메뉴 건너뛰기




Volumn 39, Issue 1, 2009, Pages 57-71

Presentation of a modified dispersion model (MDM) for hepatic drug extraction and a new methodology for the prediction of the rate-limiting step in hepatic metabolic clearance

Author keywords

Absorption; Clearance; Liver extraction model; Metabolism; Permeability; Prediction

Indexed keywords

ALBUMIN; ALPRAZOLAM; ATENOLOL; BOSENTAN; CAFFEINE; DIAZEPAM; DIGOXIN; DILTIAZEM; ENALAPRILAT; ETOPOSIDE; FLUINDOSTATIN; FLUNITRAZEPAM; FUROSEMIDE; HEXOBARBITAL; LIDOCAINE; LORAZEPAM; LORCAINIDE; METOPROLOL; NALOXONE; NICARDIPINE; NIFEDIPINE; PROBENECID; SULPIRIDE; TENIDAP; TERBUTALINE; TESTOSTERONE; TOLBUTAMIDE; TRIAZOLAM; UNINDEXED DRUG; WARFARIN;

EID: 61749103240     PISSN: 00498254     EISSN: 13665928     Source Type: Journal    
DOI: 10.1080/00498250802562652     Document Type: Article
Times cited : (7)

References (82)
  • 3
    • 14044251501 scopus 로고    scopus 로고
    • The binding of drugs to hepatocytes and its relationship to physicochemical properties
    • Austin RP, Barton P, Mohmed S, Riley RJ. (2005). The binding of drugs to hepatocytes and its relationship to physicochemical properties. Drug Metabolism and Disposition 33, 419-425.
    • (2005) Drug Metabolism and Disposition , vol.33 , pp. 419-425
    • Austin, R.P.1    Barton, P.2    Mohmed, S.3    Riley, R.J.4
  • 4
    • 0038509966 scopus 로고    scopus 로고
    • Prediction of in vivo clearance from in vitro data using cryopreserved human hepatocytes
    • Bachmann K, Byers J, Ghosh R. (2003). Prediction of in vivo clearance from in vitro data using cryopreserved human hepatocytes. Xenobiotica 33, 475-483.
    • (2003) Xenobiotica , vol.33 , pp. 475-483
    • Bachmann, K.1    Byers, J.2    Ghosh, R.3
  • 5
    • 35648935952 scopus 로고    scopus 로고
    • Kinetic determinants of hepatic clearance: Plasma protein binding and hepatic uptake
    • Baker M, Parton T. (2007). Kinetic determinants of hepatic clearance: Plasma protein binding and hepatic uptake. Xenobiotica 37, 1110-1134.
    • (2007) Xenobiotica , vol.37 , pp. 1110-1134
    • Baker, M.1    Parton, T.2
  • 6
    • 0023949942 scopus 로고
    • Physiologically based models and strategic experiments in hepatic pharmacology
    • Bass L, Keiding S. (1988). Physiologically based models and strategic experiments in hepatic pharmacology. Biochemistry and Pharmacology 37, 1425-1431.
    • (1988) Biochemistry and Pharmacology , vol.37 , pp. 1425-1431
    • Bass, L.1    Keiding, S.2
  • 7
    • 0842289324 scopus 로고    scopus 로고
    • Determination of volume of distribution at steady state with complete consideration of the kinetics of protein and tissue binding in linear pharmacokinetics
    • Berezhkovskiy LM. (2004). Determination of volume of distribution at steady state with complete consideration of the kinetics of protein and tissue binding in linear pharmacokinetics. Journal of Pharmacology Science 93, 364-374.
    • (2004) Journal of Pharmacology Science , vol.93 , pp. 364-374
    • Berezhkovskiy, L.M.1
  • 8
    • 0020073443 scopus 로고
    • Hepatic drug transport in the rat: A comparison between isolated hepatocytes, the isolated perfused liver and the liver in vivo
    • Blom A, Scaf AHJ, Meijer DKF. (1982). Hepatic drug transport in the rat: a comparison between isolated hepatocytes, the isolated perfused liver and the liver in vivo. Biochemistry and Pharmacology 31, 1553-1565.
    • (1982) Biochemistry and Pharmacology , vol.31 , pp. 1553-1565
    • Blom, A.1    Scaf, A.H.J.2    Meijer, D.K.F.3
  • 10
    • 0034454016 scopus 로고    scopus 로고
    • Determining the best animal model for human cytochrome P450 activities: A comparison of mouse, rat, rabbit, dog, micropig, monkey and man
    • Bogaards JJP, Bertrand M, Jackson P, Oudshoorn MJ, Weaver RJ, Van Bladeren PJ, Walther B. (2000). Determining the best animal model for human cytochrome P450 activities: a comparison of mouse, rat, rabbit, dog, micropig, monkey and man. Xenobiotica 30, 1131-1152.
    • (2000) Xenobiotica , vol.30 , pp. 1131-1152
    • Bogaards, J.J.P.1    Bertrand, M.2    Jackson, P.3    Oudshoorn, M.J.4    Weaver, R.J.5    Van Bladeren, P.J.6    Walther, B.7
  • 11
    • 33846405266 scopus 로고    scopus 로고
    • Evaluation of cryopreserved human hepatocytes as an alternative in-vitro system to microsomes for the prediction of metabolic clearance
    • Brown HS, Griffin M, Houston JB. (2007). Evaluation of cryopreserved human hepatocytes as an alternative in-vitro system to microsomes for the prediction of metabolic clearance. Drug Metabolism and Disposition 35, 293-301.
    • (2007) Drug Metabolism and Disposition , vol.35 , pp. 293-301
    • Brown, H.S.1    Griffin, M.2    Houston, J.B.3
  • 12
    • 3542995726 scopus 로고    scopus 로고
    • The complexities of hepatic drug transport: Current knowledge and emerging concepts
    • Chandra P, Brouwer KLR. (2004). The complexities of hepatic drug transport: current knowledge and emerging concepts. Pharmaceutical Research 21, 719-735.
    • (2004) Pharmaceutical Research , vol.21 , pp. 719-735
    • Chandra, P.1    Brouwer, K.L.R.2
  • 13
    • 0027374635 scopus 로고
    • Relationship between lipophilicity and hepatic dispersion and distribution for a homologous series of barbiturates in the isolated perfused in situ rat liver
    • Chou C-H, Evans AM, Fornasini G, Rowland M. (1993). Relationship between lipophilicity and hepatic dispersion and distribution for a homologous series of barbiturates in the isolated perfused in situ rat liver. Drug Metabolism and Disposition 21, 933-938.
    • (1993) Drug Metabolism and Disposition , vol.21 , pp. 933-938
    • Chou, C.-H.1    Evans, A.M.2    Fornasini, G.3    Rowland, M.4
  • 14
    • 0029588280 scopus 로고
    • Membrane permeability and lipophilicity in the isolated perfused rat liver: 5-ethyl barbituric acid and other compounds
    • Chou C-H, McLachlan AJ, Rowland M. (1995). Membrane permeability and lipophilicity in the isolated perfused rat liver: 5-ethyl barbituric acid and other compounds. Journal of Pharmacology and Experimental Therapeutics 275, 933-940.
    • (1995) Journal of Pharmacology and Experimental Therapeutics , vol.275 , pp. 933-940
    • Chou, C.-H.1    McLachlan, A.J.2    Rowland, M.3
  • 15
    • 0034824439 scopus 로고    scopus 로고
    • Utility of metabolic stability screening: Comparison of in vitro and in vivo clearance
    • Clarke SE, Jeffrey P. (2001). Utility of metabolic stability screening: comparison of in vitro and in vivo clearance. Xenobiotica 31, 591-598.
    • (2001) Xenobiotica , vol.31 , pp. 591-598
    • Clarke, S.E.1    Jeffrey, P.2
  • 16
    • 35648968125 scopus 로고    scopus 로고
    • Comparison of different approaches to predict metabolic drug-drug interactions
    • Einolf HJ. (2007). Comparison of different approaches to predict metabolic drug-drug interactions. Xenobiotica 37, 1257-1294.
    • (2007) Xenobiotica , vol.37 , pp. 1257-1294
    • Einolf, H.J.1
  • 17
    • 34447312263 scopus 로고    scopus 로고
    • Prediction of human pharmacokinetics - evaluation of methods for prediction of hepatic metabolic clearance
    • Fagerholm U. (2007a). Prediction of human pharmacokinetics - evaluation of methods for prediction of hepatic metabolic clearance. Journal of Pharmaceutics and Pharmacology 59, 803-828.
    • (2007) Journal of Pharmaceutics and Pharmacology , vol.59 , pp. 803-828
    • Fagerholm, U.1
  • 18
    • 34548393250 scopus 로고    scopus 로고
    • Prediction of human pharmacokinetics - evaluation of methods for prediction of volume of distribution
    • Fagerholm U. (2007b). Prediction of human pharmacokinetics - evaluation of methods for prediction of volume of distribution. Journal of Pharmaceutics and Pharmacology 59, 1181-1190.
    • (2007) Journal of Pharmaceutics and Pharmacology , vol.59 , pp. 1181-1190
    • Fagerholm, U.1
  • 19
    • 40549119872 scopus 로고    scopus 로고
    • The role of permeability in drug ADME/PK, interactions and toxicity - presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in humans
    • Fagerholm U. (2008a). The role of permeability in drug ADME/PK, interactions and toxicity - presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in humans. Pharmaceutical Research 25, 625-638.
    • (2008) Pharmaceutical Research , vol.25 , pp. 625-638
    • Fagerholm, U.1
  • 20
    • 42549095582 scopus 로고    scopus 로고
    • Prediction of human pharmacokinetics - biliary and intestinal clearance and enterohepatic circulation
    • Fagerholm U. (2008b). Prediction of human pharmacokinetics - biliary and intestinal clearance and enterohepatic circulation. Journal of Pharmaceutics and Pharmacology 60, 535-542.
    • (2008) Journal of Pharmaceutics and Pharmacology , vol.60 , pp. 535-542
    • Fagerholm, U.1
  • 21
    • 0003680152 scopus 로고    scopus 로고
    • Hardman JG, Limbird LE, Goodman Gilman A. editors, New York, NY, McGraw-Hill
    • Goodman Gilman A. (2001). In, Hardman JG, Limbird LE, Goodman Gilman A. editors. The pharmacological basis of therapeutics. New York, NY, McGraw-Hill.
    • (2001) The pharmacological basis of therapeutics
    • Goodman Gilman, A.1
  • 25
    • 0023916444 scopus 로고
    • Conformational change in plasma albumin due to interaction with isolated rat hepatocyte
    • Horie T, Mizuma T, Kasai S, Awazu S. (1988). Conformational change in plasma albumin due to interaction with isolated rat hepatocyte. American Journal of Physiology 254, G465-G470.
    • (1988) American Journal of Physiology , vol.254
    • Horie, T.1    Mizuma, T.2    Kasai, S.3    Awazu, S.4
  • 26
    • 33745130722 scopus 로고    scopus 로고
    • Prediction of in-vivo drug clearance from in-vitro data. I: Impact of inter-individual variability
    • Howgate EM, Rowland Yeo, K Proctor, NJ etal. (2006). Prediction of in-vivo drug clearance from in-vitro data. I: Impact of inter-individual variability. Xenobiotica 36, 473-497.
    • (2006) Xenobiotica , vol.36 , pp. 473-497
    • Howgate, E.M.1    Rowland Yeo, K.2    Proctor, N.J.3
  • 27
    • 17644381224 scopus 로고    scopus 로고
    • Prediction of human drug clearance from in-vitro and preclinical data using physiologically based and empirical approaches
    • Ito K, Houston JB. (2005). Prediction of human drug clearance from in-vitro and preclinical data using physiologically based and empirical approaches. Pharmaceutical Research 22, 103-112.
    • (2005) Pharmaceutical Research , vol.22 , pp. 103-112
    • Ito, K.1    Houston, J.B.2
  • 28
    • 0029950964 scopus 로고    scopus 로고
    • Prediction of in-vivo drug disposition from in-vitro data based on physiological pharmacokinetics
    • Iwatsubo T, Hirota N, Ooie T, et al. (1996). Prediction of in-vivo drug disposition from in-vitro data based on physiological pharmacokinetics. Biopharmaceutics and Drug Disposition 17, 273-310.
    • (1996) Biopharmaceutics and Drug Disposition , vol.17 , pp. 273-310
    • Iwatsubo, T.1    Hirota, N.2    Ooie, T.3
  • 29
    • 0030937636 scopus 로고    scopus 로고
    • Prediction of in-vivo drug metabolism in the human liver from in-vitro metabolism data
    • Iwatsubo T, Hirota N, Ooie T, et al. (1997). Prediction of in-vivo drug metabolism in the human liver from in-vitro metabolism data. Pharmacology and Therapy 73, 147-171.
    • (1997) Pharmacology and Therapy , vol.73 , pp. 147-171
    • Iwatsubo, T.1    Hirota, N.2    Ooie, T.3
  • 30
    • 34249742090 scopus 로고    scopus 로고
    • Expression of adenosine triphosphate-binding cassette (ABC) transporters in peripheral blood cells: Relevance for physiology and pharmacotherapy
    • Kock K, Grube M, Jedlitschky G, et al. (2007). Expression of adenosine triphosphate-binding cassette (ABC) transporters in peripheral blood cells: relevance for physiology and pharmacotherapy. Clinical Pharmacokinetics 46, 449-470.
    • (2007) Clinical Pharmacokinetics , vol.46 , pp. 449-470
    • Kock, K.1    Grube, M.2    Jedlitschky, G.3
  • 31
    • 33746089203 scopus 로고    scopus 로고
    • In vitro and in vivo correlation of hepatic transporter effects on erythromycin metabolism: Characterizing the importance of transporter-enzyme interplay
    • Lam JL, Okochi H, Huang Y, Benet LZ. (2006). In vitro and in vivo correlation of hepatic transporter effects on erythromycin metabolism: characterizing the importance of transporter-enzyme interplay. Drug Metabolism and Disposition 34, 1336-1344.
    • (2006) Drug Metabolism and Disposition , vol.34 , pp. 1336-1344
    • Lam, J.L.1    Okochi, H.2    Huang, Y.3    Benet, L.Z.4
  • 32
    • 13244297157 scopus 로고    scopus 로고
    • The hepatic sinusoid in aging and cirrhosis. Effects on hepatic substrate disposition and drug clearance
    • Le Couteur DG, Fraser R, Hilmer S, Rivory LP, McLean AJ (2005). The hepatic sinusoid in aging and cirrhosis. Effects on hepatic substrate disposition and drug clearance. Clinical Pharmacokinetics 44(2), 187-200.
    • (2005) Clinical Pharmacokinetics , vol.44 , Issue.2 , pp. 187-200
    • Le Couteur, D.G.1    Fraser, R.2    Hilmer, S.3    Rivory, L.P.4    McLean, A.J.5
  • 33
    • 0030588693 scopus 로고    scopus 로고
    • Strategies for restoration and maintenance of normal hepatic structure and function in long-term cultures of rat hepatocytes
    • LeCluyse EL, Bullock PL, Parkinson A. (1996). Strategies for restoration and maintenance of normal hepatic structure and function in long-term cultures of rat hepatocytes. Advances in Drug Delivery Reviews 22, 133-186.
    • (1996) Advances in Drug Delivery Reviews , vol.22 , pp. 133-186
    • LeCluyse, E.L.1    Bullock, P.L.2    Parkinson, A.3
  • 34
    • 0024404961 scopus 로고
    • Erythrocytes as barriers for drug elimination in the isolated liver: II
    • Lee HL, Chiou WL. (1989). Erythrocytes as barriers for drug elimination in the isolated liver: II. Propranolol. Pharmaceutical Research 6, 840-843.
    • (1989) Propranolol. Pharmaceutical Research , vol.6 , pp. 840-843
    • Lee, H.L.1    Chiou, W.L.2
  • 35
    • 0026572490 scopus 로고
    • Human jejunal unstirred layer: Evidence for extremely efficient luminal stirring
    • Levitt MD, Strocchi A, Levitt DG. (1992). Human jejunal unstirred layer: evidence for extremely efficient luminal stirring. American Journal of Physiology 262, G593-G596.
    • (1992) American Journal of Physiology , vol.262
    • Levitt, M.D.1    Strocchi, A.2    Levitt, D.G.3
  • 36
    • 0036149180 scopus 로고    scopus 로고
    • Use of allometry in predicting anatomical and physiological parameters of mammals
    • Lindstedt SL, Schaeffer PJ. (2002). Use of allometry in predicting anatomical and physiological parameters of mammals. Laboratory Animals 36, 1-19.
    • (2002) Laboratory Animals , vol.36 , pp. 1-19
    • Lindstedt, S.L.1    Schaeffer, P.J.2
  • 37
    • 17744385960 scopus 로고    scopus 로고
    • In-vitro human tissue models in risk assessment: Report of a consensus-building workshop
    • MacGregor JT, Collins JM, Sugiyama Y, et al. (2001). In-vitro human tissue models in risk assessment: report of a consensus-building workshop. Toxicology Science 29, 17-36.
    • (2001) Toxicology Science , vol.29 , pp. 17-36
    • MacGregor, J.T.1    Collins, J.M.2    Sugiyama, Y.3
  • 38
    • 0037707638 scopus 로고    scopus 로고
    • Metabolic stability for drug discovery and development. Pharmacokinetic and biochemical challenges
    • Masimirembwa CM, Bredberg U, Andersson TB. (2003). Metabolic stability for drug discovery and development. Pharmacokinetic and biochemical challenges. Clinical Pharmacokinetics 42, 515-528.
    • (2003) Clinical Pharmacokinetics , vol.42 , pp. 515-528
    • Masimirembwa, C.M.1    Bredberg, U.2    Andersson, T.B.3
  • 39
    • 34548792895 scopus 로고    scopus 로고
    • Evaluation of human pharmacokinetics, therapeutic dose and exposure predictions using marketed oral drugs
    • McGinnity DF, Collington J, Austin RP, Riley RJ. (2007). Evaluation of human pharmacokinetics, therapeutic dose and exposure predictions using marketed oral drugs. Current Drug Metabolism 463-479.
    • (2007) Current Drug Metabolism , pp. 463-479
    • McGinnity, D.F.1    Collington, J.2    Austin, R.P.3    Riley, R.J.4
  • 40
    • 0003909133 scopus 로고    scopus 로고
    • Cambridge, MA, Harvard University Press
    • McManus C. (2002). In, Right hand, left hand. Cambridge, MA, Harvard University Press.
    • (2002) Right hand, left hand
    • McManus, C.1
  • 41
    • 0024510074 scopus 로고
    • Covalent and noncovalent protein binding of drugs: Implications for hepatic clearance, storage, and cell-specific drug delivery
    • Meijer DK, Van der Sluijs P (1989). Covalent and noncovalent protein binding of drugs: Implications for hepatic clearance, storage, and cell-specific drug delivery. Pharmaceutical Research 6, 105-118.
    • (1989) Pharmaceutical Research , vol.6 , pp. 105-118
    • Meijer, D.K.1    Van der Sluijs, P.2
  • 42
    • 0033168932 scopus 로고    scopus 로고
    • Structure-hepatic disposition relationships for phenolic compounds
    • Mellick GD, Roberts MS. (1999). Structure-hepatic disposition relationships for phenolic compounds. Toxicology and Applied Pharmacology 158, 50-60.
    • (1999) Toxicology and Applied Pharmacology , vol.158 , pp. 50-60
    • Mellick, G.D.1    Roberts, M.S.2
  • 43
    • 0027447887 scopus 로고
    • Comparison of the hepatic uptake clearances of fifteen drugs with a wide range of membrane permeabilities in isolated rat hepatocytes and perfused rat livers
    • Miyauchi S, Sawada Y, Iga T, Hanano M, Sugiyama Y. (1993). Comparison of the hepatic uptake clearances of fifteen drugs with a wide range of membrane permeabilities in isolated rat hepatocytes and perfused rat livers. Pharmaceutical Research 10, 434-440.
    • (1993) Pharmaceutical Research , vol.10 , pp. 434-440
    • Miyauchi, S.1    Sawada, Y.2    Iga, T.3    Hanano, M.4    Sugiyama, Y.5
  • 44
    • 0015720236 scopus 로고
    • Patterns of nonelectrolyte permeability in human red blood cell membrane
    • Naccache P, Sha'afi RI. (1973). Patterns of nonelectrolyte permeability in human red blood cell membrane. Journal of General Physiology 62, 714-736.
    • (1973) Journal of General Physiology , vol.62 , pp. 714-736
    • Naccache, P.1    Sha'afi, R.I.2
  • 45
    • 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
    • Obach RS. (1999). 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 Metabolism and Disposition 27, 1350-1359.
    • (1999) Drug Metabolism and Disposition , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 47
    • 0030842717 scopus 로고    scopus 로고
    • Hepatic ICG removal in the pig depends on plasma protein and hematocrit: Evidence of sinusoidal binding disequilibrium and unstirred water layer effects
    • Ott P, Bass L, Keiding S. (1997). Hepatic ICG removal in the pig depends on plasma protein and hematocrit: evidence of sinusoidal binding disequilibrium and unstirred water layer effects. Hepatology 26, 679-690.
    • (1997) Hepatology , vol.26 , pp. 679-690
    • Ott, P.1    Bass, L.2    Keiding, S.3
  • 48
    • 0020694823 scopus 로고
    • Transport of propranolol and lidocaine through the rat blood brain barrier. Primary role of globulin-bound drug
    • Pardridge WM, Sakiyama R, Fierer G. (1983). Transport of propranolol and lidocaine through the rat blood brain barrier. Primary role of globulin-bound drug. Journal of Clinical Investigation 71, 900-908.
    • (1983) Journal of Clinical Investigation , vol.71 , pp. 900-908
    • Pardridge, W.M.1    Sakiyama, R.2    Fierer, G.3
  • 49
    • 0033773908 scopus 로고    scopus 로고
    • Hydrodynaic effects on the solute transport across endothelial pores and hepatocyte membranes
    • Popescu D, Movileanu L, Ion S, Flonta M-L. (2000). Hydrodynaic effects on the solute transport across endothelial pores and hepatocyte membranes. Physics in Medicine and Biology 45, N157-N165.
    • (2000) Physics in Medicine and Biology , vol.45
    • Popescu, D.1    Movileanu, L.2    Ion, S.3    Flonta, M.-L.4
  • 50
    • 0035064596 scopus 로고    scopus 로고
    • Uptake of teicoplanin by isolated rat hepatocytes: Comparison with in vivo hepatic distribution
    • Reinoso RF, Telfer BA, Brennan BS, Rowland M. (2001). Uptake of teicoplanin by isolated rat hepatocytes: comparison with in vivo hepatic distribution. Drug Metabolism and Disposition 29, 453-459.
    • (2001) Drug Metabolism and Disposition , vol.29 , pp. 453-459
    • Reinoso, R.F.1    Telfer, B.A.2    Brennan, B.S.3    Rowland, M.4
  • 51
    • 0035884143 scopus 로고    scopus 로고
    • High-resolution and high-throughput protocols for measuring drug/human serum albumin interactions using BIACORE
    • Rich RL, Yasmina SN, Morton TA, Myszka DG. (2001). High-resolution and high-throughput protocols for measuring drug/human serum albumin interactions using BIACORE. Annals of Biochemistry 296, 197-207.
    • (2001) Annals of Biochemistry , vol.296 , pp. 197-207
    • Rich, R.L.1    Yasmina, S.N.2    Morton, T.A.3    Myszka, D.G.4
  • 52
    • 23944451585 scopus 로고    scopus 로고
    • A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes
    • Riley RJ, McGinnity DF, Austin RP. (2005). A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes. Drug Metabolism and Disposition 33, 1304-1311.
    • (2005) Drug Metabolism and Disposition , vol.33 , pp. 1304-1311
    • Riley, R.J.1    McGinnity, D.F.2    Austin, R.P.3
  • 53
    • 0031661168 scopus 로고    scopus 로고
    • Relative dispersions of intra-albumin transit times across rat and elasmobranch perfusied liver, and implications for intra- and inter-species scaling of hepatic clearance using microsomal data
    • Roberts MS, Ballinger LN, Weiss M. (1998). Relative dispersions of intra-albumin transit times across rat and elasmobranch perfusied liver, and implications for intra- and inter-species scaling of hepatic clearance using microsomal data. Journal of Pharmaceutics and Pharmacology 50, 865-870.
    • (1998) Journal of Pharmaceutics and Pharmacology , vol.50 , pp. 865-870
    • Roberts, M.S.1    Ballinger, L.N.2    Weiss, M.3
  • 54
    • 0023933009 scopus 로고
    • Models of hepatic elimination: Comparison of stochastic models to describe residence time distributions and to predict the influence of drug distribution, enzyme heterogeneity, and systemic recycling of hepatic elimination
    • Roberts MS, Donaldson JD, Rowland M. (1988). Models of hepatic elimination: comparison of stochastic models to describe residence time distributions and to predict the influence of drug distribution, enzyme heterogeneity, and systemic recycling of hepatic elimination. Journal of Pharmacokinetics and Biopharmaceutics 16, 41-83.
    • (1988) Journal of Pharmacokinetics and Biopharmaceutics , vol.16 , pp. 41-83
    • Roberts, M.S.1    Donaldson, J.D.2    Rowland, M.3
  • 57
    • 0022549973 scopus 로고
    • A dispersion model of hepatic elimination: 1. Formulation of the model and bolus considerations
    • Roberts MS, Rowland M. (1986a). A dispersion model of hepatic elimination: 1. Formulation of the model and bolus considerations. Journal of Pharmacokinetics and Biopharmaceutics 14, 227-261.
    • (1986) Journal of Pharmacokinetics and Biopharmaceutics , vol.14 , pp. 227-261
    • Roberts, M.S.1    Rowland, M.2
  • 58
    • 0022552317 scopus 로고
    • A dispersion model of hepatic elimination: 2. Steady-state considerations - influence of hepatic blood flow, binding within blood, and hepatocellular enzyme activity
    • Roberts MS, Rowland M. (1986b). A dispersion model of hepatic elimination: 2. Steady-state considerations - influence of hepatic blood flow, binding within blood, and hepatocellular enzyme activity. Journal of Pharmacokinetics and Biopharmaceutics 14, 261-288.
    • (1986) Journal of Pharmacokinetics and Biopharmaceutics , vol.14 , pp. 261-288
    • Roberts, M.S.1    Rowland, M.2
  • 59
    • 0022922022 scopus 로고
    • A dispersion model of hepatic elimination: 3. Application to metabolite formation and elimination kinetics
    • Roberts MS, Rowland M. (1986c). A dispersion model of hepatic elimination: 3. Application to metabolite formation and elimination kinetics. Journal of Pharmacokinetics and Biopharmaceutics 14, 289-308.
    • (1986) Journal of Pharmacokinetics and Biopharmaceutics , vol.14 , pp. 289-308
    • Roberts, M.S.1    Rowland, M.2
  • 60
    • 0022609024 scopus 로고
    • Correlation between in-vitro microsomal enzyme activity and whole organ hepatic elimination kinetics: Analysis with a dispersion model
    • Roberts MS, Rowland M. (1986d). Correlation between in-vitro microsomal enzyme activity and whole organ hepatic elimination kinetics: analysis with a dispersion model. Journal of Pharmaceutics and Pharmacology 38, 177-181.
    • (1986) Journal of Pharmaceutics and Pharmacology , vol.38 , pp. 177-181
    • Roberts, M.S.1    Rowland, M.2
  • 65
    • 0018901053 scopus 로고
    • Transport systems of isolated hepatocytes: Studies on the transport of biliary compounds
    • Schwenk M. (1980). Transport systems of isolated hepatocytes: studies on the transport of biliary compounds. Archives of Toxicology 44, 113-126.
    • (1980) Archives of Toxicology , vol.44 , pp. 113-126
    • Schwenk, M.1
  • 66
    • 0036320379 scopus 로고    scopus 로고
    • Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: An application of serum incubation method
    • Shibata Y, Takahashi H, Chiba M, Ishii Y. (2002). Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: an application of serum incubation method. Drug Metabolism and Disposition 30, 892-896.
    • (2002) Drug Metabolism and Disposition , vol.30 , pp. 892-896
    • Shibata, Y.1    Takahashi, H.2    Chiba, M.3    Ishii, Y.4
  • 67
    • 0033670103 scopus 로고    scopus 로고
    • A convenient in vitro screening method for predicting in vivo drug metabolic clearance using isolated hepatocytes suspended in serum
    • Shibata Y, Takahashi H, Ishii Y. (2000). A convenient in vitro screening method for predicting in vivo drug metabolic clearance using isolated hepatocytes suspended in serum. Drug Metabolism and Disposition 28, 1518-1523.
    • (2000) Drug Metabolism and Disposition , vol.28 , pp. 1518-1523
    • Shibata, Y.1    Takahashi, H.2    Ishii, Y.3
  • 68
    • 34249006024 scopus 로고    scopus 로고
    • Use of hepatocytes to assess the contribution of hepatic uptake to clearance in-vivo
    • Soars MG, Grime K, Sproston JL, et al. (2007). Use of hepatocytes to assess the contribution of hepatic uptake to clearance in-vivo. Drug Metabolism and Disposition 35, 859-865.
    • (2007) Drug Metabolism and Disposition , vol.35 , pp. 859-865
    • Soars, M.G.1    Grime, K.2    Sproston, J.L.3
  • 69
    • 33749838238 scopus 로고    scopus 로고
    • Determination of the hepatocellularity number for human, dog, rabbit, rat and mouse livers from protein concentration measurements
    • Sohlenius-Sternbeck A-K. (2006). Determination of the hepatocellularity number for human, dog, rabbit, rat and mouse livers from protein concentration measurements. Toxicology In-Vitro 20, 1582-1586.
    • (2006) Toxicology In-Vitro , vol.20 , pp. 1582-1586
    • Sohlenius-Sternbeck, A.-K.1
  • 70
    • 0026693108 scopus 로고
    • A comparative investigation of hepatic clearance models: Predictions of metabolite formation and elimination
    • St-Pierre MV, Lee PI, Pang KS. (1992). A comparative investigation of hepatic clearance models: predictions of metabolite formation and elimination. Journal of Pharmacokinetics and Biopharmaceutics 20, 105-145.
    • (1992) Journal of Pharmacokinetics and Biopharmaceutics , vol.20 , pp. 105-145
    • St-Pierre, M.V.1    Lee, P.I.2    Pang, K.S.3
  • 71
    • 34547212999 scopus 로고    scopus 로고
    • Bosentan is a substrate of human OATP1B1 and OATP1B3: Inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil
    • Treiber A, Schneiter R, Häusler S, Stieger B. (2007). Bosentan is a substrate of human OATP1B1 and OATP1B3: Inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil. Drug Metabolism and Disposition 35, 1400-1407.
    • (2007) Drug Metabolism and Disposition , vol.35 , pp. 1400-1407
    • Treiber, A.1    Schneiter, R.2    Häusler, S.3    Stieger, B.4
  • 72
    • 2442691625 scopus 로고    scopus 로고
    • A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. II. Volume of distribution and mean residence time
    • Ward KW, Smith BR. (2004a). A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. II. Volume of distribution and mean residence time. Drug Metabolism and Disposition 32, 612-619.
    • (2004) Drug Metabolism and Disposition , vol.32 , pp. 612-619
    • Ward, K.W.1    Smith, B.R.2
  • 73
    • 2442680354 scopus 로고    scopus 로고
    • A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans., I. Clearance
    • Ward KW, Smith BR. (2004b). A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans., I. Clearance. Drug Metabolism and Disposition 32, 603-611.
    • (2004) Drug Metabolism and Disposition , vol.32 , pp. 603-611
    • Ward, K.W.1    Smith, B.R.2
  • 74
    • 0014546946 scopus 로고
    • Correlated morphometric and biochemical studies on the liver cell. Morphometric model, and normal morphometric data for rat liver
    • Weibel ER, Staubli W, Gnagi HR, Hess FA. (1969). Correlated morphometric and biochemical studies on the liver cell. Morphometric model, and normal morphometric data for rat liver. Journal of Cell Biology 42, 68-91.
    • (1969) Journal of Cell Biology , vol.42 , pp. 68-91
    • Weibel, E.R.1    Staubli, W.2    Gnagi, H.R.3    Hess, F.A.4
  • 75
    • 0012527385 scopus 로고
    • Dissociation from albumin: A potentially rate-limiting step in the clearance of substrates by the liver
    • Weisiger RA. (1985). Dissociation from albumin: a potentially rate-limiting step in the clearance of substrates by the liver. Proceedings of the National Academy of Sciences, USA 82, 1563-1567.
    • (1985) Proceedings of the National Academy of Sciences, USA , vol.82 , pp. 1563-1567
    • Weisiger, R.A.1
  • 76
    • 0016566218 scopus 로고
    • Commentary - a physiological approach to hepatic drug clearance
    • Wilkinson GR, Shand DG. (1975). Commentary - a physiological approach to hepatic drug clearance. Clinical Pharmacology and Therapy 18, 377-390.
    • (1975) Clinical Pharmacology and Therapy , vol.18 , pp. 377-390
    • Wilkinson, G.R.1    Shand, D.G.2
  • 78
    • 0030111263 scopus 로고    scopus 로고
    • Polarized membrane traffic in hepatocytes
    • Wilton JC, Matthews GM. (1996). Polarized membrane traffic in hepatocytes. Bioassays 18, 229-236.
    • (1996) Bioassays , vol.18 , pp. 229-236
    • Wilton, J.C.1    Matthews, G.M.2
  • 79
    • 0018180060 scopus 로고
    • Dependence of intestinal absorption in-vivo on the unstirred layer
    • Winne D. (1978). Dependence of intestinal absorption in-vivo on the unstirred layer. Naun.-Schm. Archives in Pharmacology 304, 175-181.
    • (1978) Naun.-Schm. Archives in Pharmacology , vol.304 , pp. 175-181
    • Winne, D.1
  • 80
    • 0142212163 scopus 로고    scopus 로고
    • Disposition of tacrolimus in isolated perfused rat liver: Influence of troleandomycin, cyclosporine, and GG918
    • Wu C-Y, Benet LZ. (2003). Disposition of tacrolimus in isolated perfused rat liver: Influence of troleandomycin, cyclosporine, and GG918. Drug Metabolism and Disposition 31, 1292-1295.
    • (2003) Drug Metabolism and Disposition , vol.31 , pp. 1292-1295
    • Wu, C.-Y.1    Benet, L.Z.2
  • 81
    • 33847411025 scopus 로고    scopus 로고
    • Misuse of the well-stirred model of hepatic drug clearance
    • Yang J, Jamei M, Yeo KR, et al. (2007). Misuse of the well-stirred model of hepatic drug clearance. Drug Metabolism and Disposition 35, 501-502.
    • (2007) Drug Metabolism and Disposition , vol.35 , pp. 501-502
    • Yang, J.1    Jamei, M.2    Yeo, K.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.