A novel sample preparation and on-line HPLC-DAD-MS/MS-BCD analysis for rapid screening and characterization of specific enzyme inhibitors in herbal extracts: Case study of α-glucosidase

被引:41
作者
Li, D. Q. [1 ]
Zhao, J. [1 ]
Xie, J. [1 ]
Li, S. P. [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Macao, Peoples R China
关键词
alpha-Glucosidase inhibitors; LC-DAD-MS/MS-BCD; Corilagin; Ellagic acid; PERFORMANCE LIQUID-CHROMATOGRAPHY; PHENOLIC-COMPOUNDS; IDENTIFICATION; FRUITS;
D O I
10.1016/j.jpba.2013.08.029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Drug discovery from complex mixture like Chinese herbs is a challenge and extensive false positives make the obtainment of specific bioactive compounds difficult. In the present study, a novel sample preparation method was proposed to rapidly reveal the specific bioactive compounds from complex mixtures using a-glucosidase as a case. Firstly, aqueous and methanol extracts of 500 traditional Chinese medicines were carried out with the aim of finding new sources of a-glucosidase inhibitors. As a result, the extracts of fruit of Terminalia chebula (FTC), flowers of Rosa rugosa (FRR) and Eugenia caryophyllota (FEC) as well as husk of Punica granatum (HPG) showed high inhibition on a-glucosidase. On-line liquid chromatography-diode array detection-tandem mass spectrometry and biochemical detection (HPLC-DAD-MS/MS-BCD) was performed to rapidly screen and characterize a-glucosidase inhibitors in these four extracts. After tentative identification, most of compounds with inhibitory activity in the investigated crude extracts were found to be tannins commonly recognized as non-specific enzyme inhibitors in vitro. Subsequently, the four extracts were treated with gelatin to improve specificity of the on-line system. Finally, two compounds with specific a-glucosidase inhibition were identified as corilagin and ellagic acid. The developed method could discover specific alpha-glucosidase inhibitors in complex mixtures such as plant extracts, which could also be used for discovery of specific inhibitors of other enzymes. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:130 / 135
页数:6
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