摘要
目的:建立反相高效液相色谱法测定巫山淫羊藿中朝藿定C含量和特征图谱的研究。方法:采用SUNFIRETM C18柱(250mm×4.6mm,5μm)色谱柱,以25%乙腈的水溶液为流动相进行洗脱,流速lmL·min-1,检测波长270nm,柱温30℃;通过对24份巫山淫羊藿药材HPLC图谱的检测,建立了巫山淫羊藿的HPLC特征图谱共有模式,并对11批药材进行了相似度比较。结果:巫山淫羊藿中各种成分均达到基线分离,朝藿定C的线性范围为0.071~2.82μg(r=0.9999),平均回收率(n=5)为101.3%(RSD=0.73%);得到的色谱图可为巫山淫羊藿药材专属性的特征图谱研究提供参考,为巫山淫羊藿药材的鉴别和质量控制提供了实验依据。结论:本法快速、准确、可靠,可用于巫山淫羊藿药材的质量评价。
Objective:To establish a quantitative evaluation method of epimedin C by RP-HPLC.Methods:Epimeidin C was base-isolated on the column of SUNFIRETM C18(250 mm×4.6 mm,5 μm);The mobile phase was 25% acetonitrile aqueous solution at a flow rate of 1 mL·min-1;The detection wavelength was set at 270 nm and column temperature at 30 ℃.Results:The compounds were base-isolated.The linear range of epimedin C was 0.071-2.82 μg(r =0.9999);The average recovery(n=5) was 101.3%(RSD=0.73%).The mutual mode of HPLC specific chromatograms was set up and the similar degrees to the crude drugs were compared.Conclusion:The method is rapid and reliable,and it was capable of effectively controlling the quality of Epimedium wushanense T. S. Ying.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2009年第8期1316-1319,共4页
Chinese Journal of Pharmaceutical Analysis
基金
中国药典2010版修订项目(国家药典中发[2008]99号)
陕西省教育厅基金资助项目(09JK319)