首页 | 本学科首页   官方微博 | 高级检索  
检索        

UPLC法测定莲菊感冒胶囊中3种成分的含量
引用本文:何迅,迟明艳,李勇军,王爱民,王永林,兰燕宇.UPLC法测定莲菊感冒胶囊中3种成分的含量[J].中国新药杂志,2011,20(1):79.
作者姓名:何迅  迟明艳  李勇军  王爱民  王永林  兰燕宇
作者单位:(贵阳医学院药学院,贵阳 550004)
基金项目:贵州省科技计划项目(黔科合I字[2009]4001号);贵阳市科技计划项目([2009]筑科合同字第9-3-04号)
摘    要: 目的: 建立同时测定莲菊感冒胶囊中1,5-O-二咖啡酰基-奎宁酸、3,5-O-二咖啡酰基-奎宁酸、3,4-O-二咖啡酰基-奎宁酸的超高效液相色谱(UPLC)分析方法。方法:采用Waters Acquity UPLC系统,Acquity UPLC BEH C18色谱柱(100 mm×2.1mm,1.7 μm),流动相为乙腈-0.1%磷酸,以流速为0.2 mL?min-1进行梯度洗脱;柱温:45℃;样品经50%乙醇超声提取后用UPLC-PDA进行分析检测,检测波长为325 nm。结果:1,5-O-二咖啡酰基奎宁酸、3,5-O-二咖啡酰基奎宁酸、3,4-O-二咖啡酰基奎宁酸3种被测成分在线性范围内均具有良好的线性关系(r≥0.999 8);平均回收率在99.1%~101.7%之间,RSD≤2.5%。结论:UPLC分离效果及重复性好,且快速、简便,可作为莲菊感冒胶囊的质量控制方法。

关 键 词:超高效液相色谱(UPLC)  莲菊感冒胶囊  质量控制

Simultaneous determination of 3 components in Lianju Ganmao capsule by UPLC
HE Xun,CHI Ming-yan,WANG Ai-min,LAN Yan-yu,LI Yong-jun,WANG Yong-lin.Simultaneous determination of 3 components in Lianju Ganmao capsule by UPLC[J].Chinese Journal of New Drugs,2011,20(1):79.
Authors:HE Xun  CHI Ming-yan  WANG Ai-min  LAN Yan-yu  LI Yong-jun  WANG Yong-lin
Institution:HE Xun,CHI Ming-yan,WANG Ai-min,LAN Yan-yu,LI Yong-jun,WANG Yong-lin(School of Pharmacy,Guiyang Medical College,Guiyang 550004,China)
Abstract:Objective:  To establish an ultra performance liquid chromatography (UPLC) method for simultaneous determination of 3 components in Lianju Ganmo capsule. Methods: The analyses were performed on Waters Acquity UPLC system. An Acquity UPLC BEH C18 column (100 mm×2.1 mm, 1.7 μm) was used for all analyses. The investigated compounds were separated with gradient mobile phase consisting of 0.1% phosphoric acid and acetonitrile. The flow velocity was 0.2 mL?min-1.The temperature of sample manager was set at 45℃. UPLC-PDA system was used to analysis the sample which the sample mix in 50% ethanol through ultrasound .The detection wavelength was 325 nm. Results: The investigated compounds including 1,5-O-dicaffeoyl-quinic acid 3,5-O-dicaffeoyl-quinic acid 3,4-O-dicaffeoyl-quinic acid, had a good linearity (r≥0.999 8) over the tested ranges. The average recovery was 99.1% to 101.7% with RSD≤2.5%. Conclusion: The developed UPLC method is simple, sensitive and accurate with good repeatability, which is available for quality control of Lianju Ganmao capsule.
Keywords:ultra performance liquid chromatography (UPLC)  Lianju Ganmao capsule  quality control
本文献已被 CNKI 等数据库收录!
点击此处可从《中国新药杂志》浏览原始摘要信息
点击此处可从《中国新药杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号