One-step Separation and Purification of Two Chromones and One Pyrone from Aloe barbadensis Miller: a Comparison Between Reversed-phase Flash Chromatography and High-speed Counter Current Chromatography
文献类型: 外文期刊
作者: Zhong, Jia-Sheng 1 ; Wan, Jin-Zhi 1 ; Ding, Wen-Jing 1 ; Wu, Xiao-Fang 2 ; Xie, Zhi-Yong 1 ;
作者机构: 1.Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
2.Chinese Acad Trop Agr Sci, Anal & Testing Ctr, Haikou 571101, Peoples R China
关键词: chromone;high-speed counter current chromatography;one-step;Comparison;Aloe barbadensis Miller;reversed-phase flash chromatography;pyrone
期刊名称:PHYTOCHEMICAL ANALYSIS ( 影响因子:3.373; 五年影响因子:2.959 )
ISSN: 0958-0344
年卷期: 2014 年 25 卷 3 期
页码:
收录情况: SCI
摘要: Introduction Chromones and pyrones are the major secondary metabolites of Aloe barbadensis Miller. As they are minor components of the plant, an efficient purification procedure for them is of great importance for promoting their pharmacological studies. Objective To develop efficient methods for one-step separation and purification of two chromones (5-((S)-2 '-oxo-4 '-hydroxypentyl)-2-hydroxymethylchromone (1) and 5-((4E)-2 '-oxo-pentenyl)-2-hydroxymethylchromone (3)) and one pyrone (aloenin aglycone (2)) from A. barbadensis via reversed-phase flash chromatography (RP-FC) and high-speed counter current chromatography (HSCCC). Methods The RP-FC separation was performed using methanol:water (26:74, v/v) as the mobile phase at a flow rate of 20 mL/min. A solvent system composed of dichloromethane:methanol:water (3:1.5:1, v/v/v) was used for the HSCCC separation, at a flow rate of 2.0 mL/min. Results A one-step RP-FC operation within 110 min was successfully used for the purification of compounds 1 (27.9 mg, 96.5%), 2 (32.4 mg, 98.2%) and 3 (4.1 mg, 99.0%) from 129 mg of crude sample, and a one-step HSCCC separation within 95 min was successfully implemented for the purification of compounds 1 (31.1 mg, 97.6%), 2 (35.8 mg, 96.7%) and 3 (2.7 mg, 98.1%) from 134 mg of crude sample. Conclusion The developed procedures were efficient, with low cost and high yield, which would afford sufficient amounts of high-purity compounds for chromatographic purposes and pharmacological activity screening. Copyright (c) 2014 John Wiley & Sons, Ltd.
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