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Volumn 103, Issue 2, 2008, Pages 157-165

In vitro inhibition of CYP1A2 by model inhibitors, anti-inflammatory analgesics and female sex steroids: Predictability of in vivo interactions

Author keywords

[No Author keywords available]

Indexed keywords

ANALGESIC AGENT; CELECOXIB; CIPROFLOXACIN; CYTOCHROME P450 1A2; DESOGESTREL; ETHINYLESTRADIOL; ETODOLAC; ETORICOXIB; FLUVOXAMINE; GESTODENE; MEFENAMIC ACID; NONSTEROID ANTIINFLAMMATORY AGENT; ORAL CONTRACEPTIVE AGENT; PHENACETIN; PROGESTERONE; ROFECOXIB; SEX HORMONE; TIZANIDINE; TOLFENAMIC ACID; ZOLMITRIPTAN;

EID: 47649091430     PISSN: 17427835     EISSN: 17427843     Source Type: Journal    
DOI: 10.1111/j.1742-7843.2008.00252.x     Document Type: Article
Times cited : (41)

References (61)
  • 1
    • 24744457296 scopus 로고    scopus 로고
    • Assessment of CYP1A2 activity in clinical practice: Why, how, and when?
    • Faber MS, Jetter A, Fuhr U. Assessment of CYP1A2 activity in clinical practice: why, how, and when? Basic Clin Pharmacol Toxicol 2005 97 : 125 34.
    • (2005) Basic Clin Pharmacol Toxicol , vol.97 , pp. 125-34
    • Faber, M.S.1    Jetter, A.2    Fuhr, U.3
  • 2
    • 0036667961 scopus 로고    scopus 로고
    • The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors
    • Rasmussen BB, Brix TH, Kyvik KO, Brøsen K. The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors. Pharmacogenetics 2002 12 : 473 8.
    • (2002) Pharmacogenetics , vol.12 , pp. 473-8
    • Rasmussen, B.B.1    Brix, T.H.2    Kyvik, K.O.3    Brøsen, K.4
  • 3
    • 20144370197 scopus 로고    scopus 로고
    • Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors
    • Korhonen LE, Rahnasto M, Mahonen NJ, Wittekindt C, Poso A, Juvonen RO et al. Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors. J Med Chem 2005 48 : 3808 15.
    • (2005) J Med Chem , vol.48 , pp. 3808-15
    • Korhonen, L.E.1    Rahnasto, M.2    Mahonen, N.J.3    Wittekindt, C.4    Poso, A.5    Juvonen, R.O.6
  • 4
    • 0025848751 scopus 로고
    • Evidence for the involvement of several cytochromes P-450 in the first steps of caffeine metabolism by human liver microsomes
    • Berthou F, Flinois JP, Ratanasavanh D, Beaune P, Riche C, Guillouzo A. Evidence for the involvement of several cytochromes P-450 in the first steps of caffeine metabolism by human liver microsomes. Drug Metab Dispos 1991 19 : 561 7.
    • (1991) Drug Metab Dispos , vol.19 , pp. 561-7
    • Berthou, F.1    Flinois, J.P.2    Ratanasavanh, D.3    Beaune, P.4    Riche, C.5    Guillouzo, A.6
  • 5
    • 0029018483 scopus 로고
    • Characterization of human cytochromes P450 involved in theophylline 8-hydroxylation
    • Zhang ZY, Kaminsky LS. Characterization of human cytochromes P450 involved in theophylline 8-hydroxylation. Biochem Pharmacol 1995 50 : 205 11.
    • (1995) Biochem Pharmacol , vol.50 , pp. 205-11
    • Zhang, Z.Y.1    Kaminsky, L.S.2
  • 7
    • 0032878034 scopus 로고    scopus 로고
    • Determination of the human cytochrome P450 isoforms involved in the metabolism of zolmitriptan
    • Wild MJ, McKillop D, Butters CJ. Determination of the human cytochrome P450 isoforms involved in the metabolism of zolmitriptan. Xenobiotica 1999 29 : 847 57.
    • (1999) Xenobiotica , vol.29 , pp. 847-57
    • Wild, M.J.1    McKillop, D.2    Butters, C.J.3
  • 8
    • 0022263133 scopus 로고
    • Purification and characterization of the human liver cytochromes P-450 involved in debrisoquine 4-hydroxylation and phenacetin O-deethylation, two prototypes for genetic polymorphism in oxidative drug metabolism
    • Distlerath LM, Reilly PE, Martin MV, Davis GG, Wilkinson GR, Guengerich FP. Purification and characterization of the human liver cytochromes P-450 involved in debrisoquine 4-hydroxylation and phenacetin O-deethylation, two prototypes for genetic polymorphism in oxidative drug metabolism. J Biol Chem 1985 260 : 9057 67.
    • (1985) J Biol Chem , vol.260 , pp. 9057-67
    • Distlerath, L.M.1    Reilly, P.E.2    Martin, M.V.3    Davis, G.G.4    Wilkinson, G.R.5    Guengerich, F.P.6
  • 11
    • 0026718146 scopus 로고
    • Inhibitory potency of quinolone antibacterial agents against cytochrome P450IA2 activity in vivo and in vitro
    • Fuhr U, Anders EM, Mahr G, Sorgel F, Staib AH. Inhibitory potency of quinolone antibacterial agents against cytochrome P450IA2 activity in vivo and in vitro. Antimicrob Agents Chemother 1992 36 : 942 8.
    • (1992) Antimicrob Agents Chemother , vol.36 , pp. 942-8
    • Fuhr, U.1    Anders, E.M.2    Mahr, G.3    Sorgel, F.4    Staib, A.H.5
  • 12
    • 0027380074 scopus 로고
    • Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline
    • Kunze KL, Trager WF. Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline. Chem Res Toxicol 1993 6 : 649 56.
    • (1993) Chem Res Toxicol , vol.6 , pp. 649-56
    • Kunze, K.L.1    Trager, W.F.2
  • 13
    • 1842636952 scopus 로고    scopus 로고
    • Fluvoxamine drastically increases concentrations and effects of tizanidine: A potentially hazardous interaction
    • Granfors MT, Backman JT, Neuvonen M, Ahonen J, Neuvonen PJ. Fluvoxamine drastically increases concentrations and effects of tizanidine: a potentially hazardous interaction. Clin Pharmacol Ther 2004 75 : 331 41.
    • (2004) Clin Pharmacol Ther , vol.75 , pp. 331-41
    • Granfors, M.T.1    Backman, J.T.2    Neuvonen, M.3    Ahonen, J.4    Neuvonen, P.J.5
  • 14
    • 33747072651 scopus 로고    scopus 로고
    • Rofecoxib is a potent inhibitor of cytochrome P450 1A2: Studies with tizanidine and caffeine in healthy subjects
    • Backman JT, Karjalainen MJ, Neuvonen M, Laitila J, Neuvonen PJ. Rofecoxib is a potent inhibitor of cytochrome P450 1A2: studies with tizanidine and caffeine in healthy subjects. Br J Clin Pharmacol 2006 62 : 345 57.
    • (2006) Br J Clin Pharmacol , vol.62 , pp. 345-57
    • Backman, J.T.1    Karjalainen, M.J.2    Neuvonen, M.3    Laitila, J.4    Neuvonen, P.J.5
  • 15
    • 10044260714 scopus 로고    scopus 로고
    • Ciprofloxacin greatly increases concentrations and hypotensive effect of tizanidine by inhibiting its cytochrome P450 1A2-mediated presystemic metabolism
    • Granfors MT, Backman JT, Neuvonen M, Neuvonen PJ. Ciprofloxacin greatly increases concentrations and hypotensive effect of tizanidine by inhibiting its cytochrome P450 1A2-mediated presystemic metabolism. Clin Pharmacol Ther 2004 76 : 598 606.
    • (2004) Clin Pharmacol Ther , vol.76 , pp. 598-606
    • Granfors, M.T.1    Backman, J.T.2    Neuvonen, M.3    Neuvonen, P.J.4
  • 16
    • 25844501496 scopus 로고    scopus 로고
    • Oral contraceptives containing ethinyl estradiol and gestodene markedly increase plasma concentrations and effects of tizanidine by inhibiting cytochrome P450 1A2
    • Granfors MT, Backman JT, Laitila J, Neuvonen PJ. Oral contraceptives containing ethinyl estradiol and gestodene markedly increase plasma concentrations and effects of tizanidine by inhibiting cytochrome P450 1A2. Clin Pharmacol Ther 2005 78 : 400 11.
    • (2005) Clin Pharmacol Ther , vol.78 , pp. 400-11
    • Granfors, M.T.1    Backman, J.T.2    Laitila, J.3    Neuvonen, P.J.4
  • 17
    • 33751558274 scopus 로고    scopus 로고
    • Rofecoxib is a potent, metabolism-dependent inhibitor of CYP1A2: Implications for in vitro prediction of drug interactions
    • Karjalainen MJ, Neuvonen PJ, Backman JT. Rofecoxib is a potent, metabolism-dependent inhibitor of CYP1A2: implications for in vitro prediction of drug interactions. Drug Metab Dispos 2006 34 : 2091 6.
    • (2006) Drug Metab Dispos , vol.34 , pp. 2091-6
    • Karjalainen, M.J.1    Neuvonen, P.J.2    Backman, J.T.3
  • 18
    • 34547781271 scopus 로고    scopus 로고
    • Tolfenamic acid is a potent CYP1A2 inhibitor in vitro but does not interact in vivo: Correction for protein binding is needed for data interpretation
    • Karjalainen MJ, Neuvonen PJ, Backman JT. Tolfenamic acid is a potent CYP1A2 inhibitor in vitro but does not interact in vivo: correction for protein binding is needed for data interpretation. Eur J Clin Pharmacol 2007 63 : 829 36.
    • (2007) Eur J Clin Pharmacol , vol.63 , pp. 829-36
    • Karjalainen, M.J.1    Neuvonen, P.J.2    Backman, J.T.3
  • 19
    • 33644861762 scopus 로고    scopus 로고
    • Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: Pitfalls, progress and promise
    • Bachmann KA. Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: pitfalls, progress and promise. Curr Drug Metab 2006 7 : 1 14.
    • (2006) Curr Drug Metab , vol.7 , pp. 1-14
    • Bachmann, K.A.1
  • 20
    • 0036771085 scopus 로고    scopus 로고
    • Inhibition-based metabolic drug-drug interactions: Predictions from in vitro data
    • Yao C, Levy RH. Inhibition-based metabolic drug-drug interactions: predictions from in vitro data. J Pharm Sci 2002 91 : 1923 35.
    • (2002) J Pharm Sci , vol.91 , pp. 1923-35
    • Yao, C.1    Levy, R.H.2
  • 21
    • 84971395861 scopus 로고    scopus 로고
    • Which concentration of the inhibitor should be used to predict in vivo drug interactions from in vitro data?
    • 25.
    • Ito K, Chiba K, Horikawa M, Ishigami M, Mizuno N, Aoki J et al. Which concentration of the inhibitor should be used to predict in vivo drug interactions from in vitro data? AAPS Pharm Sci 2002 4 : article 25.
    • (2002) AAPS Pharm Sci , vol.4
    • Ito, K.1    Chiba, K.2    Horikawa, M.3    Ishigami, M.4    Mizuno, N.5    Aoki, J.6
  • 22
    • 1942455361 scopus 로고    scopus 로고
    • Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
    • Ito K, Brown HS, Houston JB. Database analyses for the prediction of in vivo drug-drug interactions from in vitro data. Br J Clin Pharmacol 2004 57 : 473 86.
    • (2004) Br J Clin Pharmacol , vol.57 , pp. 473-86
    • Ito, K.1    Brown, H.S.2    Houston, J.B.3
  • 24
    • 33748946044 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4
    • Brown HS, Galetin A, Hallifax D, Houston JB. Prediction of in vivo drug-drug interactions from in vitro data: factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4. Clin Pharmacokinet 2006 45 : 1035 50.
    • (2006) Clin Pharmacokinet , vol.45 , pp. 1035-50
    • Brown, H.S.1    Galetin, A.2    Hallifax, D.3    Houston, J.B.4
  • 26
    • 27444445468 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
    • Brown HS, Ito K, Galetin A, Houston JB. Prediction of in vivo drug-drug interactions from in vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 2005 60 : 508 18.
    • (2005) Br J Clin Pharmacol , vol.60 , pp. 508-18
    • Brown, H.S.1    Ito, K.2    Galetin, A.3    Houston, J.B.4
  • 27
    • 0028093134 scopus 로고
    • Kinetic applications using high substrate and competitive inhibitor concentrations to determine Ki or Km
    • Tornheim K. Kinetic applications using high substrate and competitive inhibitor concentrations to determine Ki or Km. Anal Biochem 1994 221 : 53 6.
    • (1994) Anal Biochem , vol.221 , pp. 53-6
    • Tornheim, K.1
  • 28
    • 0013212389 scopus 로고    scopus 로고
    • In vitro approaches for studying the inhibition of drug-metabolizing enzymes and identifying the drug-metabolizing enzymes responsible for the metabolism of drugs
    • In: Rodrigues, A.D. (ed.). Merkel Dekker Inc., West Point, NY
    • Madan A, Usuki E, Burton L, Ogilvie B, Parkinson A. In vitro approaches for studying the inhibition of drug-metabolizing enzymes and identifying the drug-metabolizing enzymes responsible for the metabolism of drugs. In : Rodrigues AD (ed.). Drug-Drug Interactions. Merkel Dekker Inc., West Point, NY, 2002 217 94.
    • (2002) Drug-Drug Interactions. , pp. 217-94
    • Madan, A.1    Usuki, E.2    Burton, L.3    Ogilvie, B.4    Parkinson, A.5
  • 30
    • 10744232330 scopus 로고    scopus 로고
    • The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
    • Bjornsson TD, Callaghan JT, Einolf HJ, Fischer V, Gan L, Grimm S et al. The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos 2003 31 : 815 32.
    • (2003) Drug Metab Dispos , vol.31 , pp. 815-32
    • Bjornsson, T.D.1    Callaghan, J.T.2    Einolf, H.J.3    Fischer, V.4    Gan, L.5    Grimm, S.6
  • 32
    • 0025601732 scopus 로고
    • Quinolone inhibition of cytochrome P-450-dependent caffeine metabolism in human liver microsomes
    • Fuhr U, Wolff T, Harder S, Schymanski P, Staib AH. Quinolone inhibition of cytochrome P-450-dependent caffeine metabolism in human liver microsomes. Drug Metab Dispos 1990 18 : 1005 10.
    • (1990) Drug Metab Dispos , vol.18 , pp. 1005-10
    • Fuhr, U.1    Wolff, T.2    Harder, S.3    Schymanski, P.4    Staib, A.H.5
  • 33
    • 0029738965 scopus 로고    scopus 로고
    • Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine
    • Jeppesen U, Gram LF, Vistisen K, Loft S, Poulsen HE, Brøsen K. Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine. Eur J Clin Pharmacol 1996 51 : 73 8.
    • (1996) Eur J Clin Pharmacol , vol.51 , pp. 73-8
    • Jeppesen, U.1    Gram, L.F.2    Vistisen, K.3    Loft, S.4    Poulsen, H.E.5    Brøsen, K.6
  • 34
    • 0035215519 scopus 로고    scopus 로고
    • Fluvoxamine-theophylline interaction: Gap between in vitro and in vivo inhibition constants toward cytochrome P4501A2
    • Yao C, Kunze KL, Kharasch ED, Wang Y, Trager WF, Ragueneau I et al. Fluvoxamine-theophylline interaction: gap between in vitro and in vivo inhibition constants toward cytochrome P4501A2. Clin Pharmacol Ther 2001 70 : 415 24.
    • (2001) Clin Pharmacol Ther , vol.70 , pp. 415-24
    • Yao, C.1    Kunze, K.L.2    Kharasch, E.D.3    Wang, Y.4    Trager, W.F.5    Ragueneau, I.6
  • 35
    • 0024330642 scopus 로고
    • Ciprofloxacin-caffeine: A drug interaction established using in vivo and in vitro investigations
    • Harder S, Fuhr U, Staib AH, Wolff T. Ciprofloxacin-caffeine: a drug interaction established using in vivo and in vitro investigations. Am J Med 1989 87 : 89S 91S.
    • (1989) Am J Med , vol.87
    • Harder, S.1    Fuhr, U.2    Staib, A.H.3    Wolff, T.4
  • 36
    • 33645961595 scopus 로고    scopus 로고
    • The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions
    • Grime K, Riley RJ. The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions. Curr Drug Metab 2006 7 : 251 64.
    • (2006) Curr Drug Metab , vol.7 , pp. 251-64
    • Grime, K.1    Riley, R.J.2
  • 37
    • 28444449875 scopus 로고    scopus 로고
    • Inhibitory effect of several fluoroquinolones on hepatic microsomal cytochrome P-450 1A activities in dogs
    • Regmi NL, Abd El-Aty AM, Kuroha M, Nakamura M, Shimoda M. Inhibitory effect of several fluoroquinolones on hepatic microsomal cytochrome P-450 1A activities in dogs. J Vet Pharmacol Ther 2005 28 : 553 7.
    • (2005) J Vet Pharmacol Ther , vol.28 , pp. 553-7
    • Regmi, N.L.1    Abd El-Aty, A.M.2    Kuroha, M.3    Nakamura, M.4    Shimoda, M.5
  • 38
    • 0027452618 scopus 로고
    • Quinolone antibacterial agents: Relationship between structure and in vitro inhibition of the human cytochrome P450 isoform CYP1A2
    • Fuhr U, Strobl G, Manaut F, Anders EM, Sorgel F, Lopez-de-Brinas E et al. Quinolone antibacterial agents: relationship between structure and in vitro inhibition of the human cytochrome P450 isoform CYP1A2. Mol Pharmacol 1993 43 : 191 9.
    • (1993) Mol Pharmacol , vol.43 , pp. 191-9
    • Fuhr, U.1    Strobl, G.2    Manaut, F.3    Anders, E.M.4    Sorgel, F.5    Lopez-De-Brinas, E.6
  • 39
    • 0020583244 scopus 로고
    • Oral contraceptive steroids impair the elimination of theophylline
    • Roberts RK, Grice J, McGuffie C, Heilbronn L. Oral contraceptive steroids impair the elimination of theophylline. J Lab Clin Med 1983 101 : 821 5.
    • (1983) J Lab Clin Med , vol.101 , pp. 821-5
    • Roberts, R.K.1    Grice, J.2    McGuffie, C.3    Heilbronn, L.4
  • 40
    • 0021824615 scopus 로고
    • Impairment of caffeine clearance by chronic use of low-dose oestrogen-containing oral contraceptives
    • Abernethy DR, Todd EL. Impairment of caffeine clearance by chronic use of low-dose oestrogen-containing oral contraceptives. Eur J Clin Pharmacol 1985 28 : 425 8.
    • (1985) Eur J Clin Pharmacol , vol.28 , pp. 425-8
    • Abernethy, D.R.1    Todd, E.L.2
  • 42
    • 33846674113 scopus 로고    scopus 로고
    • Pharmacokinetic drug interactions involving 17alpha- ethinylestradiol: A new look at an old drug
    • Zhang H, Cui D, Wang B, Han YH, Balimane P, Yang Z et al. Pharmacokinetic drug interactions involving 17alpha- ethinylestradiol: a new look at an old drug. Clin Pharmacokinet 2007 46 : 133 57.
    • (2007) Clin Pharmacokinet , vol.46 , pp. 133-57
    • Zhang, H.1    Cui, D.2    Wang, B.3    Han, Y.H.4    Balimane, P.5    Yang, Z.6
  • 43
    • 29944446317 scopus 로고    scopus 로고
    • Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: Implications for drug-drug interactions
    • Ogilvie BW, Zhang D, Li W, Rodrigues AD, Gipson AE, Holsapple J et al. Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions. Drug Metab Dispos 2006 34 : 191 7.
    • (2006) Drug Metab Dispos , vol.34 , pp. 191-7
    • Ogilvie, B.W.1    Zhang, D.2    Li, W.3    Rodrigues, A.D.4    Gipson, A.E.5    Holsapple, J.6
  • 44
    • 0032239288 scopus 로고    scopus 로고
    • The role of CYP2C in the in vitro bioactivation of the contraceptive steroid desogestrel
    • Gentile DM, Verhoeven CH, Shimada T, Back DJ. The role of CYP2C in the in vitro bioactivation of the contraceptive steroid desogestrel. J Pharmacol Exp Ther 1998 287 : 975 82.
    • (1998) J Pharmacol Exp Ther , vol.287 , pp. 975-82
    • Gentile, D.M.1    Verhoeven, C.H.2    Shimada, T.3    Back, D.J.4
  • 45
    • 0019523789 scopus 로고
    • Human pharmacokinetics of tolfenamic acid, a new anti-inflammatory agent
    • Pentikäinen PJ, Neuvonen PJ, Backman C. Human pharmacokinetics of tolfenamic acid, a new anti-inflammatory agent. Eur J Clin Pharmacol 1981 19 : 359 65.
    • (1981) Eur J Clin Pharmacol , vol.19 , pp. 359-65
    • Pentikäinen, P.J.1    Neuvonen, P.J.2    Backman, C.3
  • 46
    • 0004047129 scopus 로고    scopus 로고
    • 2nd edn. Churchill Livingstone, Edinburgh, UK
    • Dollery C. Therapeutic Drugs, 2nd edn. Churchill Livingstone, Edinburgh, UK, 1999.
    • (1999) Therapeutic Drugs
    • Dollery, C.1
  • 47
    • 47649094023 scopus 로고    scopus 로고
    • FDA Celebrex (Celecoxib) Capsules Application No.: 21-156 & 20998/S007 Clinical Pharmacology. Biopharmaceutics reviews section. URL
    • FDA Celebrex (Celecoxib) Capsules Application No.: 21-156 & 20998/S007 Clinical Pharmacology Biopharmaceutics reviews section. 1999. URL: http://www.fda.gov/CDER/foi/nda/99/21156-S007_Celebrex.htm
    • (1999)
  • 48
    • 0042126736 scopus 로고    scopus 로고
    • Celecoxib inhibits metabolism of cytochrome P450 2D6 substrate metoprolol in humans
    • Werner U, Werner D, Rau T, Fromm MF, Hinz B, Brune K. Celecoxib inhibits metabolism of cytochrome P450 2D6 substrate metoprolol in humans. Clin Pharmacol Ther 2003 74 : 130 7.
    • (2003) Clin Pharmacol Ther , vol.74 , pp. 130-7
    • Werner, U.1    Werner, D.2    Rau, T.3    Fromm, M.F.4    Hinz, B.5    Brune, K.6
  • 49
    • 47649105473 scopus 로고    scopus 로고
    • EMEA Celecoxib BILAG I PRODUKTRESUME. URL
    • EMEA Celecoxib BILAG I PRODUKTRESUME. 2006. URL: http://www.emea.europa. eu/humandocs/PDFs/EPAR/onsenal/H-466-PI-da.pdf
    • (2006)
  • 50
    • 0035000968 scopus 로고    scopus 로고
    • Role of human liver cytochrome P4503A in the metabolism of etoricoxib, a novel cyclooxygenase-2 selective inhibitor
    • Kassahun K, McIntosh IS, Shou M, Walsh DJ, Rodeheffer C, Slaughter DE et al. Role of human liver cytochrome P4503A in the metabolism of etoricoxib, a novel cyclooxygenase-2 selective inhibitor. Drug Metab Dispos 2001 29 : 813 20.
    • (2001) Drug Metab Dispos , vol.29 , pp. 813-20
    • Kassahun, K.1    McIntosh, I.S.2    Shou, M.3    Walsh, D.J.4    Rodeheffer, C.5    Slaughter, D.E.6
  • 52
    • 0020679387 scopus 로고
    • In vitro activity of Bay
    • 09867, a new quinoline derivative, compared with those of other antimicrobial agents.
    • Wise R, Andrews JM, Edwards LJ. In vitro activity of Bay 09867, a new quinoline derivative, compared with those of other antimicrobial agents. Antimicrob Agents Chemother 1983 23 : 559 64.
    • (1983) Antimicrob Agents Chemother , vol.23 , pp. 559-64
    • Wise, R.1    Andrews, J.M.2    Edwards, L.J.3
  • 53
    • 0023737762 scopus 로고
    • Effect of magnesium hydroxide on the absorption of tolfenamic and mefenamic acids
    • Neuvonen PJ, Kivistö KT. Effect of magnesium hydroxide on the absorption of tolfenamic and mefenamic acids. Eur J Clin Pharmacol 1988 35 : 495 501.
    • (1988) Eur J Clin Pharmacol , vol.35 , pp. 495-501
    • Neuvonen, P.J.1    Kivistö, K.T.2
  • 54
    • 47649092919 scopus 로고    scopus 로고
    • Merck & Co. Inc. VIOXX (rofecoxib tablets and oral suspension). URL
    • Merck & Co. Inc. VIOXX (rofecoxib tablets and oral suspension). 2002. URL: http://www.merck.com/product/usa/pi_circulars/v/vioxx/vioxx_pi.pdf
    • (2002)
  • 55
    • 0037372154 scopus 로고    scopus 로고
    • Single- and multiple-dose pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase-2, in man
    • Agrawal NG, Porras AG, Matthews CZ, Rose MJ, Woolf EJ, Musser BJ et al. Single- and multiple-dose pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase-2, in man. J Clin Pharmacol 2003 43 : 268 76.
    • (2003) J Clin Pharmacol , vol.43 , pp. 268-76
    • Agrawal, N.G.1    Porras, A.G.2    Matthews, C.Z.3    Rose, M.J.4    Woolf, E.J.5    Musser, B.J.6
  • 57
    • 0030859745 scopus 로고    scopus 로고
    • The clinical pharmacokinetics of zolmitriptan
    • Dixon R, Warrander A. The clinical pharmacokinetics of zolmitriptan. Cephalalgia 1997 18 : 15 20.
    • (1997) Cephalalgia , vol.18 , pp. 15-20
    • Dixon, R.1    Warrander, A.2
  • 58
    • 23644446491 scopus 로고    scopus 로고
    • Comparison of ethinylestradiol pharmacokinetics in three hormonal contraceptive formulations: The vaginal ring, the transdermal patch and an oral contraceptive
    • van den Heuvel MW, van Bragt AJ, Alnabawy AK, Kaptein MC. Comparison of ethinylestradiol pharmacokinetics in three hormonal contraceptive formulations: the vaginal ring, the transdermal patch and an oral contraceptive. Contraception 2005 72 : 168 74.
    • (2005) Contraception , vol.72 , pp. 168-74
    • Van Den Heuvel, M.W.1    Van Bragt, A.J.2    Alnabawy, A.K.3    Kaptein, M.C.4
  • 59
    • 0025062383 scopus 로고
    • Protein binding of the contraceptive steroids gestodene, 3-keto-desogestrel and ethinylestradiol in human serum
    • Kuhnz W, Pfeffer M, al-Yacoub G. Protein binding of the contraceptive steroids gestodene, 3-keto-desogestrel and ethinylestradiol in human serum. J Steroid Biochem 1990 35 : 313 8.
    • (1990) J Steroid Biochem , vol.35 , pp. 313-8
    • Kuhnz, W.1    Pfeffer, M.2    Al-Yacoub, G.3
  • 60
    • 0030791647 scopus 로고    scopus 로고
    • Pharmacokinetics of the new progestogens and influence of gestodene and desogestrel on ethinylestradiol metabolism
    • Stanczyk FZ. Pharmacokinetics of the new progestogens and influence of gestodene and desogestrel on ethinylestradiol metabolism. Contraception 1997 55 : 273 82.
    • (1997) Contraception , vol.55 , pp. 273-82
    • Stanczyk, F.Z.1
  • 61
    • 0023757438 scopus 로고
    • Alterations in the serum levels of gestodene and SHBG during 12 cycles of treatment with 30 micrograms ethinylestradiol and 75 micrograms gestodene
    • Kuhl H, Jung-Hoffmann C, Heidt F. Alterations in the serum levels of gestodene and SHBG during 12 cycles of treatment with 30 micrograms ethinylestradiol and 75 micrograms gestodene. Contraception 1988 38 : 477 86.
    • (1988) Contraception , vol.38 , pp. 477-86
    • Kuhl, H.1    Jung-Hoffmann, C.2    Heidt, F.3


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