天然产物研究与开发 ›› 2015, Vol. 27 ›› Issue (11): 1917-1921.doi: 10.16333/j.1001-6880.2015.11.015

• 研究简报 • 上一篇    下一篇

UPLC-MS法测定羊耳菊中6种成分的含量

侯靖宇1,陆苑1,3,潘洁1,兰燕宇2,3,李春1,3,陈思颖1,3,王永林1,3*   

  1. 1 贵阳医学院 贵州省药物制剂重点实验室;2 贵阳医学院 民族药与中药开发应用教育部工程研究中心;3 贵阳医学院药学院,贵阳 550004
  • 出版日期:2015-11-30 发布日期:2015-12-02

Simultaneous Determination of Six Components in Inula cappa by UPLC-MS

HOU Jing-yu1, LU Yuan1,3, PAN Jie1, LAN Yan-yu2,3, LI Chun1,3, CHEN Si-ying1,3, WANG Yong-lin1,3*   

  1. 1 Guizhou Provincial Key Laboratory of Pharmaceutics,Guiyang Medical College;2  Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education),Guiyang Medical College; 3 School of Pharmacy,Guiyang Medical College,Guizhou Guiyang 550004,China
  • Online:2015-11-30 Published:2015-12-02

摘要: 建立了UPLC-MS/MS同时测定羊耳菊药材中东莨菪苷、1,3-O-二咖啡酰基奎宁酸、木犀草苷、3,4-O-二咖啡酰基奎宁酸、3,5-O-二咖啡酰基奎宁酸、4,5-O-二咖啡酰基奎宁酸6个成分含量的方法。采用Waters BEH C18(2.1 mm×100 mm,1.7 μm)色谱柱,用0.1%甲酸乙腈溶液-0.1%甲酸水溶液作流动相,梯度洗脱,电喷雾电离源(ESI),以多反应离子监测(MRM)检测。6种成分分别在0.058~42.000、0.178~129.630、0.087~63.400、0.288~69.930、0.172~125.500、0.184~134.130 μg/mL浓度范围线性良好,平均回收率为97.84%~105.67%(RSD<1%)。稳定性,重复性及精密度良好,本方法能简便、快捷、有效的测定羊耳菊药材中多种成分含量,为羊耳菊药材的全面质量控制提供了新的方法。

关键词: 羊耳菊, UPLC-MS/MS, 东莨菪苷, 1, 3-O-二咖啡酰基奎宁酸, 木犀草苷, 3, 4-O-二咖啡酰基奎宁酸, 3, 5-O-二咖啡酰基奎宁酸, 含量测定

Abstract: To establish a UPLC-MS/MS method for the determination of scopolin,1,3-di-O-caffeoylquinic acid,luteolin-7-O-β-D-glucoside,3,4-di-O-caffeoylquinic acid,3,5-di-O-caffeoylquinic acid and 4,5-di-O-caffeoylquinic acid in Inula cappa. Using Waters BEH C18 column (2.1 mm×100 mm,1.7 μm) with a gradient solvent system of 0.1% formic acid in acetonitrile-0.1% formic acid in water as mobile phases.Multiple reactions monitoring (MRM) mode was used as detection mode with electro-spray ionization (ESI) source.Good linearities were achieved in the ranges of 0.058-42.000, 0.178-129.630, 0.087-63.400, 0.288-69.930, 0.172~125.500 and 0.184-134.130 μg/mL for the 6 compounds,respectively.The average recoveries were 97.84%-105.67% (RSD<1%).Precision,repeatability and stability were good.The developed method was simple,rapid and effective for the determination of the components in I.cappa. It provided a new method for the quality control of I.cappa.

Key words: Inula cappa, UPLC-MS/MS;scopolin, 1,3-di-O-caffeoylquinic acid;luteolin-7-O-β-D-glucoside;3,4-di-O-caffeoylquinic acid;3,5-di-O-caffeoylquinic acid;content determination

中图分类号: 

R927.2