Cell cultures as tools in biopharmacy

被引:106
作者
Braun, A [1 ]
Hämmerle, S [1 ]
Suda, K [1 ]
Rothen-Rutishauser, B [1 ]
Günthert, M [1 ]
Krämer, SD [1 ]
Wunderli-Allenspach, H [1 ]
机构
[1] ETH Zurich, Fed Inst Technol, Dept Appl Biosci, CH-8057 Zurich, Switzerland
关键词
cell cultures; standardisation; characterisation; passive permeation; P-glycoprotein; efflux;
D O I
10.1016/S0928-0987(00)00164-0
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
A survey is given on a few selected cell culture models that are used for transport studies. They are characterised for growth, transcellular electrical resistance and cytoarchitecture. The importance of standardisation in view of their use as transport models is documented. Their potential for studies on passive permeation and P-glycoprotein-mediated transport is explored and related to published data. Transport studies are presented that were performed in a two-chamber set-up, the Costar(R) "vertical diffusion system". A series of non-homologous compounds showed similar permeability data (P-app) in the different cell cultures. The origin of the cell type had no remarkable influence on passive transcellular permeation. MDCK cells, an epithelial cell line of canine kidney origin, are perfectly suited to screen for passive permeation. They have low expression of transporter proteins and low metabolic activity. In general, they probably represent the best-known epithelial cell line with respect to genetics as well as lipid and protein composition. MDCK cells are easy to handle. Transport experiments can be done between 7 and 14 days after seeding, when the stationary growth phase is reached. To screen for P-glycoprotein substrates, efflux and uptake studies were performed with mdr1-transfected MDCK cells (MDR1-MDCK) in a one-chamber system in the presence or absence of verapamil or cyclosporin A as inhibitor. Evidence is presented why the transfected cells, which express large amounts of P-glycoprotein, are not suitable for two-chamber transport studies. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:S51 / S60
页数:10
相关论文
共 34 条
[1]
P-glycoprotein (P-gp) mediated efflux in Caco-2 cell monolayers: The influence of culturing conditions and drug exposure on P-gp expression levels [J].
Anderle, P ;
Niederer, E ;
Rubas, W ;
Hilgendorf, C ;
Spahn-Langguth, H ;
Wunderli-Allenspach, H ;
Merkle, HP ;
Langguth, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (06) :757-762
[2]
Intestinal drug absorption and metabolism in cell cultures: Caco-2 and beyond [J].
Artursson, P ;
Borchardt, RT .
PHARMACEUTICAL RESEARCH, 1997, 14 (12) :1655-1658
[3]
CORRELATION BETWEEN ORAL-DRUG ABSORPTION IN HUMANS AND APPARENT DRUG PERMEABILITY COEFFICIENTS IN HUMAN INTESTINAL EPITHELIAL (CACO-2) CELLS [J].
ARTURSSON, P ;
KARLSSON, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (03) :880-885
[4]
THE USE OF CULTURED EPITHELIAL AND ENDOTHELIAL-CELLS FOR DRUG TRANSPORT AND METABOLISM STUDIES [J].
AUDUS, KL ;
BARTEL, RL ;
HIDALGO, IJ ;
BORCHARDT, RT .
PHARMACEUTICAL RESEARCH, 1990, 7 (05) :435-451
[5]
POLARIZED MONOLAYERS FORMED BY EPITHELIAL-CELLS ON A PERMEABLE AND TRANSLUCENT SUPPORT [J].
CEREIJIDO, M ;
ROBBINS, ES ;
DOLAN, WJ ;
ROTUNNO, CA ;
SABATINI, DD .
JOURNAL OF CELL BIOLOGY, 1978, 77 (03) :853-880
[6]
Development of Caco-2 cells expressing high levels of cDNA-derived cytochrome P4503A4 [J].
Crespi, CL ;
Penman, BW ;
Hu, M .
PHARMACEUTICAL RESEARCH, 1996, 13 (11) :1635-1641
[7]
Predicting blood-brain barrier permeation from three-dimensional molecular structure [J].
Crivori, P ;
Cruciani, G ;
Carrupt, PA ;
Testa, B .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (11) :2204-2216
[8]
Dirks WG, 1999, IN VITRO CELL DEV-AN, V35, P558
[9]
Upregulation of intercellular adhesion molecule-1 expression on human endothelial cells by tumour necrosis factor-α in an in vitro model of the blood-brain [J].
Dobbie, MS ;
Hurst, RD ;
Klein, NJ ;
Surtees, RAH .
BRAIN RESEARCH, 1999, 830 (02) :330-336
[10]
Engelbertz C, 2000, BLOOD-BRAIN BARRIER AND DRUG DELIVERY TO THE CNS, P33