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Title: | Reverse-phase liquid chromatographic determination of α-lipoic acid in dietary supplements using a boron-doped diamond electrode |
Authors: | Siangproh W. Rattanarat P. Chailapakul O. |
Keywords: | Ag/AgCl Boron-doped diamond electrode Boron-doped diamond electrodes Chromatographic determination Chromatographic separations Correlation coefficient Detection limits Dietary supplements ELectrochemical detection Highly-correlated HPLC-UV Hydrodynamic voltammetry Linear relationships Lipoic acids Liquid chromatographic separations Mobile phase Optimized conditions Phase liquids Phosphate solutions Real samples Relative standard deviations Reversed phase Spiked samples Acetonitrile Acids Boron Chemical detection Chromatography Diamonds Food additives High performance liquid chromatography Liquids Nutrition Vitamins Electrochemical electrodes acetonitrile boron diamond phosphate thioctic acid accuracy article capillary electrophoresis controlled study correlation coefficient diet supplementation electrochemical detection flow rate hydrodynamics methodology oxidation pH potentiometry priority journal process optimization reversed phase liquid chromatography separation technique validation process Boron Chromatography, High Pressure Liquid Chromatography, Reverse-Phase Diamond Dietary Supplements Electrochemical Techniques Electrodes Hydrodynamics Oxidation-Reduction Reproducibility of Results Sensitivity and Specificity Thioctic Acid |
Issue Date: | 2010 |
Abstract: | A fast liquid chromatographic separation, coupled with sensitive and straightforward detection using a boron-doped diamond (BDD) electrode, was developed and validated for the determination of α-lipoic acid in dietary supplement samples. The analysis was carried out using a reversed phase C18 (150 mm × 4.6 mm, 5 μm) column with a mobile phase consisting of a 1:1 (v/v) ratio of 0.05. M phosphate solution (pH 2.5):acetonitrile, at a flow rate of 1.0. mL/min. The detection potential obtained from hydrodynamic voltammetry was 1.05. V vs. Ag/AgCl. Under optimized conditions, the chromatographic separation was performed in less than 5. min, a good linear relationship was obtained between the current and the α-lipoic concentration within the range of 0.01-60 μg/mL (correlation coefficient of 0.9971), and a detection limit of 3.0. ng/mL was determined. Furthermore, this method was successfully applied to determine α-lipoic acid concentrations in selected commercial dietary supplement samples. The recovery of α-lipoic acid in spiked samples at 0.5, 5.0 and 30 μg/mL ranged from 94.4% to 103.6% with a relative standard deviation (RSD) of between 1.2% and 3.7%. In real samples, this developed methodology produced results that were highly correlated with the standard HPLC-UV approach. Therefore, the present method can be used for fast, selective and sensitive quantification of α-lipoic acid in dietary supplements. © 2010 Elsevier B.V. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14604 https://www.scopus.com/inward/record.uri?eid=2-s2.0-78249278463&doi=10.1016%2fj.chroma.2010.10.004&partnerID=40&md5=63c9a9f60455302edc44e85d9991170b |
ISSN: | 219673 |
Appears in Collections: | Scopus 1983-2021 |
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