Magnetic ligand fishing combination with high-performance liquid chromatography-diode array detector-mass spectrometry to screen and characterize cyclooxygenase-2 inhibitors from green tea

被引:20
作者
Deng, Xu [1 ]
Shi, Shuyun [2 ]
Li, Simin [3 ]
Yang, Tianlun [1 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Cardiol, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Stomatol Hosp, Changsha 410008, Hunan, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2014年 / 973卷
基金
中国国家自然科学基金;
关键词
Cyclooxygenase-2; Magnetic ligand fishing; HPLC-DAD-MSn; Green tea; Catechin; SELECTIVE COX-2 INHIBITORS; HUMAN SERUM-ALBUMIN; BIOLOGICAL EVALUATION; BIOACTIVE COMPOUNDS; NATURAL-PRODUCTS; CANCER-CELLS; LC-MS; IDENTIFICATION; HPLC; ULTRAFILTRATION;
D O I
10.1016/j.jchromb.2014.10.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cyclooxygenase-2 (COX-2) inhibitors may be used to efficiently treat inflammation or cancer diseases. In the present study, we established a new screening assay based on magnetic Fe3O4@SiO2-COX-2 ligand fishing combination with high-performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MSn) to screen and identify COX-2 inhibitors from green tea. Optimized conditions (pH at 7.4, temperature at 30 degrees C, and incubation time for 30 min) for fishing out COX-2 inhibitors were achieved by testing positive control, celecoxib, with active and inactive COX-2. Notably, immobilized COX-2 showed high stability (remained 94.7% after ten consecutive cycles), reproducibility (RSD < 10% for batch-to-batch evaluation). Finally, eight catechins with COX-2 binding activity were screened in green tea, and their structures were characterized by ultraviolet (UV), accurate molecular weight, diagnostic fragment ions and nuclear magnetic resonance (NMR). Particularly, the COX-2 inhibitory activities of two rare catechins, [(-)-epigallocatechin-3-(3 ''-O-methyl)-gallate (3 ''-O-methyl-EGCG, IC50 = 0.17 +/- 0.03 mu M 0.16 +/- 0.01), (-)-epicatechin-3-(3 ''-O-methyl)-gallate (3 ''-O-methyl-ECG, IC50 = 0.16 +/- 0.02 mu M)], were reported for the first time. The results indicated that the proposed method was a simple, robust and reproducible approach for the discovery of COX-2 inhibitors from complex matrix. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 60
页数:6
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