-
1
-
-
0025719746
-
First-pass metabolism of cyclosporin by the gut
-
1. J. C. Kolars, W. M. Awni, R. M. Merion, and P. B. Watkins. First-pass metabolism of cyclosporin by the gut. Lancet 338:1488-1490 (1991).
-
(1991)
Lancet
, vol.338
, pp. 1488-1490
-
-
Kolars, J.C.1
Awni, W.M.2
Merion, R.M.3
Watkins, P.B.4
-
2
-
-
0026464616
-
Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes
-
2. J. C. Kolars, P. Schmiedlin-Ren, J. D. Schuetz, C. Fang, and P. B. Watkins. Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. J. Clin. Invest. 90:1871-1878 (1992).
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 1871-1878
-
-
Kolars, J.C.1
Schmiedlin-Ren, P.2
Schuetz, J.D.3
Fang, C.4
Watkins, P.B.5
-
3
-
-
0030015297
-
Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism
-
3. K. E. Thummel, D. O'Shea, M. F. Paine, D. D. Shen, K. L. Kunze, J. D. Perkins, and G. R. Wilkinson. Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clin. Pharmacol. Ther. 59:491-502 (1996).
-
(1996)
Clin. Pharmacol. Ther.
, vol.59
, pp. 491-502
-
-
Thummel, K.E.1
O'Shea, D.2
Paine, M.F.3
Shen, D.D.4
Kunze, K.L.5
Perkins, J.D.6
Wilkinson, G.R.7
-
4
-
-
0025344378
-
Cytochrome P450 isoenzymes, epoxide hydrolase and glutathione transferases in rat and human hepatic and extrahepatic tissues
-
4. I. De Waziers, P. H. Cugnenc, C. S. Yang, J.-P. Leroux, and P. H. Beaune. Cytochrome P450 isoenzymes, epoxide hydrolase and glutathione transferases in rat and human hepatic and extrahepatic tissues. J. Pharmacol. Exp. Ther. 253:387-394 (1990).
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.253
, pp. 387-394
-
-
De Waziers, I.1
Cugnenc, P.H.2
Yang, C.S.3
Leroux, J.-P.4
Beaune, P.H.5
-
5
-
-
0026457407
-
Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction
-
5. M. F. Hebert, J. P. Roberts, T. Prueksaritanont, and L. Z. Benet. Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction. Clin. Pharmacol. Ther. 52:453-457 (1992).
-
(1992)
Clin. Pharmacol. Ther.
, vol.52
, pp. 453-457
-
-
Hebert, M.F.1
Roberts, J.P.2
Prueksaritanont, T.3
Benet, L.Z.4
-
6
-
-
0029123393
-
The effects of ketoconazole on the intestinal metabolism and bioavailability of cyclosporine
-
6. D. Y. Gomez, V. J. Wacher, S. J. Tomlanovich, M. F. Hebert, and L. Z. Benet. The effects of ketoconazole on the intestinal metabolism and bioavailability of cyclosporine. Clin. Pharmacol. Ther. 58:15-19 (1995).
-
(1995)
Clin. Pharmacol. Ther.
, vol.58
, pp. 15-19
-
-
Gomez, D.Y.1
Wacher, V.J.2
Tomlanovich, S.J.3
Hebert, M.F.4
Benet, L.Z.5
-
8
-
-
0028820208
-
Differentiation of absorption and first-pass gut and hepatic metabolism in humans: Studies with cyclosporine
-
8. C.-Y. Wu, L. Z. Benet, M. F. Hebert, S. K. Gupta, M. Rowland, D. Y. Gomez, and V. J. Wacher. Differentiation of absorption and first-pass gut and hepatic metabolism in humans: Studies with cyclosporine. Clin. Pharmacol. Ther. 58:492-497 (1995).
-
(1995)
Clin. Pharmacol. Ther.
, vol.58
, pp. 492-497
-
-
Wu, C.-Y.1
Benet, L.Z.2
Hebert, M.F.3
Gupta, S.K.4
Rowland, M.5
Gomez, D.Y.6
Wacher, V.J.7
-
9
-
-
0028840847
-
Possible involvement of multiple P-glycoprotein-mediated efflux systems in the transport of verapamil and other organic cations across rat intestine
-
9. H. Saitoh and B. J. Aungst. Possible involvement of multiple P-glycoprotein-mediated efflux systems in the transport of verapamil and other organic cations across rat intestine. Pharm. Res. 12:1304-1310 (1995).
-
(1995)
Pharm. Res.
, vol.12
, pp. 1304-1310
-
-
Saitoh, H.1
Aungst, B.J.2
-
10
-
-
0029800447
-
Active secretion of drugs from the small intestinal epithelium in rats by P-glycoprotein functioning as an absorption barrier
-
10. T. Terao, E. Hisanaga, Y. Sai, I. Tamai, and A. Tsuji. Active secretion of drugs from the small intestinal epithelium in rats by P-glycoprotein functioning as an absorption barrier. J. Pharm. Pharmacol. 48:1083-1089 (1996).
-
(1996)
J. Pharm. Pharmacol.
, vol.48
, pp. 1083-1089
-
-
Terao, T.1
Hisanaga, E.2
Sai, Y.3
Tamai, I.4
Tsuji, A.5
-
11
-
-
0029028792
-
Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: Implications for drug delivery and activity in cancer chemotherapy
-
11. V. J. Wacher, C.-Y. Wu, and L. Z. Benet. Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: Implications for drug delivery and activity in cancer chemotherapy. Mol. Carcinogen. 13:129-134 (1995).
-
(1995)
Mol. Carcinogen.
, vol.13
, pp. 129-134
-
-
Wacher, V.J.1
Wu, C.-Y.2
Benet, L.Z.3
-
12
-
-
0030059953
-
Modulators and substrates of P-glycoprotein and cytochrome P4503A coordinately up-regulate these proteins in human colon carcinoma cells
-
12. E. G. Schuetz, W. T. Beck, and J. D. Schuetz. Modulators and substrates of P-glycoprotein and cytochrome P4503A coordinately up-regulate these proteins in human colon carcinoma cells. Mol. Pharmacol. 49:311-318 (1996).
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 311-318
-
-
Schuetz, E.G.1
Beck, W.T.2
Schuetz, J.D.3
-
13
-
-
12644272784
-
Role of intestinal P-glycoprotein (mdr1) in interpatient variation in the oral bioavailability of cyclosporine
-
13. K. S. Lown, R. R. Mayo, A. B. Leichtman, H. L. Hsiao, D. K. Turgeon, P. Schmiedlin-Ren, M. B. Brown, W. Guo, S. J. Rossi, L. Z. Benet, and P. B. Watkins. Role of intestinal P-glycoprotein (mdr1) in interpatient variation in the oral bioavailability of cyclosporine. Clin. Pharmacol. Ther. 62:248-260 (1997).
-
(1997)
Clin. Pharmacol. Ther.
, vol.62
, pp. 248-260
-
-
Lown, K.S.1
Mayo, R.R.2
Leichtman, A.B.3
Hsiao, H.L.4
Turgeon, D.K.5
Schmiedlin-Ren, P.6
Brown, M.B.7
Guo, W.8
Rossi, S.J.9
Benet, L.Z.10
Watkins, P.B.11
-
14
-
-
0031944723
-
Overlapping substrate specificities of cytochrome P450 3A and P-glycoprotein for a novel cysteine protease inhibitor
-
14. Y. Zhang, X. Guo, E. T. Lin, and L. Z. Benet. Overlapping substrate specificities of cytochrome P450 3A and P-glycoprotein for a novel cysteine protease inhibitor. Drug Metab. Dispos. 26:360-366 (1998).
-
(1998)
Drug Metab. Dispos.
, vol.26
, pp. 360-366
-
-
Zhang, Y.1
Guo, X.2
Lin, E.T.3
Benet, L.Z.4
-
15
-
-
0018850819
-
Quantitative mechanistic studies in simultaneous fluid flow and intestinal absorption using steroids as model solutes
-
15. I. Komiya, J. Y. Park, A. Kamani, N. F. H. Ho, and W. I. Higuchi. Quantitative mechanistic studies in simultaneous fluid flow and intestinal absorption using steroids as model solutes. Int. J. Pharm. 4:249-262 (1980).
-
(1980)
Int. J. Pharm.
, vol.4
, pp. 249-262
-
-
Komiya, I.1
Park, J.Y.2
Kamani, A.3
Ho, N.F.H.4
Higuchi, W.I.5
-
16
-
-
0027302432
-
Construction of a physiologically based pharmacokinetic model to describe the hepatobiliary excretion process of ligands: Quantitative estimation of intracellular diffusion
-
16. K. Sathirakul, H. Suzuki, K. Yasuda, M. Hanano, and Y. Sugiyama. Construction of a physiologically based pharmacokinetic model to describe the hepatobiliary excretion process of ligands: quantitative estimation of intracellular diffusion. Biol. Pharm. Bull. 16:273-279 (1993).
-
(1993)
Biol. Pharm. Bull.
, vol.16
, pp. 273-279
-
-
Sathirakul, K.1
Suzuki, H.2
Yasuda, K.3
Hanano, M.4
Sugiyama, Y.5
-
17
-
-
0025196085
-
Physiological measurements of luminal stirring in the dog and human small bowel
-
17. M. D. Levitt, J. K. Furne, A. Strocchi, B. W. Anderson, and D. G. Levitt. Physiological measurements of luminal stirring in the dog and human small bowel. J. Clin. Invest. 86:1540-1547 (1990).
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 1540-1547
-
-
Levitt, M.D.1
Furne, J.K.2
Strocchi, A.3
Anderson, B.W.4
Levitt, D.G.5
-
18
-
-
0029950964
-
Prediction of in vivo drug disposition from in vitro data based on physiological pharmacokinetics
-
18. T. Iwatsubo, N. Hirota, T. Ooie, H. Suzuki, and Y. Sugiyama. Prediction of in vivo drug disposition from in vitro data based on physiological pharmacokinetics. Biopharm. Drug Dispos. 17:273-310 (1996).
-
(1996)
Biopharm. Drug Dispos.
, vol.17
, pp. 273-310
-
-
Iwatsubo, T.1
Hirota, N.2
Ooie, T.3
Suzuki, H.4
Sugiyama, Y.5
-
19
-
-
0030937636
-
Prediction of in vivo drug metabolism in the human liver from in vitro metabolism data
-
19. 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
-
20
-
-
0031777718
-
Quantitative prediction of in vi vo drug clearance and drug interactions from in vitro data on metabolism together with binding and transport
-
20. K. Ito, T. Iwatsubo, S. Kanamitsu, Y. Nakajima, and Y. Sugiyama. Quantitative prediction of in vi vo drug clearance and drug interactions from in vitro data on metabolism together with binding and transport. Annu. Rev. Pharmacol. Toxicol. 38:461-499 (1998).
-
(1998)
Annu. Rev. Pharmacol. Toxicol.
, vol.38
, pp. 461-499
-
-
Ito, K.1
Iwatsubo, T.2
Kanamitsu, S.3
Nakajima, Y.4
Sugiyama, Y.5
-
21
-
-
0030483051
-
Strategic proposals for avoiding toxic interactions with drugs for clinical use during development and after marketing of a new drug: Pharmacokinetic consideration
-
21. Y. Sugiyama, T. Iwatsubo, K. Ueda, and K. Ito. Strategic proposals for avoiding toxic interactions with drugs for clinical use during development and after marketing of a new drug: pharmacokinetic consideration. J. Toxicol. Sci. 21:309-316 (1996).
-
(1996)
J. Toxicol. Sci.
, vol.21
, pp. 309-316
-
-
Sugiyama, Y.1
Iwatsubo, T.2
Ueda, K.3
Ito, K.4
-
22
-
-
0031723235
-
Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver
-
22. K. Ito, T. Iwatsubo, S. Kanamitsu, K. Ueda, H. Suzuki, and Y. Sugiyama. Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver. Pharmacol. Rev. 50:387-411 (1998).
-
(1998)
Pharmacol. Rev.
, vol.50
, pp. 387-411
-
-
Ito, K.1
Iwatsubo, T.2
Kanamitsu, S.3
Ueda, K.4
Suzuki, H.5
Sugiyama, Y.6
-
23
-
-
0024579134
-
A quantitative study of fluorescein isothiocyanate-dextran transport in the microcirculation of the isolated perfused rat liver
-
23. R. J. Stock, E. V. Cilento, and R. S. McCuskey. A quantitative study of fluorescein isothiocyanate-dextran transport in the microcirculation of the isolated perfused rat liver. Hepatology 9:75-82 (1989).
-
(1989)
Hepatology
, vol.9
, pp. 75-82
-
-
Stock, R.J.1
Cilento, E.V.2
McCuskey, R.S.3
-
24
-
-
0020184671
-
How crowded is the cytoplasm?
-
24. A. B. Fulton. How crowded is the cytoplasm? Cell 30:345-347 (1982).
-
(1982)
Cell
, vol.30
, pp. 345-347
-
-
Fulton, A.B.1
-
25
-
-
0030908131
-
Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Major role of CYP3A
-
25. 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
-
26
-
-
0031445547
-
Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism
-
26. 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
-
27
-
-
0025804183
-
Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells
-
27. P. Artursson and J. Karlsson. Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells. Biochem. Biophys. Res. Comm. 175:880-885 (1991).
-
(1991)
Biochem. Biophys. Res. Comm.
, vol.175
, pp. 880-885
-
-
Artursson, P.1
Karlsson, J.2
-
28
-
-
0030986812
-
Analysis of drug permeation across Caco-2 monolayer: Implication for predicting in vivo drug absorption
-
28. S. Yamashita, Y. Tanaka, Y. Endoh, Y. Taki, T. Sakane, T. Nadai, and H. Sezaki. Analysis of drug permeation across Caco-2 monolayer: implication for predicting in vivo drug absorption. Pharm. Res. 14:486-491 (1997).
-
(1997)
Pharm. Res.
, vol.14
, pp. 486-491
-
-
Yamashita, S.1
Tanaka, Y.2
Endoh, Y.3
Taki, Y.4
Sakane, T.5
Nadai, T.6
Sezaki, H.7
-
29
-
-
0030465760
-
Development of Caco2 cells expressing high levels of cDNA-derived cytochrome P4503A4
-
29. C. L. Crespi, B. W. Penman, and M. Hu. Development of Caco2 cells expressing high levels of cDNA-derived cytochrome P4503A4. Pharm. Res. 13:1635-1641 (1996).
-
(1996)
Pharm. Res.
, vol.13
, pp. 1635-1641
-
-
Crespi, C.L.1
Penman, B.W.2
Hu, M.3
|