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采用高效液相色谱-电喷雾电离质谱法对贯叶连翘的主要成分进行定量分析。

Quantitative analysis of the major constituents of St John's wort with HPLC-ESI-MS.

作者信息

Chandrasekera Dhammitha H, Welham Kevin J, Ashton David, Middleton Richard, Heinrich Michael

机构信息

Centre for Pharmacognosy and Phytotherapy, School of Pharmacy, University of London, 29-39 Brunswick Square, London WC1N 1AX, UK.

出版信息

J Pharm Pharmacol. 2005 Dec;57(12):1645-52. doi: 10.1211/jpp.57.12.0015.

DOI:10.1211/jpp.57.12.0015
PMID:16354409
Abstract

A method was developed to profile the major constituents of St John's wort extracts using high-performance liquid chromatography-electrospray mass spectrometry (HPLC-ESI-MS). The objective was to simultaneously separate, identify and quantify hyperforin, hypericin, pseudohypericin, rutin, hyperoside, isoquercetrin, quercitrin and chlorogenic acid using HPLC-MS. Quantification was performed using an external standardisation method with reference standards. The method consisted of two protocols: one for the analysis of flavonoids and glycosides and the other for the analysis of the more lipophilic hypericins and hyperforin. Both protocols used a reverse phase Luna phenyl hexyl column. The separation of the flavonoids and glycosides was achieved within 35 min and that of the hypericins and hyperforin within 9 min. The linear response range in ESI-MS was established for each compound and all had linear regression coefficient values greater than 0.97. Both protocols proved to be very specific for the constituents analysed. MS analysis showed no other signals within the analyte peaks. The method was robust and applicable to alcoholic tinctures, tablet/capsule extracts in various solvents and herb extracts. The method was applied to evaluate the phytopharmaceutical quality of St John's wort preparations available in the UK in order to test the method and investigate if they contain at least the main constituents and at what concentrations.

摘要

开发了一种使用高效液相色谱 - 电喷雾质谱法(HPLC - ESI - MS)分析圣约翰草提取物主要成分的方法。目的是使用HPLC - MS同时分离、鉴定和定量金丝桃素、金丝桃蒽酮、假金丝桃蒽酮、芦丁、金丝桃苷、异槲皮苷、槲皮苷和绿原酸。使用外标法和参考标准品进行定量。该方法包括两个方案:一个用于黄酮类化合物和糖苷的分析,另一个用于分析亲脂性更强的金丝桃蒽酮类和金丝桃素。两个方案均使用反相Luna苯基己基柱。黄酮类化合物和糖苷在35分钟内实现分离,金丝桃蒽酮类和金丝桃素在9分钟内实现分离。为每种化合物确定了ESI - MS中的线性响应范围,所有化合物的线性回归系数值均大于0.97。两个方案对所分析的成分都具有很高的特异性。质谱分析显示分析物峰内没有其他信号。该方法稳健,适用于酒精酊剂、各种溶剂中的片剂/胶囊提取物以及草药提取物。该方法用于评估英国市场上圣约翰草制剂的植物药质量,以测试该方法并调查它们是否至少含有主要成分以及含量是多少。

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