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Volumn 39, Issue 3, 2011, Pages 412-418

Simple, direct, and informative method for the assessment of CYP2C19 enzyme inactivation kinetics

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 2C19; DIBENZYLFLUORESCEIN; FLUORESCEIN; FLUORESCEIN BENZYL ESTER; FLUORESCEIN BENZYL ETHER; FLUORESCENT DYE; ISONIAZID; TICLOPIDINE; TRANYLCYPROMINE; UNCLASSIFIED DRUG;

EID: 79951897656     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.110.036376     Document Type: Article
Times cited : (15)

References (30)
  • 1
    • 0033137073 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of 3′-O-(carboxyalkyl)fluorescein labels
    • Adamczyk M, Grote J, and Moore JA (1999) Chemoenzymatic synthesis of 3′-O-(carboxyalkyl)fluorescein labels. Bioconjug Chem 10:544-547.
    • (1999) Bioconjug Chem , vol.10 , pp. 544-547
    • Adamczyk, M.1    Grote, J.2    Moore, J.A.3
  • 4
    • 0031570357 scopus 로고    scopus 로고
    • Microtiter plate assays for inhibition of human, drug-metabolizing cytochromes P450
    • Crespi CL, Miller VP, and Penman BW (1997) Microtiter plate assays for inhibition of human, drug-metabolizing cytochromes P450. Anal Biochem 248:188-190.
    • (1997) Anal Biochem , vol.248 , pp. 188-190
    • Crespi, C.L.1    Miller, V.P.2    Penman, B.W.3
  • 5
    • 0034460075 scopus 로고    scopus 로고
    • Fluorometric screening for metabolism-based drug-drug interactions
    • Crespi CL and Stresser DM (2000) Fluorometric screening for metabolism-based drug-drug interactions. J Pharmacol Toxicol Methods 44:325-331.
    • (2000) J Pharmacol Toxicol Methods , vol.44 , pp. 325-331
    • Crespi, C.L.1    Stresser, D.M.2
  • 6
    • 0035157254 scopus 로고    scopus 로고
    • A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry
    • Dierks EA, Stams KR, Lim HK, Cornelius G, Zhang H, and Ball SE (2001) A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry. Drug Metab Dispos 29:23-29.
    • (2001) Drug Metab Dispos , vol.29 , pp. 23-29
    • Dierks, E.A.1    Stams, K.R.2    Lim, H.K.3    Cornelius, G.4    Zhang, H.5    Ball, S.E.6
  • 7
    • 0031430539 scopus 로고    scopus 로고
    • Ticlopidine inhibition of phenytoin metabolism mediated by potent inhibition of CYP2C19
    • Donahue SR, Flockhart DA, Abernethy DR, and Ko JW (1997) Ticlopidine inhibition of phenytoin metabolism mediated by potent inhibition of CYP2C19. Clin Pharmacol Ther 62:572-577.
    • (1997) Clin Pharmacol Ther , vol.62 , pp. 572-577
    • Donahue, S.R.1    Flockhart, D.A.2    Abernethy, D.R.3    Ko, J.W.4
  • 8
    • 36349009310 scopus 로고    scopus 로고
    • Progress curve analysis of CYP1A2 inhibition: A more informative approach to the assessment of mechanism-based inactivation?
    • Fairman DA, Collins C, and Chapple S (2007) Progress curve analysis of CYP1A2 inhibition: a more informative approach to the assessment of mechanism-based inactivation? Drug Metab Dispos 35:2159-2165.
    • (2007) Drug Metab Dispos , vol.35 , pp. 2159-2165
    • Fairman, D.A.1    Collins, C.2    Chapple, S.3
  • 9
    • 53849084442 scopus 로고    scopus 로고
    • In vitro evaluation of reversible and irreversible cytochrome P450 inhibition: Current status on methodologies and their utility for predicting drug-drug interactions
    • Fowler S and Zhang H (2008) In vitro evaluation of reversible and irreversible cytochrome P450 inhibition: current status on methodologies and their utility for predicting drug-drug interactions. AAPS J 10:410-424.
    • (2008) AAPS J , vol.10 , pp. 410-424
    • Fowler, S.1    Zhang, H.2
  • 10
    • 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
  • 11
    • 58149242547 scopus 로고    scopus 로고
    • Mechanism-based inhibition of cytochrome P450 enzymes: An evaluation of early decision making in vitro approaches and drug-drug interaction prediction methods
    • Grime KH, Bird J, Ferguson D, and Riley RJ (2009) Mechanism-based inhibition of cytochrome P450 enzymes: an evaluation of early decision making in vitro approaches and drug-drug interaction prediction methods. Eur J Pharm Sci 36:175-191.
    • (2009) Eur J Pharm Sci , vol.36 , pp. 175-191
    • Grime, K.H.1    Bird, J.2    Ferguson, D.3    Riley, R.J.4
  • 12
    • 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
  • 13
    • 38949101404 scopus 로고    scopus 로고
    • Molecular basis for the interaction of four different classes of substrates and inhibitors with human aromatase
    • Hong Y, Cho M, Yuan YC, and Chen S (2008) Molecular basis for the interaction of four different classes of substrates and inhibitors with human aromatase. Biochem Pharmacol 75:1161-1169.
    • (2008) Biochem Pharmacol , vol.75 , pp. 1161-1169
    • Hong, Y.1    Cho, M.2    Yuan, Y.C.3    Chen, S.4
  • 14
    • 34548805504 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450 enzymes: Chemical mechanisms, structure-activity relationships and relationship to clinical drug-drug interactions and idiosyncratic adverse drug reactions
    • Kalgutkar AS, Obach RS, and Maurer TS (2007) Mechanism-based inactivation of cytochrome P450 enzymes: chemical mechanisms, structure-activity relationships and relationship to clinical drug-drug interactions and idiosyncratic adverse drug reactions. Curr Drug Metab 8:407-447.
    • (2007) Curr Drug Metab , vol.8 , pp. 407-447
    • Kalgutkar, A.S.1    Obach, R.S.2    Maurer, T.S.3
  • 15
    • 34748879042 scopus 로고    scopus 로고
    • 50 method and multiplexing high-performance liquid chromatography
    • 50 method and multiplexing high-performance liquid chromatography. J Pharm Sci 96:2485-2493.
    • (2007) J Pharm Sci , vol.96 , pp. 2485-2493
    • Lin, T.1    Pan, K.2    Mordenti, J.3    Pan, L.4
  • 16
    • 79951926973 scopus 로고    scopus 로고
    • The use of fluorescein aryl ethers in high throughput cytochrome P450 inhibition assays
    • inventors; Gentest Corp, assignee. World patent WO0114361 (A1). 2001 March 1
    • Miller VP, Stresser D, Crespi CL, and Charles L (2001), inventors; Gentest Corp, assignee.The use of fluorescein aryl ethers in high throughput cytochrome P450 inhibition assays. World patent WO0114361 (A1). 2001 March 1.
    • (2001)
    • Miller, V.P.1    Stresser, D.2    Crespi, C.L.3    Charles, L.4
  • 17
    • 81855202501 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human CYP1A2 and CYP2C19-mediated metabolism by isoniazid
    • Nishimura Y, Kurata N, Iwase M, and Yasuhara H (2003) Mechanism-based inactivation of human CYP1A2 and CYP2C19-mediated metabolism by isoniazid. Drug Metab Rev 35:50.
    • (2003) Drug Metab Rev , vol.35 , pp. 50
    • Nishimura, Y.1    Kurata, N.2    Iwase, M.3    Yasuhara, H.4
  • 18
    • 70350325443 scopus 로고    scopus 로고
    • Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel
    • Nishiya Y, Hagihara K, Kurihara A, Okudaira N, Farid NA, Okazaki O, and Ikeda T (2009) Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel. Xenobiotica 39:836-843.
    • (2009) Xenobiotica , vol.39 , pp. 836-843
    • Nishiya, Y.1    Hagihara, K.2    Kurihara, A.3    Okudaira, N.4    Farid, N.A.5    Okazaki, O.6    Ikeda, T.7
  • 19
    • 58449091215 scopus 로고    scopus 로고
    • Predicting drug-drug interactions from in vitro drug metabolism data: Challenges and recent advances
    • Obach RS (2009) Predicting drug-drug interactions from in vitro drug metabolism data: challenges and recent advances. Curr Opin Drug Discov Devel 12:81-89.
    • (2009) Curr Opin Drug Discov Devel , vol.12 , pp. 81-89
    • Obach, R.S.1
  • 21
    • 33646231768 scopus 로고    scopus 로고
    • An evaluation of potential mechanism-based inactivation of human drug metabolizing cytochromes P450 by monoamine oxidase inhibitors, including isoniazid
    • Polasek TM, Elliot DJ, Somogyi AA, Gillam EM, Lewis BC, and Miners JO (2006) An evaluation of potential mechanism-based inactivation of human drug metabolizing cytochromes P450 by monoamine oxidase inhibitors, including isoniazid. Br J Clin Pharmacol 61:570-584.
    • (2006) Br J Clin Pharmacol , vol.61 , pp. 570-584
    • Polasek, T.M.1    Elliot, D.J.2    Somogyi, A.A.3    Gillam, E.M.4    Lewis, B.C.5    Miners, J.O.6
  • 22
    • 34548283499 scopus 로고    scopus 로고
    • In vitro approaches to investigate mechanism-based inactivation of CYP enzymes
    • Polasek TM and Miners JO (2007) In vitro approaches to investigate mechanism-based inactivation of CYP enzymes. Expert Opin Drug Metab Toxicol 3:321-329.
    • (2007) Expert Opin Drug Metab Toxicol , vol.3 , pp. 321-329
    • Polasek, T.M.1    Miners, J.O.2
  • 25
  • 26
    • 68949130179 scopus 로고    scopus 로고
    • 12 inhibitors: Differences in properties and mechanisms of action and potential consequences for clinical use
    • 12 inhibitors: differences in properties and mechanisms of action and potential consequences for clinical use. Eur Heart J 30:1964-1977.
    • (2009) Eur Heart J , vol.30 , pp. 1964-1977
    • Wallentin, L.1
  • 27
    • 0035712266 scopus 로고    scopus 로고
    • Isoniazid is a mechanism-based inhibitor of cytochrome P450 1A2, 2A6, 2C19 and 3A4 isoforms in human liver microsomes
    • Wen X, Wang JS, Neuvonen PJ, and Backman JT (2002) Isoniazid is a mechanism-based inhibitor of cytochrome P450 1A2, 2A6, 2C19 and 3A4 isoforms in human liver microsomes. Eur J Clin Pharmacol 57:799-804.
    • (2002) Eur J Clin Pharmacol , vol.57 , pp. 799-804
    • Wen, X.1    Wang, J.S.2    Neuvonen, P.J.3    Backman, J.T.4
  • 28
    • 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
    • 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.
    • (2007) Curr Drug Metab , vol.8 , pp. 449-462
    • Venkatakrishnan, K.1    Obach, R.S.2
  • 29
    • 27644596457 scopus 로고    scopus 로고
    • Predicting in vivo drug interactions from in vitro drug discovery data
    • Wienkers LC and Heath TG (2005) Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov 4:825-833.
    • (2005) Nat Rev Drug Discov , vol.4 , pp. 825-833
    • Wienkers, L.C.1    Heath, T.G.2
  • 30
    • 67649382514 scopus 로고    scopus 로고
    • Application of mechanism-based CYP inhibition for predicting drug-drug interactions
    • Zhou ZW and Zhou SF (2009) Application of mechanism-based CYP inhibition for predicting drug-drug interactions. Expert Opin Drug Metab Toxicol 5:579-605.
    • (2009) Expert Opin Drug Metab Toxicol , vol.5 , pp. 579-605
    • Zhou, Z.W.1    Zhou, S.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.