## Abstract An MEKC method was developed for the determination of the five pharmaceutically important anthraquinones: chrysophanol (**1**), physcion (**2**), emodin (**3**), aloeβemodinin (**4**), and rhein **(5)** in __Cassia obtusifolia__ (Leguminosae). A buffer solution (pH 9.00) composed of 20
Separation and determination of gentiopicroside and swertiamarin in Tibetan medicines by micellar electrokinetic electrophoresis
β Scribed by Shengguo Zhao; Qing Liu; Xingguo Chen; Zhide Hu
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 194 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0269-3879
- DOI
- 10.1002/bmc.285
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β¦ Synopsis
Abstract
Micellar electrokinetic electrophoresis was employed to determine two active components, gentiopicroside (GE) and swertiamarin (SW) in one Tibetan preparation medicine named shiweilongdankeli, two Tibetan herbal medicines named Gentiana rhodantha and Gentiana kitag and three other Chinese Gentiana medicines named Gentiana scabra, Gentiana rigescens and Gentiana macrophylla. The dissociation constants of gentiopicroside and swertiamarin determined by MEKC were 7.71 and 6.25. The optimum buffer system was 70 mm borateβ10 mm sodium dodecylsulfate (SDS) β6% (v/v) ispropanol (pH 9.0). The voltage was 15 kV and detection was at 254 nm. The lower limits of detection (deο¬ned as a signalβtoβnoise ratio of about 3) were approximately 3.86 mg L^β1^ for GE and 5.88 mg L^β1^ for SW. The relative standard deviation of the migration time and peak area of the GE and SW were 2.33, 2.47 and 1.27, 2.19%, respectively and the recoveries of the two compounds were 96β104% for GE and 92β102% for SW. Copyright Β© 2003 John Wiley & Sons, Ltd.
π SIMILAR VOLUMES
Swertiamarin and gentiopicroside were quantified simultaneously using thin layer chromatography (silica gel) with densitometry (240 nrn). The single calibration graph was linear in the interval 1.0-16.0 pg in the presence of an external standard. The standard deviation did not exceed 5% and the rela
In this article, micellar electrokinetic chromatography MEKC separation of 15 N-methylcarbamate insecticides with a wide span of hydrophobicity was studied. Influences of various buffer parameters such as sodium dodecyl sulfate Ε½ . Ε½ . SDS concentration, ionic strength, and modifiers urea, cyclodext
A micellar electrokinetic capillary chromatographic method was set up for the quality control of rhubarb and its preparations. Anthraquinone derivatives were separated successfully within 10 min in the buffer solution of 50 mmol/L H 3 BO 3 -NaOH (pH 11) containing 25 mmol/L sodium deoxycholate. The