摘要
目的: 建立黄芪饮片中黄芪皂苷Ⅰ、黄芪皂苷Ⅲ和黄芪甲苷的含量测定方法并分析蜜炙对黄芪皂苷含量的影响。 方法: 采用HPLC-ELSD,色谱条件为Thermo Syncronis C18色谱柱(4.6 mm×250 mm,5 μm),流动相乙腈-0.3%甲酸溶液梯度洗脱,流速0.8 mL·min-1,柱温25 ℃,ELSD参数为漂移管温度110 ℃,氮气体积流量3.0 L·min-1。 结果: 黄芪皂苷Ⅰ、黄芪皂苷Ⅲ、黄芪甲苷的线性范围分别为0.804-8.04,0.784-7.84,0.406-4.06 μg,平均加样回收率分别为98.3%,99.3%,98.9%,RSD分别为2.46%,1.89%,2.38%。不同产地黄芪饮片中黄芪皂苷Ⅰ、黄芪皂苷Ⅲ、黄芪甲苷含量分别在0.301-0.527,0.186-0.303,0.128-0.178 mg·g-1。 结论: 建立的含量测定方法简单易行,方法学验证符合要求。炙黄芪中黄芪皂苷Ⅰ和黄芪皂苷Ⅲ的含量高于生品,但黄芪甲苷较生品降低,说明蜜炙对黄芪皂苷类成分的含量产生了一定影响。
Objective: To establish a method to determine contents of astragaloside Ⅰ,astragaloside Ⅲ and astragaloside IV from Astragali Radix,then analyzed influence of honey-processed for artragaloside content. Method: HPLC-ELSD was adopted,Thermo Syncronis C18 column(4.6 mm×250 mm,5 μm),mobile phase consisting of acetonitrile-0.3% formic acid using a gradient elution,flow rate of 0.8 mL·min-1 and column temperature at 25 ℃,drifttube temprature of ELSD parameters was 110 ℃,volume flow rate of nitrogen was 3.0 L·min-1. Result: Astragaloside Ⅰ,astragaloside Ⅲ and astragaloside IV showed a good linear relationship in the range of 0.804-8.04,0.784-7.84,0.406-4.06 μg,the average recoveries of them were 98.3%,99.3%,98.9% with RSD of 2.46%,1.89%,2.38%,respectively.Contents of astragaloside Ⅰ,astragaloside Ⅲ and astragaloside IV from Astragali Radix in different places were 0.301-0.527,0.186-0.303,0.128-0.178 mg·g-1,respectively. Conclusion: This established method was simple and reliable,methodology validation met requirements.Contents of astragaloside Ⅰ and astragaloside Ⅲ from processed Astragali Radix were higher than raw materials,but astragaloside IV was opposite,indicating that honey-processed had an effect on the content of saponins.
出处
《中国实验方剂学杂志》
CAS
北大核心
2014年第2期39-41,共3页
Chinese Journal of Experimental Traditional Medical Formulae
基金
2010-2011年中医药行业科研专项(20110700705)
山东省科技发展计划项目(2008GG30002056)