首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Separation and determination of gentiopicroside and swertiamarin in Tibetan medicines by micellar electrokinetic electrophoresis.
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Separation and determination of gentiopicroside and swertiamarin in Tibetan medicines by micellar electrokinetic electrophoresis.

机译:胶束电动电泳法分离测定藏药中龙胆苦苷和苦参碱。

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摘要

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 borate-10 mm sodium dodecylsulfate (SDS) -6% (v/v) ispropanol (pH 9.0). The voltage was 15 kV and detection was at 254 nm. The lower limits of detection (defined as a signal-to-noise ratio of about 3) were approximately 3.86 mg L(-1) for GE and 5.88 mg L(-1) 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 96-104% for GE and 92-102% for SW.
机译:胶束电动电泳用于测定一种名为世味龙丹克力的藏族制备药,两种名为龙胆秦ent和龙胆的藏药以及三种名为龙胆秦,的中药的含量。和龙胆。通过MEKC测定的龙胆苦苷和swertiamarin的解离常数为7.71和6.25。最佳缓冲液系统是70毫米硼酸盐-10毫米十二烷基硫酸钠(SDS)-6%(v / v)异丙醇(pH 9.0)。电压为15 kV,检测波长为254 nm。检测的下限(定义为约3的信噪比)对于GE约为3.86 mg L(-1),对于SW约为5.88 mg L(-1)。 GE和SW的迁移时间和峰面积的相对标准偏差分别为2.33%,2.47%和1.27%,2.19%,两种化合物的回收率GE分别为96-104%和SW的92-102%。

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