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首页|期刊导航|中国药房|NIRS结合PLS算法快速测定西洋参饮片中人参皂苷Rg1、Re、Rb1的总含量

NIRS结合PLS算法快速测定西洋参饮片中人参皂苷Rg1、Re、Rb1的总含量

左春芳 梁雪琪 喻俊峰 吕亚新 张贤良

中国药房2017,Vol.28Issue(36):5140-5143,4.
中国药房2017,Vol.28Issue(36):5140-5143,4.DOI:10.6039/j.issn.1001-0408.2017.36.26

NIRS结合PLS算法快速测定西洋参饮片中人参皂苷Rg1、Re、Rb1的总含量

Rapid Determination of Ginsenoside Rg1, Re, Rb1 in Panax quinquefolius Pieces by NIRS Combined with PLS Algorithm

左春芳 1梁雪琪 2喻俊峰 1吕亚新 1张贤良3

作者信息

  • 1. 解放军第150中心医院药剂科,河南洛阳471031
  • 2. 洛阳理工学院附属中学,河南洛阳471031
  • 3. 解放军第72660部队,河南三门峡472400
  • 折叠

摘要

Abstract

OBJECTIVE:To establish the method for rapid determination of ginsenoside Rg1,Re,Rb1 in Panax quinquefolius crude slices.METHODS:HPLC method was adopted to determine the total contents of ginsenoside Rg1,Re,Rb1 (as reference value).NIRS combined PLS algorithm were adopted to establish total quantitative correction model of ginsenoside Rg1,Re,Rb1.According to the reference,62 samples were collected.The spectrum was pretreated with multivariate scattering correction method combined with first order derivative method.The optimal ranges of wave band for ginsenoside Rg1,Re,Rb1 were 7 664.23-5 236.05 cm-1.RESULTS:Methodology validation for total content determination of ginsenoside Rg1,Re,Rb1 was in line with the requirements.For total quantitative correction model of ginsenoside Rg1,Re,Rb1,related correction set coefficient was 0.991 03,corrected mean square deviation 0.010 26.CONCLUSIONS:The method is rapid,accurate,simple and free of contamination.It can be used for rapid determination of ginsenoside Rg1,Re,Rb1 in P quinquefolius crude slices.

关键词

西洋参/人参皂苷/近红外漫反射外光谱技术/偏最小二乘法

Key words

Panax quinquefolius/Ginsenoside/NIRS/PLS

分类

医药卫生

引用本文复制引用

左春芳,梁雪琪,喻俊峰,吕亚新,张贤良..NIRS结合PLS算法快速测定西洋参饮片中人参皂苷Rg1、Re、Rb1的总含量[J].中国药房,2017,28(36):5140-5143,4.

基金项目

济南军区后勤科研面上项目(No.CJN15J074) (No.CJN15J074)

中国药房

OA北大核心CSTPCD

1001-0408

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