摘要
目的建立同时测定壮骨方煮散中抗骨质疏松有效成分朝藿定C和淫羊藿苷含量的高效液相色谱(HPLC)法。方法采用高效液相色谱法,色谱柱为Plastisil C18柱(250 mm×4.6 mm,5μm),以乙腈-水(27∶73)为流动相,流速为1.0 m L/min,检测波长为270 nm,柱温为30℃。结果朝藿定C进样量在0.050-2.016μg范围内与峰面积线性关系良好(r=0.999 9),淫羊藿苷进样量在0.032-1.280μg范围内与峰面积线性关系良好(r=0.999 9);朝藿定C和淫羊藿苷平均加样回收率分别为98.94%和100.99%,RSD分别为1.69%和1.07%(n=6)。结论该方法简便,重复性和稳定性良好,适用于壮骨方煮散中朝藿定C和淫羊藿苷的质量控制。
Objective To establish an HPLC method for the content determination of active ingredients(epimedin C and icariin)of antiosteoporosis in Zhuanggufang Zhusan.Methods HPLC was used with the Plastisil C_(18) column(250 mm × 4.6 mm,5 μm),acetonitrilewater(27:73) as the mobile phase at a flow rate of 1.0 mL/min,the detecting wavelength of 270 nm,and the column temperature at30 ℃.Results The good linear was over the range of 0.050-2.016 μg for epimedin C(r=0.999 9) and the average recovery(n=6) was 98.94%with RSD of 1.69%;the good linear was over the range of 0.032-1.280 μg for icariin(r=0.999 9) and the average recovery(n=6) was 100.99%with RSD of 1.07%.Conclusion The method is simple and with high repeatability and stability,which can be used for the quality control of Zhuanggufang Zhusan.
出处
《中国药业》
CAS
2016年第22期64-66,共3页
China Pharmaceuticals
基金
广西科学研究与科技开发计划科技攻关项目
项目编号:桂科攻14124004-1-26