-
1
-
-
0015763634
-
Classical pharmacokinetics to the frontier
-
Garrett, E.R. Classical pharmacokinetics to the frontier. J. Pharmacokinet. Biopharm. 1, 341-361 (1973).
-
(1973)
J. Pharmacokinet. Biopharm.
, vol.1
, pp. 341-361
-
-
Garrett, E.R.1
-
2
-
-
4744339424
-
In vivo comparisons of constitutive cytochrome P450 3A activity assessed by alprazolam, triazolam, and midazolam
-
Masica, A.L., Mayo G., and Wilkinson, G.R. In vivo comparisons of constitutive cytochrome P450 3A activity assessed by alprazolam, triazolam, and midazolam. Clin. Pharmacol. Ther. 76 , 341-349 (2004).
-
(2004)
Clin. Pharmacol. Ther.
, vol.76
, pp. 341-349
-
-
Masica, A.L.1
Mayo, G.2
Wilkinson, G.R.3
-
3
-
-
0020543124
-
Assessment of methods to identify sources of interindividual pharmacokinetic variation
-
Vessell, E.S. and Penno M.B. Assessment of methods to identify sources of interindividual pharmacokinetic variation. Clin. Pharmacokinet. 8, 378-409 (1983).
-
(1983)
Clin. Pharmacokinet.
, vol.8
, pp. 378-409
-
-
Vessell, E.S.1
Penno, M.B.2
-
4
-
-
0034007388
-
Phenotyping of drug-metabolizing enzymes in adults: A review of in vivo cytochrome P450 phenotyping probes
-
Streetman, D.S., Bertino J.S. Jr., and Nafziger, A.N. Phenotyping of drug-metabolizing enzymes in adults: A review of in vivo cytochrome P450 phenotyping probes. Pharmacogenetics 10, 187-216 (2000).
-
(2000)
Pharmacogenetics
, vol.10
, pp. 187-216
-
-
Streetman, D.S.1
Bertino Jr., J.S.2
Nafziger, A.N.3
-
5
-
-
0037131879
-
Genetic contribution to variable human CYP3A-mediated metabolism
-
Lamba, J.K., Lin Y.S., Schuetz, E.G., and Thummel, K.E. Genetic contribution to variable human CYP3A-mediated metabolism. Adv. Drug Deliv. Rev. 54, 1271-1294 (2002).
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 1271-1294
-
-
Lamba, J.K.1
Lin, Y.S.2
Schuetz, E.G.3
Thummel, K.E.4
-
6
-
-
17644380257
-
Predicting drug disposition via application of BCS: Transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system
-
Wu, C-Y. and Benet, L. Z. Predicting drug disposition via application of BCS: Transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm. Res. 22, 11-23 (2005).
-
(2005)
Pharm. Res.
, vol.22
, pp. 11-23
-
-
Wu, C.-Y.1
Benet, L.Z.2
-
7
-
-
0028948839
-
A theoretical basis for a biopharmaceutics drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon, G.L., Lennernas, H., Shah, V.P., and Crison J.R. A theoretical basis for a biopharmaceutics drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12, 413-420 (1995).
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
8
-
-
0003455057
-
Guidance for Industry: Waiver of in vivo bioavailability and bioequivalence studies for immediate release solid oral dosage forms based on a biopharmaceutics classification system
-
Food and Drug Administration. Food and Drug Administration, Rockville, MD Available at
-
Food and Drug Administration. Guidance for Industry: Waiver of in vivo bioavailability and bioequivalence studies for immediate release solid oral dosage forms based on a biopharmaceutics classification system. Food and Drug Administration, Rockville, MD (2000). Available at http://www.fda.gov/cder/guidance/index.htm
-
(2000)
-
-
-
9
-
-
0242585000
-
Midazolam exhibits characteristics of a highly permeable P-glycoprotein substrate
-
Tolle-Sander, S., Rautio, J., Wring, S., Polli, J.W., and Polli, J.E. Midazolam exhibits characteristics of a highly permeable P-glycoprotein substrate. Pharm. Res. 20, 757-764 (2003).
-
(2003)
Pharm. Res.
, vol.20
, pp. 757-764
-
-
Tolle-Sander, S.1
Rautio, J.2
Wring, S.3
Polli, J.W.4
Polli, J.E.5
-
10
-
-
17844386159
-
The effect of the interplay between CYP3A4 and P-gp on the metabolism of saquinavir and nifedipine in CYP3A4-transfected Caco-2 cells
-
Pharmaceutical Sciences World Congress Kyoto, Japan, June Abstract P2E-II-026
-
Watanabe, N. and Benet, L.Z. The effect of the interplay between CYP3A4 and P-gp on the metabolism of saquinavir and nifedipine in CYP3A4-transfected Caco-2 cells. Pharmaceutical Sciences World Congress, Kyoto, Japan, June, 2004, Abstract P2E-II-026.
-
(2004)
-
-
Watanabe, N.1
Benet, L.Z.2
-
11
-
-
0003344708
-
Design and optimization of dosage regimens: Pharmacokinetic data
-
(Hardman, J.G. and Limbird, L.E., eds.) 10th edition, McGraw Hill, New York
-
Thummel, K.F. and Shen D.D. Design and optimization of dosage regimens: pharmacokinetic data, in Goodman and Gilman's The Pharmacological Basis of Therapeutics (Hardman, J.G. and Limbird, L.E., eds.) pp. 1924-2023, 10th edition, McGraw Hill, New York (2001).
-
(2001)
Goodman and Gilman's The Pharmacological Basis of Therapeutics
, pp. 1924-2023
-
-
Thummel, K.F.1
Shen, D.D.2
-
12
-
-
0033323791
-
Pharmacokinetic and pharmacodynamic consequences of metabolism-based drug interactions with alprazolam, midazolam, and triazolam
-
Yuan, R., Flockhart, D.A., and Balian, J.D. Pharmacokinetic and pharmacodynamic consequences of metabolism-based drug interactions with alprazolam, midazolam, and triazolam. J. Clin. Pharmacol. 39, 1109-1125 (1999).
-
(1999)
J. Clin. Pharmacol.
, vol.39
, pp. 1109-1125
-
-
Yuan, R.1
Flockhart, D.A.2
Balian, J.D.3
-
13
-
-
0023627636
-
Urinary screening for alprazolam, triazolam, and their metabolites with EMIT d.a.u. benzodiazepine metabolite assay
-
Fraser, A.D. Urinary screening for alprazolam, triazolam, and their metabolites with EMIT d.a.u. benzodiazepine metabolite assay. J. Anal. Toxicol. 11, 263-266 (1987).
-
(1987)
J. Anal. Toxicol.
, vol.11
, pp. 263-266
-
-
Fraser, A.D.1
-
14
-
-
7944237810
-
Intravenous and oral alfentanil as in vivo probes for hepatic and first-pass cytochrome P450 3A activity: Noninvasive assessment by use of pupillary miosis
-
Kharasch, E.D., Walker, A., Hoffer, C., and Sheffels, P. Intravenous and oral alfentanil as in vivo probes for hepatic and first-pass cytochrome P450 3A activity: noninvasive assessment by use of pupillary miosis. Clin. Pharmacol. Ther. 76, 452-466 (2004).
-
(2004)
Clin. Pharmacol. Ther.
, vol.76
, pp. 452-466
-
-
Kharasch, E.D.1
Walker, A.2
Hoffer, C.3
Sheffels, P.4
-
15
-
-
0033160860
-
Intraindividual variability in male hepatic CYP3A4 activity assessed by alfentanil and midazolam clearance
-
Kharasch, E.D., Jubert, C., Senn, T, Bowdle, T.A., and Thummel, K.E. Intraindividual variability in male hepatic CYP3A4 activity assessed by alfentanil and midazolam clearance. J. Clin. Pharmacol. 39, 664-669 (1999).
-
(1999)
J. Clin. Pharmacol.
, vol.39
, pp. 664-669
-
-
Kharasch, E.D.1
Jubert, C.2
Senn, T.3
Bowdle, T.A.4
Thummel, K.E.5
-
16
-
-
14044268352
-
Evaluation of first-pass cytochrome P4503A (CYP3A) and P-glycoprotein activities using alfentanil and fexofenadine in combination
-
Kharasch, E.D., Walker, A., Hoffer, C., and Sheffels, P. Evaluation of first-pass cytochrome P4503A (CYP3A) and P-glycoprotein activities using alfentanil and fexofenadine in combination. J. Clin. Pharmacol. 45, 79-88 (2005).
-
(2005)
J. Clin. Pharmacol.
, vol.45
, pp. 79-88
-
-
Kharasch, E.D.1
Walker, A.2
Hoffer, C.3
Sheffels, P.4
-
17
-
-
0032927254
-
Drug, meal and formulation interactions influencing drug absorption after oral administration. Clinical implications
-
Fleischer, D., Li, C., Zhou, Y., Pao, L.H., and Karim, A. Drug, meal and formulation interactions influencing drug absorption after oral administration. Clinical implications. Clin. Pharmacokinet. 36, 233-254 (1999).
-
(1999)
Clin. Pharmacokinet.
, vol.36
, pp. 233-254
-
-
Fleischer, D.1
Li, C.2
Zhou, Y.3
Pao, L.H.4
Karim, A.5
-
18
-
-
2442719906
-
Unmasking the dynamic interplay between efflux transporters and metabolic enzymes
-
Benet, L.Z., Cummins, C.L., and Wu, C-Y. Unmasking the dynamic interplay between efflux transporters and metabolic enzymes. Int. J. Pharm. 277, 3-9 (2004).
-
(2004)
Int. J. Pharm.
, vol.277
, pp. 3-9
-
-
Benet, L.Z.1
Cummins, C.L.2
Wu, C.-Y.3
-
19
-
-
1342302110
-
Ex situ inhibition of hepatic uptake and efflux significantly changes metabolism: Hepatic enzyme-transporter interplay
-
Lau, Y.Y., Wu, C-Y., Okochi, H., and Benet, L.Z. Ex situ inhibition of hepatic uptake and efflux significantly changes metabolism: Hepatic enzyme-transporter interplay. J. Pharmacol. Exp. Ther. 308, 1040-1045 (2004).
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.308
, pp. 1040-1045
-
-
Lau, Y.Y.1
Wu, C.-Y.2
Okochi, H.3
Benet, L.Z.4
-
20
-
-
6944219986
-
Hepatic microsome studies are insufficient to characterize in vivo hepatic metabolic clearance and metabolic drug-drug interacations: Studies of digoxin metabolism in primary rat hepatocytes versus microsomes
-
Lam, J. L. and Benet L.Z. Hepatic microsome studies are insufficient to characterize in vivo hepatic metabolic clearance and metabolic drug-drug interacations: Studies of digoxin metabolism in primary rat hepatocytes versus microsomes. Drug Metab. Dispos. 32, 1311-1316 (2004).
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 1311-1316
-
-
Lam, J.L.1
Benet, L.Z.2
-
21
-
-
12644272784
-
Role of intestinal P-glycoprotein (mdr1) in interpatient variation in the oral bioavailability of cyclosporine
-
Lown, K.S., Mayo, R.R., Leichtman, A.B. et al. 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
|