evaluation of this exper-
iment were the Bartlett test and the F-test, which provide a measure of the homo-
geneity of the standard deviations and arithmetic means. Iterations of these two
tests were continued until no further significances were obtained. Finally, all the
individual data for each parameter were summarized as a single overall arithmetic
mean, overall standard deviation, and a total number of scores. If one looks at
the experiment in conjunction with the mathematical evaluation as described, it
can be seen that the results from the different laboratories are largely comparable,
and produced very similar qualitative sensory profiles (see Table 2 and Fig. 9).
A detailed examination shows that in the case of nine parameters, all the
laboratories showed no significant differences concerning arithmetic means. As
for the standard deviations, in four parameters one laboratory in each case stood
out by reason of a lower standard deviation. The circumstance that in three of
these cases the laboratory in question was the one where the method had origi-
nally been developed can be explained by the far higher level of training its judges
had received. As far as the parameters stickiness and oiliness are concerned, two
laboratories stand out by reason of a high standard deviation. A possible explana-
tion for this is that these parameters, in the case of the test cream, were assessed
differently depending on the time when they were assessed. Presumably these
two laboratories carried out part of the assessment somewhat earlier than laid
down in the test regulations.
Summarizing the results of this experiment, it is apparent that very similar
sensory profiles were obtained for the same test cream in the different labora-
tories. From a statistical point of view as well, the results from the different
laboratories are comparable. In view of the brief, one-off training received by
the judges, and the high scatter usual in subjective testing methods, this result
provides confirmation that the method presented here really can achieve replica-
ble results with a relatively inexpensive and short period of training.
III. SENSORY ASSESSMENT OF GALENIC CONCEPTS

IN COSMETICS
When developing cosmetic preparations, it is often important to design products

with very specific characteristics using appropriate galenic formulations. The
method of sensory assessment outlined above can be used to very good effect
to test the effect of galenic concepts quickly and without undue expense [13].
In addition, it will reveal any unintended ‘‘side effects’’.
When various galenic concepts are implemented in cosmetics, a role is
often played not only by particular active constituents but also by lipids and their
derivatives—for example, emollients, consistency-giving factors, emulsifiers, or
refatting agents. In the following section, with the help of several examples, we
shall discuss what influences systematic galenic modifications of a cream formu-
lation have on its sensory characteristics.
We chose as our starting formulation an oil-in-water (O/W) cream, based
on ethoxylated cetylstearylalcohol as emulsifier and cetylstearylalcohol and glyc-
erine monostearate as co-emulsifiers, and an oil phase consisting of dicaprylyl
ether, hexyldecanol, hexyldecyl laurate, cocoglycerides, and almond oil. Glycer-
ine was chosen as moisturizer. The emulsifier/thickening system accounted for
approximately 8%, the oil phase 20%, and the moisturizer 5% of the formulation.
Classification of the emulsion thus produced showed that it could most appropri-
Figure 10 Base emulsions for proof of galenic concept.
ately be used as intensive skin care or night care cream. The thickening system,
the emulsifier, the oil phase, and the moisturizer were now systematically varied
and the sensory changes recorded using the sensory profile sheets shown already
in Figure 7 (Fig. 10).
A. Modification of the Consistency-Giving Factors

Where emulsions are concerned, a whole range of different compounds are used
as consistency-giving factors. The fatty alcohols and partial glycerides used in
the initial formulation exercise their consistency-giving effect largely by forming
a coherent lamellar gel network in the aqueous phase together with the hydro-
philic emulsifiers. This process also takes place in the absence of an oil phase,
and leads then to so-called complex emulsifiers or surfactant gels. If an oil phase
is present, this can in itself lead to increased viscosity if the proportions are
appropriate.
Another group of frequently-used thickeners are polymer compounds such
as polyacrylates or various polysaccharides. In the case of polyacrylates, the
thickening effect comes from the way the molecules arrange themselves follow-
ing the neutralization of the free acrylic acid side groups in the aqueous phase
of the emulsion. The polyacrylate gels thus formed are, in contrast to the hydro-
philic gels formed by polysaccharides, highly shear- and electrolyte-sensitive.
In the case of W/O emulsions, the consistency-giving factors here de-
scribed are ineffectual, because the consistency is determined first and foremost
by the nature, amount, and viscosity of the emulsifiers and the oil phase, and
also by physical properties, such as particle size and the proportion of dispersed
aqueous phase.
In order, by way of example, to register the sensorily relevant changes
when a consistency-giving system is modified, formulations were produced and
subjected to sensory assessment; the quantities of consistency-giving factors pres-
ent in the initial formulation were doubled or else largely replaced by a polysac-
charide or a polyacrylate. The results (Fig. 11) show that when the amount of
consistency-giving factor is doubled, the consistency of the product increases as
expected, and along with this, it is more difficult to spread; also, peaking and
cushion are somewhat increased, and it is harder to get the cream out of the pot.
The higher proportion of fatty alcohol and partial glyceride also leads to greater
waxiness. All in all, however, the sensory profile does not undergo any fundamen-
tal change. The relevant properties of the initial formulation, which in any case
Figure 11 Modification of consistency-giving factors.

already has a high proportion of the factor, are increased, but without any addi-
tional effects.
If the initial thickening system is strongly reduced, and a polyacrylate used
instead, the sensory characteristics change markedly. First of all, the formulation
is more difficult to remove from the container. This is because the polyacrylate,
besides its thickening properties, is both shear-sensitive and sensitive to electro-
lytes, which means that skin contact alone causes the formulation to partially
break down when it is taken from the container. The reduction in peaking and
cushion can be explained in the same way. As the polymer leaves residues on
the skin, stickiness is increased while the smoothness of the skin is somewhat
reduced. The sensory changes resulting from these changes in formulation would
be assessed as negative if we were talking, for example, about a face cream. If,
however, the preparation were intended to be applied to a large area of skin, as
a body lotion for example, the use of these polymer thickeners could be entirely
positive.
Finally, the use of a polysaccharide in combination with a reduced quantity
of fatty alcohol leads to a product that shows a marked increase in peaking and
cushion effects, while at the same time the polysaccharide increases skin smooth-
ness and facilitates the removal from the container. The effects are due to the
fact that while this polymer only thickened the emulsion slightly, it did not itself
show any noticeable shear-sensitivity or sensitivity to electrolytes.
B. Modification of the Emulsifier

The choice of emulsifier system is of fundamental importance for the sensory
characteristics of the emulsion. First, it is the emulsifier that determines whether
the oil or the water forms the outer phase of the emulsion. Second, the differences
in chemical structure, even within one type of emulsion where the formulation
is otherwise identical, lead to a marked change in sensory characteristics when
the emulsifier is changed. Among the reasons are the different physical properties
and the different propensities of different emulsifiers to form liquid-crystalline
associates. Among the O/W (oil-in-water) emulsifiers commonly used in cosmet-
ics are such different compounds as ethoxylated fatty alcohols, partial glycerides
or sorbitan fatty acid esters, alkyl polyglucosides, polyglycerol esters, alkyl phos-
phates, fatty alcohol sulfates, alkali salts of fatty acids, and amphiphile polymer
compounds, to name but a few.
To illustrate this, first of all an ethoxylated cetylstearylalcohol in the model
formulation was exchanged for a cetylstearyl glucoside. The basic properties of
the cream remained unchanged (Fig. 12). Because of the particularly strongly
marked propensity of alkyl glucoside to form liquid-crystalline gel phases, the
consistency and the cushion effect both increase. The remaining parameters are
largely unchanged.
When the complete emulsifier/thickener system is replaced by polyglyc-
Figure 12 Modification of the emulsifier-system.
eryl-2-dipolyhydroxystearate, the result is a thin W/O emulsion. This can be

spread easily and, despite its low consistency, shows a relatively high cushion
effect. This is typical of W/O creams, which mostly have a high cushion score.
In their absorption score, as in the other parameters, there are only small devia-
tions from that of the initial O/W formulation. As a result of the change described
here, therefore, merely changing the emulsifier system, while keeping the same
oil phase, can result in a rich, semi-solid cream being turned into a low-viscous,
easily spread lotion that leaves behind a strongly ‘‘caring’’ impression.
C. Modification of the Oil Phase

Cosmetic oils are often used specifically to implement certain galenic concepts.
There is a range of emollients to choose from, a whole range of different chemical
classes, such as ester oils, glycerides, hydrocarbons, ether, guerbet alcohols, or

silicone derivatives. Within the various groups, in turn, substances can be chosen
with quite different viscosity or spreadability or other physical properties. In
general, increasing the quantity of emollient will lead to richer formulations that
take longer to absorb. If the amount of oil-phase is kept constant, the physico-
chemical properties of their composition will in turn affect the sensory character-
istics.
In order to illustrate these correspondences, the relatively high proportion
of cosmetic oils in the initial formulation was first reduced in the model formula-
tion. The sensory assessment (Fig. 13) shows two conspicuous sensory changes:
first, the formulation is absorbed much more quickly and is much less oily; sec-
ond, the cream has a much higher consistency, and a larger quantity of waxy
Figure 13 Modification of the emollients.

residue could be detected. These effects are due to a relative disproportion of

consistency-giving factors. Altogether, the result was a more compact cream that
left a less ‘‘caring’’ impression. For particular applications, as in a warm humid
climate, a formulation of this kind might well be positive.
A formulation that omits high-spreading dicaprylyl ether and replaces it
by low-spreading almond oil results in some surprising changes: in spite of the
higher viscosity of the almond oil, the consistency of the cream is reduced. This
result can be explained by the fact that the oil phase in total is more polar
and thus dissolves more fatty alcohols, which are then no longer available as
consistency-giving factors to form the liquid-crystalline surfactant phases that
determine viscosity. The increased subjective stickiness, the slower absorption,
and the greater waxiness that result when the high-spreading factor is omitted
are, by contrast, all to be expected. The experiment shows that the implementation
of galenic concepts by a change in the oil phase must always be accompanied
by an adjustment in the emulsifier/co-emulsifier system if the desired effect is
to be achieved without unintended side effects.
D. Variation of the Moisturizers

One of the most important tasks of skin-care emulsions is to supply moisture.
To retain moisture in the external layers of the skin, moisturizers are normally
employed, typically various polyols. These substances really do improve the
moisture of the skin, but their maximum concentration has an upper limit. Using
sensory assessment, for example, it can be proved that an increase in the glycerol
content to 20% results in a very marked increase in stickiness (Fig. 14). Because
of the co-solvent effect of glycerol, there is also a reduction in the liquid-crystal-
line surfactant phases, and thus a reduction in the consistency of the cream.
It is interesting that glycerol carbonate, which can also be used as a moistur-
izer, does not result in either a marked change in consistency or in the high
stickiness associated with glycerol, even when used in concentrations of 20%.
Compounds with properties of this kind allow the formulation of elegant cosmetic
emulsions with a very long-lasting moisturizing effect.
E. Multiple Emulsions
Multiple emulsions are characterized by the presence of one or more additional
inner phases. In the case of W/O/W emulsions, oil droplets are distributed within
a coherent aqueous phase; the oil droplets in their turn contain small droplets of
water.
In the investigation described below, the question to be answered was
whether there are any sensory characteristics associated specifically with multiple
emulsions. For this purpose, three different products were subjected to sensory
Figure 14 Modification of the moisturizer.
assessment. One product was based on a polymer emulsifier with a polyacrylate

as thickening agent; a second on polyglycerol ester and ethoxylated fatty alco-
hols; and a third product on ethoxylated fatty acids and partial glycerides.
The sensory profiles of the creams investigated (Fig. 15) are different. The
formulation thickened with polyacrylates rapidly broke down after being applied
to the skin, and the cream felt quite watery. Then the formulation was quickly
absorbed, evincing a certain stickiness. The other emulsions show sensory pro-
files that are markedly different in several parameters.
These investigations show that there is no set of sensory characteristics
specific to all W/O/W creams. Only in the case of one product can the multiple
emulsion be directly detected by the senses, in that it feels very watery when
first applied, and then producing, if anything, an oily and sticky impression.
Figure 15 Different W/O/W creams.
The actual usefulness of multiple emulsions lies in the fact that they make it
theoretically possible to keep certain normally incompatible ingredients separate
during storage. In this way, it has been possible to prepare unstable formulations
that allow novel or long-term effects.
F. Sensory Assessment of Water-Free Emollients

Cosmetic lipids are usually one component of formulations and are used together
with numerous other substances, mostly emulsifiers. As shown above, the sensory
characteristics of the finished product are always the result of a complicated inter-
action of all the ingredients. In certain cases, such as in skin oils or other formula-
tions with a high lipid content, the emollients are the only, or at least the clearly
dominant, factor as far as the formulation’s sensory characteristics are concerned.
Cosmetic emollients are the subjects of detailed description elsewhere in

this book. In principle, the emollients differ along the following parameters:
Polarity: nonpolar emollients—paraffins, iso-paraffins; polar emollients—
triglycerides, straight-chained, branched and unsaturated esters
Molecular weight
Degree of branching
Viscosity
Surface tension
Functional groups
An important parameter of emollients is their spreadability, as it makes an impor-
tant contribution to absorbability and to the time taken for fatting. Zeidler [14]
has examined the connections between the spreading speed of different emollients
on the skin and their physicochemical and chemical properties. The results
showed that within functionally similar product series, the spreading values in-
creased with increasing molecular weight. In addition, moderately hydrophobic
lipids with ester groups (i.e., fats and wax esters) spread—although molecular
Figure 16 Comparative evaluation of various emollients. (From Ref. 14.)

weights were comparable—more strongly than nonpolar hydrocarbons; and

branched lipids spread more strongly than nonbranched.
Further connections between the sensory characteristics of emollients and
their chemical and physicochemical properties are described elsewhere [15,16]
(Fig. 16). Nonpolar emollients are, compared with polar substances, heavy and
draggy. Branched substances are if anything light and smooth, as are substances
with low viscosity and low molecular weight. Nacht et al. [17] describe an inverse
proportionality between perceived greasiness and the skin friction coefficient.
The connections described are confirmed by the following sensory profile,
Figure 17 Sensory profile of dicaprylyl ether and capric/caprylic triglyceride.

in which dicaprylyl ether (low viscous, nonpolar) and caprylic/capric triglycer-

ides (low viscous, polar) were compared in pairs with a mineral oil as reference
(Fig. 17). It can clearly be seen that the low-viscous or polar oil components
were, overall, assessed as being the lighter, more quickly absorbed oils. This
sensory assessment was carried out as a pair comparison, whereby the sensory
parameters were defined in similar fashion to those for the emulsions described
above.
G. Sensory Assessment of Lipids in Surfactant-Based

Rinse-Off Products
Sensory assessment can also be applied to other cosmetic product categories.
Depending on the product category concerned, individual sensory parameters and
Figure 18 Sensory assessment (direct comparison) of formula 2–4 versus reference.

reference products must be developed. For surfactant-based body-cleansing prod-

ucts for example, foaming and post-use skin-feel are the chief parameters; in
the case of shampoos, other parameters are more important (e.g., volume, care,
combability, gloss, or stylability).
In the field of surfactant-based body-cleansing preparations, in the early
1980s more surfactants that are gentler to the skin and hair came on the market.
This concept, however, is no longer regarded as original. The topic of refatting
or moisturizing is interesting in this connection. This is due on the one hand to
changed consumer habits: today, people take showers and wash their hair as a
rule several times a week, which leads to repeated removal of skin lipids with the
result that the barrier function of the stratum corneum can be gradually weakened,
resulting in turn in increasing dryness of the skin. Second, demographic shift
means that the older section of the community is growing markedly. This con-
sumer group suffers particularly severely from dry, itchy, and taut skin. Particu-
larly important for them are not only gentle but, above all, refatting surfactant
preparations.
Sensory assessment has been employed to determine the efficacy of novel
refatting agents [18]. A compound of glycerol monooleate and APG and a wax
particle dispersion were tested. In both cases, a clear improvement in skin softness
and skin moisture was registered after treatment with refatting shower-baths (Fig.
Figure 19 Sensory assessment of hair.

Figure 20 Shampoo with a nonionic conditioner versus placebo.
18). Interesting in this connection are the marked differences in foaming charac-
teristics that were discovered in this sensory investigation.
The other big surfactant-based product category is shampoos, which may
contain functional ingredients designed, for example, to increase hair gloss or to
develop a conditioning effect. Typically, alongside various polymers, silicone
derivatives or other conditioning lipids are employed. The effects on the hair are
usually determined by half-side tests in hair studios; the sensory assessment is
carried out by hairdressers.
Another possibility consists in treating strands of hair and having a panel

of experts assess these strands along precisely defined parameters. In Figure 19,
the test procedures for the parameters hardness, smoothness, and softness of ends
are shown by way of example. The effects following application of a shampoo
containing a conditioning lipid are shown in Figure 20. Positive effects were
detected above all for combability, smoothness, and tactile feel.
IV. CORRELATION OF SENSORY ASSESSMENT

AND CONSUMER TESTS
What all the forms of practical implementation of sensory assessment described

above have in common is the fact that the panelists are more or less highly trained
experts. If sensory assessment is also to result in statements on the potential
market acceptance of a newly developed or modified product, therefore, there is
a definite need to know about any correlations between the results of sensory
assessment and consumer tests.
Below, the results of an investigation are presented in which three moistur-
izing creams of type O/W (creams A, B, C) were examined in a sensory assess-
ment (paired comparison test) and in a typical consumer test.
A. Sensory Assessment
The three products were compared in pairs in a paired comparison test (A versus
B, A versus C, and B versus C) along certain sensory parameters. The sensory
profiles resulting from this investigation showed that product A was markedly
different from the other products in respect to the majority of sensory parameters.
Samples B and C showed only minor differences in the sensory parameters inves-
tigated.
B. Consumer Test
The three products were subjected in parallel to consumer tests in Germany and
France, each using 60 participants. These consumer tests also showed up differ-
ences between product A and samples B and C. But it transpired that not all the
established differences (e.g., between samples A and C) were perceived. Table
3 lists the respective parameters for which differences were noted in the sensory
assessment and in the consumer test.
Overall, the comparison shows that the consumer tests, which cost much
more in terms of money and, in particular, time, came up with fewer differences
in the descriptive analysis of the three samples than the sensory assessment. It
is interesting that this survey was also able to register the influence of language/
Table 3 Product Comparison A versus C, Distinguishable Parameters
Sensory assessment German consumer panel French consumer panel

Appearance Appearance Appearance
Color Color
Pick-up Consistency Consistency
Peaking
Cushion
Consistency Consistency Consistency
Distribution Distribution
Absorption Absorption
Smoothness
Stickiness
Oiliness
Waxiness
Fragrance
Shine Skin gloss Skin gloss
cultural background on the product assessment, as revealed in the varying ability

of the consumers to register differences.
The advantage of the consumer tests is that they provide a direct statement
on whether consumers like the product or not. In the present case, the different
consumer panels agreed in the ranking of the three test products as far as con-
sumer acceptance was concerned: cream C ⬎ cream B ⬎⬎ cream A.
Only exact knowledge of the correlations between the results of expert
assessment and consumer acceptance of the product enables sensory assessment
to be used to make a forecast on product acceptance. The exact evaluation of
such parallel tests could therefore be used to dispense with consumer tests in
future.
V. RHEOLOGY AND SENSORY CHARACTERISTICS
In view of the relative expenditure of time and money, sensory assessment has
the advantage over the consumer test. However, it still involves considerable
expense in view of the relatively large number of people involved. For this reason,
attempts have been made to establish test systems that can come up with state-
ments on sensory characteristics of consumer goods without involving human
subjects at all. In this connection, it is above all the rheological characteristics
that have been subjected to more detailed investigation.
In the literature, there has been controversial debate on the question of

whether the sensory characteristics of lipid-containing topical emulsions correlate
with their rheological characteristics. Moscowitz, for example, describes the de-
pendence of the sensory attributes of skin-care fluids on their rheological charac-
teristics [19]; Brummer [20] finds a correlation of primary skin feeling with the
shear stress at the onset of flow τ F and the dynamic viscosity η dyn and secondary
skin feeling with the value of stationary viscosity η for the rate of shear prevailing
at the end of application to the skin.
S. Wang measured TEWL and skin capacitance using several emulsions
that contained the same oil but had different rheological properties and found no
effect from rheology on moisturizing efficacy [21]. This study, as well as another
[22], could detect no clear correlation with various sensory characteristics.
Basically, the rheological characteristics of lipid-containing emulsions in
W/O systems are determined by the phase/volume relationship between oil and
aqueous phase, whereas in O/W formulations the dominant influence on the flow
behavior comes from the co-emulsifiers and thickeners. Examples of this can be
found in Förster [23] (Figs. 21 and 22). This source also provides an example
of the correlation between particular sensory and rheological parameters. Thus,
it could be shown that the consistency determined by sensory assessment corre-
lates with viscosity at low shear rates, and the dispersability (or distribution) of
the product accords well with the viscosity at higher shear rates (Fig. 23).
Taking a general view, it seems to be the case that rheological measure-
ments may be suited for making forecasts of certain simple sensory parameters,
Figure 21 Viscosity curves of differently thickened emulsions.

Figure 22 Strain-sweep curves of differently thickened emulsions: upper set of curves

shows G′, lower set G″.
Figure 23 Estimation of sensory properties of creams.

depending on the formulation. In the case of certain complex parameters, such

as skin feel, absorption, or skin smoothness, rheological measurements are not
capable of delivering a reliable forecast.
VI. SUMMARY
In this chapter, we have discussed the basics and various test methods for the
sensory investigation of lipid-containing cosmetic preparations. The sensory as-
sessment of lipids in leave-on and rinse-off products such as emulsions and sur-
factant-based formulations for skin and hair care has been presented with numer-
ous examples. In addition, we have pointed out correspondences between the
physicochemical and galenic characteristics of cosmetics on the one hand, and
the subjectively perceptible characteristics profile on the other.
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Index
Acylglutamate, 301 [Ceramide]

Alkyl chain nature-identical, 15
all-trans conformation of, 81, 85 precursor, 14
conformation, 107 synthesis of, 103, 111
trans fraction of, 81, 90 synthetic, 13, 42
Alkyl ether sulfate, 300, 309 type-1, 3, 7, 12, 15, 279, 280
Alkyl glucoside, 303, 309, 311 type-2, 7, 12, 77, 281
Alkyl sulfate, 300 type-3, 3, 7, 17, 18, 29, 30, 42
Amino acid content, 106 type-4, 3, 7, 138, 281
Area per lipid, 81, 86 type-5, 3, 7, 12, 138, 140, 279, 281
Arm flex wash test, 310, 311 type-6, 3, 7, 138, 140
Ascorbate (see Ascorbic acid) type-7, 138, 140
Ascorbic acid Cleansing (see Washing)
cofactor in lipogenesis, 138 milk, 248
and lipid profile, 140 Cholesterogenesis, 102
Cholesterol, 5, 12, 42, 43, 45, 51, 52,
Barrier (see Skin barrier) 79, 84, 85, 92, 102, 109, 138,
Betaine, 302, 310 173, 283, 286
Blister technique, 156, 157 addition of, 240, 288
Body wash product (see Surfactant) and ceramide and fatty acid (see Skin
barrier lipid)
Ceramide, 1, 6, 8, 14, 42, 79, 92, 228, effect on area per lipid, 86
270, 271, 280, 307 synthesis of, 111
analogue, 15, 16, 17 Cholesterol sulfate, 101, 104, 166, 172,
and cholesterol and fatty acid (see 228, 246
Skin barrier lipid) Chromameter, 215
composition and aging, 110 Collagen
glycosyl, 5, 8, 14, 28, 101, 104, 137, 281 type I, 133
in skin models, 137, 138 type III, 133
syntase, 103 type V, 133
353
354 Index
[Collagen] Elastin, 128

type VII, 133 Emollient, 188, 202, 214, 307, 341, 342
type XII, 128 absorbability, 342
type XIV, 128 spreadability, 343
Confocal laser scanning microscopy Emulsifier, 214, 257, 258, 303, 327,
(CLSM), 56, 58, 215, 275 333, 334, 336, 341
Consumer test, 325, 347, 348 Emulsion (see Cream)
Corneometer, 188 Epidermal
and capacitance, 189 barrier, 3
and conductance, 189 cell division, 14
and phase angle, 189 lipids, 210
Corneosurfametry, 209
Cornified envelope, 37, 107, 112, 113 Fat (see Triacylglyceride)
Cream, 228, 275, 286 Fatty acid/ester ratio, 237, 246
absorption, 330 Fibrillin-1, 133
cold, 256 Fibronectin, 133
consistency, 330, 335, 338, 339 Filaggrin, 133
cushion, 330, 336 Foam, 299, 301, 302, 311, 345
lamellar, 249, 250 Fourier transform infrared spectroscopy
multiple, 339 (FTIR) (see Infrared spectros-
oiliness, 330, 333 copy)
oil-in-water, 273, 285, 333, 347 Frictionmeter, 216
peaking, 330, 335, 336 Free fatty acid, 8, 43, 45, 102, 160,
pick-up, 330 167, 171, 172
and restoration of lipid film, 305 addition of, 288
spreadability, 273, 274, 338 in aged skin, 279
stickiness, 330, 333, 336, 339, 340 area per lipid, 86
water-in-oil, 248, 249, 273, 285, 334, and ceramide and cholesterol (see
337 Skin barrier lipid)
waxiness, 330, 335, 338, 339 removal of, 246, 303
Culture in skin models, 138, 140
fibroblast, 122 synthesis of, 103, 111
keratinocyte, 122 Freeze fracture electron microscopy
Cutometer, 204 (FFEM), 38, 47, 56
Defatting, 303 Gas-bearing electrodynamometer, 204

Dermal-epidermal junction, 128, 130 Gas chromatography, 165
Desmosome, 207 Gas-liquid chromatography, 171
Desquamation, 206 and extracting solvent, 171
degree of, 207 Greasiness, 237
process, 139, 160
rate of, 207 Hydrolipidic film, 210
Differentiation
marker, 133, 160 Infrared spectroscopy, 38, 43, 58, 76,
and proliferation, 136 77, 85, 107, 137, 138, 189, 228,
DSC (see Thermal analysis) 229, 232, 282
Index 355
[Infrared spectroscopy] [Lipid]

and assignment of bands, 235 packing order, 244, 249, 282
and ATR technique, 230 profile, 163, 164, 173
Interlayer distance, 10, 39, 45 Liposome, 43, 48, 49, 55
gel-state, 49, 51
Keratin, 10, 14, 130, 133 liquid-state, 49, 51
Keratinocytes of skin lipids, 51
differentiation of, 128
and retinoids, 130 Magnetic resonance imaging, 215
joined by desmosomes, 129 Model
collagen gel, 127
Lamellar body, 5, 99, 100, 101, 104, addition of adipocytes to, 128
136, 137, 138 support of hair follicles by, 128
Lamellar granules, 129 dermal analogue (see Dermal sub-
Laminin, 133 strate)
Lanolin, 256, 265, 287 dermal equivalent, 121
Laser-Doppler-flowmeter, 282, 283 dermal substrate
Lecithin, 257 based on collagen, 126
Lipid, 327 based on collagen-glycosaminogly-
alkyl chain order, 47, 238, 246 can-chitosan, 127, 128, 133
barrier composition noncollagenous, 127
and age, 150 epidermis, 121–124, 140, 159, 242
and anatomical site, 150 horny layer lipid, 9, 76
and dietary influences, 151 membrane system, 42
and exposure to UV, 152, 154 skin barrier, 77
and hormonal effects, 151 skin equivalent, 121–124, 242
and location in the epidermis, 163 inclusion of endothelial cells in,
and race, 151 124
and seasonal variations, 152 inclusion of Langerhans cells in,
and sex, 150 124
and winter xerosis, 150, 152 inclusion of melanocytes in, 124
bilayer, 4, 10, 12, 76, 78, 80, 99, and lipids, 159
106, 228 stratum corneum (SC) lipid (see
protective function of, 100 horny layer lipid)
lamellae, 38 Moisturizer, 258, 307, 333
arrangement of, 84 Molecular modeling, 75
swelling of, 47
water content of, 47 Natural moisturizing factor (NMF), 188
lamellar structure of, 4, 12, 13, 37, 43 Nuclear magnetic resonance spectros-
lateral packing of, 41 copy (NMR), 76, 92, 189, 228
layer (see Bilayer)
metabolism Occlusivity, 276, 277, 278, 280, 287,
and calcium, 112 288, 289
and enzymes, 111 Oil
and magnesium, 112 ester, 266, 278
and potassium, 112 Jojoba, 266
356 Index
Optical coherence tomography, 215 Sebum, 5, 99, 100, 102, 107, 108–110,
Order parameter, 87, 88, 92 210,
excretion rate of, 211, 247
Packing parameter, 76 effect of age on, 211
Paraffin, 256, 262, 264 effect of sex on, 211
Patch test, 308 effect of body site on, 211
Periodicity (see Interlayer distance) wash off by surfactants, 303
Penetration, 281 Sebumeter, 212
enhancer, 52, 55, 241, 281, 282, 283, Sebutape, 211
284 Second messenger, 14
of lipids, 54, 275, 276, 288 Sensory assessment, 273, 275, 319, 335, 345
of surfactants, 304 comparative, 326
of water, 275 correlation with consumer test, 347
Percutaneous absorption (see Penetra- correlation with rheology, 348
tion) guidelines for, 324
Permeation study, 49, 137 and language, 320
Petrolatum, 256, 278, 286, 287, 305 and psychological factors, 320
Phase test set-up for, 322
behavior, 45 Sensory characteristic (see Sensory as-
of stratum corneum lipids, 238 sessment)
diagram, 10 Sensory profile
gel, 84, 240 of cleansing products, 345
lamellar, 39, 41, 45 of creams, 332, 334, 340
separation, 42, 43, 59 of emollients, 341, 343
Phosphatidylcholine, 84 Shower gel (see Surfactant)
bilayer, 79 Silicone, 268, 275, 278, 307, 338, 346
Phospholipid, 6, 8, 101, 174 Skin
membrane, 47 absorption, 273, 274, 351
saturated, 50 atopic, 279, 285
unsaturated, 50 color, 215
vesicle, 51 compatibility, 188
Phytosterol, 286 of cleansing agent, 188, 189, 306,
Polymer, 262, 307, 336, 340, 346 309, 310, 311
Profilometer, 198 dry, 105, 106, 110, 152, 154, 187,
Pseudoceramide, 15, 17, 18, 19, 20–24, 194, 207, 243, 244, 248, 279,
29, 30, 270, 271 280, 285, 313, 315, 345
Psoriasis, 279 and aging, 109
elasticity, 202
Raman spectroscopy, 84, 228, 231, 232 extensibility, 202
and assignment of bands, 235 and aging, 205
Refatting, 305, 312, 345 feel, 273, 351
Rheological modifier (see Thickener) flexibility, 202
Rheology, 272, 349 greasy, 244
hydration (see Moisture)
Scanning electron microscopy (SEM), irritation, 283, 303, 305
199 of cleansing products, 209, 310
Index 357
[Skin] [Skin barrier]

moisture, 14, 106, 193, 237, 243, and sex, 150
246, 249, 250, 339 after topical application, 108
moisturization, 187, 202, 284, 286, repair, 13, 107, 111, 112
288, 289, 307, 345 strengthening of, 191, 194, 248, 249
and humectants, 188, 191 Soap, 299, 300
and occlusive products, 193 Solvent mixture, 160
pH, 216 Sphingolipids, 160, 228
redness, 195, 311 signaling role of, 14
replica, 197 sphinganine, 1
rheometer, 205 sphingosine, 1, 15, 16
roughness, 14, 152, 197, 200, 280, sphingomyeline, 101
284, 289, 313 Squalene, 5, 12, 102, 107, 108, 166,
scaly, 106, 110, 152, 207, 208 210
surfactant induced, 107, 305, 306, Squamometry, 209
311 Stratum corneum
smoothness, 286, 330, 336, 351 barrier (see Skin barrier)
softness, 203, 286 lipid (see Skin barrier lipid)
surface lipids, 210 thickness, 97, 129, 215
swelling, 311 turnover, 207
temperature, 216 Sulfosuccinate ester, 301
texture Surface area (see Area per lipid)
and age, 197 Surface tension, 273, 274, 275
and weather, 197 Surfactant, 188, 228, 247, 299, 307,
and topical application, 197 312, 315, 345
thickness, 201, 215, 280 amphoteric, 302
type, 212, 244, 248 damaging effect of, 195, 196, 277,
xerosis, 15, 110, 194 285, 309, 311
Skin barrier
damage, 13, 99, 194, 195, 303 Tackiness, 275
prevention of, 196 Tape stripping, 155, 156
disruption, 109 by adhesive tape, 155
formation and barrier disruption, 107, 156
and nuclear hormone receptor, 113 by cyanoacrylate resin, 156, 162
function, 14, 37, 97, 102, 105, 137, and lipid gradient, 163
193 and scaling, 110, 208
and histamine receptor, 113 Thermal analysis, 77, 85, 228, 239, 282,
homeostasis, 98, 99, 114 283
lipid (SBL), 7, 9, 17, 25, 38, 77, 89, Thickener, 257, 327, 333, 334, 340
101, 136, 166, 193, 278, 279, Thin-layer chromatography, 137, 138,
285 165
recovery, 286 and ceramide profiles, 165
and circadian rhythm, 98 and eluting solvent, 167
by creams, 196 and pure lipid standards, 166
after psychological stress, 98 and total lipid determination, 165
by replacement of lipids, 284, 285 Tocopherol, 108, 138, 268
358 Index
Topical application Two-photon excitation microscopy, 59,

of mevalonic acid, 111 61
of petrolatum, 108
of retinoic acid, 113
Ultrasound measurement, 214
of stratum corneum lipids, 108
Topometry, in vivo, 199, 313
Torquemeter, 204 Vaseline, 262
Transepidermal water loss (TEWL), 13, Vesicle, 59
107, 249, 280, 281, 283, 285, nonionic surfactant, 50
305, 349 Viscosity, 273, 274, 275, 303, 311, 334,
in dry environment, 97 338, 339, 349
in the elderly, 110 Vitamin C (see Ascorbic acid)
and film formation, 277 Vitamin E (see Tocopherol)
and healthy skin, 19
and impairment of skin barrier, 304
Washing, 189, 246, 247, 299, 304, 307,
inhibiting of, 265
311
normalization of, 196
dehydrating effect of, 189
and occlusivity, 278, 287
Water-binding capacity, 13
and skin irritation, 311
Water domains, 48
in skin models, 137
Wax, 256, 259, 264, 270, 278, 286,
Transfersome, 52, 54, 55, 58
310, 342
Transglutaminase, 133
Wrinkles, 197, 200
Transmission electron microscopy
(TEM), 59, 76, 133, 137
Triacylglyceride (see Triglyceride) X-linked ichthyosis, 109, 279
Triacylglycerol (see Triglyceride) X-ray scattering, 38, 43, 47, 280
Triglyceride, 6, 7, 110, 167, 173, 210, 342 small-angle (SAXS), 10, 39, 44, 76,
addition of, 288 137, 138, 139, 228
in creams, 256, 267 wide-angle (WAXS), 39, 41, 44, 76,
in skin models, 137, 138, 140 105

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ISBN: 0-8247-0664-1

This book is printed on acid-free paper.

Eastern Hemisphere Distribution

World Wide Web

Copyright  2002 by Marcel Dekker, Inc. All Rights Reserved.

Current printing (last digit):

PRINTED IN THE UNITED STATES OF AMERICA

cations, and pragmatic presentations. Contributors are encouraged to present their

Series Introduction Eric Jungermann iii

PART I. CHEMISTRY AND STRUCTURE OF SKIN LIPIDS

1. The Chemistry of Natural and Synthetic Skin Barrier Lipids 1

2. Structure of Stratum Corneum Lipid Layers and Interactions

3. Computer Modeling of Skin Barrier Lipid Layers by Molecular

PART II. BIOLOGICAL FUNCTION OF SKIN LIPIDS

4. Role of Lipids in Skin Barrier Function 97

5. Investigating Human Skin Barrier Lipids with In Vitro Skin

PART III. ANALYSIS OF SKIN LIPIDS AND THEIR EFFECTS

6. Analytical Techniques for Skin Lipids 149

7. Biophysical Methods for Stratum Corneum Characterization 185

8. Detection of Cosmetic Changes in Skin Surface Lipids by

PART IV. LIPIDS IN COSMETIC PRODUCTS

9. Lipidic Ingredients in Skin Care Formulations 255

10. Benefits of Lipidic Refatters in Surfactant Products 299

11. Sensory Assessment of Lipids in Leave-On and Rinse-Off

Peter Busch, Ph.D. Department of Biophysics and Sensorics/Product Perfor-

Odile Damour, Ph.D. Director of Laboratoire des Substituts Cutanés, Hôpital

Kristien De Paepe, Ph.D. Department of Toxicology, Vrije Universiteit Brus-

Mitsuhiro Denda, Ph.D. Skin Biology Research Laboratory, Shiseido Life

Thomas Förster, Ph.D. Department of Cosmetics, Henkel KgaA, Düsseldorf,

Thomas Gassenmeier, M.D. Department of Skin Biochemistry, Henkel KgaA,

Monika Höltje, Ph.D. Department of Pharmaceutical Chemistry, Institute of

Ulrich Issberner, M.D. Department of Care Chemicals, Cognis Deutschland

Hans Lambers, Ph.D. Department of Innovation Cosmetics, Sara Lee House-

Ghita Lanzendörfer, Ph.D. Advanced Development, Decorative Cosmetics

Hinrich Möller, Ph.D. Department of Cosmetics, Henkel KgaA, Düsseldorf,

Thomas Prasch, Ph.D. Department of Analytics of Chemical Products, Henkel

Hans Pronk, M.Sc. Department of Biophysical Evaluation, Sara Lee House-

Vera Rogiers, Ph.D. Department of Toxicology, Vrije Universiteit Brussel,

Kordula Schlotmann, M.D. Department of Skin Biochemistry, Henkel KgaA,

II. CHEMICAL STRUCTURE

Figure 1 Sphinganine derivatives.

Figure 2 Ceramide structures.

III. LOCALIZATION AND CREATION

Figure 3 Multiple intercellular lamellae of pig stratum corneum [5].

Figure 4 Barrier model of intercellular horny layer lipids.

IV. COMPOSITION OF THE EPIDERMAL LIPIDS

Table 1 Composition of Lipids from Human

Triacylglycerols are the main component of the sebaceous lipids—about

Table 2 Composition of Human Stratum Corneum Lipids [9,10]

Table 3 Composition of Ceramides Found in

Figure 7 Change in lipid composition during epidermal cell differentiation [13].

Table 4 Model for Stratum Corneum Lipid [14]

Free fatty acids 17

Figure 9 Scheme of x-ray reflection off lipid bilayers.

VI. EFFECTS OF CERAMIDES

The different effects of the ceramides are shown in Table 5.

Table 5 Activity of Ceramides

Modulation of lamellar gel crystal of the horny layer lipids

mide 2 possess a pronounced role in building lamellar structures as well as the