Three-dimensional cell bioreactor coupled with high performance liquid chromatography-mass spectrometry for the affinity screening of bioactive components from herb medicine

被引:8
|
作者
Mou, Zhao-Li [1 ]
Qi, Xiao-Ni [2 ]
Liu, Rui-Lin [2 ]
Zhang, Jing [1 ]
Zhang, Zhi-Qi [1 ,2 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Analyt Chem Life Sci Shaanxi Prov, Xian 710062, Peoples R China
[2] Shaanxi Normal Univ, Minist Educ, Key Lab Med Resources & Nat Pharmaceut Chem, Xian 710062, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell bioreactor; Dynamic seeding; Perfusion culture; On-line affinity screening; Herb medicine; High performance liquid chromatography-mass spectrometry; CULTURE; GROWTH; MICROARRAYS; SCAFFOLDS; PROTEINS; DEVICE; AGENTS; PROBE;
D O I
10.1016/j.chroma.2012.04.041
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An efficient and convenient method, three-dimensional (3-D) cell bioreactor coupled with high performance liquid chromatography-mass spectrometry was developed for affinity screening and analysis of multiple bioactive components from herbal medicines. Cancer cells were cultured on a porous scaffold to form a 3-D cell bioreactor. After interacting with live and fixed cells, the HPLC fingerprinting chromatograms of herbal medicine extract were compared to evaluate the binding properties of herbal components on cells. Model anticancer drugs (paclitaxel and resveratrol) and non-anticancer drugs (ketoprofen and penicillin G) were chosen to investigate the feasibility. When cell-drug interaction time was 30 min. the binding degrees of paclitaxel and resveratrol (each 15 mu g/ml)were 82.2 +/- 7.2% and 66.1 +/- 4.1%, and for ketoprofen and penicillin G (each 15 mu g/ml) were less than 3%. This method was used to screen bioactive components from Polygonum cillinerve (Nakai) Ohwi (PCO) extract, and the binding degrees of two main components in PCO extract (10 mu g/ml), aristolochic acid A and aristolochic acid B, were 63.0 +/- 5.1% and 18.8 +/- 0.9%, respectively. These results demonstrated that this method was highly specific, efficient and convenient for affinity screening and analysis of bioactive components interacted with cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 38
页数:6
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