天然产物研究与开发 ›› 2025, Vol. 37 ›› Issue (1): 122-130.doi: 10.16333/j.1001-6880.2025.1.014 cstr: 32307.14.1001-6880.2025.1.014

• 开发研究 • 上一篇    下一篇

基于一测多评法的不同药材中6个环烯醚萜苷类成分的含量测定研究

申凤霞1,2,马   云1,2,李   倩1,2,李蔚群1,2,孙   艳1,2,沈素芹1,2,姜佳峰2*,范建伟1,2*   

  1. 1鲁南制药集团股份有限公司 经方与现代中药融合创新全国重点实验室;2鲁南厚普制药有限公司 中药制药共性技术山东省工程研究中心,临沂 276006
  • 出版日期:2025-01-22 发布日期:2025-01-22
  • 基金资助:
    山东省重点研发计划(重大科技创新工程)(2021CXGC010508)

Content determination of six iridoid glycosides in different medicinal materials by QAMS method

SHEN Feng-xia1,2,MA Yun1,2,LI Qian1,2,LI Wei-qun1,2,SUN Yan1,2,SHEN Su-qin1,2,JIANG Jia-feng2*,FAN Jian-wei1,2*   

  1. 1State Key Laboratory of Integration and Innovation of Classic Formula and Modern Chinese Medicine,Lunan Pharmaceutical Group Co.,Ltd.;2 Shandong Engineering Research Center of Generic Manufacture Technology of Traditional Chinese Medicine,Lunan Hope Pharmaceutical Co.,Ltd.,Linyi 276006,China
  • Online:2025-01-22 Published:2025-01-22

摘要:

基于一测多评法建立同时测定栀子、山茱萸、胡黄连、玄参4种药材中莫诺苷、栀子苷、马钱苷、胡黄连苷Ⅱ、胡黄连苷Ⅰ和哈巴俄苷6个环烯醚萜苷类成分的含量测定方法。采用超高效液相色谱-四极杆/静电场轨道阱高分辨质谱(UPLC-Q-Exactive Orbitrap-MS)技术确定栀子等4种药材中各环烯醚萜苷类成分的专属性;采用高效液相色谱(HPLC)法,以栀子苷为内参照物,采用多点校正法,计算得莫诺苷、马钱苷、胡黄连苷Ⅱ、胡黄连苷Ⅰ、哈巴俄苷5个待测组分的相对校正因子,建立一测多评(quantitative analysis of multi-components by single-marker,QAMS)含量测定方法,并与外标法(external standard method,ESM)实测值进行比较。通过多点校正法计算得到莫诺苷、马钱苷、胡黄连苷Ⅱ、胡黄连苷Ⅰ、哈巴俄苷的相对校正因子分别为0.894 8、1.096 8、1.284 9、1.700 8、1.405 1,QAMS与ESM测定值无显著差异,相对标准偏差小于1.0%。基于一测多评法建立了一种同时测定栀子中栀子苷、山茱萸中莫诺苷和马钱苷、胡黄连中胡黄连苷Ⅱ和胡黄连苷Ⅰ以及玄参中哈巴俄苷6个环烯醚萜苷类成分的含量测定方法,该方法准确、可行,可用于栀子、山茱萸、胡黄连、玄参药材的质量评价,并为其他药材质量评价提供参考。

关键词: 环烯醚萜, 一测多评, 相对校正因子, 含量测定

Abstract:

Based on the concept of "quantitative analysis of multi-components by single-marker",this study aims to establish a method for simultaneously determining the content of six cyclic terpenoid glycosides,namely morroniside,gardenoside,loganin,picroside II,picroside I,and harpagoside,in four medicinal materials:Gardeniae Fructus,Corni Fructus,Picrorhizae Rhizoma,and Scrophulariae Radix.The specificity of each iridoid glycoside in four medicinal herbs were determined using ultra-high performance liquid chromatography coupled with quadrupole/electrostatic field orbitrap high-resolution mass spectrometry (UPLC-Q-Exactive Orbitrap-MS) technology.For the high-performance liquid chromatography (HPLC) method,gardenoside served as the internal reference,and a multi-point calibration method was utilized to calculate the relative correction factors for five components to be tested,namely quantitative analysis of multi-components by single-marker (QAMS),morroniside,loganin,picroside II,picroside I,and harpagoside.A quantitative analysis of multi-components by QAMS method was established and compared with the measured values obtained using the external standard method (ESM).The relative correction factors for morroniside,loganin,picroside II,picroside I,and harpagoside were calculated using the multi-point calibration method,with values of 0.894 8,1.096 8,1.284 9,1.700 8 and 1.405 1,respectively.There was no significant difference in QAMS and ESM measurements,the relative standard deviation is less than 1.0%.Based on the concept of "quantitative analysis of multi-components by single-marker",a method for simultaneously determining the content of six cyclic terpenoid glycosides,including gardenoside in Gardeniae Fructus,morroniside and loganin in Corni Fructus,picroside II and picroside I in Picrorhizae Rhizoma,and harpagoside in Scrophulariae Radix,has been established.This method is accurate and feasible,and can be used for the quality evaluation of Gardeniae Fructus,Corni Fructus,Picrorhizae Rhizoma,and Scrophulariae Radix,which provides a reference for the quality evaluation of other medicinal materials.

Key words: iridoids, quantitative analysis of multi-components by single marker, relative correction factor, content determination

中图分类号:  R284