Predicting oral drug absorption and hepatobiliary clearance: Human intestinal and hepatic in vitro cell models

被引:24
作者
Fearn, RA [1 ]
Hirst, BH [1 ]
机构
[1] Univ Newcastle, Sch Med, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会;
关键词
intestine; liver; drug absorption; hepatobiliary clearance; bioavailability; membrane transport;
D O I
10.1016/j.etap.2005.06.002
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Membrane transport proteins control the uptake and efflux of many drugs in tissues including the intestine, liver and kidneys and thus play important roles in drug absorption, distribution and excretion. With the development of high throughput screening in an industrial environment, the importance of having appropriate in vitro systems to study drug transporter function, regulation, and interactions are invaluable. Cell lines are efficient tools in screening individual transport processes. In this review, we focus on the processes involved in the absorption and hepatobiliary clearance of drugs and the potential of cell lines to model such process, paying particular attention to the use of Caco-2 and HepG2 cells. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:168 / 178
页数:11
相关论文
共 88 条
[1]   Comparative studies on in vitro methods for evaluating in vivo function of MDR1 P-glycoprotein [J].
Adachi, Y ;
Suzuki, H ;
Sugiyama, Y .
PHARMACEUTICAL RESEARCH, 2001, 18 (12) :1660-1668
[2]   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
[3]   The drug efflux-metabolism alliance: biochemical aspects [J].
Benet, LZ ;
Cummins, CL .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 50 :S3-S11
[4]  
BENET LZ, 1990, GOODMAN GILMANS PHAR, P1707
[5]   Characterization of MPP+ secretion across human intestinal Caco-2 cell monolayers:: role of P-glycoprotein and a novel Na+-dependent organic cation transport mechanism [J].
Bleasby, K ;
Chauhan, S ;
Brown, CDA .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (03) :619-625
[6]   Expression of drug-metabolizing enzymes, nuclear transcription factors and ABC transporters in Caco-2 cells [J].
Borlak, J ;
Zwadlo, C .
XENOBIOTICA, 2003, 33 (09) :927-943
[7]   Efficient in vitro vectorial transport of a fluorescent conjugated bile acid analogue by polarized hepatic hybrid WIF-B and WIF-B9 cells [J].
Bravo, P ;
Bender, V ;
Cassio, D .
HEPATOLOGY, 1998, 27 (02) :576-583
[8]   Predicting drug absorption: How nature made it a difficult problem [J].
Burton, PS ;
Goodwin, JT ;
Vidmar, TJ ;
Amore, BM .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 303 (03) :889-895
[9]   MRP2, a human conjugate export pump, is present and transports fluo 3 into apical vacuoles of Hep G2 cells [J].
Cantz, T ;
Nies, AT ;
Brom, M ;
Hofmann, AF ;
Keppler, D .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (04) :G522-G531
[10]   Transport and epithelial secretion of the cardiac glycoside, digoxin, by human intestinal epithelial (Caco-2) cells [J].
Cavet, ME ;
West, M ;
Simmons, NL .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (06) :1389-1396