Analytical Application Using Modern Electrochemical Techniques
Analytical Application Using Modern Electrochemical Techniques
Analytical Application Using Modern Electrochemical Techniques
ELECTROCHEMICAL
SCIENCE
www.electrochemsci.org
Review
1. INTRODUCTION
Electrochemical techniques are powerful and versatile analytical techniques that offer high
sensitivity, accuracy, and precision as well as large linear dynamic range, with relatively low-cost
instrumentation. After developing more sensitive pulse methods, the electroanalytical studies are more
regularly used on industrial , environmental applications and on the drug analysis in their dosage
forms and especially in biological samples. However, electroanalytical techniques can easily solve
many problems of pharmaceutical interest with a high degree of accuracy, precision, sensitivity, and
selectivity employing this approach. Some of the most useful electroanalytical techniques are based on
the concept of continuously changing the applied potentials to the electrode-solution interface and the
resulting measured current (Kissinger and Heineman 1996; J. Wang 2006; Smyth and Vos 1992;
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Ozkan, Uslu, and Aboul-Enein 2003; Bard and Faulkner 2001; Kellner et al. 2004; Hart 1990 ; Bengi
Uslu and Sibel A. Ozkan 2010,). Most of the chemical compounds were found to be as
electrochemically active [261], During the past years, there has been extraordinary acceleration of
progress in the discovery, synthesis, sensitive electrochemical analysis [262-269].
The aim of the present review is to give the basic information about electroanalytical analysis
methods, working electrodes, techniques, and their industrial, pharmaceutical, and environmental
applications. An attempt was made to choose some readily available publications describing some
advances in methodology and applications.
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started to appear in 1947-1960, fast linear sweep voltammetry was the first [11-13] followed by the
development of square wave and pulse Polarography by Barker et al [14-16].
An Hg
deposition
HgA ne
(3)
The sensitivity of CSV depends on the amount of that can be plated in a given period, the
density of the formed insoluble salt film and the dissociation rate of the insoluble mercury compound
during the stripping step [21].
stripping
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The measured parameters in cyclic voltammetry are anodic and cathodic peak potential (Epa
and Epc), anodic and cathodic peak current (Ipa and Ipc) and the half peak potentials (Ep/2) at which the
cathodic and anodic currents reach half of their peak value.
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electrode surface with the solution of the selected polymer and allowing the solvent to evaporate. Also,
electroploymerization may be used to make the polymer film on the electrode surface.
As a new type of CMEs, pre concentrated CMEs were described [39-42]. Such modified
electrodes have surface characterized by ability for reacting and binding the target analyte. Pre
concentrating agent used in such modifications is usually incorporated in the electrode matrix (as done
with carbon paste electrode [43, 44]) or may be binding with functionalized polymeric film on the
electrode surface [23].
1.7. Potentiometry
Potentiometry is a classical analytical technique provides us information about the composition
of the sample through the potential appearing between tow electrodes [23]. Recently, this method was
developed by suggestion of use ion selective electrode (ISE). This electrode characterized by its
selectivity and sensitivity. The equipment used in potentiometric measurement consists of ion selective
electrode (ISE), reference electrode and potential measuring device.
The main idea of ion selective electrode is use membrane-based devices. The composition of
such membrane will bind the analyte ions with high sensitivity and selectivity leaving the co-ions
behind [23]. Such electrodes show fast response, wide linear range, not affected by color or turbidity,
not destructive and very inexpensive.
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The electrochemical behavior of sulpiride at a HMDE was investigated. Linear sweep cathodic
stripping voltammetry was used to determine sulpiride in the presence of acetate buffer of pH 10.5
[57]. The linear concentration range is from 0.68 to 17.1 ng mL-1 sulpiride. Furthermore, a theoretical
detection limit of 0.068 ng mL-1 sulpiride was calculated.
Differential pulse stripping voltammetric method was developed for the determination of
paracetamol and phenobarbital in pharmaceuticals assisted by chemometrics [58]. Both of these
analytes gave well-defined oxidation peaks in the BrittonRobinson buffer (pH 5.72) at a glassy
carbon electrode. A linear relationship between current and concentration of paracetamol [ranges:
0.09-0.93 mg L-1 (r2 = 0.999) and 0.9-11.7 mg L-1 (r2 = 0.999)], and phenobarbital [1.0-22.0 mg L-1
(r2 = 0.999)]. The proposed method was applied for the determination of paracetamol and
phenobarbital in several commercial tablets with satisfactory results.
Direct electrochemical method based on the electrochemical oxidation of paracetamol was
described for the determination of paracetamol in plasma [59]. A nanogold modified indium tin oxide
(ITO) electrode was used for the determination of paracetamol at pH 7.2 [60]. Linear calibration curve
is obtained over the range 2x10-7-1.5x10-3 M with a correlation coefficient of 0.997. The detection
limit (3) was estimated to be 1.8x10-7 M. The practical analytical utility of the method is illustrated
by determination of paracetamol in pharmaceutical preparations.
Square-wave adsorptive cathodic stripping voltammetric procedure was described for the trace
determination of chlordiazepoxide in bulk form, pharmaceutical formulation and human serum at a
mercury electrode [61]. This procedure show lower limits of detection (LOD) (4.4x1010 M and
6.6x1010 M) and limits of quantitation (LOQ) (1.5x109 M and 2.2x109 M), respectively in
pharmaceutical formulation and spiked human serum.
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Voltammetric study of the interaction of lomefloxacin (LMF)-Mg(II) complex with DNA and
its analytical application at a mercury electrode is reported [69]. In NH3-NH4Cl buffer (pH~9.1), the
adsorption phenomena of the LMF-Mg(II) complex were observed by linear sweep voltammetry. In
the presence of calf thymus DNA (ctDNA), the peak current of LMF-Mg(II) complex decreased
considerably, and a new well-defined adsorptive reduction peak appeared at -1.63 V. The new peak
currents of LMF-Mg(II)-DNA system increased linearly correlated to the concentration of DNA in the
4x107-2.6x106 g mL1 range when the concentrations of LMF-Mg(II) complex was fixed at 5x106
mol L1, with the detection limits of 2.3x107 g mL1.
The adsorptive and electrochemical behavior of norfloxacin on a glassy carbon electrode was
investigated by cyclic and square-wave voltammetry [70]. In acetate buffer of pH 5.0, norfloxacin gave
a sensitive adsorptive oxidative peak at 0.9 V. Applicability to measurement of norfloxacin at
submicromolar levels in urine samples was illustrated. The peak current was linear with the
norfloxacin concentration in the range 5-50 g mL1 urine. The detection limit was 1.1g mL1 urine.
Square-wave adsorptive anodic stripping voltammetric procedure was described to assay of
both the rifampicin (RIF) and isoniazid (INH) drugs separately or combined in pharmaceutical
formulations and human serum has been investigated at a carbon paste electrode [71]. The proposed
procedure was also successfully applied to simultaneous assay of rifampicin and isoniazid drugs
combined in pharmaceutical formulations. Moreover, the proposed procedure was successfully applied
to simultaneous assay of both drugs in human serum samples with limits of detection and quantitation
of 5x108 and 1.7x107 M for RIF and 6.1x108 and 2x107 M for INH.
A systematic study of the adsorption and association of the cancerostatic drug actinomycin-C1
(ACT) at a hanging mercury drop electrode has been conducted using phase-sensitive a.c. voltammetry
and cyclic voltammetry [72]. Also, Adsorptive accumulation in stripping voltammetry has been
applied for trace measurements of the ACT [73]. Accumulation is achieved by controlled adsorption of
ACT film on the hanging mercury drop electrode (HMDE). The limit of detection after 5 minutes
preconcentration is 8x10-10 M.
Cephalosporins (such as rocephin and cefobid), were determined by several voltammetric
techniques [74-82]. Sulfadiazine was determined in artificial gastric and intestinal juices using
differential pulse voltammetry [83]. Indirect differential pulse voltammetry was used for the
determination of sulfonamide [84]. This procedure depend diazotization and coupling occurs between
1-naphthol and sulfonamide in alkaline medium.
Different antibacterial drugs were determined in dosage forms, plasma and urine by several
voltammetric and polarographic methods using hanging mercury drop electrode (HMDE) and
membrane selective electrode (MSE) [85-91].
Voltammetric behavior of chloroquine was investigated using cyclic voltammetry and
differential pulse voltammetry [92]. DNA-modified carbon paste electrode was used in this study.
Voltammogram obtained show linearity range of 1x10-7-1x10-5 mol L-1with detection limit 3x10-8 mol
L-1.
Dc-polarography, cyclic voltammetry, controlled-potential coulometry and square-wave
adsorptive stripping voltammetry techniques were used to study the electrochemical behavior of
cefazolin sodium (CFZ) in Britton-Robinson buffer (pH 2-11) at the mercury electrode [93]. Square-
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wave adsorptive cathodic stripping voltammetric procedure was described for the trace determination
of CFZ in bulk form up to limits of detection and quantitation of 2.6x1010 M and 8.6x1010 M,
respectively. The method was successfully applied for determination of CFZ in pharmaceutical
preparation.
Different types of electrodes namely: dropping mercury electrode (DME), static mercury drop
electrode (SMDE), glassy carbon electrode (GCE), carbon paste electrode (CPE), and modified carbon
paste electrode (MCPE) were used to investigate the electrochemical behavior of the monobactam
antibiotic aztreonam at different electrodes and in biological fluids [94]. Differential pulse stripping
voltammetry (DPSV) and Osteryoung square-wave stripping voltammetry (OSWSV) were utilized for
the drug determination in either aqueous medium or in urine samples. Detection limits of 2x108 M
and 8x108 M aztreonam were achieved in aqueous and urine samples, respectively.
2.1.3. Antineoplastic drugs:
Modified carbon paste electrode was used for electrochemical studying of interaction between
mitoxantrone and double-standard DNA (dsDNA) and single-standard DNA (ssDNA) [95]. This study
was carried out using DNA-modified carbon paste electrode in combination with cyclic voltammetry
and differential pulse voltammetry.
5-Fluorouracil was determined using cathodic stripping voltammetry in presence of trace
concentrations of Cu(II) [96]. Linearity range of 5x10-9-6x10-8 mol dm-3 of 5-fluorouracil with
detection limit 4.6x10-10 mol dm-3 was obtained. Another method for the determination of 5fluorouracil was suggested utilizing flow injection system with voltammetric detection [97].
Carboplatin was determined by differential pulse voltammetry using DNA-modified glassy
carbon electrode [98]. This method was applied for determination in serum. Also, it was applied to
pharmacokinetic studies on patients receiving carboplatin treatment.
The electrochemical oxidation and reduction behavior of adsorbed species of tarabine PFS at an
in situ-mercury film electrode is studied using cyclic voltammetry and Osteryoung square-wave
stripping voltammetry (OSWSV) [99]. The drug is easily detected as 0.134 ng mL-1.
A sensitive procedure for trace measurement of tamoxifen is described [100]. The method is
based on controlled adsorptive accumulation of the drug at an electrochemically treated glassy carbon
electrode, followed by chronopotentio-metric measurement of the surface species.
A carbon paste electrode modified by hydrophobic molecules of hydroxypropyl -cyclodextrin
to form enantioselective membrane sensor was used for the enantioseparation of racemic methotrexate
[101]. Also, determination of its enantiomeric purity in some pharmaceuticals in suggested.
Trace measurements of 2-thiouracil and 4-thiouridine in presence of Cu(II) is described
[102]. In this method the adsorption and redox behavior occurs on hanging mercury drop electrode,
and the reduction current of the accumulated complex is measured by cathodic stripping voltammetry.
2.1.4. Cardiovascular drugs:
Indapamide was determined by an adsorptive stripping method using carbon paste electrode
modified by castor oil [103]. Utilizing anodic stripping differential pulse voltammetry procedure, the
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calibration plot was linear in the range 18.3-36.5 ng mL-1 indapamide with detection limit of 1.8 ng
mL-1. The method was applied for the determination of indapamide in spiked serum.
Analytical method based on the adsorptive accumulation of Cu(II)-indapamide complex
followed by the reduction of the complexed copper was developed for the indapamide determination
[104]. Under the optimal experimental conditions, a linear calibration graph in the range 20-200 nmol
L-1 and detection limit of 5 nmol L-1 were calculated.
1,4-Dihydropyridine derivatives such as nitrendipine, nifedipine, dehydro- nifedipine and other
calcium antagonist members were determined by different voltammetric techniques [105-114].
Differential-pulse voltammetric method was developed for the determination of amlodipine
based on the oxidation of the dihydropyridine group on the surface of glassy carbon electrode under
stationary and rotating conditions [115]. The limit of detection (LOD) and the limit of quantitative
(LOQ) for the rotating and stationary techniques were found to be 0.004 and 0.0072 mg mL-1 (for S/N
= 3.3) and (LOQ) 0.012 and 0.022 mg mL-1 (for S/N = 10), respectively. The proposed method was
applied to the tablets containing amlodipine and according to the statistical evaluations acceptable
results were obtained at the 95 % probability level.
Captopril was subjected for different voltammetric techniques. The voltammetric behavior was
studied [116, 117]. Carbon-paste electrode modified with cobalt-5-nitrolsalophen was used as a
sensitive voltammetric sensor for detection of captopril [118]. Captopril was determined using
adsorptive cathodic differential pulse stripping voltammetry with the HMDE [119]. Square-wave
voltammetric determination of captopril also was suggested [120, 121]. Quite fast and inexpensive
voltammetric method was suggested for the determination of captopril using differential pulse
polarography in presence of oxygen [122]. Adsorptive cathodic stripping voltammetry is used for the
determination of trace levels of captopril in phosphoric acid (pH 2.3) [123]. The method was applied to
determine the mentioned drug in pharmaceutical formulations, urine and blood-serum. The limit of
detection was 0.019 ng/ml
Cyclic voltammetry, direct current polarography, differential pulse polarography and
alternating current polarography were used to study the voltammetric behavior of ramipril [124].
Verapamil was determined by adsorptive stripping voltammetry [125]. The suggested procedure shows
linearity range of 1x10-8-1x10-6 M with detection limit 5x10-10 M. This procedure was successfully
applied for the determination of verepamil in urine and in dosage forms
Diltiazem as an antihypertensive agent was determined in capsules and urine using adsorptive
stripping voltammetry [126]. The calculated detection limit of diltiazem in aqueous solution in 2.7 ng
mL-1.
The square-wave adsorptive cathodic stripping voltammogram of terazosin exhibited a single
well-defined two-electron irreversible cathodic peak which may be attributed to the reduction of C=O
double bond of the drug molecule [127]. The described procedure was suitable for the determination of
terazosin in bulk form, tablets and human serum. Limits of detection (LOD) and quantitation (LOQ) of
1.5x1011 and 5x1011 M bulk terazosin were achieved, respectively. The proposed procedure was
successfully applied to determination of the drug in tablets and human serum samples.
DC polarography and the determination of doxazosin employing different polarographic
techniques are described in this study [128]. Since the sensitivity of suggested procedure was higher
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than the others, the determination of doxazosin was performed in filtered and unfiltered tablet solutions
containing 4 mg active material.
Square wave voltammetry of antihipertensive doxazosin at nafion modified carbon paste
electrode has been carried out [129]. The detection limit reached using square wave voltammetry was
2.33x1011 M and the variation coefficient at 2.0x109 M level was 3.54%. The suggested procedure
can be used to determine the drug at trace level in human urine samples with good recoveries.
A polarographic procedure of suffocate sensitivity for the determination of bulk amiloride drug
in BrittonRobinson buffer at pH 2 using mercury electrodes is described [130]. The calibration graph
was obtained over the concentration range 2.5x105-2.5x104 M amiloride. The limits of detection
(LOD) and quantitation (LOQ) of the procedure were 1x105 and 3.3x104 M bulk amiloride,
respectively. Moreover, a differential-pulse adsorptive cathodic stripping voltammetric procedure has
been described to assay of the drug at lower concentration levels. The calibration graph was obtained
over the concentration range 2x108-1x106 M for bulk amiloride. Both procedures were successfully
applied to the determination of amiloride in tablets.
2.1.6. Flavonoids:
Characterization of voltammetric behavior and antioxidative activity for selected four
flavonoids (quercetin, rutin, catechin and epigallocatechin gallate) was suggested using carbon paste
electrode modified with dsDNA [134].
Square wave anodic stripping voltammetry was used for the determination of quercetin is
investigated [135]. Under the optimal experimental conditions, the linear concentration ranged from
67.66 to 338.3 ppb quercetin. The detection limit of 6.77 ppb quercetin at 15 s accumulation time.
Electrochemical behavior of quercetin was studied in detail by field emission scanning electron
microscope (FE-SEM), UV-spectroelectrochemical and various electrochemical methods [136]. A
highly sensitive adsorptive stripping voltammetric measurement (AdSV) for quercetin was also shown
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2.1.7. Vitamins:
Water soluble vitamins (thiamine, riboflavin, pyridoxine and ascorbic acid) were determined by
linear sweep voltammetry at carbon paste electrode [137]. Thiamine (vitamin B1) was determined by
different voltammetric methods [138-140]. Also, riboflavin was determined by square wave adsorptive
stripping voltammetry at mercury film electrode [141-143].
Ascorbic acid was determined using different voltammetric techniques. Using modified carbon
paste electrode to study the electrocatalytic determination of ascorbic acid in aqueous solution [144].
Also, ascorbic acid was determined in fruits and vegetables [145, 146]. Differential pulse voltammetric
determination of ascorbic acid has been realized on the carbon paste electrode (CPE) [147]. The
developed method has been applied to the direct determination of vitamin C in pharmaceutical tablets
and in different types of fruit juices. Limits of determination are 1.5x10 7 M, 8x107 M and 1x105 M
for tablets, dehydrated and liquid juices, respectively.
Ascorbic acid is simultaneously determined by voltammetric techniques; with uric acid [148,
149], with epinephrine [150] and with dopamine [151, 152]. Simultaneous determination of dopamine,
ascorbic acid and uric acid at modified glassy carbon electrode is suggested [153]. Also, ascorbic acid,
epinephrine and uric acid were determined at glassy carbon electrode modified with caffeic acid [154].
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voltammetry using polymer modified carbon paste electrode [162], fatty acid carbon paste electrode
[163], platinum and activated glassy carbon electrode [164]. At lipid-coated glassy carbon electrode
and lipid-coated carbon paste electrode, the desipramine, imipramine and trimipramine were
determined by voltammetry [165].
Electrochemical behavior of trazodone-HCl was investigated using carbon paste electrode
[166] and platinum electrode [167]. Also, direct current (DCt), differential pulse (DPP) and alternating
current (ACt) polarography were used to study the voltammetric behavior of trazodone-HCl [168].
The electrochemical oxidation of tryptophan at graphite electrodes has been studied in aqueous
solutions [169]. A simple, fast and sensitive method is proposed for tryptophan determination in
pharmaceutical formulations containing other non-electroative amino acids, vitamins and
hydroxycobalamines was suggested using carbon paste electrode [170].
2.2. Electroanalytical application for the trace determination of metals:
Modern electroanalytical methods show a remarkable sensitivity, broad scope and very low
quantitation limit. Different electroanalytical methods, especially stripping analysis, widely used for
the trace metals determination in environmental, industrial and in biological samples. Various stripping
techniques were used for the determination of 30 trace elements [23].
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Bismuth film electrodes were prepared ex-situ by pulsed potential electrodeposition. The
analytical performances of these electrodes for adsorptive cathodic stripping voltammetry of nickel
were evaluated in nondeaerated solutions using dimethylglyoxime as complexing agent [175]. Linear
calibration curves were obtained for Ni+2 concentrations ranging from 1x10-8-1x10-7 mol L-1 and from
1x10-7-1x10-6 mol L-1 with relative standard deviations of 5% (n = 15) at 1x10-7 mol L-1 level. The
analytical methodology was successfully applied to monitor Ni+2 content in industrial electrolytic
baths, ground water and tap water.
Differential pulse cathodic stripping voltammetry (DPCSV) and linear sweep cathodic
stripping voltammetry (LSCSV) were used for the determination of trace amounts Cr(VI) ions in
neutral phosphate media [176]. Detection limit was 5x10-9 mol L-1 and 1x10-9 mol L-1 using LSCSV
and DPCSV, respectively.
Differential pulse cathodic and anodic stripping voltammetry were applied for the
determination f trace ions Cd(II), Co(II), Cu(II), Pb(II), Mn(II), Ni(II) and Zn(II) which are found in
different grades of common salt as contaminants [177].
A procedure for the determination of lead in paints by differential-pulse anodic-stripping
voltammetry is presented [178].
Differential pulse anodic stripping voltammetry with a hanging mercury drop electrode has
been used for the determination of trace amounts of Cu(II), Cd(II), Pb(II) and Zn(II) ions in white cane
sugar [179, 180].
Trace amounts of Zn(II), Cd(II) and Pb(II) were determined in refined beet sugar by differential
pulse anodic stripping voltammetry (DPASV) at a hanging mercury drop electrode [181]. The
procedure was applied to the determination of toxic elements in commercial beet sugar samples and
levels of metals below 35 mg kg-1 Pb(II), 80 mg kg-1 Zn(II) and 10 mg kg-1 Cd(II) were found.
Determination of heavy metals (Cu(II), Cd(II), Pb(II) and Zn(II)) in concentrated refined sugar
and raw syrups with differential pulse polarography and anodic stripping voltammetry was described
[182]. Using differential pulse polarography, trace determinations down to 10-7 M were measured. But
using anodic stripping voltammetry at a mercury film electrode, it was found that the refined sugar of
alimentary grade contained: 57 Cu(II), 34 Zn(II), 1 Cd(II), and 6 Pb(II) g/kg of dry sugar.
Anodic stripping voltammetry with a hanging mercury drop electrode was used for the
determination of trace amounts of Zn(II), Pb(II) and Cu(II) in sugar cane spirit from different sources:
commercial, oak-cask matured and home-made [183].
Experiments have been carried out to assess the potential of differential pulse voltammetry and
potential stripping analysis for determining Pb(II), Cu(II) and Cd(II) directly in dissolved honey
samples [184].
Se(IV) is determined by differential pulse anodic stripping voltammetry using gold electrodes
[185]. A wide linear response range 0.5-291 ng mL-1, was obtained using a 5.0 mm diameter gold
electrode.
Mo(VI) is determined by anodic stripping voltammetry using a carbon paste electrode modified
in situ with cetyltrimethylammonium bromide (CTAB) [186]. Differential pulse anodic stripping
voltammetry exploiting the reoxidation signal is used for the determination of trace levels of
molybdenum(VI). Linearity between current and concentration exists for a range of 0.5-500 g L1
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Mo(VI) with proper preconcentration times; the limit of detection is 0.04 g L1 with an accumulation
period of 10 min.
A chemically modified carbon paste electrode was developed for the determination of silver by
incorporating the strong acid ion-exchanger into a conventional graphite-Nujol oil paste using by
square wave anodic stripping voltammetry [187]. For 5 min of accumulation, the linear range was from
1.62 g L 1 to 0.8 mg L 1 with a detection limit of 0.27 g L 1. Another type of chemically modified
carbon paste electrode was suggested for the determination of silver [188]. Using differential pulse
stripping voltammetry, the appropriate calibration graph for Ag(I) was obtained between 5x10 -7 M and
1.5x10 -6 M and detection limit was 2x10 -7 M.
Determination of lead and antimony in firearm discharge residues on hands by anodic stripping
voltammetry using a mercury-coated graphite electrode are established [189].
Anodic stripping voltammetric determination of trace amounts of titanium has been studied
using glassy carbon electrode modified with thymol blue (TB) [190]. The method has been
successfully applied to determine titanium in two standard reference material Portland cement samples,
then to Portland cement and cement clinker.
A voltammetric method has been used for the determination of the contents of toxic heavy
metals in domestic waste and in compost produced from it [191]. Cu(II), Pb(II), Zn(II) and Cd(II) were
determined in wet-digested samples of domestic waste, compost produced of that waste and in
compost mixed with sewage sludge by anodic stripping voltammetry.
An indirect voltammetric method is described for determination of cyanide ions and hydrogen
cyanide, using the effect of cyanide on cathodic adsorptive stripping peak height of Cu-adenine using
mercury electrode [192]. The detection limit was obtained as 1x10-8 M for 60 s accumulation time. The
method was applied to the determination of cyanide in various industrial waste waters such as
electroplating waste water and also for determination of hydrogen cyanide in air samples.
Simultaneous determination of Cu(II), Zn(II) and Pb(II) by adsorptive stripping voltammetry in
the presence of Morin was suggested [193]. With an accumulation time of 60 s, the peak currents are
proportional to the concentration of copper, lead and zinc over the 1-60, 0.3-80 and 1-70 ng/mL range
with detection limits of 0.06, 0.08 and 0.06 ng/mL, respectively. The procedure was applied to the
simultaneous determination of Cu(II), Zn(II) and Pb(II) in some real and synthetic artificial real
samples.
Ni(II) and Co(II) have been determined simultaneously by means of adsorptive cathodic
stripping voltammetry (AdCSV) in a computerized flow injection system [194].The selectivity of the
method was demonstrated for the analysis of high purity iron.
A voltammetric method is presented for the determination of trace levels of Cr(VI) in the
presence of cupferron as ligand [195]. This method based on using square wave adsorptive stripping
voltammetry (SWAdSV) in conjunction with the electrochemical batch injection analysis technique at
mercury thin-film electrodes. An analytical method has been developed for the determination of
dissolved chromium at concentrations less than 2 g/L in PWR coolant by differential-pulse adsorptive
stripping voltammetry at a hanging mercury drop electrode [196].
Mo(VI) has been determined by differential-pulse adsorptive stripping voltammetry in a pH 2
phosphate buffer utilising the strong adsorption of 12-molybdophosphoric acid at a hanging mercury
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drop electrode [197]. Calibration graphs are rectilinear up to the 7x107 M Mo(VI). A clearly defined
stripping peak was observed at the 5.6x109 M level with 2 min accumulation.
Adsorptive stripping voltammetry at a static mercury drop electrode for the determination of
Al(III) and Fe(III) in Portland cement has been employed [198].
An analytical procedure for the determination of Fe(III) and total iron in wines based on
adsorptive stripping voltammetry is described [199]. Fe(III) was determined by using Solochrome
Violet Red as chelating agent while catechol was used for the determination of the total iron content.
A sensitive stripping voltammetric procedure for quantifying thorium is described [200]. The
chelate of thorium with the azo dye mordant blue 9 is adsorbed on the hanging mercury drop electrode.
The detection limit is 4x1010 M (4-min accumulation), a linear current-concentration relationship is
observed up to 1.3x107 M.
Square wave adsorptive stripping voltammetric method for the determination of Ti(IV) is
described [201]. The method is based on Ti(IV) complexed with hydroxynaphthol blue (HNB) at the
static mercury drop electrode. The limit of detection was found to be 0.18 g/L and the limit of
determination to be 1.09 g/L, both using 30 s of preconcentration time.
Simultaneous determination of tin and lead by differential pulse polarography with addition of
hyamine-2389 is described [202]. Calibration plots are linear up to 5x105 M for tin and 1.3x104 M
for lead, with detection limits of 8.4x107 M and 2.4x107 M, respectively. Simple methods are
proposed for the determination of tin in solders and canned fruit juices.
Traces of Fe(III) were determined by differential pulse polarography in solar-grade silicon
[203]. Differential pulse polarography provides a detection limit of about 0.15 g g-1 with a precision
of 1-2% and linear calibration graphs up to 0.5 g mL-1 Fe(III).
Differential pulse polarographic determination of Cr(VI) in semiconductor gallium arsenide
based on the catalytic current produced by nitrate in the electrolytic reduction of the Cr(VI)diethylenetriaminepentaacetate complex [204]. This method is suitable for determinations of Cr(VI) at
levels as low as about 1 g g1 with about 50 mg of sample.
Mo(VI) was determined in steel by differential-pulse polarography [205]. The method is
applicable to the determination of molybdenum in the 0.001-5% of Mo(VI) range and good agreement
is reported for a number of certified British Chemical Standard and commercial steels.
Ternary mixtures of metals can be resolved by using the ratio derivative polarography without
the need for any pre-separation step [206]. The method is based on the simultaneous use of the first
derivative of ratios of polarograms and measurements of zero-crossing potentials. The method has
been successfully applied for resolving ternary mixtures of Cu(II), Cd(II) and Ni(II), which have
overlapped polarograms. The concentration ranges to be determined are 0.30-1.40 mg L1 for Cu(II),
0.90-4.50 mg L1 for Cd(II) and 0.20-1.20 mg L1 for Ni(II).
An electrochemical method for the quantitative determination of boron in minerals and ceramic
materials is described [207]. It is based on the abrasive attachment of mixtures of ZnO plus sample to
modified graphite electrodes.
A method for determining trace level of V(V) has been developed [208]. The reaction is the
polarographic reduction of the bromate, catalyzed by this metal ion, in the presence of cupferron. A
linear current-concentration relationship is observed between 2x10-8 and 3x10-7 M, with a detection
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limit of 6x10-9 M. The procedure is very selective and has been successfully applied to a certified steel
sample.
Voltammetric determination of the iodide ion with a quinine copper(II) complex modified
carbon paste electrode employing linear sweep and differential pulse voltammetry [209]. Using linear
sweep voltammetry, a calibration curve was attained over the concentration ranges 1x10-42.5x10-6 M
of the iodide ion at deposition time of 10 min, with the detection limit 1x10-6 M. Using differential
pulse voltammetry, linear response range for the iodide ion was between 10-6 and 10-8 M, and the
detection limit was 1x10-8 M. This method was evaluated by analyzing the iodide ion content in a
commercial disinfectant.
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performed on synthetic solutions containing Cd(II), Pb(II), and Cu(II) as target ions. In particular,
linear calibration curves over the range 5x10 8-1x10 6 M for Cd(II) and Pb(II), detection limits of 7.8
and 2.9 nM for Cd(II) and Pb(II), respectively. This method was applying for the determination of
Pb(II) and Cu(II)in drinking water, wine, and tomato sauce.
An analytical procedure regarding the determination of Cu(II), Pb(II), Cd(II), Zn(II) and Sb(III)
in matrices involved in foods and food chain as wholemeal, wheat and maize meal is proposed [217].
Differential pulse anodic stripping voltammetry (DPASV) was employed for simultaneously
determining all the elements. The limits of detection were in the range 0.009-0.096 g/g
A method for the determination of Pb(II) in soft drinks and fruit juices by potentiometric
stripping analysis is described [218].
Trace levels of tin can be determined by voltammetry after controlled adsorptive
preconcentration of the tin-tropolone complex on a hanging mercury drop electrode [219]. For a 8-min
preconcentration period, the detection limit is 2.3x1010 M. The method was applied for the
determination of tin in orange-juice samples.
The application of potentiometric stripping analysis (PSA) to simultaneous determination of
lead and tin has been investigated using a continuous flow system.[220]. The suggested procedure was
applied for the determination of lead and tin in fruit juices and soft drinks are also described.
A square wave adsorptive stripping voltammetric (SWAdSV) method for the indirect
determination of trace amounts of Mg(II) with thiopentone sodium (TPS) as an electroactive ligand, at
carbon paste mercury film electrode (CP-MFE) is proposed [221]. a linear relation in the range 6x10-9
to 9x10-8 M Mg(II) (0.142.16 ppb), at 60 s deposition time, is obtained. The detection limit of Mg(II)
is 0.14 ppb for 60 s deposition time.
The complex formation between uric acid and Zn(II), Cd(II) and Pb(II) has been investigated
using differential pulse polarography [222]. A sensitive voltammetric method is developed for the
quantitative determination of uric acid. This method is based on controlled adsorptive preconcentration
of uric acid on the hanging mercury drop electrode (HMDE), followed by tracing the voltammogram
in the cathodic going potential scan. The modes used are direct current stripping voltammetry (DCSV)
and differential pulse stripping voltammetry (DPSV). The detection limits found were 8x10 9 M
(quiescent period 15 sec) by DPSV and 1.6x108 M by DCSV.
Controlled adsorptive accumulation of Mo(VI)-2-benzylideneiminobenzo hydroxamic acid
(BIBH) at the hanging mercury drop electrode (HMDE) provides the basis for the direct stripping
measurement of Mo(VI) in nanomolar concentration [223]. A differential pulse cathodic stripping
voltammetric method for the determination of Mo(VI) with 2-BIBH in urine is proposed.
The modified carbon paste electrode (CPE) responding simultaneously to Pb(II), Cu(II), and
Hg(II) ions has been constructed by incorporating humic acid (HA) into the graphite powder with
Nujol oil [224]. Here, the detection limit for Pb(II), Cu(II), and Hg(II) ions were 5x10 -9 M, 8x10-9 M,
and 810-9 M, respectively, for 20 minutes of deposition time. Satisfactory results were acquired for
the determination of the test metal ions in certified standard urine.
Determination of traces of thallium in urine by anodic stripping AC voltammetry [225].
Determination of thallium by measuring the current peak which results from the fundamental harmonic
ac stripping voltammogram recorded.
3307
Concentrations of heavy metals such as Pb(II), Cd(II), Cu(II), and Zn(II) have been determined
by using differential pulse anodic stripping voltammetry (DPASV) in air particulates, diet, and
children's blood residing [226]. The determination of Zn(II) in human eye tissues by anodic stripping
voltammetry was introduced [227].
Arsenic was determined in ancient bone samples was determined using a gold tipped rotating
disc electrode and differential pulse anodic stripping voltammetry [228]. For a deposition time of
120 sec, the lowest detection limit (LOD) for arsenic was 1.078 g/L.
Differential-pulse adsorption voltammetry for the simultaneous determination of nickel and
cobalt in bovine liver [229]. The limits of detection obtained under the conditions of this study were
0.01 g g1 and 0.02 g g1 for cobalt and nickel, respectively,
Application of stripping voltammetry to trace Pb(II) analysis in intermediates and final
products of syntheses of pharmaceuticals [230]. The method showed a good linearity up to 50-100
ppm Pb(II) with a detection limit less than 10 ppb.
The determination of Pb(II) and Cd(II) biological materials was carried out by potentiometric
stripping analysis [231]. The method was applied to different standard reference materials (leaves,
needles, hair).
Differential pulse cathodic stripping voltammetry (DPCSV) have been used for the
determination of selenium in plants[232]. The selenium content in capsules and in seeds was
evaluated; the seed contains 5000 mg kg 1 as total selenium, of which almost 50% is soluble in
solvents.
Simultaneous determination of Cd(II), Cu(II), Pb(II) and Zn(II) in amino acid parenteral
nutrition solutions by anodic stripping voltammetry and sample digestion by UV irradiation [233]. The
metal concentrations ranged between 1.3-4.4 for Cd(II), 2.9-40.8 for Cu(II), 4.4-16.8 for Pb(II), and
1.4-208.5 for Zn(II).
Bismuth film electrode is presented as a promising alternative to mercury electrodes for the
simultaneous determination of trace Co(II) and Ni(II) in non-deoxygenated solutions [234]. This
method show low detection limits of 0.08
g L1 for Co(II) and 0.26 g L1 for Ni(II) employing a
deposition time of 60 s.
Square wave stripping voltammetry of Pb(II), Cu(II), and Hg(II) was performed on the
modified gold electrode [235]. The detection limits of 0.16, 0.15, and 0.14 ppb for Pb(II), Cu(II) and
Hg(II) were obtained, respectively.
3308
Mo(VI) and Cr(VI). The detection limits of these metal ions were 0.03, 0.4, 0.04, 0.1, 0.15, 0.05, 0.2,
and 3.2 ug/kg for Cd(II), Pb(II), Cu(II), Zn(II), Co(II), Ni(II), Cr(VI), and Mo(VI), respectively
A method was described for the determination of selenium in soils and plants by differential
pulse cathodic-stripping voltammetry (DPCSV) at a hanging mercury-drop electrode [237].
An ultrasensitive adsorptive catalytic stripping (voltammetric and potentiometric) procedure for
determining trace levels of chromium in the presence of cupferron is described [238]. A
preconcentration time of 1 min results in a detection limit of 1.0 ng L1. The stripping potentiometric
scheme allows convenient measurements of chromium in the presence of dissolved oxygen. The
identical stripping response for Cr(III) and Cr(VI) solutions makes the method applicable to the
measurement of the total chromium content. The simultaneous determination of chromium and
uranium is illustrated. The merits of the proposed procedure are demonstrated by the analysis of soil
and groundwater samples.
A differential pulse stripping voltammetry method for the trace determination of Mo(VI) in
water and soil has been developed [239]. The suggested procedure can be used for determining
Mo(VI) in the range 51010 to 7109 M, with a detection limit of 11010 M (4 min accumulation).
Direct and simultaneous voltammetric analysis of heavy metals in tap water samples at Assiut
city was developed [240]. Tap water samples are analyzed to determine the total content of Cd(II),
Cu(II), Pb(II) and Zn(II) by differential pulse anodic stripping voltammetry (DPASV) while Ni(II) and
Co(II) are determined by a new simple differential pulse adsorptive stripping voltammetry (DPAdSV),
using dimethylglyoxime (DMG) as the complexing agent. This method uses sodium sulfite as the
supporting electrolyte, which facilitates the removal of oxygen interference without the traditional
necessity of purging with inert gas
Graphite Electrodes Modified by 8-hydroxyquinolines exhibited an affinity to chelating Cu(II)
forming a Cu(II) complex, which was employed for Cu(II) trace analysis [241]. A differential pulse
voltammetry, combined with a preconcentrating-stripping process and a standard addition method was
used for the analysis. A detection limit for trace copper determination in water, such as 5.110-9 mol L1
, was obtained.
Catalytic adsorptive stripping voltammetry determination of ultra trace amount of Mo(VI) is
proposed [242]. The method is based on adsorptive accumulation of the Mo(VI)-pyrocatechol violet
(PCV) complex on to a hanging mercury drop electrode, followed by reduction of the adsorbed species
by voltammetric scan using differential pulse modulation Mo(VI) can be determined in the range 1103
-100.0 ng mL-1 with a limit of detection of 0.2 pg mL-1. The procedure was applied to the
determination of Mo(VI) in mineral water and some analytical grade substances with satisfactory
results.
Differential pulse adsorptive cathodic stripping voltammetric method has been developed for
trace determination of Mo(VI) in presence of alizarin red S as complexing agent [243]. The peak
current is proportional to the concentration of Mo(VI) over the concentration range of 1-25 ppb with a
detection limit of 0.25 ppb. The method has been applied to the determination of Mo(VI) in water
samples.
Carbon paste electrode modified with diacetyldioxime used for the simultaneous determination
of Pb(II) and Cd(II) [244]. Calibration graphs were linear in the concentration ranges of 1.0x10 -7-
3309
1.5x10-5 mol/L (Pb(II)) and 2.5x10-7-2.5x10-5 mol/L (Cd(II)), respectively. For 5 min preconcentration,
detection limits of 1x10-8 mol/L (Pb(II)) and 4x10-8 mol/L (Cd(II)) were obtained. The diacetyldioxime
modified carbon paste electrode was applied to the determination of Pb(II) and Cd(II) in water samples.
Electrochemical method is described for the determination of inorganic arsenic in water at the
g/L level, applicable in the laboratory and in the field, based on differential pulse cathodic stripping
voltammetry [245]. Determination of total As is performed by reducing As(V) to As(III) using sodium
meta-bisulfite/sodium thiosulfate reagent stabilized with ascorbic acid. As(V) is quantified by
difference The detection limit was 0.5 g/L with a linear range from 4.5 to 180 g/L.
Adsorptive stripping voltammetric determination of Pb(II) in presence of 2,2-dipyridyl2,4dioxybenzoic acid molecular complex was proposed [246]. The compounds formed by Pb(II) and 2,2dipyridyl2,4-dioxybenzoic acid molecular complex (DDOB) are adsorbed on the mercury electrode.
Linear dependence between the current and Pb(II) concentration in the solution was observed in the
range 1.210 8-3.510 7 M Pb(II), for accumulation time 60 s and stationary diffusion. This method
was applied for the determination of the Pb(II) in the natural waters.
Anodic stripping voltammetric method with a mercury thin film electrode is reported for the
establishment of baseline concentrations of Cd(II), Pb(II) and Cu(II) in natural waters [247].
A voltammetric method based on chelate adsorption at the hanging mercury electrode is
described for the simultaneous determination of Cu(II), Pb(II), Cd(II), Ni(II) and Co(II) by
adsorptive stripping voltammetry using quercetin as complexing agent [248]. The method was applied
successfully for the simultaneous determination of the five metals in tap water samples.
Diffrential pulse anodic stripping voltammetry was used for the determination of Zn(II), Cd(II),
Pb(II) and Cu(II) in the underground water [249]. The trace elements levels found are in the ranges
0.01-0.37, 1.27-49.5, 0.41-29.8 and 0.13-98.09 ug/L for Cd(II), Cu(II), Pb(II) and Zn(II), respectively.
The method was applied with satisfactory results for the determination of these metals in underground
water samples.
Adsorptive cathodic stripping voltammetric determination of Mo(VI) in synthetic solutions and
environmental samples was proposed [250]. This method is based on controlled adsorptive
preconcentration of Mo(VI) species on the hanging mercury drop electrode (HMDE) using mixtures of
nitrate and phosphate as supporting electrolytes. The method used is cathodic linear sweep stripping
voltammetry (CLSSV). The detection limit found was 110-8 M using 120 s. as accumulation time.
This method has been applied for the determination of Mo(VI) in environmental samples; e.g., soil,
natural water and indoor airborne particulate.
Determination of iron in seawater using cathodic stripping voltammetry preceded by adsorptive
collection with the hanging mercury drop electrode [251] The detection limit for the determination of
iron in seawater of pH 6.9 was 61010 M in the presence of 4104 M catechol and after a collection
period of 3 min. The peak current increased linearly with the metal concentration up to about 5108
M, but the linear range could be increased by using a shorter collection period.
Direct determination of sub-nanomolar levels of Zn(II) in seawater by cathodic stripping
voltammetry is presented [252]. The zinc complex with ammonium pyrrolidine dithiocarbamate is
adsorbed on a hanging mercury drop electrode and the reduction current of zinc is measured by
voltammetry. The detection limit for Zn(II) is 31011 M, with 10-min collection time.
3310
3. CONCLUSION:
The previous survey shows that the number of publications dealing with the application of
some selected modern electrochemical techniques (voltammetric techniques) to determine
pharmaceuticals and metals in different samples. The importance of such applications increased
steadily, and this due to the following advantages:
3311
1Voltammetric methods have been very popular and have made valuable contributions to
trace elements speciation because they combine the requirements of accuracy and sensitivity.
2The sensitivity is sufficiently high and can be increased more by modifications of
classical voltammetric techniques (modified microelectrodes and ultramicroelectrodes) that enhance
significantly sensitivity and selectivity of the method.
3Voltammetry coupled with different separation methods such as (HPLC, Flow Injection
(FI) and Capillary Electrophoresis (CE)) enhancing the analytical properties for complex mixtures in
different compounds.
4Turbid and colored solutions, which are a problem with other methods, can be easily
analyzed. The separation of the excipients, in pharmaceutical analysis, is in many cases not necessary
and this simplified the preparation of samples.
5Only small volumes of samples are necessary.
6Modern voltammetry also continues to be a potent tool used by various kinds of
chemists interested in studying oxidation and reduction process in various media, adsorption process
on surfaces and electron transfer mechanism at chemically modified electrodes surfaces.
7Electroanalytical stripping procedures have been developed for the measuring down to
sub-g/L level.
8Also, these techniques combine low maintenance costs with high sensitivity and
selectivity that allows the determination of low levels of analytes with out prior treatments of the
samples.
9These techniques have been developed for various cations, anions and organic
molecules.
10Elelctroanalytical techniques (specially stripping analysis) are well known as excellent
procedures for the determination of trace chemical species.
11The developed stripping voltammetric methods are simple, time saving, selective and
more sensitive for the simultaneous determination of trace substances.
12Electroanalytical methods especially square wave voltammetry is a very sensitive and
rapid analytical method due to it is high scan rate in all cases where the reacting species is accumulated
by adsorption on the electrode surface.
13The short analysis time in these methods makes it very attractive for routine
determination of the analytes in different samples.
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