摘要
目的对附桂骨痛颗粒中有效成分芍药苷的质量比测定方法进行研究。方法采用反相高效液相色谱(RP-HPLC)法测定附桂骨痛颗粒中芍药苷的质量比。结果测得附桂骨痛颗粒中芍药苷质量比为3.301mg/5g。结论采用RP-HPLC法测定附桂骨痛颗粒中芍药苷的质量比可作为附桂骨痛颗粒的定量标准,测定方法简便、准确、可靠、重现性好。
Objective To study the paeoniflorin＇s determination method of paeoniae radix as the principal drug in Fuguigutong Granule. Methods RP - HPLC was adopted to determine the mass ratio of paeoniflorin. Results The mass ratio of paeoniflorin was 3. 301 mg/5 g. Conclusion The mass ratio determined by this method can be as the quantitation standard of Fuguigutong Granule, and the determination method is simple, accurate, reliable and reproducible.
出处
《中国药业》
CAS
2009年第20期31-32,共2页
China Pharmaceuticals
