메뉴 건너뛰기




Volumn 5, Issue 2, 2005, Pages 79-83

There are no useful CYP3A probes that quantitatively predict the in vivo kinetics of other CYP3A substrates and no expectation that one will be found

Author keywords

[No Author keywords available]

Indexed keywords

ALFENTANIL; ALPRAZOLAM; AMIODARONE; BENZODIAZEPINE DERIVATIVE; CARBAMAZEPINE; CYCLOSPORIN; CYTOCHROME P450 2C19; CYTOCHROME P450 2D6; CYTOCHROME P450 3A; CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; DAPSONE; DEBRISOQUINE; DEXTROMETHORPHAN; ERYTHROMYCIN; ERYTHROMYCIN DERIVATIVE; FEXOFENADINE; HYDROCORTISONE; LIDOCAINE; MEPHENYTOIN; MIDAZOLAM; NIFEDIPINE; OMEPRAZOLE; PHENAZONE; RANITIDINE; SAQUINAVIR; TRIAZOLAM; TROLEANDOMYCIN; UNINDEXED DRUG; VERAPAMIL;

EID: 17844393071     PISSN: 15340384     EISSN: None     Source Type: Journal    
DOI: 10.1124/mi.5.2.5     Document Type: Review
Times cited : (38)

References (21)
  • 1
    • 0015763634 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.