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脏连丸质量标准研究
引用本文:卢祖庆,季申.脏连丸质量标准研究[J].中国基层医药,2008,15(4).
作者姓名:卢祖庆  季申
作者单位:上海市食品药品检验所中药室,上海市,201203
摘    要:目的 建立脏连丸的质量控制标准.方法 对脏连丸制剂中黄连、槐角、槐花采用薄层色谱法进行了定性鉴别;采用HPLC法测定黄芩中黄芩苷的含量.Intersil C18色谱柱,2%冰醋酸溶液-甲醇(45:55)为流动相;检测波长280 nm.结果 黄芩苷在0.0434~4.34 μg范围内进样量与峰面积呈线性关系,黄芩苷的平均回收率99.2%,相对标偏差(RSD)为1.10%.薄层图谱斑点清晰,空白无干扰.结论 方法简便、准确、重现性好,可用于该制剂的质量控制标准.

关 键 词:脏连丸  质量控制  黄芩苷

Study on the quality specification of Zanglian Pill
LU Zu-qing,JI Shen.Study on the quality specification of Zanglian Pill[J].Chinese Journal of Primary Medicine and Pharmacy,2008,15(4).
Authors:LU Zu-qing  JI Shen
Abstract:Objective To establish the quality specification of Zanglian Pill. Methods Rhizoma coptidia,fructus sophorae and flos sophorae were identified by TLC. Radix scuteUariae was determined by HPLC. Intersit Cas column was used with the mobile phase of 2 % acetic acid-methanol(45:55 ), at the detection wavelength of 280nm.Results The calibration curve was linear in the range of 0. 0434~4.34 μg. The average recovery rate of baiealin was 99.2 % with RSD of 1.10 %. The TLC spots developed were fairly clear, and the blank test showed no interference. Conclusion The method developed is simple and accurate with a good reproducibility,and the method can be used for the quality control of Zanglian Pill.
Keywords:Zanglian Pill  Quality eontrol  Baicalin
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