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出 处:《中成药》2007年第9期1321-1324,共4页Chinese Traditional Patent Medicine
摘 要:目的:建立复方参桂胶囊的质量标准。方法:采用TLC法对复方参桂胶囊中甘草、三七、丹参和川芎进行定性鉴别,采用HPLC法测定制剂中甘草酸铵和丹参酮ⅡA含量。结果:在薄层色谱中能检出甘草、三七、丹参和川芎;甘草酸铵在0.5-4μg和丹参酮ⅡA在0.04-0.32μg范围内线性良好,回归系数r分别为0.999 8和0.999 6,平均回收率分别为98.9%,97.8%。结论:建立的分析方法简便可行,专属性强,可用于复方参桂胶囊质量控制。AIM: To establish quality standard for Compound Shengui Capsules. METHODS: Glycyrrhiza uralensis Fisch. ,Panax notoginseng (Burk.) F. H. Chen, Salvia miltiorrhiza Bge. and Ligusticum chuartxiong Hort. were identified by TLC. Ammonium glycyrrhizinate and tanshinone ⅡA were determined by HPLC. RESULTS: TLC spots developed were fairly clear and the blank test showed no interference. The linear rangers were 0.5 -41μg(r =0. 999 8)for ammonium glycyrrhizinate ;0. 04 -0. 321μg(r =0. 999 6) for tanshinone ⅡA. The average recoveries of them were 98.9% ,97.8%, respectively. CONCLUSION: The methods is effective for the quality control of Compound Shengui Capsules.
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