天然产物研究与开发 ›› 2024, Vol. 36 ›› Issue (1): 86-93.doi: 10.16333/j.1001-6880.2024.1.010

• 研究简报 • 上一篇    下一篇

基于HPLC-QQQ-MS技术探讨炮制对肉苁蓉中5个活性成分的含量影响

雷慧博,余雅婷,韩   璐,吴   岩,原永芳,俞晓艳*   

  1. 上海交通大学医学院附属第九人民医院药剂科,上海 200011
  • 出版日期:2024-01-23 发布日期:2024-01-23
  • 基金资助:
    上海交通大学医学院附属第九人民医院基础研究助推计划种子基金(JYZZ160)

Influence of processing on the content of five active components in Cistanche tubulosa based on HPLC-QQQ-MS technology

LEI Hui-bo,YU Ya-ting,HAN Lu,WU Yan,YUAN Yong-fang,YU Xiao-yan*   

  1. Department of Pharmacy,Shanghai Ninth People′s Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai 200011,China
  • Online:2024-01-23 Published:2024-01-23

摘要:

炮制一般会对中药材的成分及药效产生重要作用,本文为了探讨炮制加工对肉苁蓉成分的影响,建立了同时测定炮制前后肉苁蓉中肉苁蓉苷F、毛蕊花糖苷、毛蕊花糖苷、2′-乙酰基毛蕊花糖苷和松果菊苷的含量的高效液相色谱-串联三重四极杆质谱法(high-performance liquid chromatography-tandem triple quadrupole mass spectrometry,HPLC-QQQ-MS)的检测方法。采用50%甲醇溶液提取药物粉末,在Agilent Zorbax Eclipse Plus C18(2.1 mm × 150 mm,1.8 μm)的色谱柱上,以0.1%甲酸水(A)-乙腈(B)为流动相进行梯度洗脱,选取负离子多反应监测(multiple reaction monitoring,MRM)模式,以木通苯乙醇苷为内标成分,以进样量1 μL,流速0.3 mL/min,柱温35 ℃,样品管理器温度8 ℃于HPLC-QQQ-MS进行同一批次炮制前后肉苁蓉中这五种成分的含量测定。结果显示5种成分在各自范围内线性关系良好,相关系数(r)在0.992 9~0.998 5之间,平均加样回收率在98.15%~100.2%,相对标准偏差(relative standard deviation,RSD)小于4.6%。所建立的研究方法简便准确,可用于肉苁蓉的质量控制,并用于评价炮制对肉苁蓉含量及药效的影响。

关键词: 肉苁蓉, 炮制, 化学成分, 含量测定, HPLC-QQQ-MS

Abstract:

Processing often plays an important role in determining the components and pharmacological effects of Chinese herbal medicines.In order to investigate the impact of processing on the components of Cistanche tubulosa,a high-performance liquid chromatography-tandem triple quadrupole mass spectrometry (HPLC-QQQ-MS) method was established to simultaneously determine the content of cistanoside F,acteoside,isoacteoside,2′-acetylacteoside and echinacoside in C. tubulosa before and after processing.The medicinal powder was extracted with a 50% methanol solution.The chromatographic separation was achieved on an Agilent Zorbax Eclipse Plus C18 column (2.1 mm × 150 mm,1.8 μm) using a gradient elution of 01% formic acid water (A) and acetonitrile (B) as the mobile phase.Negative ion multiple reaction monitoring (MRM) mode was selected,with calceolarioside B used as the internal standard.The sample injection volume was 1 μL,flow rate was 0.3 mL/min,column temperature was 35 ℃,and the temperature of the autosampler was set at 8 ℃ during the analysis by HPLC-QQQ-MS for the determination of these five components in C. tubulosa before and after processing in the same batch.The results showed good linearity within their respective ranges,with correlation coefficients (r) ranging from 0.992 9 to 0.998 5.The average recovery rates were between 98.15% and 100.2%,and the relative standard deviations (RSD) were less than 4.6%.The established method is simple,accurate,and can be used for quality control of C. tubulosa,as well as evaluating the impact of processing on its content and pharmacological effects.

Key words: Cistanche tubulosa, processing, chemical composition, content determination, HPLC-QQQ-MS

中图分类号:  R927