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Volumn 11, Issue 1, 2009, Pages 155-166

Modelling and PBPK simulation in drug discovery

Author keywords

Absorption; Clearance; Distribution; PBPK; Pharmacokinetics

Indexed keywords

ALPRENOLOL; DICLOFENAC; DILTIAZEM; FELODIPINE; KETOCONAZOLE; METOPROLOL; NICARDIPINE; OMEPRAZOLE; PHENYTOIN;

EID: 65549096369     PISSN: 15507416     EISSN: None     Source Type: Journal    
DOI: 10.1208/s12248-009-9088-1     Document Type: Article
Times cited : (164)

References (63)
  • 1
    • 0019974098 scopus 로고
    • Interspecies scaling, allometry, physiological time, and the ground plan of pharmacokinetics
    • H. Boxenbaum. Interspecies scaling, allometry, physiological time, and the ground plan of pharmacokinetics. J. Pharmacokinet. Biopharm. 10:201-227 (1982).
    • (1982) J. Pharmacokinet. Biopharm. , vol.10 , pp. 201-227
    • Boxenbaum, H.1
  • 2
    • 0029918773 scopus 로고    scopus 로고
    • Interspecies scaling: Predicting pharmacokinetic parameters of antiepileptic drugs in humans from animals with special emphasis on clearance
    • I. Mahmood, and J. D. Balian. Interspecies scaling: Predicting pharmacokinetic parameters of antiepileptic drugs in humans from animals with special emphasis on clearance. J. Pharm. Sci. 85:411-414 (1996).
    • (1996) J. Pharm. Sci. , vol.85 , pp. 411-414
    • Mahmood, I.1    Balian, J.D.2
  • 4
    • 0032921527 scopus 로고    scopus 로고
    • Prediction of hepatic metabolic clearance based on interspecies allometric scaling techniques and in vitro - In vivo correlations
    • T. Lave, P. Coassolo, and B. Reigner. Prediction of hepatic metabolic clearance based on interspecies allometric scaling techniques and in vitro - in vivo correlations. Clin. Pharmacokinet. 36:211-231 (1999a).
    • (1999) Clin. Pharmacokinet. , vol.36 , pp. 211-231
    • Lave, T.1    Coassolo, P.2    Reigner, B.3
  • 5
    • 0034102018 scopus 로고    scopus 로고
    • Dose-dependent pharmacokinetics of cyclosporin A in rats: Events in tissues
    • C. Tanaka, R. Kawai, and M. Rowland. Dose-dependent pharmacokinetics of cyclosporin A in rats: Events in tissues. Drug Metab. Dispos. 28:582-589 (2000).
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 582-589
    • Tanaka, C.1    Kawai, R.2    Rowland, M.3
  • 6
    • 0042161645 scopus 로고    scopus 로고
    • Whole body pharmacokinetic models
    • I. Nestorov. Whole body pharmacokinetic models. Clin. Pharmacokinet. 42:883-908 (2003).
    • (2003) Clin. Pharmacokinet. , vol.42 , pp. 883-908
    • Nestorov, I.1
  • 7
    • 0028342648 scopus 로고
    • Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
    • J. B. Houston. Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance. Biochem. Pharmacol. 47:1469-1479 (1994).
    • (1994) Biochem. Pharmacol. , vol.47 , pp. 1469-1479
    • Houston, J.B.1
  • 9
    • 0030911863 scopus 로고    scopus 로고
    • The use of human hepatocytes to select compounds based on their expected hepatic extraction ratios in humans
    • T. Lave, S. Dupin, C. Schmitt, B. Valles, G. Ubeaud, R. C. Chou, D. Jaeck, and P. Coassolo. The use of human hepatocytes to select compounds based on their expected hepatic extraction ratios in humans. Pharm. Res. 14:152-155 (1997).
    • (1997) Pharm. Res. , vol.14 , pp. 152-155
    • Lave, T.1    Dupin, S.2    Schmitt, C.3    Valles, B.4    Ubeaud, G.5    Chou, R.C.6    Jaeck, D.7    Coassolo, P.8
  • 10
    • 0032733974 scopus 로고    scopus 로고
    • Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
    • R. S. Obach. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metab. Dispos. 27:1350-1359 (1999).
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 11
    • 0033966128 scopus 로고    scopus 로고
    • A priori prediction of tissue: Plasma partition coefficients of drugs to facilitate the use of physiologically-based pharmacokinetic models in drug discovery
    • P. Poulin, and F. P. Theil. A priori prediction of tissue: Plasma partition coefficients of drugs to facilitate the use of physiologically-based pharmacokinetic models in drug discovery. J. Pharm. Sci. 89:16-35 (2000).
    • (2000) J. Pharm. Sci. , vol.89 , pp. 16-35
    • Poulin, P.1    Theil, F.P.2
  • 12
    • 0035044107 scopus 로고    scopus 로고
    • Prediction of adipose tissue: Plasma partition coefficients for structurally unrelated drugs
    • P. Poulin, K. Schoenlein, and F. P. Theil. Prediction of adipose tissue: plasma partition coefficients for structurally unrelated drugs. J. Pharm. Sci. 90:436-447 (2001).
    • (2001) J. Pharm. Sci. , vol.90 , pp. 436-447
    • Poulin, P.1    Schoenlein, K.2    Theil, F.P.3
  • 13
    • 0036144815 scopus 로고    scopus 로고
    • Prediction of pharmacokinetics prior to in vivo studies. 1. Mechanism-based prediction of volume of distribution
    • P. Poulin, and F. P. Theil. Prediction of pharmacokinetics prior to in vivo studies. 1. Mechanism-based prediction of volume of distribution. J. Pharm. Sci. 91:129-156 (2002a).
    • (2002) J. Pharm. Sci. , vol.91 , pp. 129-156
    • Poulin, P.1    Theil, F.P.2
  • 14
    • 2642536176 scopus 로고    scopus 로고
    • Volume of distribution at steady state for a linear pharmacokinetic system with peripheral elimination
    • L. M. Berezhkovskiy. Volume of distribution at steady state for a linear pharmacokinetic system with peripheral elimination. J. Pharm. Sci. 93(6):1628-40 (2004).
    • (2004) J. Pharm. Sci. , vol.93 , Issue.6 , pp. 1628-1640
    • Berezhkovskiy, L.M.1
  • 15
    • 21344469211 scopus 로고    scopus 로고
    • Physiologically based pharmacokinetic modeling 1: Predicting the tissue distribution of moderate-to-strong bases
    • T. Rodgers, D. Leahy, and M. Rowland. Physiologically based pharmacokinetic modeling 1: Predicting the tissue distribution of moderate-to-strong bases. J. Pharm. Sci. 94:1259-1276 (2005).
    • (2005) J. Pharm. Sci. , vol.94 , pp. 1259-1276
    • Rodgers, T.1    Leahy, D.2    Rowland, M.3
  • 16
    • 33745055239 scopus 로고    scopus 로고
    • Physiologically based pharmacokinetic modeling 2: Predicting the tissue distribution of acids, very weak bases, neutrals and zwitterions
    • T. Rodgers, and M. Rowland. Physiologically based pharmacokinetic modeling 2: Predicting the tissue distribution of acids, very weak bases, neutrals and zwitterions. J. Pharm. Sci. 95(6):1238-57 (2006).
    • (2006) J. Pharm. Sci. , vol.95 , Issue.6 , pp. 1238-1257
    • Rodgers, T.1    Rowland, M.2
  • 17
    • 34247556082 scopus 로고    scopus 로고
    • Mechanistic approaches to volume of distribution predictions: Understanding the processes
    • T. Rodgers, and M. Rowland. Mechanistic approaches to volume of distribution predictions: Understanding the processes. Pharm. Res. 24(5):918-33 (2007).
    • (2007) Pharm. Res. , vol.24 , Issue.5 , pp. 918-933
    • Rodgers, T.1    Rowland, M.2
  • 18
    • 0036075799 scopus 로고    scopus 로고
    • Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition
    • P. Poulin, and F. P. Theil. Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition. J. Pharm. Sci. 91:1358-1370 (2002b).
    • (2002) J. Pharm. Sci. , vol.91 , pp. 1358-1370
    • Poulin, P.1    Theil, F.P.2
  • 19
    • 0037452445 scopus 로고    scopus 로고
    • Utility of physiologically based pharmacokinetic models to drug development and rational drug discovery candidate selection
    • F. P. Theil, T. W. Guentert, S. Haddad, and P. Poulin. Utility of physiologically based pharmacokinetic models to drug development and rational drug discovery candidate selection. Toxicol. Lett. 138:29-49 (2003).
    • (2003) Toxicol. Lett. , vol.138 , pp. 29-49
    • Theil, F.P.1    Guentert, T.W.2    Haddad, S.3    Poulin, P.4
  • 20
    • 27944458924 scopus 로고    scopus 로고
    • An evaluation of the utility of physiologically based models of pharmacokinetics in early drug discovery
    • N. Parrott, N. Paquereau, P. Coassolo, and T. Lave. An evaluation of the utility of physiologically based models of pharmacokinetics in early drug discovery. J. Pharm. Sci. 94:2327-2343 (2005).
    • (2005) J. Pharm. Sci. , vol.94 , pp. 2327-2343
    • Parrott, N.1    Paquereau, N.2    Coassolo, P.3    Lave, T.4
  • 21
    • 29944443496 scopus 로고    scopus 로고
    • Application of a generic physiologically-based pharmacokinetic model to the estimation of xenobiotic levels in rat plasma
    • F. A. Brightman, D. E. Leahy, G. E. Searle, and S. Thomas. Application of a generic physiologically-based pharmacokinetic model to the estimation of xenobiotic levels in rat plasma. Drug Metab. Dispos. 34:84-93 (2006a).
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 84-93
    • Brightman, F.A.1    Leahy, D.E.2    Searle, G.E.3    Thomas, S.4
  • 22
    • 29944443496 scopus 로고    scopus 로고
    • Application of a generic physiologically-based pharmacokinetic model to the estimation of xenobiotic levels in human plasma
    • F. A. Brightman, D. E. Leahy, G. E. Searle, and S. Thomas. Application of a generic physiologically-based pharmacokinetic model to the estimation of xenobiotic levels in human plasma. Drug Metab. Dispos. 34:94-101 (2006b).
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 94-101
    • Brightman, F.A.1    Leahy, D.E.2    Searle, G.E.3    Thomas, S.4
  • 23
    • 33646124969 scopus 로고    scopus 로고
    • A novel strategy for physiologically based predictions of human pharmacokinetics
    • H. M. Jones, N. Parrott, K. Jorga, and T. Lave. A novel strategy for physiologically based predictions of human pharmacokinetics. Clin. Pharmacokinet. 45(5):511-542 (2006).
    • (2006) Clin. Pharmacokinet. , vol.45 , Issue.5 , pp. 511-542
    • Jones, H.M.1    Parrott, N.2    Jorga, K.3    Lave, T.4
  • 24
    • 34748925493 scopus 로고    scopus 로고
    • Prediction of human pharmacokinetics using physiologically based modeling: A retrospective analysis of 26 clinically tested drugs
    • S. S. De Buck, V. K. Sinha, L. A. Fenu, M. J. Nijsen, C. E. Mackie, and R. A. H. J. Gilissen. Prediction of human pharmacokinetics using physiologically based modeling: A retrospective analysis of 26 clinically tested drugs. Drug Metab. Dispos. 35(10):1766-80 (2007a).
    • (2007) Drug Metab. Dispos. , vol.35 , Issue.10 , pp. 1766-1780
    • De Buck, S.S.1    Sinha, V.K.2    Fenu, L.A.3    Nijsen, M.J.4    Mackie, C.E.5    Gilissen, R.A.H.J.6
  • 25
    • 40549113994 scopus 로고    scopus 로고
    • Evaluation of a generic physiologically based pharmacokinetic model for lineshape analysis
    • S. A. Peters. Evaluation of a generic physiologically based pharmacokinetic model for lineshape analysis. Clin. Pharmacokinet. 47(4):261-75 (2008).
    • (2008) Clin. Pharmacokinet. , vol.47 , Issue.4 , pp. 261-275
    • Peters, S.A.1
  • 26
    • 34248680469 scopus 로고    scopus 로고
    • Physiologically based pharmacokinetics in drug development and regulatory science: A workshop report (Georgetown University, Washington, DC, May 29-30, 2002)
    • M. Rowland, L. Balant, and C. Peck. Physiologically based pharmacokinetics in drug development and regulatory science: A workshop report (Georgetown University, Washington, DC, May 29-30, 2002). AAPS PharmSci. 6:E6 (2004).
    • (2004) AAPS PharmSci. , vol.6
    • Rowland, M.1    Balant, L.2    Peck, C.3
  • 27
    • 0027275566 scopus 로고
    • Physiological parameters in laboratory animals and humans
    • B. Davies, and T. Morris. Physiological parameters in laboratory animals and humans. Pharm. Res. 10:1093-1095 (1993).
    • (1993) Pharm. Res. , vol.10 , pp. 1093-1095
    • Davies, B.1    Morris, T.2
  • 30
    • 0023033053 scopus 로고
    • Man versus beast: Pharmacokinetic scaling in mammals
    • J. Mordenti. Man versus beast: Pharmacokinetic scaling in mammals. J. Pharm. Sci. 75:1028-1040 (1986).
    • (1986) J. Pharm. Sci. , vol.75 , pp. 1028-1040
    • Mordenti, J.1
  • 31
    • 0033016936 scopus 로고    scopus 로고
    • Interspecies pharmacokinetic comparisons and allometric scaling of napsagatran, a low molecular weight thrombin inhibitor
    • T. Lave, R. Portmann, G. Schenker, A. Gianni, A. Guenzi, M. A. Girometta, and M. Schmitt. Interspecies pharmacokinetic comparisons and allometric scaling of napsagatran, a low molecular weight thrombin inhibitor. J. Pharm. Pharmacol. 51: 85-91 (1999b).
    • (1999) J. Pharm. Pharmacol. , vol.51 , pp. 85-91
    • Lave, T.1    Portmann, R.2    Schenker, G.3    Gianni, A.4    Guenzi, A.5    Girometta, M.A.6    Schmitt, M.7
  • 32
    • 23944515735 scopus 로고    scopus 로고
    • A novel model for prediction of human drug clearance by allometric scaling
    • H. Tang, and M. Mayersohn. A novel model for prediction of human drug clearance by allometric scaling. Drug Metab. Dispos. 33: 1297-1303 (2005).
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 1297-1303
    • Tang, H.1    Mayersohn, M.2
  • 33
    • 65549144913 scopus 로고    scopus 로고
    • A global examination of allometric scaling for predicting tested drugs
    • H. Tang, and M. Mayersohn. A global examination of allometric scaling for predicting tested drugs. Drug Metab. Dispos. 35:1766-1780 (2007).
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 1766-1780
    • Tang, H.1    Mayersohn, M.2
  • 34
    • 33747154776 scopus 로고    scopus 로고
    • Prediction of human drug clearance from animal data: Application of the rule of exponents and 'fu corrected intercept method' (FCIM)
    • I. Mahmood. Prediction of human drug clearance from animal data: Application of the rule of exponents and 'fu corrected intercept method' (FCIM). J. Pharm. Sci. 95(8):1810-1821 (2006).
    • (2006) J. Pharm. Sci. , vol.95 , Issue.8 , pp. 1810-1821
    • Mahmood, I.1
  • 36
    • 0031723045 scopus 로고    scopus 로고
    • Correlation of plasma clearance of 54 extensively metabolized drugs between humans and rats: Mean allometric coefficient of 0.66
    • W. L. Chiou, G. Robbie, S. M. Chung, T. C. Wu, and C. Ma. Correlation of plasma clearance of 54 extensively metabolized drugs between humans and rats: Mean allometric coefficient of 0.66. Pharm. Res. 15(9):1474-9 (1998).
    • (1998) Pharm. Res. , vol.15 , Issue.9 , pp. 1474-1479
    • Chiou, W.L.1    Robbie, G.2    Chung, S.M.3    Wu, T.C.4    Ma, C.5
  • 37
    • 0344333422 scopus 로고    scopus 로고
    • Prediction of hepatic clearance from microsomes, hepatocytes, and liver slices
    • J. B. Houston, and D. J. Carlile. Prediction of hepatic clearance from microsomes, hepatocytes, and liver slices. Drug Metab. Rev. 29:891-922 (1997).
    • (1997) Drug Metab. Rev. , vol.29 , pp. 891-922
    • Houston, J.B.1    Carlile, D.J.2
  • 38
    • 3543026365 scopus 로고    scopus 로고
    • Comparison of the use of liver models for predicting drug clearance using in vitro kinetic data from hepatic microsomes and isolated hepatocytes
    • K. Ito, and J. B. Houston. Comparison of the use of liver models for predicting drug clearance using in vitro kinetic data from hepatic microsomes and isolated hepatocytes. Pharm. Res. 21:785-792 (2004).
    • (2004) Pharm. Res. , vol.21 , pp. 785-792
    • Ito, K.1    Houston, J.B.2
  • 39
    • 4143108324 scopus 로고    scopus 로고
    • Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations
    • H. M. Jones, and J. B. Houston. Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations. Drug Metab. Dispos. 32:973-982 (2004).
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 973-982
    • Jones, H.M.1    Houston, J.B.2
  • 40
    • 0036891948 scopus 로고    scopus 로고
    • The influence of nonspecific microsomal binding on apparent intrinsic clearance, and its prediction from physicochemical properties
    • R. P. Austin, P. Barton, S. L. Cockroft, M. C. Wenlock, and R. J. Riley. The influence of nonspecific microsomal binding on apparent intrinsic clearance, and its prediction from physicochemical properties. Drug Metab. Dispos. 30:1497-1503 (2002).
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 1497-1503
    • Austin, R.P.1    Barton, P.2    Cockroft, S.L.3    Wenlock, M.C.4    Riley, R.J.5
  • 41
    • 14044251501 scopus 로고    scopus 로고
    • The binding of drugs to hepatocytes and its relationship to physicochemical properties
    • R. P. Austin, P. Barton, S. Mohmed, and R. J. Riley. The binding of drugs to hepatocytes and its relationship to physicochemical properties. Drug Metab. Dispos. 33:419-425 (2005).
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 419-425
    • Austin, R.P.1    Barton, P.2    Mohmed, S.3    Riley, R.J.4
  • 42
    • 33645100073 scopus 로고    scopus 로고
    • Binding of drugs to hepatic microsomes: Comment and assessment of current prediction methodology with recommendation for improvement
    • D. Hallifax, and J. B. Houston. Binding of drugs to hepatic microsomes: Comment and assessment of current prediction methodology with recommendation for improvement. Drug Metab. Dispos. 34(4):724-26 (2006).
    • (2006) Drug Metab. Dispos. , vol.34 , Issue.4 , pp. 724-726
    • Hallifax, D.1    Houston, J.B.2
  • 44
    • 0030850023 scopus 로고    scopus 로고
    • Scaling factors to relate drug metabolic clearance in hepatic microsomes, isolated hepatocytes, and the intact liver: Studies with induced livers involving diazepam
    • D. J. Carlile, K. Zomorodi, and J. B. Houston. Scaling factors to relate drug metabolic clearance in hepatic microsomes, isolated hepatocytes, and the intact liver: Studies with induced livers involving diazepam. Drug Metab. Dispos. 25:903-911 (1997).
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 903-911
    • Carlile, D.J.1    Zomorodi, K.2    Houston, J.B.3
  • 47
    • 0021746592 scopus 로고
    • Prediction of the volumes of distribution of basic drugs in humans based on data from animals
    • Y. Sawada, M. Hanano, Y. Sugiyama, H. Harashima, and T. Iga. Prediction of the volumes of distribution of basic drugs in humans based on data from animals. J. Pharmacokinet. Biopharm. 12:587-596 (1984).
    • (1984) J. Pharmacokinet. Biopharm. , vol.12 , pp. 587-596
    • Sawada, Y.1    Hanano, M.2    Sugiyama, Y.3    Harashima, H.4    Iga, T.5
  • 48
    • 0032888376 scopus 로고    scopus 로고
    • A compartmental absorption and transit model for estimating oral drug absorption
    • L. X. Yu, and G. L. Amidon. A compartmental absorption and transit model for estimating oral drug absorption. Int. J. Pharm. 186:119-125 (1999).
    • (1999) Int. J. Pharm. , vol.186 , pp. 119-125
    • Yu, L.X.1    Amidon, G.L.2
  • 49
    • 0035478779 scopus 로고    scopus 로고
    • Predicting the impact of physiological and biochemical processes on oral drug bioavailability
    • B. Agoram, W. S. Woltosz, and M. B. Bolger. Predicting the impact of physiological and biochemical processes on oral drug bioavailability. Adv. Drug Deliv. Rev. 50 (Suppl 1):S41-67 (2001).
    • (2001) Adv. Drug Deliv. Rev. , vol.50 , Issue.SUPPL. 1
    • Agoram, B.1    Woltosz, W.S.2    Bolger, M.B.3
  • 51
    • 0344084044 scopus 로고    scopus 로고
    • A physiologic model for simulating gastrointestinal flow and drug absorption in rats
    • S. Willmann, W. Schmitt, J. Keldenich, and J. B. Dressman. A physiologic model for simulating gastrointestinal flow and drug absorption in rats. Pharm. Res. 20:1766-1771 (2003).
    • (2003) Pharm. Res. , vol.20 , pp. 1766-1771
    • Willmann, S.1    Schmitt, W.2    Keldenich, J.3    Dressman, J.B.4
  • 52
    • 3242778534 scopus 로고    scopus 로고
    • A physiological model for the estimation of the fraction dose absorbed in humans
    • S. Willmann, W. Schmitt, J. Keldenich, J. Lippert, and J. B. Dressman. A physiological model for the estimation of the fraction dose absorbed in humans. J. Med. Chem. 47:4022-4031 (2004).
    • (2004) J. Med. Chem. , vol.47 , pp. 4022-4031
    • Willmann, S.1    Schmitt, W.2    Keldenich, J.3    Lippert, J.4    Dressman, J.B.5
  • 53
    • 34249694908 scopus 로고    scopus 로고
    • Evaluation of a basic physiologically based pharmacokinetic model for simulating the first-time-in-animal study
    • M. Germani, P. Crivori, M. Rocchetti, P. S. Burton, A. G. E. Wilson, M. E. Smith, and I. Poggesi. Evaluation of a basic physiologically based pharmacokinetic model for simulating the first-time-in-animal study. Eur. J. Pharm. Sci. 31:190-201 (2007).
    • (2007) Eur. J. Pharm. Sci. , vol.31 , pp. 190-201
    • Germani, M.1    Crivori, P.2    Rocchetti, M.3    Burton, P.S.4    Wilson, A.G.E.5    Smith, M.E.6    Poggesi, I.7
  • 54
    • 34047157087 scopus 로고    scopus 로고
    • The prediction of drug metabolism, tissue distribution, and bioavailability of 50 structurally diverse compounds in rat using mechanism-based absorption, distribution, and metabolism prediction tools
    • S. S. De Buck, V. K. Sinha, L. A. Fenu, R. A. H. J. Gilissen, C. E. Mackie, and M. J. Nijsen. The prediction of drug metabolism, tissue distribution, and bioavailability of 50 structurally diverse compounds in rat using mechanism-based absorption, distribution, and metabolism prediction tools. Drug Metab. Dispos. 35:649-659 (2007b).
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 649-659
    • De Buck, S.S.1    Sinha, V.K.2    Fenu, L.A.3    Gilissen, R.A.H.J.4    Mackie, C.E.5    Nijsen, M.J.6
  • 55
    • 17644381224 scopus 로고    scopus 로고
    • Prediction of human drug clearance from in vitro and preclinical data using physiologically based and empirical approaches
    • K. Ito, and J. B. Houston. Prediction of human drug clearance from in vitro and preclinical data using physiologically based and empirical approaches. Pharm. Res. 22:103-112 (2005).
    • (2005) Pharm. Res. , vol.22 , pp. 103-112
    • Ito, K.1    Houston, J.B.2
  • 56
    • 0037403950 scopus 로고    scopus 로고
    • Utility of hepatocytes in predicting drug metabolism: Comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro
    • Y. Naritomi, S. Terashita, A. Kagayama, and Y. Sugiyama. Utility of hepatocytes in predicting drug metabolism: Comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro. Drug Metab. Dispos. 31:580-588 (2003).
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 580-588
    • Naritomi, Y.1    Terashita, S.2    Kagayama, A.3    Sugiyama, Y.4
  • 57
    • 33846405266 scopus 로고    scopus 로고
    • Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance
    • H. S. Brown, M. Griffin, and J. B. Houston. Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance. Drug Metab. Dispos. 35:293-301 (2007).
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 293-301
    • Brown, H.S.1    Griffin, M.2    Houston, J.B.3
  • 58
    • 6944226371 scopus 로고    scopus 로고
    • Evaluation of fresh and cryopreserved hepatocytes as in vitro drug metabolism tools for the prediction of metabolic clearance
    • D. F. McGinnity, M. G. Soars, R. A. Urbanowicz, and R. J. Riley. Evaluation of fresh and cryopreserved hepatocytes as in vitro drug metabolism tools for the prediction of metabolic clearance. Drug Metab. Dispos. 32:1247-1253 (2004).
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 1247-1253
    • McGinnity, D.F.1    Soars, M.G.2    Urbanowicz, R.A.3    Riley, R.J.4
  • 59
    • 0033670103 scopus 로고    scopus 로고
    • A convenient in vitro screening method for predicting in vivo drug metabolic clearance using isolated hepatocytes suspended in serum
    • Y. Shibata, H. Takahashi, and Y. Ishii. A convenient in vitro screening method for predicting in vivo drug metabolic clearance using isolated hepatocytes suspended in serum. Drug Metab. Dispos. 28:1518-1523 (2000).
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 1518-1523
    • Shibata, Y.1    Takahashi, H.2    Ishii, Y.3
  • 60
    • 23944451585 scopus 로고    scopus 로고
    • A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes
    • R. J. Riley, D. F. McGinnity, and R. P. Austin. A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes. Drug Metab. Dispos. 33:1304-1311 (2005).
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 1304-1311
    • Riley, R.J.1    McGinnity, D.F.2    Austin, R.P.3
  • 61
    • 0034824439 scopus 로고    scopus 로고
    • Utility of metabolic stability screening: Comparison of in vitro and in vivo clearance
    • S. E. Clarke, and P. Jeffrey. Utility of metabolic stability screening: Comparison of in vitro and in vivo clearance. Xenobiotica. 31:591-598 (2001).
    • (2001) Xenobiotica , vol.31 , pp. 591-598
    • Clarke, S.E.1    Jeffrey, P.2
  • 62
    • 33645961595 scopus 로고    scopus 로고
    • The impact of in vitro binding on in vitro - In vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions
    • K. Grime, and R. J. Riley. The impact of in vitro binding on in vitro - in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions. Curr. Drug Metab. 7:251-264 (2006).
    • (2006) Curr. Drug Metab. , vol.7 , pp. 251-264
    • Grime, K.1    Riley, R.J.2
  • 63
    • 0036893242 scopus 로고    scopus 로고
    • Development of a novel in vitro model to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes
    • Y. Y. Lau, E. Sapidou, X. Cu, R. E. White, and K. C. Cheng. Development of a novel in vitro model to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes. Drug. Metab. Dispos. 30:1446-1454 (2002).
    • (2002) Drug. Metab. Dispos. , vol.30 , pp. 1446-1454
    • Lau, Y.Y.1    Sapidou, E.2    Cu, X.3    White, R.E.4    Cheng, K.C.5


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