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离子对高效液相色谱法测定甘草及其制剂中甘草酸的含量

[Determination of glycyrrhizin in glycyrrhiza and it's preparations by ion-pair HPLC].

作者信息

Liu S, Jiang X, Zheng Y, Xu P

出版信息

Hua Xi Yi Ke Da Xue Xue Bao. 1993 Mar;24(1):111-4.

PMID:8340083
Abstract

Glycyrrhizin is the main component of glycyrrhiza. In this article an Ion-pair high performance liquid chromatography (HPLC) method is described for the determination of glycyrrhizin in two kinds of glycyrrhiza from different origins and twelve kinds of Chinese traditional patent medicine containing glycyrrhiza. A reversed phase system was used, including an ODS column with water and methanol (36:64) as the mobile phase which contained 5mmol/L tetra-n-butyl ammonium hydroxide and was adjusted to pH 6.0 by phosphoric acid. The column temperature was 35 degrees C; the detection was performed at 254 nm. Under this condition glycyrrhizin could be separated from other components. The limit of detection was 13ng, and the average recovery was 99.85%. During the experiments, we studied the concentration of counter-ion, the mixing ratio of methanol to water, the pH of the mobile phase and column temperature and their effect on the capacity factor of compound and resolution. We also studied the method of pre-treatment for the samples. The determination method is simple and accurate.

摘要

甘草酸是甘草的主要成分。本文描述了一种离子对高效液相色谱(HPLC)法,用于测定两种不同产地的甘草及十二种含甘草的中成药中的甘草酸。采用反相系统,使用ODS柱,以水和甲醇(36:64)为流动相,流动相中含有5mmol/L四丁基氢氧化铵,并用磷酸调节至pH 6.0。柱温为35℃;检测波长为254nm。在此条件下,甘草酸可与其他成分分离。检测限为13ng,平均回收率为99.85%。实验过程中,研究了反离子浓度、甲醇与水的混合比例、流动相pH值和柱温及其对化合物容量因子和分离度的影响。还研究了样品的预处理方法。该测定方法简单准确。

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