首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Separation and analysis of glycyrrhizin, 18 beta-glycyrrhetic acid and 18 alpha-glycyrrhetic acid in liquorice roots by means of capillary zone electrophoresis
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Separation and analysis of glycyrrhizin, 18 beta-glycyrrhetic acid and 18 alpha-glycyrrhetic acid in liquorice roots by means of capillary zone electrophoresis

机译:甘草根中甘草甜素,18β-甘草次酸和18α-甘草次酸的分离和分析通过毛细管区带电泳

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摘要

Glycyrrhizin is the main active compound of Glycyrrhiza glabra root extracts; according to recent studies, glycyrrhizin and its aglycon, glycyrrhetic acid, have interesting therapeutic properties. A new capillary electrophoretic method has been developed for the separation and quantification of glycyrrhizin, beta-glycyrrhetic acid and its isomer a-glycyrrhetic acid. Separation of the analytes was achieved in less than 3 min on a fused silica capillary, by injecting the samples at the short end of the capillary (effective length: 8.5 cm). The background electrolyte was composed of pH 10.0 carbonate buffer, methanol and ethylene glycol (80/10/10) and contained 0.4% beta-cyclodextrin; indomethacin was used as the internal standard. Diode array detection was used, with quantitative assays carried out at 254 nm. Linearity was found over the 5-200 and 2.5-100 mu g mL(-1) concentration ranges for glycyrrhizin and glycyrrhetic acid, respectively. This method has been applied to the determination of the analytes in different matrices (liquorice roots and commercial confectionery products), and to the purity control of beta-glycyrrhetic acid obtained from the hydrolysis of glycyrrhizin. When analysing beta-glycyrrhetic acid and its epimer in roots, the samples were purified by means of a suitable solid-phase extraction (SPE) procedure with Oasis HLB cartridges, which granted good selectivity, eliminating matrix interference. (c) 2005 Elsevier B.V. All rights reserved.
机译:甘草甜素是甘草根提取物的主要活性成分。根据最近的研究,甘草甜素及其糖苷配基,甘草次酸具有令人感兴趣的治疗特性。已经开发出一种新的毛细管电泳方法,用于分离和定量甘草甜素,β-甘草次酸及其异构体α-甘草次酸。通过在毛细管的短端(有效长度:8.5 cm)注入样品,在熔融石英毛细管上不到3分钟即可完成分析物的分离。背景电解质由pH 10.0的碳酸盐缓冲液,甲醇和乙二醇(80/10/10)组成,并包含0.4%的β-环糊精。消炎痛用作内标。使用二极管阵列检测,并在254 nm进行定量分析。线性分别在5-200和2.5-100μg mL(-1)浓度范围内的甘草甜素和甘草次酸中发现。此方法已应用于测定不同基质(甘草根和商业糖果产品)中的分析物,以及控制由甘草甜素水解获得的β-甘草次酸的纯度。当分析根中的β-甘草次酸及其差向异构体时,样品采用Oasis HLB柱通过合适的固相萃取(SPE)程序纯化,具有良好的选择性,消除了基质干扰。 (c)2005 Elsevier B.V.保留所有权利。

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