Physiologically based pharmacokinetic modelling 2: Predicting the tissue distribution of acids, very weak bases, neutrals and zwitterions
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Poulin, 2000, A priori prediction of tissue:plasma partition coefficients of drugs to facilitate the use of physiologically-bed pharmacokinetic models in drug discovery, J Pharm Sci, 89, 16, 10.1002/(SICI)1520-6017(200001)89:1<16::AID-JPS3>3.0.CO;2-E
Poulin, 2001, Prediction of adipose tissue:plasma partition coefficients for structurally unrelated drugs, J Pharm Sci, 90, 436, 10.1002/1520-6017(200104)90:4<436::AID-JPS1002>3.0.CO;2-P
Poulin, 2002, Prediction of pharmacokinetics prior to in vivo studies. I. Mechanism-based prediction of volume of distribution, J Pharm Sci, 91, 129, 10.1002/jps.10005
Poulin, 1995, A biologically based algorithm for prediction human tissue:blood partition coefficients of organic chemicals, Hum Exp Toxicol, 14, 273, 10.1177/096032719501400307
Poulin, 1995, An algorithm for prediction human tissue:blood partition coefficients of organic chemicals from n-octanol:water partition coefficient data, J Toxicol Environ Health, 46, 101, 10.1080/15287399509532021
Rodgers, 2005, Tissue distribution of basic drugs: accounting for enantiomeric, compound and regional differences amongst β-blocking drugs in rats, J Pharm Sci, 94, 1237, 10.1002/jps.20323
Rodgers, 2005, Physiologically-based pharmacokinetic modeling 1: predicting the tissue distribution of moderate-to-strong bases, J Pharm Sci, 94, 1259, 10.1002/jps.20322
Bree, 1989, Binding to alpha 1-acid glycoprotein and relevant apparent volume of distribution, Progress in Clin Biol Res, 300, 321
1992, Applied pharmacokinetics, principles of therapeutic drug monitoring
Chen, 2004, Studies of phenytoin binding to human serum albumin by high-performance affinity chromatography, J Chromatogr B, 809, 137, 10.1016/j.jchromb.2004.06.012
Aubry, 1995, Comparison of drug binding interactions on human, rat and rabbit serum albumin using high-performance displacement chromatography, Comp Biochem Physiol, 112C, 257
Rahman, 1993, Studies of interaction of caprofen and its enantiomers with albumin I: mechanism of binding studied by dialysis and spectroscopic methods, Biochem Pharmacol, 46, 1721, 10.1016/0006-2952(93)90576-I
1982, Phospholipids, 2p
Nelson, 1967, The phospholipids composition of plasma in various mammalian species, Lipids, 2, 323, 10.1007/BF02532119
Kawai, 1994, Physiologically based pharmacokinetic study on a cyclosporine derivative, SDZ IMM 125, J Pharmacokin Biopharm, 22, 327, 10.1007/BF02353860
Ballard, 2003, Prediction of in vivo tissue distribution from in vitro data. 3. Correlation between in vitro and in vivo tissue distribution of a homologous series of nine 5-n-alkyl-5-ethyl barbituric acids, Pharm Res, 20, 864, 10.1023/A:1023912318133
Berezhkovskiy, 2004, Volume of distribution at steady state for a linear pharmacokinetic system with peripheral elimination, J Pharm Sci, 93, 1628, 10.1002/jps.20073
Bjorkman, 1990, Comparative tissue concentration profiles of fentanyl and alfentanil in humans predicted from tissue/blood partition data obtained in rats, Anaesthesiology, 72, 865, 10.1097/00000542-199005000-00017
Gueorguieva, 2004, Development of a whole body physiologically based model to characterise the pharmacokinetics of benzodiazepines 1: estimation of rat tissue-plasma partition coefficients, J Pharmacokin Pharmacodyn, 31, 269, 10.1023/B:JOPA.0000042737.14033.c6
Igari, 1983, Prediction of diazepam disposition in the rat and man by a physiologically based pharmacokinetic model, J Pharmacokin Biopharm, 11, 577, 10.1007/BF01059058
Bjorkman, 1996, Determination of the steady state distribution of midazolam in the rat, J Pharm Sci, 85, 887, 10.1021/js960113+
Tsuji, 1983, Physiologically based pharmacokinetic model for β-lactam antibiotics I: tissue distribution and elimination in rats, J Pharm Sci, 72, 1239, 10.1002/jps.2600721103
Yamazaki, 2004, Computational prediction of the plasma protein-binding percent of diverse pharmaceutical compounds, J Pharm Sci, 93, 1480, 10.1002/jps.20059
Lee, 1988, Kinetics and mechanisms of etodolac degradation in aqueous solutions, J Pharm Sci, 77, 81, 10.1002/jps.2600770116
Brooks, 1990, The pharmacokinetics of etodolac enantiomers in the rat: lack of pharmacokinetic interaction between enantiomers, Drug Metab Dispos, 18, 471
Sawada, 1985, Prediction of the disposition of nine weakly acidic and six weakly basic drugs in humans from pharmacokinetic parameters in rats, J Pharmacokin Biopharm, 13, 477, 10.1007/BF01059331
Zhao, 2002, High-throughput LogP measurement using parallel Liquid chromatography/ultraviolet/mass spectrometry and sample pooling, Rapid Commum Mass Spectrom, 16, 1548, 10.1002/rcm.749
Chatton, 1990, Salictclic acid permeability properties of the rabbit cortical collecting duct, Am J Physiol, 259, F613
Yoshikawa, 1984, Effect of pregnancy on tissue distribution of salicylate in rats, J Pharm Sci, 12, 500
Guntert, 1986, Acceleration of the elimination of tenoxicam by cholestyramine in the dog, J Pharmacol Exp Ther, 238, 295
Kwon, 1987, Physiological pharmacokinetic model for the distribution and elimination of tenoxicam, Int J Pharmaceut, 37, 219, 10.1016/0378-5173(87)90032-9
Worboys, 1997, Kinetics of metabolism in rat liver slices III. Relationship between metabolic clearance and slice uptake, Drug Metab Dispos, 25, 460
Kessel, 2001, Continuum solvent model studies of the interactions of an anticonvulsant drug with a lipid bilayer, Biophys J, 80, 2536, 10.1016/S0006-3495(01)76225-X
Tanaka, 2000, Dose-dependant pharmacokinetics of cyclosporine A in rats: events in tissues, Drug Metab Dispos, 28, 582
Poulin, 2002, Prediction of pharmacokinetics prior to in vivo studies.II. Generic physiologically based pharmacokinetic models of drug disposition, J Pharm Sci, 91, 1358, 10.1002/jps.10128
Sakiya, 1985, Prediction of ftorafur disposition in rats and man by a physiologically based pharmacokinetic model, Int J Pharm, 25, 347, 10.1016/0378-5173(85)90174-7
Okezaki, 1988, Structure-tissue distribution relationship based on physiological pharmacokinetics for NY-198, a new antimicrobial agent, and the related pyridonecarboxylic acids, Drug Metab Dispos, 16, 865
Naber, 2003, Antibiotic therapy-rationale and evidence for optimal drug concentrations in prostatic and seminal fluid and in prostatic tissue, Andrologia, 35, 331, 10.1111/j.1439-0272.2003.tb00868.x
Martin, 1993
Davies, 1993, Physiological parameters in laboratory animals and humans, Pharm Res, 10, 1093, 10.1023/A:1018943613122
1995, Clinical pharmacokinetics: Concepts and applications, 502
Bjorkman, 2002, Prediction of the volume of distribution of a drug: which tissue-plasma partition coefficients are needed?, J Pharm Pharmacol, 54, 1237, 10.1211/002235702320402080
Tsuji, 1989, Age-related change in tissue-to-plasma partition coefficient of cefazolin for noneliminating organs in the rat, J Pharm Sci, 78, 535, 10.1002/jps.2600780705
Kang, 1997, Physiologically based pharmacokinetic models of 2′, 3′-dideoxyinosine, Pharm Res, 14, 337, 10.1023/A:1012002206007
Brooks, 1991, Enantioselective pharmacokinetics of etodolac in the rat: tissue distribution, tissue binding and in vitro metabolism, J Pharm Sci, 80, 1058, 10.1002/jps.2600801112
Yoshikawa, 1984, Effect of pregnancy on tissue distribution of salicylate in rats, Drug Metab Dispos, 12, 500
Ebling, 1994, From piecewise to full physiologic pharmacokinetic modelling: applied to thiopental disposition, J Pharmacokin Biopharm, 22, 252, 10.1007/BF02353622
Harrison, 1977, Physiologically based pharmacokinetic model for digoxin distribution and elimination in the rat, J Pharm Sci, 66, 1138, 10.1002/jps.2600660822
Funakoshi, 2005, Role of organic anion transporting polypeptide 2 in pharmacokinetics of digoxin and -methyldigoxin in rats, J Pharm Sci, 94, 1196, 10.1002/jps.20346
Lin, 1982, In vitro and In vivo evaluation of the tissue-to-blood partition coefficient for physiological pharmacokinetic models, J Pharmacokin Biopharm, 10, 637, 10.1007/BF01062545
Granero, 1998, Distribution of ceftazidime in rat tissues, Biopharm Drug Dispos, 19, 473, 10.1002/(SICI)1099-081X(199810)19:7<473::AID-BDD125>3.0.CO;2-M
Olanoff, 1979, Controlled release of tetracycline II: development of an in vivo flow-limited pharmacokinetic model, J Pharm Sci, 68, 1151, 10.1002/jps.2600680925
1995, Clinical pharmacokinetics: Concepts and applications, 149
Ooie, 1997, Quantitiaive brain microdialysis study on the mechanism of quinolones distribution in the central nervous system, Drug Metab Dispos, 25, 784
Takasawa, 1997, Distributed model analysis of 3′-Azido-3′-deoxythymidine and 2′,3′-dideoxyinosine distribution in brain tissue and cerebrospinal fluid, J Pharmacol Exp Ther, 282, 1509
Yu, 1995, Analysis of tissue distribution of valproate in guinea-pigs: evidence for its capacity limited distribution, Pharm Res, 12, 421, 10.1023/A:1016264821127
Jusko, 1976, Plasma and tissue protein binding of drugs in pharmacokinetics, Drug Metab Rev, 5, 43, 10.3109/03602537608995839
Kullak-Ublick, 1999, Regulation of organic anion and drug transporters of the sinusoidal membrane, J Hepatol, 31, 563, 10.1016/S0168-8278(99)80054-3
Ayrton, 2001, Role of transport proteins in drug absorption, distribution and excretion, Xenobiotic, 31, 469, 10.1080/00498250110060969
Olanoff, 1980, Controlled release of tetracycline III: a physiological pharmacokinetic model of the pregnant rat, J Pharmacokin Biopharm, 8, 599, 10.1007/BF01060056
Funakoshi, 2003, Role of P-glycoprotein in pharmacokinetics and drug interactions of digoxin and -methyldigoxin in rats, J Pharm Sci, 92, 1455, 10.1002/jps.10416
Fichtl, 1991, Tissue binding versus plasma binding of drugs: general principles and pharmacokinetic consequences, Adv Drug Res, 20, 117, 10.1016/B978-0-12-013320-8.50006-X
Schuhman, 1987, Prediction of drug distribution in vivo on the basis of in vitro binding data, Biopharm Drug Dispos, 8, 73, 10.1002/bdd.2510080109
Pierson, 1978, Extracellular water measurements: organ tracer kinetics of bromide and sucrose in rats and man, Am J Physiol, 235, F254