中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Separation of Four Homoisoflavonoids from Caesalpinia sappan by High-speed Counter-current Chromatography

文献类型:期刊论文

作者Xu, Pingping; Guan, Shuhong; Feng, Ruihong; Tang, Renneng; Guo, Dean
刊名PHYTOCHEMICAL ANALYSIS
出版日期2012-05
卷号23期号:3页码:228-231
关键词HSCCC brazilin 3-deoxysappanone B homoisoflavonoid Caesalpinia sappan
ISSN号0958-0344
DOI10.1002/pca.1347
文献子类Article
英文摘要Introduction - The main chemical constituents of Caesalpinia sappan are homoisoflavonoids. Conventional column chromatographic techniques used for isolation of this type of compounds are tedious, time-consuming and waste solvents. High-speed counter-current chromatography (HSCCC) could be a suitable alternative for the enrichment and purification of these target compounds from traditional Chinese medicine (TCM). Objective - To establish a method to isolate four homoisoflavonoids in one-step separation from C. sappan by HSCCC. Methodology - The crude extract of C. sappan was fractionated by HSCCC using a two-phase solvent system consisting of chloroform-methanol-water (4:3:2, v/v/v). The separation conditions were:flow rate, 1.0mL/min; revolution speed, 900 rpm; detection wavelength, 280 nm; separation temperature, 25 degrees C; sample size, 120 mg crude sample dissolved in a mixture of the upper and lower phases (10 mL each). The retention of the stationary phase was 83%. Results - Five milligrams of 3'-deoxysappanol, 8 mg of 3-deoxysappanone B, 20 mg of 4-O-methylsappanol and 18 mg of brazilin were obtained in one-step separation from 120 mg of an ethyl acetate extracted fraction of C. sappan. Their purities were 99%, 97%, 90% and 85% by HPLC analysis. The mean recoveries of the four compounds were 83%, 86%, 93% and 85%, respectively. Conclusion - The study has shown that HSCCC is effective for the separation and enrichment of the target compounds at a large scale. Copyright (C) 2011 John Wiley & Sons, Ltd.
WOS关键词NITRIC-OXIDE SYNTHASE ; ABSOLUTE-CONFIGURATIONS ; PREPARATIVE ISOLATION ; 3 FLAVONOIDS ; BRAZILIN ; PURIFICATION ; CELLS ; L.
资助项目National Science and Technology Major Project 'Key New Drug Creation and Manufacturing Program', China[2009ZX09308-005] ; National Science and Technology Major Project 'Key New Drug Creation and Manufacturing Program', China[2009ZX09311-001] ; National Science and Technology Major Project 'Key New Drug Creation and Manufacturing Program', China[2009ZX09502-020] ; National Science and Technology Major Project 'Key New Drug Creation and Manufacturing Program', China[2009ZX09304-002] ; Chinese Academy of Sciences[KSCX2-YW-R-166]
WOS研究方向Biochemistry & Molecular Biology ; Plant Sciences ; Chemistry
语种英语
WOS记录号WOS:000302292300006
出版者WILEY-BLACKWELL
源URL[http://119.78.100.183/handle/2S10ELR8/278105]  
专题上海中药现代化研究中心
通讯作者Guo, Dean
作者单位Chinese Acad Sci, Shanghai Res Ctr Modernizat Tradit Chinese Med, Shanghai Inst Mat Med, Natl Engn Lab TCM Standardizat Technol, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Xu, Pingping,Guan, Shuhong,Feng, Ruihong,et al. Separation of Four Homoisoflavonoids from Caesalpinia sappan by High-speed Counter-current Chromatography[J]. PHYTOCHEMICAL ANALYSIS,2012,23(3):228-231.
APA Xu, Pingping,Guan, Shuhong,Feng, Ruihong,Tang, Renneng,&Guo, Dean.(2012).Separation of Four Homoisoflavonoids from Caesalpinia sappan by High-speed Counter-current Chromatography.PHYTOCHEMICAL ANALYSIS,23(3),228-231.
MLA Xu, Pingping,et al."Separation of Four Homoisoflavonoids from Caesalpinia sappan by High-speed Counter-current Chromatography".PHYTOCHEMICAL ANALYSIS 23.3(2012):228-231.

入库方式: OAI收割

来源:上海药物研究所

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