Simultaneous determination of five anthraquinones in medicinal plants and pharmaceutical preparations by HPLC with fluorescence detection

被引：105

作者：

He, Dongxiu ^{[1
,2
]}

Chen, Bo ^{[1
]}

Tian, Qingqing ^{[1
]}

Yao, Shouzhou ^{[1
]}

机构：

[1] Hunan Normal Univ, Minist Educ, Key Lab Chem Biol & Tradit Chinese Med Res, Changsha 410081, Peoples R China

[2] Univ S China, Sch Life Sci & Technol, Hengyang 421001, Peoples R China

来源：

JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS | 2009年 / 49卷 / 04期

关键词：

Anthraquinones; HPLC-fluorescence detection; HPLC-UV detection; Traditional Chinese medicine; Pharmaceutical preparation; PERFORMANCE LIQUID-CHROMATOGRAPHY; COUNTER-CURRENT CHROMATOGRAPHY; CAPILLARY-ZONE-ELECTROPHORESIS; MIXED MICELLAR SYSTEM; ELECTROKINETIC CHROMATOGRAPHY; ALOE-EMODIN; RHEUM-EMODI; RHUBARB ANTHRAQUINONES; SODIUM CHOLATE; DERIVATIVES;

D O I：

10.1016/j.jpba.2009.02.014

中图分类号：

O65 [分析化学];

学科分类号：

070302 [分析化学];

摘要：

A reversed-phase high-performance liquid chromatography (RP-HPLC) method with fluorescence detection for simultaneous determination of five anthraquinones in Rhubarb collected from nine different locations in China, Polygonum cuspidatum, Polygoni multiflori and three pharmaceutical preparations is proposed and validated. Chromatography was carried out at 25 degrees C on a Hypersil C18 column with the isocratic mobile phase of methanol-0.1% aqueous formic acid (85:15, v/v) at a flow rate of 1.0 ml/min. The excitation and emission wavelengths were set at 440 and 540 nm, respectively. A comprehensive validation of the method included tests of sensitivity, linearity, precision and accuracy. The linear regressions were acquired with r > 0.999. Satisfactory intra- and inter-day precisions were achieved with R.S.D.s less than 3.95% and the average recovery factors obtained were in the range of 93.2-103.8%. (C) 2009 Elsevier B.V. All rights reserved.

引用

页码：1123 / 1127

页数：5

共 36 条

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