活力素胶囊质量标准的研究  

A Study of the Quality Standard of Huolisu Capsules

作　　者：葛皓玲[1] 阮金兰[1] 钟家平[2] 

机构地区：[1]华中科技大学同济医学院药学院,武汉430030 [2]武汉莱奇尔中药现代化有限公司,430030

出　　处：《医药导报》2004年第6期411-413,共3页Herald of Medicine

基　　金：武汉市科技局科技攻关项目(基金编号:2002780)

摘　　要：目的:研究活力素胶囊的质量标准。方法:采用薄层色谱法对活力素胶囊进行定性鉴别;采用高效液相色谱法(HPLC)对活力素中人参皂苷Re的含量进行测定。结果:人参皂苷Re的线性范围0.315～4.725μg,平均回收率99.84％,RSD=0.73％。结论:该方法可行,重复性好,可作为活力素胶囊质量标准的重要指标。Objective: To study the quality standard of huolisu capsules. Methods: Thin layer chromatography (TLC) was used for the qualitative discrimination of huolisu capsules and the content of ginsenoside Re in the capsules determined with high performance liquid chromatography (HPLC). Results: The linear range of ginsenoside Re was 0.315～4.725 μg and the average recovery rate, 99.84%, RSD=0.73%. Conclusion: The method was shown to be feasible, with good reproducibility, and can be used for the effective quality control of huolisu capsules.

关 键 词：活力素胶囊 人参皂苷 质量标准 

分 类 号：R286[医药卫生—中药学] R927.2[医药卫生—中医学]