摘要
目的:完善馥感啉口服液质量标准。方法:采用薄层色谱法鉴别馥感啉口服液中西洋参;采用高效液相色谱法测定黄芪甲苷的含量。结果:西洋参鉴别斑点圆整,分离度好。含量测定黄芪甲苷平均回收率为95.44%,RSD为3.37%。结论:方法简便、准确、重现性好,能更好的控制馥感啉口服液的质量。
Objective：To improve the quality standard for Fuganlin Oral Solution. Methods：TLC was used to identify American Ginseng and HPLC-ELSD was used to determine the contents of Astragaloside Ⅳ. Results： American Ginseng was well separated and identified by TLC,and average recovery was 95.44% with RSD 3.37%. Conclusion：The method is quick, simple and repeatable for the quality control of Fuganlin Oral Solution.
出处
《中国药品标准》
CAS
2009年第3期179-181,共3页
Drug Standards of China
关键词
馥感啉口服液
西洋参
黄芪甲苷
质量标准
Fuganlin Oral Solution
American Ginseng
Astragaloside IV
quality standard
