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舒肝止痛丸的质量标准研究
引用本文:林绿萍,林德晖,程怡,徐锌锌,郑品劲.舒肝止痛丸的质量标准研究[J].北方药学,2012,9(3):12-13.
作者姓名:林绿萍  林德晖  程怡  徐锌锌  郑品劲
作者单位:广州中医药大学,广州510006
摘    要:目的:建立舒肝止痛丸质量标准。方法:采用薄层色谱法对处方中的木香进行定性鉴别;采用高效液相色谱法测定制剂中黄芩苷的含量。结果:薄层色谱斑点清晰,专属性强,易于识别;黄芩苷在(0.3~1.8)μg呈良好的线性关系(r=0.9999),平均加样回收率为100.25%,RSD=1.45%。结论:所建立的方法简便、准确、重复性好,可用于舒肝止痛丸的质量控制。

关 键 词:舒肝止痛丸  质量标准  黄芩苷  高效液相色谱法

Studies on Quality Standar of Shugan Zhitong Wan
Lin Lueping Lin Dehui Cheng Yi Xu Xinxin Zheng Pinjin.Studies on Quality Standar of Shugan Zhitong Wan[J].BEIFANG YAOXUE,2012,9(3):12-13.
Authors:Lin Lueping Lin Dehui Cheng Yi Xu Xinxin Zheng Pinjin
Institution:Lin Lueping Lin Dehui Cheng Yi Xu Xinxin Zheng Pinjing (Guangzhou university of Traditional Chinese Medicine, Guangzhou, 510006, China)
Abstract:Objective:To establish the quality standard for Shugan Zhitong Wan. Methods: Aucklandia lappa Decne. was identified by TLC. The content of baicalin in Shugan Zhitong Wan was determined by HPLC. Result: TLC spots were clear with strong specificity and easy identification. Baicalin was linear in the range of 0.3-1.8μg (r=0.9999). The average recovery was 100.25% with RSD of 1.45%. Conclusion: The methods are simple, accurate, and repeatable and can be used for the quality control of Shugan Zhitong Wan.
Keywords:Shugan Zhitong Wan Quality standard Baicalin HPLC
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