摘要
目的建立超高效液相色谱(UPLC)法测定龙胆药材中活性成分的方法。方法采用L9(34)正交表安排实验,确定最佳提取条件。色谱柱:Shimadzu C18(3.0 mm×75 mm,1.7μm);流动相:乙腈-0.1%磷酸(V∶V=5.5∶94.5),流速0.80 ml/min;检测波长235,270 nm;柱温为40℃。结果獐芽菜苦苷、龙胆苦苷分别在0.154 8~1.858 0 mg/ml,0.322~5.152mg/ml范围内呈良好的线性关系,平均回收率分别为102.09%,RSD=1.68%(n=6);103.80%,RSD=1.11%(n=6)。结论采用UPLC法控制龙胆质量,操作简单,结果准确,方法可行。
Objective To establish a method for the determination of swertiamarin and gentiopicroside in root of Gentiana scabra Bge. by UPLC. Methods By L9 ( 34 ) orthogonal design, an optimal condition was confirmed. The separation was performed on Shimadzu C18(3.0 mm ×75 mm,1.7μm) column, the mobile phase was Acetonitrile -0. 1% Phosphorylation(V: V = 5.5: 94.5 ). The flow rate was 0.8 ml/min, the detection 'wavelength was 235nm, 270nm, and the column temperature was 40℃. Resuits This method had good linearity in the range of 0. 322 -5. 152mg/ml,and the average recovery was102.09 % with RSD of 1.68% for swertiamarin. It had good linearity in the range of 0. 1548 - 1. 858 mg/ml , and the average recovery was 103.80% with RSD of 1.11% for gentiopicroside. Conclusion This method is simple , accurate , and suitable for the quality control of root of Gentiana scabra Bge. by UPLC.
出处
《时珍国医国药》
CAS
CSCD
北大核心
2009年第5期1079-1080,共2页
Lishizhen Medicine and Materia Medica Research
基金
国家科技支持计划(No.2006DAI06A05-08)