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胶束电动毛细管色谱法分析构树叶中罕见的黄酮 C-糖苷。

Analysis of rare flavonoid C-glycosides in Celtis australis L. by micellar electrokinetic chromatography.

机构信息

Institute of Pharmacy, Pharmacognosy, University of Innsbruck, Innrain 52, 6020 Innsbruck, Austria.

出版信息

J Pharm Biomed Anal. 2010 Apr 6;51(5):1165-8. doi: 10.1016/j.jpba.2009.11.028. Epub 2009 Dec 1.

DOI:10.1016/j.jpba.2009.11.028
PMID:20022443
Abstract

This manuscript reports on the first analytical procedure for the determination of flavonoids in Celtis australis. The capillary electrophoretic separation of 8 compounds, most of them flavone C-glycosides, was possible using a borax buffer with pH 9.0, which contained 25mM SDS as detergent and 7.5% of n-butanol as organic modifier. Method validation revealed that the developed assay is repeatable (sigma(rel)<or=4.0%), precise (inter-day sigma(rel)<or=6.7%, intra-day sigma(rel)</=3.9%), accurate (recovery rates from 96.8 to 102.3%), sensitive (LOD: 2.2-1.6microg/ml) and linear (R(2)>or=0.9996) within the tested concentration range. The quantitative analysis of several C. australis samples showed that isovitexin is the most abundant representative (0.06-0.09%), at a rather uniform content of total flavonoids of approx. 0.3% in all specimens.

摘要

这篇手稿报告了首个分析方法,用于测定朴树中的类黄酮。使用 pH 值为 9.0 的硼砂缓冲液,其中含有 25mM SDS 作为去污剂和 7.5%的正丁醇作为有机改性剂,实现了 8 种化合物(大多数为黄酮 C-糖苷)的毛细管电泳分离。方法验证表明,所开发的测定法具有可重复性(sigma(rel)<or=4.0%)、精确性(日间 sigma(rel)<or=6.7%,日内 sigma(rel)</=3.9%)、准确性(回收率为 96.8%至 102.3%)、灵敏度(LOD:2.2-1.6μg/ml)和线性(R(2)>or=0.9996),测试浓度范围内。对几种朴树样本的定量分析表明,异荭草苷是最丰富的代表(0.06-0.09%),所有标本中总类黄酮的含量约为 0.3%,相当均匀。

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