摘要
目的:增加麻仁丸的含量测定方法,建立同时检测芍药苷,柚皮苷及橙皮苷的测定方法。方法:采用C18色谱柱;水-乙腈为流动相,进行梯度洗脱;流速1.0mL·min-1;检测波长230nm。结果:线性范围:芍药苷0.03075~0.2050g·L-1(r2=0.9997),柚皮苷0.1148~0.7650g·L-1,r2=0.9997,橙皮苷0.01275~0.08500g·L-1(r2=0.9996);平均回收率:芍药苷99.4%,RSD=0.9%(n=6),柚皮苷99.7%,RSD=1.2%(n=6),橙皮苷98.6%,RSD=2.0%(n=6)。结论:该方法操作简便、准确,重复性好,可用于麻仁丸的质量控制。
Objective:The method of determination of the paeoniflorin,naringin and hesperidin in Maren Pills processed by HPLC was established. Methods:The column was C18 Column, the mobile phase was water acetonitrile for gradient elution, the flow rate was 1.0 mL·min-1 and the detection wavelength was 230 nm. Results:The linear range of Paeoniflorin was 0.030 75~0.205 0 g·L-1 (r2=0.999 7), the average recovery was 99.4%, RSD=0.9%(n=6).The linear range of naringin was 0.012 75~0.085 00 g·L-1 (r2=0.999 7), the average recovery was 99.7%,RSD=1.2%(n=6).The linear range of hesperidin was 0.012 75~0.085 00 g·L-1 (r2=0.999 6), the average recovery was 98.6%, RSD=2.0%(n=6).Conclusions: This method is simple,rapid and accurate with good reproducibility,it is suitable for the quality control of Maren Pills processed.
出处
《中国药品标准》
CAS
2010年第6期442-446,共5页
Drug Standards of China