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一种使用超高效液相色谱法同时测定三七中11种皂苷的快速方法。

A rapid method for the simultaneous determination of 11 saponins in Panax notoginseng using ultra performance liquid chromatography.

作者信息

Guan J, Lai C M, Li S P

机构信息

Institute of Chinese Medical Sciences, University of Macau, Taipa, Macao.

出版信息

J Pharm Biomed Anal. 2007 Aug 15;44(4):996-1000. doi: 10.1016/j.jpba.2007.03.032. Epub 2007 Apr 4.

Abstract

A rapid ultra performance liquid chromatography coupled with photo diode array detection method (UPLC-PDA) was developed for the simultaneous determination of 11 saponins, namely notoginsenoside R1, ginsenoside Rg1, Re, Rf, Rb1, Rg2, Rc, Rb2, Rb3, Rd and Rg3 in Panax notoginseng. The analysis was performed on Acquity UPLC system with Acquity UPLC BEH C(18) column and gradient elution of water and acetonitrile in 12 min. The high correlation coefficient (r(2)>0.9968) values indicated good correlations between the investigated compounds' concentrations and their peak areas within the test ranges. The LOQ and LOD were lower to 0.2-2.4 and 0.1-1.8 ng on column, respectively. The overall intra- and inter-day variations (R.S.D.) of 11 saponins were lower than 3.1%. The developed method was successfully used for the analysis of saponins in P. notoginseng with overall recovery of 93.0-101.6% for the analytes. The results show that UPLC is a powerful tool for analysis of components in Chinese medicines.

摘要

建立了一种快速超高效液相色谱-光电二极管阵列检测法(UPLC-PDA),用于同时测定三七中的11种皂苷,即三七皂苷R1、人参皂苷Rg1、Re、Rf、Rb1、Rg2、Rc、Rb2、Rb3、Rd和Rg3。采用Acquity UPLC系统,在Acquity UPLC BEH C(18)柱上进行分析,水和乙腈梯度洗脱12分钟。高相关系数(r(2)>0.9968)值表明在所研究化合物的浓度与测试范围内的峰面积之间具有良好的相关性。柱上的定量限(LOQ)和检测限(LOD)分别低至0.2 - 2.4 ng和0.1 - 1.8 ng。11种皂苷的日内和日间总体变化(相对标准偏差,R.S.D.)低于3.1%。所建立的方法成功用于三七中皂苷的分析,分析物的总体回收率为93.0 - 101.6%。结果表明,UPLC是分析中药成分的有力工具。

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