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葛根素的高效液相色谱分离和含量测定
引用本文:房其年,吴鹏,杨林. 葛根素的高效液相色谱分离和含量测定[J]. 药学学报, 1983, 18(9): 695-699
作者姓名:房其年  吴鹏  杨林
作者单位:中国医学科学院药物研究所 北京(房其年,吴鹏),中国医学科学院药物研究所 北京(杨林)
摘    要:本文用反相高效液体色谱法对葛根素进行分离和含量测定。色谱柱为partisil-10μmODS,流动相为MeOH-H2O-CHCl8系统,葛根总黄酮在40分钟内可以完全分离。以外标法,在254nm检测对葛根素进行含量测定。本文还报道了利用C10反相制备型液体色谱柱对葛根素和与它难分离的另一组分(暂名OMe葛根素)的制备分离。

关 键 词:反相液相色谱  C16反相柱  葛根素  OMe葛根素  制备型液相色谱
收稿时间:1982-06-02

THE SEPARATION AND DETERMINATION OF PUERARIN BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY
FANG Qi-nian,WU peng and YANG lin. THE SEPARATION AND DETERMINATION OF PUERARIN BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY[J]. Acta pharmaceutica Sinica, 1983, 18(9): 695-699
Authors:FANG Qi-nian  WU peng  YANG lin
Abstract:This paper reports the separation and quantitative determination of puerarin by HPLC method. The column used was Partisil-10μODS with MeOH:H2O:CHCl3 system as the mobile phase. Total flavonoid of pueraria can be separated within 40 minutes. The content of puerarin was determined at 254 nm by external standard method.Preparation and isolation by C16 reverse phase column of a constituent(tentatively named OMe-puerarin) which is separated from puerarin only with much difficulty is also described.
Keywords:Reverse phase liquid chromatography  Preparative liquid chromatography  C_(16) column  Puerarin  OMe-Puerarin  
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