In Vitro Methods to Study the Interplay of Drug Metabolism and Efflux in the Intestine

被引:13
作者
Siissalo, Sanna [1 ]
Heikkinen, Aki T. [2 ]
机构
[1] Univ Groningen, Dept Pharm, Div Pharmacokinet Toxicol & Targeting, NL-9713 AV Groningen, Netherlands
[2] F Hoffmann La Roche & Cie AG, Nonclin Safety, pRED Pharma Res & Early Dev, Basel, Switzerland
关键词
Absorption pharmacokinetics; drug metabolism; efflux-metabolism interplay; efflux transporters; in vitro methods; intestinal absorption; CACO-2 CELL MONOLAYER; P-GLYCOPROTEIN; MULTIDRUG-RESISTANCE; 1ST-PASS METABOLISM; UDP-GLUCURONOSYLTRANSFERASES; GENE-EXPRESSION; TRANSPORT; PREDICTION; ABSORPTION; PERMEABILITY;
D O I
10.2174/138920013804545241
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review provides an overview of the in vitro methods currently used in studies of intestinal drug metabolism and active efflux with a special emphasis on the efflux-metabolism interplay. These methods include e. g. expressed enzymes or efflux transporters, fractionated intestinal cells, cell lines, primary cells, intestinal segments and other tissue preparations. Pharmacokinetics of efflux-metabolism interplay is often very complicated, possibly involving saturation, stimulation and/or inhibition of one or both of these mechanisms. Parent drug and/or metabolite(s) can be substrates for several enzymes and/or efflux proteins. These detoxifying proteins may alter the exposure of drugs to each other and, consequently, their contributions to the overall drug elimination. Depending on the complexity of the in vitro system used, different kinds of information can be extracted from the results. Simple methods concentrating on single mechanisms provide easily interpretable information, but neglect the interplay between various mechanisms influencing the kinetics in a whole organism. More complex experimental systems mimic the mechanistic complexity of in vivo setting better, but at the same time the interpretation and utilization of the results becomes more challenging. Advantages and limitations of various in vitro systems are addressed and consideration is given to the physiological relevance of the results obtained and there is discussion of approaches for in vitro - in vivo translation of the data.
引用
收藏
页码:102 / 111
页数:10
相关论文
共 101 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]   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
[3]  
BACK D J, 1987, Alimentary Pharmacology and Therapeutics, V1, P339
[4]   Scaling factors for the extrapolation of in vivo metabolic drug clearance from in vitro data:: Reaching a consensus on values of human microsomal protein and hepatocellularity per gram of liver [J].
Barter, Zoe E. ;
Bayliss, Martin K. ;
Beaune, Philip H. ;
Boobis, Alan R. ;
Carlile, David J. ;
Edwards, Robert J. ;
Houston, J. Brian ;
Lake, Brian G. ;
Lipscomb, John C. ;
Pelkonen, Olavi R. ;
Tucker, Geoffrey T. ;
Rostami-Hodjegan, Amin .
CURRENT DRUG METABOLISM, 2007, 8 (01) :33-45
[5]   BDDCS Applied to Over 900 Drugs [J].
Benet, Leslie Z. ;
Broccatelli, Fabio ;
Oprea, Tudor I. .
AAPS JOURNAL, 2011, 13 (04) :519-547
[6]   The Drug Transporter-Metabolism Alliance: Uncovering and Defining the Interplay [J].
Benet, Leslie Z. .
MOLECULAR PHARMACEUTICS, 2009, 6 (06) :1631-1643
[7]   The steady-state Michaelis-Menten analysis of P-glycoprotein mediated transport through a confluent cell monolayer cannot predict the correct Michaelis constant Km [J].
Bentz, J ;
Tran, TT ;
Polli, JW ;
Ayrton, A ;
Ellens, H .
PHARMACEUTICAL RESEARCH, 2005, 22 (10) :1667-1677
[8]   HIV Protease Inhibitors: Garlic Supplements and First-pass Intestinal Metabolism Impact on the Therapeutic Efficacy [J].
Berginc, Katja ;
Trdan, Tina ;
Trontelj, Jurij ;
Kristl, Albin .
BIOPHARMACEUTICS & DRUG DISPOSITION, 2010, 31 (8-9) :495-505
[9]   Simulations of the Nonlinear Dose Dependence for Substrates of Influx and Efflux Transporters in the Human Intestine [J].
Bolger, Michael B. ;
Lukacova, Viera ;
Woltosz, Walter S. .
AAPS JOURNAL, 2009, 11 (02) :353-363
[10]   The use of isolated enterocytes to study Phase I intestinal drug metabolism: validation with rat and pig intestine [J].
Bonnefille, Philippe ;
Sezgin-Bayindir, Zerrin ;
Belkhelfa, Haouaria ;
Arellano, Cecile ;
Gandia, Peggy ;
Woodley, John ;
Houin, Georges .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2011, 25 (01) :104-114