Separation and purification of alkaloids from Sophora flavescens Ait. by focused microwave-assisted aqueous two-phase extraction coupled with reversed micellar extraction

被引:52
作者
Zhang, Wei [1 ]
Liu, Xiaoqin [2 ]
Fan, Huajun [2 ,3 ]
Zhu, Dan [2 ]
Wu, Xuehao [2 ]
Huang, Xiaowen [2 ]
Tang, James [3 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Basic Courses, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Guangdong, Peoples R China
[3] Wolverhampton Univ, Fac Sci & Engn, Wolverhampton WV1 1LY, W Midlands, England
关键词
Focused microwave-assisted aqueous two-phase extraction; Reversed micellar extraction; Sophora flavescens Ait; Alkaloids; High performance liquid chromatography; LIQUID-LIQUID-EXTRACTION; SYSTEM; MATRINE; OXYMATRINE; CHROMATOGRAPHY; ULTRASOUND; APOPTOSIS; CELLS; ACID;
D O I
10.1016/j.indcrop.2016.03.052
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Based on advantages of microwave-assisted extraction (MAE), aqueous two-phase extraction (ATPE) and reversed micellar extraction (RME), a novel method of extraction and purification of alkaloids from Sophora flavescens Ait. was put forward by using focused microwave-assisted aqueous two-phase extraction (FMAATPE) coupled with the reversed micellar extraction (RME). The aqueous two-phase system (ATPS) consisted of ethanol and ammonia sulfate was used as extracting solvent, FMAATPE conditions such as the compositions of ATPS, and the extraction temperature, extraction time and solvent-to materials ratio were optimized by orthogonal test through HPLC analysis. Then alkaloids extracted by FMAATPE were further purified with reverse micelles of sodium dodecyl benzene sulfonate/isooctane/n-octanol. The relative purity of total alkaloids in the product was improved greatly by RME from 58.30% to 88.75% (w/w), and purification recovery was higher than that of solvent extraction, ion exchange resin and macroporous adsorption resin. Moreover, the reverse micelles used could be readily recycled by adding salt and water, keeping better extraction performance with about 80% (w/w) of recovery. Thus, the proposed method is easy to adjust, operate and enlarge for better application prospect; the purity of alkaloids obtained meets the requirements of the compound drug preparation. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 238
页数:8
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