摘要
目的:建立补肾口服液中淫羊藿苷的高效液相色谱定量方法。方法:采用ZORBAX SB-C18(4.6mm×250mm,5μm)色谱柱,流动相为甲醇-水(63:37),流速1.0 mL/min,检测波长为270nm,柱温25℃。结果:淫羊藿苷浓度为0.0224~0.448mg范围内线性关系良好(r=0.9995),平均加样回收率为100.08%,RSD为1.25%(n=6)。结论:该方法简便、准确、灵敏度高、专属性强、重现性好,可作为补肾口服液的质量控制方法。
Objective: To establish an HPLC method for detemination of Icariin in busen oral liquid.Method: The separation was per formed on a ZORBAX SB-C18 column(4.6mm× 250mm,5μm).The mobile phase was CH3OH-H2O(63:37).gradient elution at flow rate of 1mL/min,the eluent monitored by a DAD detector at 270 nm,The column temperature was 25℃.Result: The linear range of Icariin was 0.0224~0.448mg,r=0.9995。The average recovery was 100.08%,RSD=1.25%。Conclusion: The method is simple,ac curate,sensitive,specific and reproducible.it can be used for quality evaluation and quality control of busen oral liquid.
出处
《江西中医学院学报》
2012年第3期48-50,共3页
Journal of Jiangxi College of Traditional Chinese Medicine