-
1
-
-
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
-
2
-
-
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
-
3
-
-
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
-
4
-
-
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. Pharmacokin. Biopharm. 10:201-227 (1982).
-
(1982)
J. Pharmacokin. Biopharm.
, vol.10
, pp. 201-227
-
-
Boxenbaum, H.1
-
5
-
-
0025045663
-
Interspecies metabolism and pharmacokinetic scaling of theophylline disposition
-
F. Gaspari and M. Bonati. Interspecies metabolism and pharmacokinetic scaling of theophylline disposition. Drug Metab. Rev. 22:179-207 (1990).
-
(1990)
Drug Metab. Rev.
, vol.22
, pp. 179-207
-
-
Gaspari, F.1
Bonati, M.2
-
6
-
-
0029828960
-
Interspecies scaling: Predicting clearance of drugs in humans. Three different approaches
-
I. Mahmood and J. D. Balian. Interspecies scaling: predicting clearance of drugs in humans. Three different approaches. Xenobiotica 9:887-895 (1996).
-
(1996)
Xenobiotica
, vol.9
, pp. 887-895
-
-
Mahmood, I.1
Balian, J.D.2
-
7
-
-
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
-
8
-
-
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. 15:1474-1479 (1998).
-
(1998)
Pharm. Res.
, vol.15
, pp. 1474-1479
-
-
Chiou, W.L.1
Robbie, G.2
Chung, S.M.3
Wu, T.-C.4
Ma, C.5
-
9
-
-
0034835463
-
Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans
-
Y. Naritomi, S. Terashita, S. Kimura, A. Suzuki, A. Kagayama, and Y. Sugiyama. Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans. Drug Metab. Dispos. 29: 1316-1324 (2001).
-
(2001)
Drug Metab. Dispos.
, vol.29
, pp. 1316-1324
-
-
Naritomi, Y.1
Terashita, S.2
Kimura, S.3
Suzuki, A.4
Kagayama, A.5
Sugiyama, Y.6
-
10
-
-
0030918716
-
Integration of in vitro data into allometric scaling to predict hepatic metabolic clearance in man: Application to 10 extensively metabolized drugs
-
T. Lave, S. Dupin, C. Schmitt, R. C. Chou, D. Jaeck, and P. Coassolo. Integration of in vitro data into allometric scaling to predict hepatic metabolic clearance in man: Application to 10 extensively metabolized drugs. J. Pharm. Sci. 86:584-590 (1997).
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 584-590
-
-
Lave, T.1
Dupin, S.2
Schmitt, C.3
Chou, R.C.4
Jaeck, D.5
Coassolo, P.6
-
11
-
-
0034897160
-
Prediction of hepatic metabolic clearance: Comparison and assessment of prediction models
-
J. Zuegge, G. Schneider, P. Coassolo, and T. Lave. Prediction of hepatic metabolic clearance: Comparison and assessment of prediction models. Clin. Pharmacokin. 40:553-563 (2001).
-
(2001)
Clin. Pharmacokin.
, vol.40
, pp. 553-563
-
-
Zuegge, J.1
Schneider, G.2
Coassolo, P.3
Lave, T.4
-
13
-
-
0029565574
-
Regional drug delivery II: Relationship between drug targeting index and pharmacokinetic parameters for three non-steroidal anti-inflammatory drugs using the rat air pouch model of inflammation
-
A. J. Stevens, S. W. Martin, B. S. Brennan, A. McLachlan, L. A. Gifford, M. Rowland, and J. B. Houston. Regional drug delivery II: relationship between drug targeting index and pharmacokinetic parameters for three non-steroidal anti-inflammatory drugs using the rat air pouch model of inflammation. Pharm. Res. 12: 1987-1996 (1995).
-
(1995)
Pharm. Res.
, vol.12
, pp. 1987-1996
-
-
Stevens, A.J.1
Martin, S.W.2
Brennan, B.S.3
McLachlan, A.4
Gifford, L.A.5
Rowland, M.6
Houston, J.B.7
-
14
-
-
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
-
15
-
-
0030781510
-
Prediction of species differences (rats, dogs, humans) in the in vivo metabolic clearance of YM796 by the liver from in vitro data
-
T. Iwatsubo, H. Suzuki, and Y. Sugiyama. Prediction of species differences (rats, dogs, humans) in the in vivo metabolic clearance of YM796 by the liver from in vitro data. J. Pharmacol. Exp. Ther. 283:462-469 (1997).
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 462-469
-
-
Iwatsubo, T.1
Suzuki, H.2
Sugiyama, Y.3
-
16
-
-
0030908131
-
Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Major role of CYP3A
-
M. Chiba, M. Hensleigh, and J. H. Lin. Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Major role of CYP3A. Biochem. Pharmacol. 53:1187-1195 (1997).
-
(1997)
Biochem. Pharmacol.
, vol.53
, pp. 1187-1195
-
-
Chiba, M.1
Hensleigh, M.2
Lin, J.H.3
-
17
-
-
0030467480
-
Disposition of indinavir, a potent HIV-1 protease inhibitor, after an oral dose in humans
-
S. K. Balani, E. J. Woolf, V. L. Hoagland, M. G. Sturgill, P. J. Deutsch, K. C. Yeh, and J. H. Lin. Disposition of indinavir, a potent HIV-1 protease inhibitor, after an oral dose in humans. Drug Metab. Dispos. 24:1389-1394 (1996).
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 1389-1394
-
-
Balani, S.K.1
Woolf, E.J.2
Hoagland, V.L.3
Sturgill, M.G.4
Deutsch, P.J.5
Yeh, K.C.6
Lin, J.H.7
-
18
-
-
0029974065
-
Species differences in the pharmacokinetics and metabolism of indinavir, a potent human immunodeficiency virus protease inhibitor
-
J. H. Lin, M. Chiba, S. K. Balani, I.-W. Chen, G. Y.-S. Kwei, K. J. Vastag, and J. A. Nishime. Species differences in the pharmacokinetics and metabolism of indinavir, a potent human immunodeficiency virus protease inhibitor. Drug Metab. Dispos. 24: 1111-1120 (1996).
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 1111-1120
-
-
Lin, J.H.1
Chiba, M.2
Balani, S.K.3
Chen, I.-W.4
Kwei, G.Y.-S.5
Vastag, K.J.6
Nishime, J.A.7
-
19
-
-
0030459494
-
Identification of 2,6-xylidine as a major lidocaine metabolite in human liver slices
-
R. J. Parker, J. M. Collins, and J. M. Strong. Identification of 2,6-xylidine as a major lidocaine metabolite in human liver slices. Drug Metab. Dispos. 24:1167-1173 (1996).
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 1167-1173
-
-
Parker, R.J.1
Collins, J.M.2
Strong, J.M.3
-
20
-
-
0028840740
-
Multiple forms of cytochrome P450 are involved in the metabolism of ondansetron in humans
-
C. M. Dixon, P. V. Colthup, C. J. Serabjit-Singh, B. M. Kerr, C. C. Boehlert, G. R. Park, and M. H. Tarbit. Multiple forms of cytochrome P450 are involved in the metabolism of ondansetron in humans. Drug Metab. Dispos. 23:1225-1230 (1995).
-
(1995)
Drug Metab. Dispos.
, vol.23
, pp. 1225-1230
-
-
Dixon, C.M.1
Colthup, P.V.2
Serabjit-Singh, C.J.3
Kerr, B.M.4
Boehlert, C.C.5
Park, G.R.6
Tarbit, M.H.7
-
21
-
-
0029683112
-
Antipyrine as a probe for human oxidative drug metabolism: Identification of the cytochrome P450 enzymes catalyzing 4-hydroxyantipyrine, 3-hydroxymethylantipyrine, and norantipyrine formation
-
G. Engel, U. Hofmann, H. Heidemann, J. Cosme, and M. Eichelbaum. Antipyrine as a probe for human oxidative drug metabolism: identification of the cytochrome P450 enzymes catalyzing 4-hydroxyantipyrine, 3- hydroxymethylantipyrine, and norantipyrine formation. Clin. Pharmacol. Ther. 59:613-623 (1996).
-
(1996)
Clin. Pharmacol. Ther.
, vol.59
, pp. 613-623
-
-
Engel, G.1
Hofmann, U.2
Heidemann, H.3
Cosme, J.4
Eichelbaum, M.5
-
22
-
-
0028856279
-
Determination of P4501A2 activity in human liver microsomes using [3-14C-methyl]caffeine
-
J. C. Bloomer, S. E. Clarke, and R. J. Chenery. Determination of P4501A2 activity in human liver microsomes using [3-14C-methyl]caffeine. Xenobiotica 25:917-927 (1995).
-
(1995)
Xenobiotica
, vol.25
, pp. 917-927
-
-
Bloomer, J.C.1
Clarke, S.E.2
Chenery, R.J.3
-
23
-
-
0026005081
-
Stereoselective metabolism of felodipine in liver microsomes from rat, dog, and human
-
U. G. Eriksson, J. Lundahl, C. Baarnhielm, and C. G. Regardh. Stereoselective metabolism of felodipine in liver microsomes from rat, dog, and human. Drug Metab. Dispos. 19:889-894 (1991).
-
(1991)
Drug Metab. Dispos.
, vol.19
, pp. 889-894
-
-
Eriksson, U.G.1
Lundahl, J.2
Baarnhielm, C.3
Regardh, C.G.4
-
24
-
-
0024993542
-
Propranolol oxidation by human liver microsomes - The use of cumene hydroperoxide to probe isoenzyme specificity and regio- and stereoselectivity
-
S. V. Otton, E. M. Gillam, M. S. Lennard, G. T. Tucker, and H. F. Woods. Propranolol oxidation by human liver microsomes - the use of cumene hydroperoxide to probe isoenzyme specificity and regio- and stereoselectivity. Br. J. Clin. Pharmacol. 30:751-760 (1990).
-
(1990)
Br. J. Clin. Pharmacol.
, vol.30
, pp. 751-760
-
-
Otton, S.V.1
Gillam, E.M.2
Lennard, M.S.3
Tucker, G.T.4
Woods, H.F.5
-
25
-
-
0026769890
-
Induction of propranolol metabolism by the azo dye sudan III in rats
-
R. Ishida, S. Obara, Y. Masubuchi, S. Narimatsu, S. Fujita, and T. Suziki. Induction of propranolol metabolism by the azo dye sudan III in rats. Biochem. Pharmacol. 43:2489-2492 (1992).
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 2489-2492
-
-
Ishida, R.1
Obara, S.2
Masubuchi, Y.3
Narimatsu, S.4
Fujita, S.5
Suziki, T.6
-
26
-
-
0021866744
-
A carrier-protein receptor is not a prerequisite for avid hepatic elimination of highly bound compounds: A study of propranolol elimination by the isolated perfused rat liver
-
D. B. Jones, M. S. Ching, R. A. Smallwood, and D. J. Morgan. A carrier-protein receptor is not a prerequisite for avid hepatic elimination of highly bound compounds: A study of propranolol elimination by the isolated perfused rat liver. Hepatology 5:590-593 (1985).
-
(1985)
Hepatology
, vol.5
, pp. 590-593
-
-
Jones, D.B.1
Ching, M.S.2
Smallwood, R.A.3
Morgan, D.J.4
-
27
-
-
0017603437
-
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
-
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. Pharmacokin. Biopharm. 5:625-653 (1977).
-
(1977)
J. Pharmacokin. Biopharm.
, vol.5
, pp. 625-653
-
-
Pang, K.S.1
Rowland, M.2
-
30
-
-
0025265465
-
Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose
-
G. M. Pollack, K. L. R. Brouwer, K. B. Demby, and J. A. Jones. Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose. Drug Metab. Dispos. 18:197-202 (1999).
-
(1999)
Drug Metab. Dispos.
, vol.18
, pp. 197-202
-
-
Pollack, G.M.1
Brouwer, K.L.R.2
Demby, K.B.3
Jones, J.A.4
-
31
-
-
0018170924
-
Complications in the estimation of hepatic blood flow in vivo by pharmacokinetic parameters
-
K. S. Pang and J. R. Gillette. Complications in the estimation of hepatic blood flow in vivo by pharmacokinetic parameters. Drug Metab. Dispos. 6:567-576 (1978).
-
(1978)
Drug Metab. Dispos.
, vol.6
, pp. 567-576
-
-
Pang, K.S.1
Gillette, J.R.2
-
32
-
-
0019604592
-
Some suggestions for measuring predictive performance
-
L. B. Sheiner and S. L. Beal. Some suggestions for measuring predictive performance J. Pharmacokin. Biopharm. 9:503-512 (1981).
-
(1981)
J. Pharmacokin. Biopharm.
, vol.9
, pp. 503-512
-
-
Sheiner, L.B.1
Beal, S.L.2
-
33
-
-
0036194124
-
In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance
-
M. G. Soars, B. Burchell, and R. J. Riley. In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance. J. Pharmacol. Exp. Ther. 301:382-390 (2002).
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.301
, pp. 382-390
-
-
Soars, M.G.1
Burchell, B.2
Riley, R.J.3
-
34
-
-
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
-
35
-
-
0035154850
-
The potential pharmacological and toxicological impact of P450 screening
-
R. J. Riley. The potential pharmacological and toxicological impact of P450 screening. Curr. Opin. Drug Discov. Devel. 4:45-54 (2001).
-
(2001)
Curr. Opin. Drug Discov. Devel.
, vol.4
, pp. 45-54
-
-
Riley, R.J.1
-
36
-
-
0036075799
-
Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models for drug disposition
-
P. Poulin. and F-P Theil. Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models for drug disposition. J. Pharm. Sci. 91:1358-1370 (2002).
-
(2002)
J. Pharm. Sci.
, vol.91
, pp. 1358-1370
-
-
Poulin, P.1
Theil, F.-P.2
-
37
-
-
0034105896
-
In vitro-in vivo scaling of CYP kinetic data not consistent with the classical Michaelis-Menten model
-
J. B. Houston and K. E. Kenworthy. In vitro-in vivo scaling of CYP kinetic data not consistent with the classical Michaelis-Menten model. Drug Metab. Dispos. 28:246-254 (2000).
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 246-254
-
-
Houston, J.B.1
Kenworthy, K.E.2
-
38
-
-
0031445547
-
Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism
-
M. F. Paine, M. Khalighi, J. M. Fisher, D. D. Shen, K. L. Kunze, C. L. Marsh, J. D. Perkins, and K. E. Thummel. Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. J. Pharmacol. Exp. Ther. 283:1552-1562 (1997).
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 1552-1562
-
-
Paine, M.F.1
Khalighi, M.2
Fisher, J.M.3
Shen, D.D.4
Kunze, K.L.5
Marsh, C.L.6
Perkins, J.D.7
Thummel, K.E.8
-
39
-
-
0033022765
-
Characterization of human small intestinal cytochromes P-450
-
Q. Y. Zhang, D. Dunbar, A. Ostrowska, S. Zeisloft, J. Yang, and L. S. Kaminsky. Characterization of human small intestinal cytochromes P-450. Drug Metab. Dispos. 27:804-809 (1999).
-
(1999)
Drug Metab. Dispos.
, vol.27
, pp. 804-809
-
-
Zhang, Q.Y.1
Dunbar, D.2
Ostrowska, A.3
Zeisloft, S.4
Yang, J.5
Kaminsky, L.S.6
-
40
-
-
0033009998
-
Is the role of the small intestine in first-pass metabolism overemphasized?
-
H. J. Lin, M. Chiba, and T. A. Baillie. Is the role of the small intestine in first-pass metabolism overemphasized? Pharmacol. Rev. 51:135-157 (1999).
-
(1999)
Pharmacol. Rev.
, vol.51
, pp. 135-157
-
-
Lin, H.J.1
Chiba, M.2
Baillie, T.A.3
|