Spectrophotometry 0

SPECTROPHOTOMETRY
SPECTROPHOTOMETRY
It is that technique that measures the amount of light
absorbed or transmitted by a substance.
It is one of the most important technique in analytical
biochemistry.
Unknown compounds can be identified by their characteristic
absorption spectra in the ultraviolet, visible or infrared
regions.
Concentrations of known compounds in solutions can be
determined by measuring the light absorption at one or more
wavelengths.
SPECTROPHOTOMETRY
CONT’D
Spectrophotometry is used for both and quantitative and
qualitative analysis .
Enzyme catalyzed reactions can be followed by measuring

the absorption of the substrate or product .
SPECTROPHOTOMETRY
CONT’D
Regions X-Ray Ultraviolet Visible Infrared microwave
Wave 0.1 -100 nm 100 - 400 nm 400 - 800 nm 800 nm - 100 µm 100 µm - 30 cm
length
The ultra violet and the visible regions are the ones that we
usually use in the spectrophotometry.
1 nm = 10-9 m
1 A° = 10-10 m
1 µm = 10-6 m
λ is the symbol of wavelength.
SPECTROPHOTOMETRY
CONT’D
Wave number is the reciprocal of the wavelength
1
wave number = cm-1
wavelength
THE ESSENTIAL
COMPONENTS OF
SPECTROPHOTOMETER
1- Light source:
• It can be two kinds:
• Tungsten lamp ; produces light at visible region.
• Hydrogen lamp; produces light at ultraviolet region.
2- Collimator:
• It is a focusing device that transmits an intense straight beam
of light.
3- Monochromator:
• It is a device that divides the light beam into it’s component
wavelengths.
THE ESSENTIAL COMPONENTS
OF SPECTROPHOTOMETER
CONT’D
4- Selector:
• It selects the required wavelength.
5- Cuvette:
• It is a compartment in which the sample is placed.
• Two kinds:
• Glass cuvettes; used in the visible region.
• Quartz cuvettes; used in the ultraviolet region.
• The glass cuvettes absorbs light in the ultraviolet region ..
Thus the amount of light measured by spectrophotometer will
be the absorbance of sample + the glass cuvette.
CONT’D
6- Photocell (photodetector):
• It detects the amount of light transmitted.
7- Electrical meter:
• It records the output of the detector.
CONT’D
Collimator
Cuvette
Light’s sample
band λ1 container
λ2
λ3
λ4
Light Monochromator Potometer

source Photocell
Prism Slit
Wavelength
selector
CONT’D
CONT’D
The fraction of the incident light I0 that is absorbed by a
solution depends on three factors:
• 1- The thickness of the sample or path length.

• 2- The concentration of the absorbing sample.
• 3- The chemical nature of the compound.
The relationship between the concentration, path length, and

the amount of light absorbed or transmitted can be exposed
mathematically in two laws: the Beer law and Lambert law.
BEER LAW
It states that the intensity of the light transmitted by an
absorbing media decreases with increasing concentration of
the absorbing compound.
Log I0 / I α a c
I0 = intensity of the incident light

I = intensity of the transmitted light
a = a constant for every compound at a specific wavelength
c = concentration of absorbing compound
BEER LAW CONT’D
The amount of light absorbed = I0 – I
Log I0 / I represents the fraction of light absorbed
LAMBERT’S LAW
It states that the intensity of the light transmitted by an
absorbing media decreases as the thickness or path length
of the absorbing media increases.
Log I0 / I α a L
L = is the path length
The two law’s can be combined in one law which is Lambert-

Beer Law
LAMBERT-BEER LAW
Log I0 / I = a c L
a = is the extinction coefficient which is a constant for each

substance but it differs at different wavelength and it is constant
at a specific wavelength
• Molar absorption coefficient (am); in M
• Specific absorption coefficient (as); in g/l
• am340 = is the molar absorption coefficient of a substance at a
wavelength = 340 nm
• am = as Mwt
am is most commonly used in biochemistry, and the path length

L is almost always 1 cm, thus the units for am is M-1 cm-1.
The absorption coefficient varies in different substances, it also

varies with varying wave-lengths also.
LAMBERT-BEER LAW
Log I0 / I = A
• A = absorbance or optical density O.D.
Ø A = a c l
BLANK SOLUTION
Is a solution that is necessary in all spectrophotometry studies.
It should contain all components of the assay or test solution

except the component who’s absorbance is being measured.
Purpose of the Blank:

The blank will cancel out the absorbance of the substances in
the background so that the absorbance of the tests will be that
of the compound under study only.
Ø Note: Glass cuvettes are not to be used in the U.V region,
since the glass itself will absorb light thus leading to a false
high result.
Ø In the U.V region Quartz cuvettes are to be used!
PROTEIN
DETERMINATIONS
Proteins in solutions can be determined spectrophotometrically by two
methods:
a) Colorimetrical method:
Biuret method: it is based on the reaction of Cu2+ with peptides in an
alkaline solution producing a purple complex that has an absorption
maximum at 540 nm.
alkaline media
Proteins + Biuret reagent purple complex (max absorbance at 540nm)
b) Direct spectrophotomety:
The absorbance at 280nm can be used to determine protein
concentration in solutions.
(Because proteins have a distinct absorbance maximum at 280nm due
to their aromatic amino acids).
SOLUTIONS CONTAINING
ONE ABSORBING
SUBSTANCE
Example:
A solution containing 2 g/l of a light absorbing substance
in a 1 cm cuvette transmits 75% of the incident light at
260 nm. Calculate the transmission of a solution
containing
a) 4 g/l.
b) 6 g/l.
c) If the Mwt is 250, calculate am.
d) What type of cuvette should you use here? Why?
ONE ABSORBING
SUBSTANCE
A = Log I0 / I
A = log 1.0 /0.75 = 0.124
A = as c l
as = A / c l = 0.124 / 2 × 1
as = 0.0625
a) log I° / I = as c l
Log 1.0 – log I = 0.06 x c x l
0 – log I = 0.0625 x c x l
- log I = 0.0625 x 4 x 1 = - 0.25
I = antilog - 0.25 = 0.562 è 56.2%
ONE ABSORBING
SUBSTANCE
b) Log I0 / l = as c l
Log 1.0 - log I = 0.0625 x 6 x1.
- log I = 0.375
Log I = - 0.375
I = antilog - 0.375 = 0.422 è 42.2%
C) am = as x Mwt = 0.0625 x 250 = 15.63

D) Quartz cuvettes should be used at the U.V range.
ONE ABSORBING
SUBSTANCE
A solution containing 10-5 M ATP, has a
transmission 0.702 (70.2%) at 260 nm in a 1 cm
cuvette. Calculate:
a) The transmission of the solution in a 3 cm
cuvette.
b) The absorbance of the solution in a 1 cm and 3
cm cuvette.
c) The absorbance if the concentration increased
to 5x 10-5 M of ATP, in a 1 cm cuvette.
ONE ABSORBING
SUBSTANCE
a) A = Log I° / I = am c l b) A in a 1 cm cuvette.
A = log 1.0 / 0.702 = 0.152 A = 15200 x 10-5 x 1 = 0.15
0.152 = am x 10-5 x 1 A in a 3 cm cuvette.
am = 0.152 / 10-5 = A = 15200 x 10-5 x 3 =
15200 M-1 cm-1 0.456
A = 15200 x 10-5 x 3 =
0.456
c) A = 15200 x (5 x 10-5) x
Ø A = Log I° / I 1 = 0.76
Ø 0.456 = log 1.0 / I
0.456 = log1 – log I = 0 –
log I = - log I
Thus I = antilog - 0.456 =
0.349 è 34.9%
ONE ABSORBING
SUBSTANCE
A protein solution (0.3 ml) was diluted with 0.9 ml of
water. To 0.5 ml of this diluted solution, 4.5 ml of
biuret reagent was added and the color was allowed
to develop.
The absorbance of the mixture at 540 nm was 0.18 in a
1 cm diameter tube. A standard solution (0.5 ml
containing 4 mg of protein/ml) plus 4.5 ml of biuret
reagent gave an absorbance of 0.12 in the same size
test tube.
a) Calculate the protein concentration in the undiluted
unknown solution.
b) What is the composition of the blank here ?
ONE ABSORBING
SUBSTANCE
A) Concentration of standard Cst = 4 mg/ml
Thus Cst = 4 g/L
Astandard = as x C x l
0.12 = as x 4 x 1
So as = 0.12 / 4 = 0.03
Atest = as x C x l
0.18 = 0.03 x C x1
So Ctest = 0.18 / 0.03 = 6 g/L = 6 mg/ml
The concentration of protein in the undiluted solution:
Cundiluted = 6 x (1.2/0.3) = 24 mg/ml .
é Dilution factor
b) The blank should contain 4.5 ml of biuret and 0.5 ml of distilled
water only.
TWO ABSORBING
SUBSTANCE
A solution containing NAD+ and NADH had an absorbance of 0.311 in a 1 cm
cuvette at 340 nm, and 1.2 at 260 nm. Calculate the concentration of the
oxidized and reduced forms of the coenzyme in the solution. Both NAD+ and
NADH absorb at 260nm, but only NADH absorbs at 340nm.
am
Compound 260nm 340nm
NAD+ 18000 0.0
NADH 15000 6220
Absorbance at 340nm represents the absorbance of NADH only since NAD+

does not absorb at that wavelength. So the concentration of NADH can be
obtained.
A340nm = ANADH = am x C x l
0.311 = 6220 x C x 1
So CNADH = 0.311/6220 = 5 x 10-5 M
A260nm = ANADH + ANAD+ ( since both absorb at this wavelength )
TWO ABSORBING
SUBSTANCE
ANADH = am x C x l = 15000 x 5 x 10-5 x 1 = 0.75

Thus ANAD+ = A total - ANADH = 1.2 – 0.75 = 0.45
Since ANAD+ = am x CNAD+ x l
0.45 = 18000 x CNAD+ x 1
CNAD+ = 0.45 / 18000 = 2.5 x 10-5 M

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SPECTROPHOTOMETRY

Enzyme catalyzed reactions can be followed by measuring

Light Monochromator Potometer

• 1- The thickness of the sample or path length.

The relationship between the concentration, path length, and

I0 = intensity of the incident light

L = is the path length

The two law’s can be combined in one law which is Lambert-

a = is the extinction coefficient which is a constant for each

am is most commonly used in biochemistry, and the path length

The absorption coefficient varies in different substances, it also

It should contain all components of the assay or test solution

Purpose of the Blank:

C) am = as x Mwt = 0.0625 x 250 = 15.63

Absorbance at 340nm represents the absorbance of NADH only since NAD+

ANADH = am x C x l = 15000 x 5 x 10-5 x 1 = 0.75

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