Caco-2 monolayers in experimental and theoretical predictions of drug transport (Reprinted from Advanced Drug Delivery Reviews, vol 22, pg 67-84, 1996)

被引:1038
作者
Artursson, P [1 ]
Palm, K
Luthman, K
机构
[1] Uppsala Univ, Dept Pharmaceut, Uppsala Biomed Ctr, Box 580, S-75123 Uppsala, Sweden
[2] Uppsala Univ, Dept Organ Pharmaceut Chem, Uppsala Biomed Ctr, S-75123 Uppsala, Sweden
关键词
drug transport; drug absorption; intestinal epithelium; Caco-2; cell monolayer; partition coefficient; hydrogen bonding potential; desolvation energy; molecular surface area; in vitro-in vivo correlation;
D O I
10.1016/S0169-409X(00)00128-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review examines the use of Caco-2 monolayers in the prediction of intestinal drug absorption. First, the different routes of drug transport in Caco-2 monolayers are compared with those seen in vivo. Second, the prediction of drug absorption in vivo from transport experiments in cell monolayers is discussed for different classes of drugs. Finally, the use of Caco-2 monolayers as a reference model in physico-chemical and theoretical predictions of drug absorption is discussed. We conclude that Caco-2 monolayers can be used to identify drugs with potential absorption problems, and possibly also to select drugs with optimal passive absorption characteristics from series of pharmacologically active molecules generated in drug discovery programs. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:27 / 43
页数:17
相关论文
共 113 条
[81]   INTERACTION OF PRISTINAMYCIN I-A WITH P-GLYCOPROTEIN IN HUMAN INTESTINAL EPITHELIAL-CELLS [J].
PHUNGBA, V ;
WARNERY, A ;
SCHERMAN, D ;
WILS, P .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 288 (02) :187-192
[82]   IAM CHROMATOGRAPHY - AN IN-VITRO SCREEN FOR PREDICTING DRUG MEMBRANE-PERMEABILITY [J].
PIDGEON, C ;
ONG, SW ;
LIU, HL ;
QIU, XX ;
PIDGEON, M ;
DANTZIG, AH ;
MUNROE, J ;
HORNBACK, WJ ;
KASHER, JS ;
GLUNZ, L ;
SZCZERBA, T .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (04) :590-594
[83]  
PINTO M, 1983, BIOL CELL, V47, P323
[84]   THE INFLUENCE OF MOLECULAR VOLUME AND HYDROGEN-BONDING ON PEPTIDE-TRANSPORT ACROSS EPITHELIAL MEMBRANES [J].
POTTS, RO ;
GUY, RH .
PHARMACEUTICAL RESEARCH, 1993, 10 (04) :635-636
[85]   Use of a Biophysical-Kinetic Model to Understand the Roles of Protein Binding and Membrane Partitioning on Passive Diffusion of Highly Lipophilic Molecules Across Cellular Barriers [J].
Raub, Thomas J. ;
Barsuhn, Craig L. ;
Williams, Lawrence R. ;
Deckers, Douglas E. ;
Sawada, Geri A. ;
Ho, Norman F. H. .
JOURNAL OF DRUG TARGETING, 1993, 1 (04) :269-286
[86]   COMPARISON OF THE PERMEABILITY CHARACTERISTICS OF A HUMAN COLONIC EPITHELIAL (CACO-2) CELL-LINE TO COLON OF RABBIT, MONKEY, AND DOG INTESTINE AND HUMAN DRUG ABSORPTION [J].
RUBAS, W ;
JEZYK, N ;
GRASS, GM .
PHARMACEUTICAL RESEARCH, 1993, 10 (01) :113-118
[87]  
RUBAS W, 1995, STP PHARMA SCI, V5, P93
[88]   TRANSCELLULAR PERMEABILITY OF CHLORPROMAZINE DEMONSTRATING THE ROLES OF PROTEIN-BINDING AND MEMBRANE PARTITIONING [J].
SAWADA, GA ;
HO, NFH ;
WILLIAMS, LR ;
BARSUHN, CL ;
RAUB, TJ .
PHARMACEUTICAL RESEARCH, 1994, 11 (05) :665-673
[89]   A METHOD TO DETERMINE THE ABILITY OF DRUGS TO DIFFUSE THROUGH THE BLOOD-BRAIN-BARRIER [J].
SEELIG, A ;
GOTTSCHLICH, R ;
DEVANT, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :68-72
[90]  
Stein W. D., 1967, MOVEMENT MOL CELL ME, P65