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1
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0017603437
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Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred" model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepato cellular enzymatic activity on hepatic drug clearance
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K. S. Pang and M. Rowland. Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred" model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearance. J. Pharmacokinet. Biopharm. 5:625-653 (1977).
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0018190444
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Hepatic elimination of flowing substrates: The distributed model
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L. Bass, P. Robinson, and A. J. Bracken. Hepatic elimination of flowing substrates: the distributed model. J. Theor. Biol. 72:161-184 (1978).
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Bass, L.1
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3
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0018163388
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Hepatic transport kinetics and plasma disappearance curves: Distributed modeling vs. conventional approach
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E. L. Forker and B. Luxon. Hepatic transport kinetics and plasma disappearance curves: distributed modeling vs. conventional approach. Am. J. Physiol. 235:E648-660 (1978).
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Forker, E.L.1
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4
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0022549973
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A dispersion model of hepatic elimination: 1. Formulation of the model and bolus considerations
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M. S. Roberts and M. Rowland. A dispersion model of hepatic elimination: 1. Formulation of the model and bolus considerations. J. Pharmacokinet. Biopharm. 14:227-260 (1986).
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Roberts, M.S.1
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5
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0023142478
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The series-compartment model for hepatic elimination
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M. R. Gray and Y. K. Tam. The series-compartment model for hepatic elimination. Drug. Metab. Dispos. 15:27-31 (1987).
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Gray, M.R.1
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6
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0023933009
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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 on hepatic elimination
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M. S. Roberts, J. D. Donaldson, and M. Rowland. 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 on hepatic elimination. J. Pharmaeokinet. Biopharm. 16:41-83 (1988).
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Roberts, M.S.1
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8
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0033592241
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Interconnected-tubes model of hepatic elimination: Steady-state considerations
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Y. G. Anissimov, A. J. Bracken, and M. S. Roberts. Interconnected-tubes model of hepatic elimination: steady-state considerations. J. Theor. Biol. 199:435-447 (1999).
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Anissimov, Y.G.1
Bracken, A.J.2
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9
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0001244133
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A linear method for determining liver sinusoidal and extravascular volumes
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C. A. Goresky. A linear method for determining liver sinusoidal and extravascular volumes. Am. J. Physiol. 204:626-640 (1963).
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Am. J. Physiol.
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Goresky, C.A.1
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10
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0015620354
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On the uptake of materials by the intact liver. The transport and net removal of galactose
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C. A. Goresky, G. C. Bach, and B. E. Nadeau. On the uptake of materials by the intact liver. The transport and net removal of galactose. J. Clin. Invest. 52:991-1009 (1973).
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Goresky, C.A.1
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11
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0021034742
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Kinetic interpretation of hepatic multiple-indicator dilution studies
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C. A. Goresky. Kinetic interpretation of hepatic multiple-indicator dilution studies. Am. J. Physiol. 245:G1-12 (1983).
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Am. J. Physiol.
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Goresky, C.A.1
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12
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0033500591
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Modelling of hepatic elimination and organ distribution kinetics with the extended convection-dispersion model
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M. S. Roberts and Y. G. Anissimov. Modelling of hepatic elimination and organ distribution kinetics with the extended convection-dispersion model. J. Pharmacokinet. Biopharm. 27:343-382 (1999).
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Roberts, M.S.1
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13
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0031224992
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On the validity of the dispersion model of hepatic drug elimination when intravascular transit time densities are long-tailed
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M. Weiss, C. Stedtler, and M. S. Roberts. On the validity of the dispersion model of hepatic drug elimination when intravascular transit time densities are long-tailed. Bull. Math. Biol. 59:911-929 (1997).
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Bull. Math. Biol.
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Weiss, M.1
Stedtler, C.2
Roberts, M.S.3
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14
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-
0024955759
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Availability predictions by hepatic elimination models for Michaelis-Menten kinetics
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M. S. Roberts, J. D. Donaldson, and D. Jackett. Availability predictions by hepatic elimination models for Michaelis-Menten kinetics. J. Pharmacokinet. Biopharm. 17:687-719 (1989).
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J. Pharmacokinet. Biopharm.
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Roberts, M.S.1
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Jackett, D.3
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15
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-
0032423390
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Analysis of nonlinear and nonsteady state hepatic extraction with the dispersion model using the finite difference method
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A. Hisaka and Y. Sugiyama. Analysis of nonlinear and nonsteady state hepatic extraction with the dispersion model using the finite difference method. J. Pharmacokinet. Biopharm. 26:495-519. (1998).
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Hisaka, A.1
Sugiyama, Y.2
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16
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0034982023
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A whole-body physiologically based pharmacokinetic model incorporating dispersion concepts: Short and long time characteristics
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R. E. Oliver, A. F. Jones, and M. Rowland. A whole-body physiologically based pharmacokinetic model incorporating dispersion concepts: short and long time characteristics. J. Pharmacokinet. Biopharm. 28:27-55 (2001).
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Oliver, R.E.1
Jones, A.F.2
Rowland, M.3
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18
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-
0025787031
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A two-compartment dispersion model describes the hepatic outflow profile of diclofenac in the presence of its binding protein
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A. M. Evans, Z. Hussein, and M. Rowland. A two-compartment dispersion model describes the hepatic outflow profile of diclofenac in the presence of its binding protein. J. Pharm. Pharmacol. 43:709-714 (1991).
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Evans, A.M.1
Hussein, Z.2
Rowland, M.3
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19
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0031790353
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Application of the dispersion model for description of the outflow dilution profiles of noneliminated reference indicators in rat liver perfusion studies
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A. J. Schwab, W. Geng, and K. S. Pang. Application of the dispersion model for description of the outflow dilution profiles of noneliminated reference indicators in rat liver perfusion studies. J. Pharmacokinet. Biopharm. 26:163-181 (1998).
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Schwab, A.J.1
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Pang, K.S.3
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20
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0033914033
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Cytoplasmic binding and disposition kinetics of diclofenac in the isolated perfused rat liver
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M. Weiss, O. Kuhlmann, D. Y. Hung, and M. S. Roberts. Cytoplasmic binding and disposition kinetics of diclofenac in the isolated perfused rat liver. Br. J. Pharmacol. 130:1331-1338 (2000).
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Weiss, M.1
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21
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0032940054
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Analysis of nonlinear hepatic clearance of a cyclopentapeptide, BQ-123, with the multiple indicator dilution method using the dispersion model
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A. Hisaka, T. Nakamura, and Y. Sugiyama. Analysis of nonlinear hepatic clearance of a cyclopentapeptide, BQ-123, with the multiple indicator dilution method using the dispersion model. Pharm. Res. 16:103-109. (1999).
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Hisaka, A.1
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22
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0032924999
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Analysis program based on finite element method, MULTI(FEM), for evaluation of dose-dependent local disposition of drug in liver
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K. Fukumura, K. Yamaoka, M. Higashimori, and T. Nakagawa. Analysis program based on finite element method, MULTI(FEM), for evaluation of dose-dependent local disposition of drug in liver. J. Pharm. Sci. 88:538-543 (1999).
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Fukumura, K.1
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23
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0032723479
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Notes on the inverse gaussian distribution and choice of boundary conditions for the dispersion model in the analysis of local pharmacokinetics
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A. Hisaka and Y. Sugiyama. Notes on the inverse gaussian distribution and choice of boundary conditions for the dispersion model in the analysis of local pharmacokinetics. J. Pharm. Sci. 88:1362-1365 (1999).
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Hisaka, A.1
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24
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Problems of mixed boundary conditions for convection-dispersion models in the analysis of local pharmacokinetics
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A. Hisaka and Y. Sugiyama. Problems of mixed boundary conditions for convection-dispersion models in the analysis of local pharmacokinetics. J. Pharm. Sci. 89:1587-1588 (2000).
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Hisaka, A.1
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25
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0033639240
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Commentary: Using the convection-dispersion model and transit time density functions in the analysis of organ distribution kinetics
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M. S. Roberts, Y. G. Anissimov, and M. Weiss. Commentary: using the convection-dispersion model and transit time density functions in the analysis of organ distribution kinetics. J. Pharm. Sci. 89:1579-1586. (2000).
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Roberts, M.S.1
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Weiss, M.3
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26
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0031827417
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Hepatic structure-pharmacokinetic relationships: The hepatic disposition and metabolite kinetics of a homologous series of O-acyl derivatives of salicylic acid
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D. Y. Hung, G. D. Mellick, Y. G. Anissimov, M. Weiss, and M. S. Roberts. Hepatic structure-pharmacokinetic relationships: the hepatic disposition and metabolite kinetics of a homologous series of O-acyl derivatives of salicylic acid. Br. J. Pharmacol. 124:1475-1483 (1998).
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Hung, D.Y.1
Mellick, G.D.2
Anissimov, Y.G.3
Weiss, M.4
Roberts, M.S.5
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27
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0021798973
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Hepatic elimination - Dispersion model
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M. S. Roberts and M. Rowland. Hepatic elimination - dispersion model. J. Pharm. Sci. 74:585-587 (1985).
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(1985)
J. Pharm. Sci.
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Roberts, M.S.1
Rowland, M.2
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28
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0029836290
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The disposition of aspirin and salicylic acid in the isolated perfused rat liver: The effect of normal and retrograde flow on availability and mean transit time
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G. D. Mellick and M. S. Roberts. The disposition of aspirin and salicylic acid in the isolated perfused rat liver: the effect of normal and retrograde flow on availability and mean transit time. J. Pharm. Pharmacol. 48:738-743 (1996).
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Mellick, G.D.1
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30
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0029759461
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Tissue distribution kinetics as determinant of transit time dispersion of drugs in organs: Application of a stochastic model to the rat hindlimb
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M. Weiss and M. S. Roberts. Tissue distribution kinetics as determinant of transit time dispersion of drugs in organs: application of a stochastic model to the rat hindlimb. J. Pharmacokinet. Biopharm. 24:173-196 (1996).
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Weiss, M.1
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31
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0022625742
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The hepatic sinusoid is not well-stirred: Estimation of the degree of axial mixing by analysis of lobular concentration gradients formed during uptake of thyroxine by the perfused rat liver
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R. A. Weisiger, C. M. Mendel, and R. R. Cavalieri. The hepatic sinusoid is not well-stirred: estimation of the degree of axial mixing by analysis of lobular concentration gradients formed during uptake of thyroxine by the perfused rat liver. J. Pharm. Sci. 75:233-237 (1986).
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Weisiger, R.A.1
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32
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0021498023
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Extension of the theory of the multiple indicator dilution technique to variable systems with an arbitrary number of rate constants
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A. J. Schwab. Extension of the theory of the multiple indicator dilution technique to variable systems with an arbitrary number of rate constants. Math. Biosci. 71:57-79 (1984).
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Schwab, A.J.1
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33
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0026447133
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A new method for quantitating intracellular transport: Application to the thyroid hormone 3,5,3′-triiodothyronine
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B. A. Luxon and R. A. Weisiger. A new method for quantitating intracellular transport: application to the thyroid hormone 3,5,3′-triiodothyronine. Am. J. Physiol. 263:G733-741 (1992).
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Luxon, B.A.1
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0030842164
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Effect of fasting on the uptake of bilirubin and sulfobromophthalein by the isolated perfused rat liver
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U. Gartner, T. Goeser, and A. W. Wolkoff. Effect of fasting on the uptake of bilirubin and sulfobromophthalein by the isolated perfused rat liver. Gastroenterology 113:1707-1713 (1997).
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Gartner, U.1
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Wolkoff, A.W.3
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35
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0010431101
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Enterohepatic circulation: Physiological, pharmacokinetic and clinical implications
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Accepted
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M. Roberts, B. Magnusson, F. Burczynski, and M. Weiss. Enterohepatic circulation: Physiological, pharmacokinetic and clinical implications. Clin. Pharmacokin., Accepted 2001.
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Clin. Pharmacokin.
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Roberts, M.1
Magnusson, B.2
Burczynski, F.3
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36
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0019350665
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Functional implications of liver cell heterogeneity
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J. J. Gumucio, and D. L. Miller. Functional implications of liver cell heterogeneity. Gastroenterology 80:393-403 (1981).
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Gumucio, J.J.1
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Enzymatic elimination of substrates flowing through the intact liver
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L. Bass, S. Keiding, K. Winkler, and N. Tygstrup. Enzymatic elimination of substrates flowing through the intact liver. J. Theor. Biol. 61:393-409 (1976).
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Bass, L.1
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38
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0022684662
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Convection-dispersion modeling of hepatic elimination
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L. Bass. Convection-dispersion modeling of hepatic elimination. J. Pharm. Sci. 75:321-322 (1986).
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Bass, L.1
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39
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0031412577
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A physiologically based pharmacokinetic model incorporating dispersion principles to describe solute distribution in the perfused rat hindlimb preparation
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R. E. Oliver, A. C. Heatherington, A. F. Jones, and M. Rowland. A physiologically based pharmacokinetic model incorporating dispersion principles to describe solute distribution in the perfused rat hindlimb preparation. J. Pharmacokinet. Biopharm. 25:389-412 (1997).
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Oliver, R.E.1
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Jones, A.F.3
Rowland, M.4
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