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高效液相色谱法同时测定含丹参的中药制剂中隐丹参酮、丹参酮Ⅰ和丹参酮ⅡA的含量

Simultaneous determination of cryptotanshinone, tanshinone I and tanshinone IIA in traditional Chinese medicinal preparations containing Radix salvia miltiorrhiza by HPLC.

作者信息

Shi Zhihong, He Jiantao, Yao Tingting, Chang Wenbao, Zhao Meiping

机构信息

Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, PR China.

出版信息

J Pharm Biomed Anal. 2005 Mar 9;37(3):481-6. doi: 10.1016/j.jpba.2004.11.015. Epub 2004 Dec 23.

DOI:10.1016/j.jpba.2004.11.015
PMID:15740907
Abstract

A reversed-phase high performance liquid chromatographic method was established for the simultaneous determination of tanshinones in five kinds of traditional Chinese medicinal preparations (TCMPs) containing Radix salvia miltiorrhiza (Chinese herbal name: Danshen). Tanshinones including cryptotanshinone, tanshinone I and tanshinone IIA were successfully separated on a Diamonsil C18 column (150 mm x 4.6 mm i.d., 5 microm). The mobile phase was a mixture of methanol, tetrahydrofuran, water and glacial acetic acid (20:35:44:1, v/v/v/v), employing isocratic elution at a flow rate of 1.0 mL/min. Detection was accomplished at 254 nm. The compounds were identified by comparing their retention times and UV spectra in the 200-400 nm range with authentic standards. Regression equations revealed good linear relationship between the peak areas of the constituents and their concentrations (correlation coefficients: 0.9998 for cryptotanshinone, 0.9999 for tanshinone I and 1.0000 for tanshinone IIA). The relative standard deviations (n=6) of retention time and peak area were less than 0.25% and 1.00%, respectively. The recoveries were between 96.2% and 102.5%. The proposed method has been successfully applied to the simultaneous determination of the tanshinones in five kinds of Chinese herbal preparations containing Danshen within 20 min.

摘要

建立了一种反相高效液相色谱法,用于同时测定五种含丹参的传统中药制剂中的丹参酮。隐丹参酮、丹参酮Ⅰ和丹参酮ⅡA等丹参酮在Diamonsil C18柱(150 mm×4.6 mm内径,5μm)上成功分离。流动相为甲醇、四氢呋喃、水和冰醋酸的混合物(20:35:44:1,v/v/v/v),采用等度洗脱,流速为1.0 mL/min。检测波长为254 nm。通过将其保留时间和200 - 400 nm范围内的紫外光谱与标准品进行比较来鉴定化合物。回归方程显示各成分的峰面积与其浓度之间具有良好的线性关系(相关系数:隐丹参酮为0.9998,丹参酮Ⅰ为0.9999,丹参酮ⅡA为1.0000)。保留时间和峰面积的相对标准偏差(n = 6)分别小于0.25%和1.00%。回收率在96.2%至102.5%之间。所建立的方法已成功应用于在20分钟内同时测定五种含丹参的中药制剂中的丹参酮。

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