血人参水溶性化学成分的UHPLC-DAD-Q-TOF-MS/MS分析

杨雅欣; 廖尚高; 王正; 李勇军; 梁妍; 郝小燕; 王永林

doi:10.13422/j.cnki.syfjx.2014230063

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血人参水溶性化学成分的UHPLC-DAD-Q-TOF-MS/MS分析

化学与分析 | 更新时间：2024-01-04

- 血人参水溶性化学成分的UHPLC-DAD-Q-TOF-MS/MS分析
- Analysis of Water-soluble Chemical Constituents of Indigoferae Stachyoidis Radix by UHPLC-DAD-Q-TOF-MS/MS
- 中国实验方剂学杂志 2014年20卷第23期页码：63-67
- 作者机构：
- 作者简介：
- 基金信息：
  
  贵州省中药现代化科技产业研究开发专项(黔科合ZY字[2013]3006号,黔科合中药字[2011]5081号,黔科合重G字[2013]4001号);贵阳市现代药业计划项目(筑科合同[2011204]号)
- DOI：10.13422/j.cnki.syfjx.2014230063
  中图分类号： R284.1
- 纸质出版日期：2014
- 稿件说明：
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杨雅欣, 廖尚高, 王正, 等. 血人参水溶性化学成分的UHPLC-DAD-Q-TOF-MS/MS分析[J]. 中国实验方剂学杂志, 2014,20(23):63-67.

YANG Ya-xin, LIAO Shang-gao, WANG Zheng, et al. Analysis of Water-soluble Chemical Constituents of Indigoferae Stachyoidis Radix by UHPLC-DAD-Q-TOF-MS/MS[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(23): 63-67.
杨雅欣, 廖尚高, 王正, 等. 血人参水溶性化学成分的UHPLC-DAD-Q-TOF-MS/MS分析[J]. 中国实验方剂学杂志, 2014,20(23):63-67. DOI： 10.13422/j.cnki.syfjx.2014230063.

YANG Ya-xin, LIAO Shang-gao, WANG Zheng, et al. Analysis of Water-soluble Chemical Constituents of Indigoferae Stachyoidis Radix by UHPLC-DAD-Q-TOF-MS/MS[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(23): 63-67. DOI： 10.13422/j.cnki.syfjx.2014230063.

摘要

目的: 采用超高压液相色谱-二级管阵列检测器-四级杆-飞行时间质谱(UHPLC-DAD-Q-TOF-MS/MS)联用技术

在负离子模式下开展血人参水煎煮提取物中化学成分的一级及二级质谱研究

分析血人参的水溶性化学成分. 方法: 液相色谱条件为Synergi Hydro-RP色谱柱(2.0 mm×100 mm

2.5 μm)

0.1%甲酸乙腈-0.1%甲酸水溶液梯度洗脱.质谱条件为Bruker Daltonics micro TOF-Q质谱仪

电喷雾离子源

负离子模式

毛细管电压2 800 V

二级质谱碰撞能量11～25 eV;源内碰撞诱导裂解(CID)及其二级质谱条件:源内CID能量25～35 eV

碰撞能量12～17 eV. 结果: 共推测出15个化合物的化学结构

分别为没食子酸、原儿茶酸-3-O-葡萄糖苷、原儿茶酸、原儿茶醛、丁香酸葡萄糖苷、龙胆酸、儿茶素、表儿茶素、原花青素B类同分异构体4个、棕儿茶素A类同分异构体3个. 结论: 除化合物表儿茶素外

其他14个化合物均为该植物首次报道.研究结果为血人参及其制剂的开发和质量标准制定提供了依据.

Abstract

Objective: An ultra-high-pressure liquid chromatography-diode-array detection-quadrupole time-of-flight mass spectrometric (UHPLC-DAD-Q-TOF-MS/MS) method was established to analyze the chemical constituents of the decoction of Indigoferae Stachyoidis Radix. Method: The chromatographic separation was performed on a Synergi Hydro-RP (2.00 mm×100 mm

2.5 μm) column using a mobile phase consisting of 0.1% formic acid in water(A)and 0.1% formic acid in acetonitrile (B). The flow rate was 0.3 g· L-1 and the mass spectrometer was Bruker Daltonics micro TOF-Q equipped with an electrospray ionization (ESI) source. The MS and MS/MS spectra were recorded in the negative ion mode.The capillary voltage is 2 800 V. The range of collision energy of MS2 is 11 eV from 25 eV. And a condition of Endogenous collision induced dissociation (CID) is 25 eV from 35 eV

the corresponded MS2 energy is 12 eV from 17 eV. Result: 15 compounds in the decoction of Indigoferae Stachyoidis Radix were well isolated and identified as gallic acid

protocatechuic acid-3-O-glucoside

protocatechuic aldehyde

protocatechuic acid

glucosyringic acid

gentisic acid

catechin

epicatechin

four procyanidines and three gambiriins. Conclusion: In addition to the compound epicatechin

the other 14 compounds were first reported in this plant. The results have formed the basis for the exploitation of Indigoferae Stachyoidis Radix and the establishment of a quality control method for Indigoferae Stachyoidis Radix.

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