摘要
目的:制定复方青娥丸的质量标准。方法:采用HPLC对处方中松脂醇二葡萄糖苷(PDG)含量进行定量测定。结果:HPLC法测定松脂醇二葡萄糖苷在4.43~443 mg.L-1线性关系良好,回归方程为Y=28 849X-2 119.5(r=0.999 9),平均加样回收率为100.99%(RSD 2.17%),符合分析要求。结论:所建立定量检测方法操作简便、准确可靠、灵敏度高、专属性强,可有效控制青娥丸的质量。
Objective: To establish the quality standard for Qing'e Wan. Method: ( + ) -Pinoresinol di-O-13-D-glucopyranoside (PDG) was determined by HPLC. Result: The results of quantitative evaluation showed that ( + ) -pinoresinol di-O-fl-D-glucopyranoside (PDG) concentration was linear in the range of 4.43-443 mg· L-1 (r=0.999 9), the average recovery rate was 100.99% (RSD 2. 17%). This method met the analysis requirement. Conclusion: The established quantitative methods were simple, accurate, reliable and reproducible, which can be effectively used for the quality control of Qing'e Wan.
出处
《中国实验方剂学杂志》
CAS
北大核心
2012年第20期112-115,共4页
Chinese Journal of Experimental Traditional Medical Formulae
基金
国家自然科学青年基金项目(30901952)
国家药典委员会项目(ZH-398)
上海市中医药事业发展三年行动计划项目
关键词
青娥丸
杜仲
质量标准
Qing'e Wan
Eucommiae Cortexg
pinoresinol di-glucopyranoside
quality standard