Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14604
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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