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Non‐aqueous capillary electrophoresis for simultaneous separation and determination of three major active components in traditional medicinal preparations
Author(s) -
Li Cunhong,
Zhang Jiyou,
Chen Anjia,
Xie Jianping,
Chen Xingguo,
Hu Zhide
Publication year - 2005
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.459
Subject(s) - chromatography , chemistry , puerarin , capillary electrophoresis , daidzein , analyte , ammonium acetate , aqueous solution , detection limit , high performance liquid chromatography , medicine , alternative medicine , pathology , genistein
A simple and sensitive non‐aqueous capillary electrophoresis method has been developed for simultaneous assay of three bioactive components (puerarin, daidzein and wogonin) in three traditional medicinal preparations for the rst time. Optimum separation of the analytes was obtained on a 47 cm × 75 µm i.d. capillary using a non‐aqueous buffer system of 20% acetonitrile, 25 m m ammonium acetate and apparent pH 9.00, with applied voltage and capillary temperature of 20 kV and 16°C, respectively. The relative standard deviations (RSDs) of the migration times and the peak areas of the three analytes were in the ranges 2.5–4.0% and 3.2–3.9%, respectively. Detection limits of puerarin, daidzein and wogonin were 0.090, 0.145 and 0.090 µg mL −1 , respectively. In the tested concentration range, good linear relationships (correlation coefcients: 0.9998 for puerarin, 0.9998 for daidzein and 0.9978 for wogonin) between peak areas and concentrations of the analytes were observed. This method has been successfully applied to simultaneous determination of the three bioactive components with recoveries from 91.0 to 114.0%. Copyright © 2004 John Wiley & Sons, Ltd.