메뉴 건너뛰기




Volumn 39, Issue 11, 2011, Pages 2085-2092

Determination of time-dependent inactivation of CYP3A4 in cryopreserved human hepatocytes and assessment of human drug-drug interactions

Author keywords

[No Author keywords available]

Indexed keywords

ALPRAZOLAM; CYCLOSPORIN; CYTOCHROME P450 3A4; DILTIAZEM; ERYTHROMYCIN; METOPROLOL; MIDAZOLAM; NIFEDIPINE; SILDENAFIL; SIMVASTATIN; THEOPHYLLINE; TRIAZOLAM; TROLEANDOMYCIN; VERAPAMIL;

EID: 80054733298     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.111.040634     Document Type: Article
Times cited : (51)

References (21)
  • 1
    • 29944446485 scopus 로고    scopus 로고
    • Prediction of time-dependent CYP3A4 drug-drug interactions: Impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
    • DOI 10.1124/dmd.105.006874
    • Galetin A, Burt H, Gibbons L, and Houston JB (2006) Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition. Drug Metab Dispos 34:166-175. (Pubitemid 43042658)
    • (2006) Drug Metabolism and Disposition , vol.34 , Issue.1 , pp. 166-175
    • Galetin, A.1    Burt, H.2    Gibbons, L.3    Houston, J.B.4
  • 2
    • 33645980647 scopus 로고    scopus 로고
    • A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation
    • Ghanbari F, Rowland-Yeo K, Bloomer JC, Clarke SE, Lennard MS, Tucker GT, and Rostami- Hodjegan A (2006) A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation. Curr Drug Metab 7:315-334.
    • (2006) Curr Drug Metab , vol.7 , pp. 315-334
    • Ghanbari, F.1    Rowland-Yeo, K.2    Bloomer, J.C.3    Clarke, S.E.4    Lennard, M.S.5    Tucker, G.T.6    Rostami- Hodjegan, A.7
  • 3
    • 67649389519 scopus 로고    scopus 로고
    • The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: A perspective of the pharmaceutical research and manufacturers of America
    • Grimm SW, Einolf HJ, Hall SD, He K, Lim HK, Ling KH, Lu C, Nomeir AA, Seibert E, Skordos KW, et al. (2009) The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: a perspective of the pharmaceutical research and manufacturers of America. Drug Metab Dispos 37:1355-1370.
    • (2009) Drug Metab Dispos , vol.37 , pp. 1355-1370
    • Grimm, S.W.1    Einolf, H.J.2    Hall, S.D.3    He, K.4    Lim, H.K.5    Ling, K.H.6    Lu, C.7    Nomeir, A.A.8    Seibert, E.9    Skordos, K.W.10
  • 4
    • 0038311984 scopus 로고    scopus 로고
    • Prediction of the in vivo interaction between midazolam and macrolides based on in vitro studies using human liver microsomes
    • DOI 10.1124/dmd.31.7.945
    • Ito K, Ogihara K, Kanamitsu S, and Itoh T (2003) Prediction of the in vivo interaction between midazolam and macrolides based on in vitro studies using human liver microsomes. Drug Metab Dispos 31:945-954. (Pubitemid 36759066)
    • (2003) Drug Metabolism and Disposition , vol.31 , Issue.7 , pp. 945-954
    • Ito, K.1    Ogihara, K.2    Kanamitsu, S.-I.3    Itoh, T.4
  • 7
    • 79956136652 scopus 로고    scopus 로고
    • Complex drug interactions of HIV protease inhibitors 1: Inactivation, induction and inhibition of cytochrome P450 3A by ritonavir or nelfinavir
    • Kirby BJ, Collier AC, Kharasch ED, Whittington D, Thummel KE, and Unadkat JD (2011) Complex drug interactions of HIV protease inhibitors 1: inactivation, induction and inhibition of cytochrome P450 3A by ritonavir or nelfinavir. Drug Metab Dispos 39:1070-1078.
    • (2011) Drug Metab Dispos , vol.39 , pp. 1070-1078
    • Kirby, B.J.1    Collier, A.C.2    Kharasch, E.D.3    Whittington, D.4    Thummel, K.E.5    Unadkat, J.D.6
  • 8
    • 80054774673 scopus 로고    scopus 로고
    • Physiologically-based pharmacokinetic (PBPK) models for prediction of time-dependent enzyme inhibition (TDI): effect of diltiazem on midazolam and quinidine. Poster presented at the American Association of Pharmaceutical Scientists, Arlington, VA
    • Lukacova V, Chung JI, Woltosz WS, Bolger MB. Physiologically-based pharmacokinetic (PBPK) models for prediction of time-dependent enzyme inhibition (TDI): effect of diltiazem on midazolam and quinidine. Poster presented at the American Association of Pharmaceutical Scientists Annual Meeting and Exposition; 2010 Nov 14-18; New Orleans, LA. American Association of Pharmaceutical Scientists, Arlington, VA.
    • American Association of Pharmaceutical Scientists Annual Meeting and Exposition; 2010 Nov 14-18; New Orleans, la
    • Lukacova, V.1    Chung, J.I.2    Woltosz, W.S.3    Bolger, M.B.4
  • 9
    • 0033831197 scopus 로고    scopus 로고
    • An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation
    • Mayhew BS, Jones DR, and Hall SD (2000) An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation. Drug Metab Dispos 28:1031-1037. (Pubitemid 30660356)
    • (2000) Drug Metabolism and Disposition , vol.28 , Issue.9 , pp. 1031-1037
    • Mayhew, B.S.1    Jones, A.D.R.2    Hall, S.D.3
  • 10
    • 33746047547 scopus 로고    scopus 로고
    • Evaluation of time-dependent cytochrome P450 inhibition using cultured human hepatocytes
    • DOI 10.1124/dmd.106.009969
    • McGinnity DF, Berry AJ, Kenny JR, Grime K, and Riley RJ (2006) Evaluation of timedependent cytochrome P450 inhibition using cultured human hepatocytes. Drug Metab Dispos 34:1291-1300. (Pubitemid 44079869)
    • (2006) Drug Metabolism and Disposition , vol.34 , Issue.8 , pp. 1291-1300
    • McGinnity, D.F.1    Berry, A.J.2    Kenny, J.R.3    Grime, K.4    Riley, R.J.5
  • 11
    • 33846449874 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions
    • DOI 10.1124/dmd.106.012633
    • Obach RS, Walsky RL, and Venkatakrishnan K (2007) Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions. Drug Metab Dispos 35:246-255. (Pubitemid 46148737)
    • (2007) Drug Metabolism and Disposition , vol.35 , Issue.2 , pp. 246-255
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3
  • 12
    • 13244287685 scopus 로고    scopus 로고
    • 'In silico' simulations to assess the 'in vivo' consequences of 'in vitro' metabolic drug-drug interactions
    • DOI 10.1016/j.ddtec.2004.10.002, PII S174067490400037X
    • Rostami-Hodjegan A and Tucker GT (2004) 'In silico' simulations to assess the 'in vivo' consequences of 'in vitro' metabolic drug-drug interactions. Drug Discov Today Tech 1:441-448. (Pubitemid 40186348)
    • (2004) Drug Discovery Today: Technologies , vol.1 , Issue.4 , pp. 441-448
    • Rostami-Hodjegan, A.1    Tucker, G.2
  • 13
    • 34548738229 scopus 로고    scopus 로고
    • Drug-drug interactions via mechanism-based cytochrome P450 inactivation: Points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation
    • DOI 10.2174/138920007780866861
    • Venkatakrishnan K and Obach RS (2007) Drug-drug interactions via mechanism-based cytochrome P450 inactivation: points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation. Curr Drug Metab 8:449-462. (Pubitemid 47603409)
    • (2007) Current Drug Metabolism , vol.8 , Issue.5 , pp. 449-462
    • Venkatakrishnan, K.1    Obach, R.S.2
  • 14
    • 77953787344 scopus 로고    scopus 로고
    • Confidence assessment of the Simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors
    • Wang YH (2010) Confidence assessment of the Simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors. Drug Metab Dispos 38:1094-1104.
    • (2010) Drug Metab Dispos , vol.38 , pp. 1094-1104
    • Wang, Y.H.1
  • 15
    • 0842282550 scopus 로고    scopus 로고
    • Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites
    • DOI 10.1124/dmd.32.2.259
    • Wang YH, Jones DR, and Hall SD (2004) Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites. Drug Metab Dispos 32:259-266. (Pubitemid 38176944)
    • (2004) Drug Metabolism and Disposition , vol.32 , Issue.2 , pp. 259-266
    • Wang, Y.-H.1    Jones, D.R.2    Hall, S.D.3
  • 16
    • 71049127036 scopus 로고    scopus 로고
    • Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator
    • Xu L, Chen Y, Pan Y, Skiles GL, and Shou M (2009) Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator. Drug Metab Dispos 37:2330-2339.
    • (2009) Drug Metab Dispos , vol.37 , pp. 2330-2339
    • Xu, L.1    Chen, Y.2    Pan, Y.3    Skiles, G.L.4    Shou, M.5
  • 19
    • 47749122616 scopus 로고    scopus 로고
    • Cytochrome p450 turnover: Regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions
    • Yang J, Liao M, Shou M, Jamei M, Yeo KR, Tucker GT, and Rostami-Hodjegan A (2008) Cytochrome p450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions. Curr Drug Metab 9:384-394.
    • (2008) Curr Drug Metab , vol.9 , pp. 384-394
    • Yang, J.1    Liao, M.2    Shou, M.3    Jamei, M.4    Yeo, K.R.5    Tucker, G.T.6    Rostami-Hodjegan, A.7
  • 20
    • 18844445670 scopus 로고    scopus 로고
    • Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes
    • DOI 10.1124/dmd.104.002832
    • Zhao P, Kunze KL, and Lee CA (2005) Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes. Drug Metab Dispos 33:853-861. (Pubitemid 40686640)
    • (2005) Drug Metabolism and Disposition , vol.33 , Issue.6 , pp. 853-861
    • Zhao, P.1    Kunze, K.L.2    Lee, C.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.