详细信息

Preparative isolation of ganoderic acid S, ganoderic acid T and ganoderol B from Ganoderma lucidum mycelia by high-speed counter-current chromatography  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Preparative isolation of ganoderic acid S, ganoderic acid T and ganoderol B from Ganoderma lucidum mycelia by high-speed counter-current chromatography

作者:Feng, Na[1,2,3];Wei, Yutian[4];Feng, Jie[1,2,3];Tang, Qingjiu[1,2,3];Zhang, Zhong[1,2,3];Zhang, Jingsong[1,2,3];Han, Wei[4]

机构:[1]Natl Engn Res Ctr Edible Fungi, Minist Agr, Shanghai, Peoples R China;[2]Shanghai Acad Agr Sci, Inst Edible Fungi, Natl R&D Ctr Edible Fungi Proc, Shanghai, Peoples R China;[3]Key Lab Edible Fungi Resources & Utilizat South, Shanghai, Peoples R China;[4]East China Univ Sci & Technol, Sch Pharm, Shanghai, Peoples R China

年份:2018

卷号:32

期号:10

外文期刊名:BIOMEDICAL CHROMATOGRAPHY

收录:;EI(收录号:20232414241772);WOS:【SCI-EXPANDED(收录号:WOS:000445175600001)】;

基金:Key Technology and Application of Ganoderma Trieterpenes Preparation, Grant/Award Number: No. 17391903300

语种:英文

外文关键词:bioactive triterpenes; Ganoderma lucidum; high-performance liquid chromatography; high-speed counter-current chromatography

摘要:Ganoderic acid S, ganoderic acid T and ganoderal B are the main bioactive triterpenes of Ganoderma lucidum. In this study, mycelia of G. lucidum were obtained by two-stage fermentation and then extracted by ethanol and petroleum ether sequentially to obtain crude triterpenes. The crude sample was further purified by recycling high-speed counter-current chromatography with n-hexane-ethyl acetate-methanol-water (7:12:11:5, v/v/v/v) as the optimized two-phase solvent system. A 16.4 mg aliquot of ganoderol B with a purity of 90.4% was separated from 300 mg of the crude sample in a single run. After employing the recycling elution mode of HSCCC with n-hexane-ethyl acetate-methanol-water (6:10:8:4.5, v/v/v/v) for five cycles, 25.7 mg ganoderic acid T and 3.7 mg ganoderic acid S with purities of 97.8 and 83.0%, respectively, were obtained. The purities of three compounds were determined by high-performance liquid chromatography and their chemical structures were identified by NMR and MS data.

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