摘要
目的:建立HPLC同时测定竹节参中竹节参皂苷Ⅴ和Ⅳa的含量测定方法,并对不同产地的竹节参药材进行含量测定。方法:采用Hibar C18色谱柱,以乙腈-0.1%磷酸溶液为流动相,梯度洗脱,柱温30℃,检测波长203 nm。结果:竹节参皂苷Ⅴ在0.36--7.20μg(r〉0.999)范围内线性关系良好,平均加样回收率为96.0%,(RSD=0.73%,n=6);竹节参皂苷Ⅳa在0.57~11.40μg(r〉0.999)范围内线性关系良好,平均加样回收率为104.2%(RSD=0.86%,n=6)。结论:该方法结果准确、重复性好,可用于竹节参药材的质量控制。
Objective : To develop an RP-HPLC method for simultaneous determination of ehikusetsusaponin V and IV a in Panax japonieus of 7 different origins. Methods : Chromatographic separation was performed on a Hibar C18 column, using a step gradient program with the mobile phase of aeetonitrile-0.1% phosphoric acid water solution. The temperature of column was 30 ℃ and the detective wavelength was 203 nm. Results : Chikusetsusaponin V and IV a showed good linear relationships in the ranges of 0.36-7.20 μ g and 0.57-11.40 μg (r〉0.999), respectively. The average recoveries were 96.0% ( RSD=0.73%, n=6 ) and 104.2% ( RSD=0.86%, n=6 ), respectively. Conclusions : The HPLC method is accurate, simple and reproduetive. It is helpful to control the quality of Panaxjaponieus.
出处
《辽宁中医药大学学报》
CAS
2015年第1期52-54,共3页
Journal of Liaoning University of Traditional Chinese Medicine
基金
国家自然科学基金项目(81403095)
北京市市属高校青年拔尖人才培育项目(CIT&TCD201404175
CIT&TCD201404184)
首都中医药护理专项项目(12ZYH08)