Abstract
Micellar electrokinetic chromatography (MEKC) was examined for the separation and determination of Mo(VI), Cr(VI), Ni(II), Pd(II), and Co(III) as diethyl dithiocarbamate (DDTC) chelates. The separation was achieved from fused silica capillary (52βcmβΓβ75βmβid) with effective length 40βcm, background electrolyte (BGE) borate buffer pHβ9.1 (25βmM), CTAB 30% (100βmM), and 1% butanol in methanol (70β:β30β:β5βv/v/v) with applied voltage of β10βkV using reverse polarity. The photodiode array detection was achieved at 225βnm. The linear calibration for each of the element was obtained within 0.16β10βg/mL with a limit of detection (LOD) 0.005β0.0167βg/mL. The separation and determination was repeatable with relative standard deviation (RSD) within 2.4β3.3% () in terms of migration time and peak height/peak area. The method was applied for the determination of Mo(VI) from potatoes and almond, Ni(II) from hydrogenated vegetable oil, and Co(III) from pharmaceutical preparations with RSD within 3.9%. The results obtained were checked by standard addition and rechecked by atomic absorption spectrometry.
1. Introduction
Capillary electrophoresis (CE) is coming up as an alternative analytical technique for the elemental analysis in parallel with liquid chromatography [1]. However, CE requires small sample volume (10β50βnL) with less running cost, and analysis could be completed with shorter analysis time. A number of chelating reagent are available, which could complex with different metal ions, thus making simultaneous determination of metal with CE possible [1, 2]. A number of groups have indicated CE as a useful analytical technique for metal ions [3β8]. Capillary zone electrophoresis (CZE) is used to separate water-soluble ionic compounds, but less water-soluble nonionic compounds could better be addressed by micellar electrokinetic chromatography (MEKC). Surfactants are added to buffer solution in MEKC to make up critical concentration. The separation in the MEKC is based on differential partition between buffered aqueous mobile phase and the micellar (pseudo) stationary phase [9]. Diethyl dithiocarbamate (DDTC) is more frequently used as complexing reagent for metal ions, because it forms intensely coloured complexes with a number of metal ions [10]. DDTC has been used as reagent for spectrophotometry [11], liquid chromatography [12, 13], gas chromatography [14], and high-performance liquid chromatography inductively coupled plasma mass spectrometry of metal ions [15β18]. DDTC mostly forms coordinating saturated neutral metal chelates, extractable in nonaqueous organic molecules [19]. Hilder et al. have reported separations of metal chelates of bis(2-hydroxyethyl) dithiocarbamate by MEKC by direct photometric detection using anionic micelles of sodium dodecyl sulphate (SDS) [20, 21]. The present work examines the separation of the metal chelates of DDTC using cationic and neutral micelles, including the use of organic modifiers. The conditions are optimized for the separation of Mo(VI), Cr(VI), Ni(II), Pd(II), and Co(III) chelates. Linear calibration range, limits of detection (LOD), limits of quantitation (LOQ), repeatability, and accuracy are ascertained for application of the method for the sample analysis.
2. Experimental
2.1. Chemicals and Equipment
Sodium diethyl dithiocarbamates (Na-DDTC) (Fluka, Switzerland), nickel(II) chloride, cobalt(II) acetate, palladium(II) chloride, ammonium molybdate(VI), and potassium bicarbonate (E-Merck, Germany) were used. The chemical methanol (RDH, Germany), acetonitrile, and chloroform (E-Merck, Germany) were used. Guaranteed reagent grade hydrochloric acid (37%), potassium chloride, acetic acid, sodium acetate, ammonium acetate, sodium tetraborate, boric acid, sodium bicarbonate, sodium carbonate, ammonium chloride, and ammonia solution were form E-Merck, Germany. Buffer solution pH 1β10 at unit interval was prepared from the following; hydrochloric acid-potassium chloride (pH 1-2), acetic acid-sodium acetate (3β6), ammonium acetate (pH 7) boric acid-sodium tetraborate (8β9.5), sodium bicarbonate-sodium carbonate (pH 9), and ammonium chloride-ammonium solution (pH10). The pH measurements were performed with an Orian 420A pH meter with combined glass electrode and reference interval electrode (Orian Inc. Boston, USA). The spectrophotometric study was carried out with double beam Perkin Elmer 35 spectrophotometer (Perkin Elmer, Singapore) with 1βcm quartz cuvettes. The spectrophotometer was controlled by the computer with software. The determination of nickel, cobalt, and molybdenum was carried out with Perkin Elmer AA 800 (Perkin Elmer, Singapore); atomic absorption spectrometer with standard burner head and an air-acetylene flame under the conditions recommended was determined in quadruplet (). The capillary electrophoresis system consists of a Beckman Coulter P/ACE MDQ instrument (Beckman Instruments Inc., Fullerton, CA) equipped with an auto sampler, photodiode array detector, and a data system comprising an IBM personal: computer and P/ACE system MDQ (32 Karate) software. Uncoated fused silica capillaries were obtained from Beckman Instruments Inc. with total length 52βcm, effective length 40βcm, 75βΞΌm i.d, and 375βΞΌm o.d. The temperature of the capillary and sample was maintained at 25Β°C. Prior to the sample run, each day, or at the time of observation of any distortion in the peak shape in the electropherogram during the day, the capillary was regenerated and conditioned with methanol, for 1βmin, followed by water for 0.5βmin, hydrochloric acid (0.1βM) for 2βmin, water for 0.5βmin, sodium hydroxide (0.1βM) for 2βmin, water for 0.5βmin, finally run buffer for 2βmin. Before each sample injection, the capillary was washed with sodium hydroxide (0.1βM) for 1βmin, water for 0.5βmin, and then equilibrated with run buffer for 2βmin. The washing and conditioning of the capillary was carried out as recommended by manufacturer. The sample was injected by an auto sampler with a pressure of 0.5βpsi 3.45βkPa for 4 to 6βsec. The solution 0.1% w/v of NaDDTC was prepared by dissolving appropriate amount in 0.01βM NaOH. Metal ion solutions containing 1βmg/mL of each metal were prepared by dissolving appropriate amount of potassium dichromate, nickel chloride, cobalt acetate, and ammonium molybdate in deionized double-distilled water containing a few drops of appropriate acid. Weighed amount of palladium chloride was added 2βmL of hydrochloric acid (37%) and heated gently, till most of the PdCl2 dissolved. More acid was added if required. The solution was concentrated to about 0.5βmL, and the solution was dissolved in water and volume was adjusted to the mark.
2.2. Analytical Procedure
The solution (1-2βmL) containing Mo(VI) (1.6β30.0βΞΌg), Co(III) (4.0β40.0βΞΌg), Pd(II) (20.0β100.0βΞΌg), Ni(II) (4.0β120.0βΞΌg), and Cr(VI) (2.5β20.0βΞΌg), was transferred to a separating funnel and was added 2βmL acetic acid-sodium acetate buffer pH 5. Freshly prepared reagent Na-DDTC solution (2βmL) and 2βmL chloroform were then added. The content was mixed well and layers were allowed to separate. The organic layers were collected and extraction was repeated with 2βmL of chloroform. The combined solvent from organic layer was evaporated under a nitrogen-solvent system, and residue was dissolved in 10βmL of solvent system comprising borate buffer pH 9 (25βmM) cetyltrimethylammonium bromide (CTAB) (30βmM)βbutanol (1% v/v in methanol) (40β:β40β:β10 v/v/v). The solution 2βmL was transferred to septum-capped sample vial. The solution was injected by an autosampler, and electropherograms were recorded by the migration of the chelates with background electrolyte consisting of borate buffer pH 9.1 (25βmM)-CTAB (100βmM)-butanol (1% v/v in methanol), (70β:β30β:β5 v/v/v) with applied voltage β10βkV at reverse polarity. Photodiode array detection was achieved at 225βnm.
2.2.1. Analysis of Nickel(II) from Hydrogenated Vegetable Oil (Ghee)
Three samples of hydrogenated vegetable oil (Ghee) were collected from local market (Hyderabad, Pakistan); (1) Pak Ghee (Pakistan oil mills (Pvt) Karachi), (2) Naz Ghee (Tallu oil Mills, Hyderabad, Pakistan), (3) unbranded Ghee. Sample (20βgm each) was transferred to separate conical flak and was added nitric acid (1βM) (30βmL). The contents were shaken on the mechanical shaker for 1 hour. The layers were allowed to separate and aqueous layer was collected. The aqueous layer was concentrated to 5βmL and final volume was adjusted to 10βmL. The solution (0.5βmL) was processed as analytical procedure after adjustment of the pH to 5. The amount of nickel was evaluated from external calibration curves based on linear regression equation, .
2.2.2. Analysis of Molybdenum(VI) from Food Samples
Potato and Almond samples collected from local market (Jamshoro, Pakistan) were properly washed and outer skin peeled off. The remaining mass was cut into small pieces, and 40βg of potato and 20βg of Almond was burned in the furnace at 700Β°C and 650Β°C, respectively, for 10 hours. The ash of each sample was treated separately with 5βmL of H2SO4 (0.1βM). The content was mixed well and filtered with Whatman 9 filter paper. The pH of each solution was adjusted to 5 and final volume was made up to 10 and 15βmL, respectively, for potato and almond samples. The solution 1βmL was processed as analytical procedure. The amount of molybdenum was calculated from external calibration curves.
2.2.3. Determination of Cobalt(III) from Pharmaceutical Preparations
Cobalmine injection (1βmL) (Merck, Marker (Pvt.) Ltd, Germany) or 4 tablet of Neurobion (Merck, Marker (Pvt.) Ltd, Germany) were weighed and grinded to powder and each added 5βmL of aqua regia (HCl-HNO3 3β:β1 v/v). The contents were heated gently to near dryness. The residue was dissolved in distilled water and filtered. The pH of the solution was adjusted to 5, and final volume was made up to 20βmL. The solution (1βmL) was taken and analyzed following analytical procedure.
2.2.4. Sample Analysis by Standard Addition
The samples for the analysis of nickel, molybdenum, and cobalt were also analyzed by standard addition. The solutions 0.5βmL in duplicate were taken from the prepared solution after acid extraction of nickel from Ghee. A solution was added nickel 10βΞΌg, and both solutions were analyzed as analytical procedure. Similarly, the samples of potatoes and almonds prepared by dry ashing for the analysis of molybdenum were also analyzed by standard addition. the prepared solutions of potato (1βmL) and almonds (2βmL) were taken in duplicate. 10βΞΌg of Mo were added in one of the aliquot and both solutions were analyzed by following analytical procedure. The solution (1βmL each) in duplicate was taken from prepared solution of cobalmine injection and Neurobion tablets. A solution was added Co(III) 10βΞΌg and both solution were processed as analytical procedure. The quantitation was carried out from the linear calibration curves and from increase in response (peak height) with added standards.
3. Results and Discussions
DDTC is reported to react with a number of metal ions to form complexes extractable in organic solvents [22, 23]. The metal ions Ni(II), Co(III), Pd(II), Mo(VI), and Cr(VI) reacted with DDTC at pH above 5 to form the complexes extractable in chloroform. However, the use of organic-solvent resulted in the drop of electric current in CE, thus the organic solvent of the metal chelates was evaporated under nitrogen atmosphere and redissolved in water miscible solvent, close to background electrolyte: borate buffer (9.1) (25βmM)-CTAB (30βmM)-butanol (1% v/v in methanol) (40β:β40β:β20 v/v/v), (40β:β30β:β30 v/v/v), and (40β:β40β:β10 v/v/v). The solvent mixture containing 40β:β40β:β10 v/v/v gave better results and also maintained the current and was selected. The ligand DDTC forms water insoluble neutral metal chelates [23], thus MEKC was considered as better choice and was examined.
3.1. Optimization of Background Electrolyte
DDTC metal chelates indicate less solution stability in acidic medium [11], thus buffer systems within pH 7β10 were examined. Borate, phosphate, and carbonate buffers were considered; borate buffer indicated somewhat electrophoretic mobilities for the metal chelates and was, therefore, further investigated. The effect of pH, nature of surfactant added, concentration of buffer and surfactant added and possible addition of organic modifier on the electrophoretic mobilities, and separation of metal chelates were examined. The pH was varied from 8 to 10. All the metal chelates had same mobility upto 8 (Figure 1), a difference in the migration behaviour was observed at pH 8.6, but the chelating ligand was long retained. It was observed that migration time decreased by increasing the pH, and an optimal migration time was observed at pH 9.1 and was selected. MEKC depends upon the pseudostationary phase, and initially SDS and borate buffer pH 9.1, were examined. Different concentrations of SDS were investigated, but an improvement of separation was not observed. The cationic surfactant CTAB, along with borate buffer pH 9.1 was examined. The cationic surfactant generally interact with the negatively charged silica capillary wall and reverse the direction of electrostatic flow (EFO) [24], thus the polarity of an electrode was reversed to elute the solute through detection window. An improvement in the separation and peak shape was observed. The concentration of an electrolyte plays an important role in the separation and controls the joules heating effect created on the surface of capillary. Different concentrations of borate buffer pH 9.1 between 10β100βmM at an interval of 10βmM were examined. Concentrations above 40βmM resulted into the merger of the peaks with short migration time (Figure 2). However, an improvement in the separation was observed at concentration below 40βmM and at 25βmM an acceptable resolution was obtained.
The impact of the concentration of CTAB and the effect of the ratio of buffer and surfactant on the separation of metal chalets was examined. A significant improvement in the separation and electrophoretic mobility of Pd(II), Ni(II), and Co(III) was observed with cationic surfactant CTAB, particularly at higher concentration. However, at the higher concentration of CTAB current inside the capillary was developed, which again affected the separation. In order to avoid this effect, volume of added CTAB (thus the concentration) was varied from 1βmL to 5βmL at an interval of 1βmL. The electrophoretic mobility of the metal chelates remained nearly constant (Figure 3), but 3βmL was selected to obtain short analysis time. In order to further improve the separation selectivity, the addition of organic modifier was considered. Methanol and acetonitrile have been extensively used as modifier [12, 20, 25, 26], and propanol has also been tried with CTAB to improve the resolution [19].
The solvent systems were examined, but no significant improvement in the separation was observed. An improvement in the separation was observed when n-butanol in methanol used. The percentage of n-butanol in methanol was varied between 1 to 7% at an interval of 1%. However, a better separation was obtained using 1% n-butanol in methanol (Figure 4). The addition of the 1% n-butanol in background electrolyte was varied in the ratio from 5 to 15 at an interval of 5, but an optimal separation was obtained using borate buffer pH 9.1 (25βmM), CTAB (30βmM), n-butanol 1% in methanol (65β:β30β:β5 v/v/v) (Figure 4).
3.2. Optimization of Voltage
The applied voltage affects the retention factor as well as the environment developed inside the capillary by creating the joule heating effects. The use of cationic surfactant reversed the direction of EOF, and negative voltage was applied to induce the migration of analyte towards the selection window. The effect of applied voltage was investigated within β5βkV to β20βkV at an interval of β2βkV. An acceptable separation between all the five metal chelates and reagent was observed within β10βkV to β15βkV, and β10βkV was selected owing to better separation with lower applied voltage. A final separation of all five metal complexes along with reagent is presented in Figure 5.
3.3. Quantitation
Linear calibration curves for simultaneous determination were drawn by recording average peak height () versus concentrations at the optimized conditions, within the range of 0.16β12.0βmg/mL with good coefficient of determination (0.998β0.995) (Table 1). The limit of detection (LOD) measured as three times signal-to-noise ratio (S/N) was observed in the range 0.005β0.017βmg/mL (Table 1). Mo(VI) indicated highest and Pd(II) lowest sensitivity. The limits of quantitation measured as S/N ratio (10β:β1) were calculated within 0.016β0.20βΞΌg/mL. The separation was repeatable with relative standard deviation (RSD) () within 2.4β3.34%, in terms of migration time and peak height/peak area. The analysis was repeated by the same person on the same day () and on different days () at the different concentrations within calibration range and the RSD did not exceed 3.8% in terms of migration time and peak height/peak area. The analysis of test mixtures () within calibration range was carried, and the relative errors were obtained within Β±40%. DDTC reacts with a number of metal ions to form colored complexes, and their possible interfering effects on the determinations were examined. Cu(II) and Fe(III) chelates indicate poor mobility in the background electrolyte system used for the separation, and did not affect the determination of the metal ions.
3.4. Sample Analysis
Vegetable oils hydrogenated using Ni as catalyst was analyzed for the contents of Ni, after extraction of nickel in nitric acid. The amounts found were 3.66β4.18βΞΌg/g with RSD within 3.51β4.5%. The nickel samples were also spiked with Ni(II) standard solution and an increase in the response (peak height) was obtained without change in migration time (Figures 6(a) and 6(b)). The results obtained on MEKC were verified by standard AAS procedure, and an acceptable correlation was achieved (Table 3). Finally two pharmaceutical preparation cobalmine and Neurobion tablets were analysed for the content of cobalt. The amount found was correlated with the labeled values of the manufactures (Table 4). The samples for cobalt were also spiked with cobalt and corresponding increase in the response was observed without change in the peak shape (Figures 7(a) and 7(b)). The amount of cobalt was also rechecked by AAS and good agreement was observed (Table 4). The method was used also for the analysis of Mo(VI) from potatoes (Figure 8) and almonds, Ni(II) from edible oils, and Co(III) from pharmaceutical preparations. Mo(VI) in potatoes and almonds was analysed after dry ashing and average amounts found () were 0.293βΞΌg/g and 0.702βΞΌg/g with RDS 3.1% and 1.02%, respectively. The amounts were also analyzed using AAS and results agreed with the observed values of MEKC (Table 2).
(a)
(b)
(a)
(b)
4. Conclusion
A simple and sensitive MEKC method has been described for the determination of Mo(VI), Cr(VI), Pd(II), Ni(II), and Co(III). The separation was obtained within migration time within 12 minutes with LODs within 0.005β0.0176βΞΌg/mL. The procedure is repeated with RSD within 3.3% (). Precapillary derivatization is achieved using DDTC chelating reagent. BGE consist, of borate buffer and contain surfactant CTAB and n-butanol applied as cosurfactant. Analysis of Mo(VI), Ni(II), and Co(VI) from real samples shows that method is applicable to real matrices.
Conflict of Interests
All the authors of the paper declare that they do not have a direct financial relation with any commercial identity mentioned in the paper that might lead to a conflict of interests for any of the authors.