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白三七及近源种药材指纹图谱与识别模式的构建及其应用研究
引用本文:伍红年,谭诗涵,王元清,雷雅婷,刘瑞莲,Rida Ahme,刘乐平,严建业,王炜.白三七及近源种药材指纹图谱与识别模式的构建及其应用研究[J].中草药,2019,50(1):217-224.
作者姓名:伍红年  谭诗涵  王元清  雷雅婷  刘瑞莲  Rida Ahme  刘乐平  严建业  王炜
作者单位:湖南中医药大学药学院, 湖南 长沙 410208;湖南中医药大学科技创新中心, 湖南 长沙 410208,湖南中医药大学药学院, 湖南 长沙 410208;湖南中医药大学科技创新中心, 湖南 长沙 410208,中南林业科技大学生命科学与技术学院 生物技术与工程实验室, 湖南 长沙 410004,湖南中医药大学药学院, 湖南 长沙 410208;湖南中医药大学科技创新中心, 湖南 长沙 410208,湖南中医药大学附属中西医结合医院 药剂科, 湖南 长沙 410208,湖南中医药大学药学院, 湖南 长沙 410208,湖南中医药大学科技创新中心, 湖南 长沙 410208,湖南中医药大学药学院, 湖南 长沙 410208;湖南中医药大学科技创新中心, 湖南 长沙 410208;中药成药性与制剂制备湖南省重点实验室, 湖南 长沙 410208,湖南中医药大学药学院, 湖南 长沙 410208
基金项目:湖南省中医药管理局重点项目(201811号);湖南中医药大学一层次学科中药学资助(湘教通[2011]76号)
摘    要:目的建立并识别不同产地白三七药材HPLC指纹图谱,为其质量控制及标准制定提供参考。方法采用HPLC法建立白三七指纹图谱,同时应用相似度评价、聚类分析和主成分分析(PCA)对实验数据进行识别,以分析不同产地白三七药材间及同科同属5种药材的相似性及差异性,并通过总量统计矩法对白三七药材共有峰进行定性定量分析。结果白三七指纹图谱共标定16个共有峰,并指认了人参皂苷Rg1、Re、Rb1及竹节参皂苷V、IV、IVa色谱峰;其中竹节参皂苷V和IV在不同批次白三七样品中的质量波动较小;各产地白三七样品除产自四川大凉山样品(S7)外相似度在0.90以上;聚类分析及主成分分析均将白三七样品分为3类;五加科人参属5种药材成分总量统计矩参数差异较大。结论建立的白三七HPLC指纹图谱和化学识别模式可为其质量控制和区分同科同属5种药材提供科学依据。

关 键 词:白三七  五加科  指纹图谱  总量统计矩  聚类分析  主成分分析  人参皂苷Rg1  人参皂苷Re  人参皂苷Rb1  竹节参皂苷V  竹节参皂苷IV  竹节参皂苷IVa
收稿时间:2018/5/9 0:00:00

Establishment and application of chemical fingerprint and pattern recognition for Panacis Japonici Rhizoma
WU Hong-nian,TAN Shi-han,WANG Yuan-qing,LEI Ya-ting,LIU Rui-lian,Rida Ahme,LIU Le-ping,YAN Jian-ye and WANG Wei.Establishment and application of chemical fingerprint and pattern recognition for Panacis Japonici Rhizoma[J].Chinese Traditional and Herbal Drugs,2019,50(1):217-224.
Authors:WU Hong-nian  TAN Shi-han  WANG Yuan-qing  LEI Ya-ting  LIU Rui-lian  Rida Ahme  LIU Le-ping  YAN Jian-ye and WANG Wei
Institution:School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China;Institute of Innovation and Applied Research in Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China,School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China;Institute of Innovation and Applied Research in Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China,Laboratory of Biotechnology and Engineering, College of Life Science and Technology, Central South University of Forestry and Technology, Changsha 410004, China,School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China;Institute of Innovation and Applied Research in Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China,Department of Pharmacy, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha 410208, China,School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China,Institute of Innovation and Applied Research in Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China,School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China;Institute of Innovation and Applied Research in Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China;Hunan Key Laboratory of Druggability and Preparation Modification for Traditional Chinese Medicine, Changsha 410208, China and School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China
Abstract:Objective To establish and identify HPLC fingerprints of Panacis Japonici Rhizoma from different regions, and provide a scientific method for quality its control and standardization.Methods The fingerprints of Panacis Japonici Rhizoma were established based on HPLC method. The similarity evaluation, cluster analysis (CA), and principal component analysis (PCA) were applied for the experimental data, in order to find out the similarities and differences among the 10 batches of Panacis Japonici Rhizoma from different regions. Meanwhile, the qualitatively and quantitatively analyze were adopted in the common peaks of Panacis Japonici Rhizoma by total statistical moment method.Results The HPLC fingerprint with 16 common peaks was established, for the common chemical components, six were identified as ginsenoside Rg1, ginsenoside Re, ginsenoside Rb1, chikusetsusaponin V, chikusetsusaponin IV, an chikusetsusaponin IVa, respectively. Among them, the contents of chikusetsusaponin V and IV in different batches of Panacis JaponiciRhizoma samples showed little differences. The similarities of samples from various regions except S7 were over 0.90. The samples were classified into three categories by CA and PCA methods. The parameters of total statistical moment for five species of Panax genus showed significantly differences.Conclusion The developed HPLC fingerprint of Panacis Japonici Rhizoma combined with chemical pattern recognition can provide a scientific instruction for the quality control of Panacis Japonici Rhizoma and the differentiation of five herb medicines from Panax genus.
Keywords:Panacis Japonici Rhizoma  Araliaceae  fingerprint  total statistical moment  cluster analysis  PCA  ginsenoside Rg1  ginsenoside Re  ginsenoside Rb1  chikusetsusaponin V  chikusetsusaponin IV  chikusetsusaponin IVa
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