摘要
目的:建立测定七归滴丸中阿魏酸、三七皂苷R1、人参皂苷Rg1、人参皂苷Rb1的含量测定方法。方法:采用C18柱(4.6 mm×150 mm,5μm),流动相为甲醇-0.6%冰醋酸(30∶70),检测波长为323 nm,测定阿魏酸;采用C18柱(4.6 mm×250 mm,5μm),乙腈-水梯度洗脱,流速0.8 mL·min-1,检测波长203 nm,测定三七皂苷R1、人参皂苷Rg1、人参皂苷Rb1。结果:阿魏酸的回收率为99.18%(RSD 1.4%);三七皂苷R1、人参皂苷Rg1、人参皂苷Rb1的回收率分别为98.77%(RSD1.71%),98.94%(RSD 1.58%),99.48%(RSD 1.65%)。结论:此法准确、可靠,重复性好,可用于控制七归滴丸的质量。
Objective: To develop a method for the determination of ferulic acid,notoginsenoside R1,ginsenoside Rg1 and Rb1 in Qigui drop pill by HPLC.Method: The content of ferulic acid was quantified by HPLC.A C18 column was used with the mobile phase of methanol-0.6% glacial acetic acid solution(30∶ 70),at the detection wavelength of 323 nm.The content of sanchi notoginsenoside R1,ginsenoside Rg1 and Rb1 was quantified by HPLC.A C18 column was used with the mobile phase of acetonitrile-water gradient elution.Equilibrium was 0.8 min and the wavelength of detector was set at 203 nm.Result: The average recovery of ferulic acid was 99.18%(RSD 1.4%).The average recoveries of notoginsenoside R1,ginsenoside Rg1 and Rb1 were 98.77%(RSD 1.71%),98.94%(RSD 1.58%) and 99.48%(RSD 1.65%).Conclusion: The method is accurate,reliable and reproducible.It can be used for the quality control of Qigui drop pill.
出处
《中国实验方剂学杂志》
CAS
北大核心
2012年第15期112-116,共5页
Chinese Journal of Experimental Traditional Medical Formulae