-
1
-
-
0019974098
-
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
-
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
-
3
-
-
0030799001
-
The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
-
R. S. Obach, J. G. Baxter, T. E. Liston, B. M. Silber, B. C. Jones, F. MacIntyre, D. J. Rance, and P. Wastall. The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J. Pharmacol. Exp. Ther. 283:46-58 (1997).
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 46-58
-
-
Obach, R.S.1
Baxter, J.G.2
Liston, T.E.3
Silber, B.M.4
Jones, B.C.5
MacIntyre, F.6
Rance, D.J.7
Wastall, P.8
-
4
-
-
0032921527
-
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
-
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
-
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
-
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
-
8
-
-
0030937636
-
Prediction of in vivo drug metabolism in the human liver from in vitro metabolism data
-
T. Iwatsubo, N. Hirota, T. Ooie, H. Suzuki, N. Shimada, K. Chiba, T. Ishizaki, C. E. Green, C. A. Tyson, and Y. Sugiyama. Prediction of in vivo drug metabolism in the human liver from in vitro metabolism data. Pharmacol. Ther. 73:147-171 (1997).
-
(1997)
Pharmacol. Ther.
, vol.73
, pp. 147-171
-
-
Iwatsubo, T.1
Hirota, N.2
Ooie, T.3
Suzuki, H.4
Shimada, N.5
Chiba, K.6
Ishizaki, T.7
Green, C.E.8
Tyson, C.A.9
Sugiyama, Y.10
-
9
-
-
0030911863
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
28
-
-
0030806348
-
Physiological parameter values for physiologically based pharmacokinetic models
-
R. P. Brown, M. D. Delp, S. L. Lindstedt, L. R. Rhomberg, and R. P. Beliles. Physiological parameter values for physiologically based pharmacokinetic models. Toxicol. Ind. Health. 13:407-484 (1997).
-
(1997)
Toxicol. Ind. Health.
, vol.13
, pp. 407-484
-
-
Brown, R.P.1
Delp, M.D.2
Lindstedt, S.L.3
Rhomberg, L.R.4
Beliles, R.P.5
-
30
-
-
0023033053
-
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
-
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
-
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
-
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
-
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
-
35
-
-
37149008003
-
Predicting oral clearance in humans how close can we get with allometry?
-
V. K. Sinha, S. S. De Buck, L. A. Fenu, J. W. Smit, M. Nijsen, R. A. H. J. Gilissen, A. Van Peer, K. Lavrijsen, and C. E. Mackie. Predicting oral clearance in humans how close can we get with allometry? Clin. Pharmacokinet. 47(1):35-45 (2008).
-
(2008)
Clin. Pharmacokinet.
, vol.47
, Issue.1
, pp. 35-45
-
-
Sinha, V.K.1
De Buck, S.S.2
Fenu, L.A.3
Smit, J.W.4
Nijsen, M.5
Gilissen, R.A.H.J.6
Van Peer, A.7
Lavrijsen, K.8
Mackie, C.E.9
-
36
-
-
0031723045
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
43
-
-
65549135680
-
Prediction of non-specific hepatic microsomal binding from readily available physicochemical properties
-
Manchester, UK
-
D. B. Turner, A. Rostami-Hodjegan, G. T. Tucker, and K. Rowland-Yeo. Prediction of non-specific hepatic microsomal binding from readily available physicochemical properties. 9th European ISSX Meeting June 4th-7th, Manchester, UK. (2006).
-
(2006)
9th European ISSX Meeting June 4th-7th
-
-
Turner, D.B.1
Rostami-Hodjegan, A.2
Tucker, G.T.3
Rowland-Yeo, K.4
-
44
-
-
0030850023
-
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
-
45
-
-
0141839733
-
Inter-individual variability in levels of human microsomal protein and hepatocellularity per gram of liver
-
Z. E. Wilson, A. Rostami-Hodjegan, J. L. Burn, A. Tooley, J. Boyle, S. W. Ellis, and G. T. Tucker. Inter-individual variability in levels of human microsomal protein and hepatocellularity per gram of liver. Br. J. Clin. Pharmacol. 56:433-440 (2003).
-
(2003)
Br. J. Clin. Pharmacol.
, vol.56
, pp. 433-440
-
-
Wilson, Z.E.1
Rostami-Hodjegan, A.2
Burn, J.L.3
Tooley, A.4
Boyle, J.5
Ellis, S.W.6
Tucker, G.T.7
-
46
-
-
33845996187
-
Scaling factors for the extrapolation of in vivo microsomal protein and hepatocellularity per gram of liver
-
A. E. Barter, P. H. Beaune, A. R. Boobis, D. J. Carlile, R. J. Edwards, J. B. Houston, J. B. Lipscomb, O. R. Pelkonen, G. T. Tucker, and A. Rostami Hodjegan. Scaling factors for the extrapolation of in vivo microsomal protein and hepatocellularity per gram of liver. Curr. Drug. Metab. 8(1):33-45 (2007).
-
(2007)
Curr. Drug. Metab.
, vol.8
, Issue.1
, pp. 33-45
-
-
Barter, A.E.1
Beaune, P.H.2
Boobis, A.R.3
Carlile, D.J.4
Edwards, R.J.5
Houston, J.B.6
Lipscomb, J.B.7
Pelkonen, O.R.8
Tucker, G.T.9
Rostami Hodjegan, A.10
-
47
-
-
0021746592
-
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
-
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
-
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
-
50
-
-
65549113334
-
Supersaturation properties of poorly soluble weak bases are key factors in determining drug absorption: A simulation study of nifedipine using the ADAM model (Simcyp v7.1)
-
October 1-2, 2007, Athens, Greece
-
D. B. Turner, M. Jamei, G. T. Tucker, and A. Rostami-Hodjegan. Supersaturation properties of poorly soluble weak bases are key factors in determining drug absorption: A simulation study of nifedipine using the ADAM model (Simcyp v7.1). "EUFEPS & COST B25 Conference on Bioavailability and Bioequivalence: Focus on physiological factors and variability. October 1-2, 2007, Athens, Greece. (2007).
-
(2007)
"EUFEPS & COST B25 Conference on Bioavailability and Bioequivalence: Focus on Physiological Factors and Variability
-
-
Turner, D.B.1
Jamei, M.2
Tucker, G.T.3
Rostami-Hodjegan, A.4
-
51
-
-
0344084044
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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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