메뉴 건너뛰기




Volumn 73, Issue 4, 2003, Pages 322-329

Effect of itraconazole on the pharmacokinetics of rosuvastatin

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; CYTOCHROME P450 3A4; CYTOCHROME P450 INHIBITOR; GLYCOPROTEIN P; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; ITRACONAZOLE; PLACEBO; ROSUVASTATIN;

EID: 0344453812     PISSN: 00099236     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-9236(02)17633-8     Document Type: Article
Times cited : (98)

References (20)
  • 1
    • 0035451307 scopus 로고    scopus 로고
    • Effect of rosuvastatin on low-density lipoprotein cholesterol in patients with hypercholesterolemia
    • Olsson AG, Pears J, McKellar J, Mizan J, Raza A. Effect of rosuvastatin on low-density lipoprotein cholesterol in patients with hypercholesterolemia. Am J Cardiol 2001;88:504-8.
    • (2001) Am J Cardiol , vol.88 , pp. 504-508
    • Olsson, A.G.1    Pears, J.2    McKellar, J.3    Mizan, J.4    Raza, A.5
  • 2
    • 0033745108 scopus 로고    scopus 로고
    • Itraconazole alters the pharmacokinetics of atorvastatin to a greater extent than either cerivastatin or pravastatin
    • Mazzu AL, Lasseter KC, Shamblen EC, Agarwal V, Lettieri J, Sundaresen P, et al. Itraconazole alters the pharmacokinetics of atorvastatin to a greater extent than either cerivastatin or pravastatin. Clin Pharmacol Ther 2000;68:391-400.
    • (2000) Clin Pharmacol Ther , vol.68 , pp. 391-400
    • Mazzu, A.L.1    Lasseter, K.C.2    Shamblen, E.C.3    Agarwal, V.4    Lettieri, J.5    Sundaresen, P.6
  • 3
    • 0031847115 scopus 로고    scopus 로고
    • Effect of itraconazole on the pharmacokinetics of atorvastatin
    • Kantola T, Kivistö KT, Neuvonen PJ. Effect of itraconazole on the pharmacokinetics of atorvastatin. Clin Pharmacol Ther 1998;64:58-65.
    • (1998) Clin Pharmacol Ther , vol.64 , pp. 58-65
    • Kantola, T.1    Kivistö, K.T.2    Neuvonen, P.J.3
  • 4
    • 0031892901 scopus 로고    scopus 로고
    • Simvastatin but not pravastatin is very susceptible to interaction with the CYP3A4 inhibitor itraconazole
    • Neuvonen PJ, Kantola T, Kivistö KT. Simvastatin but not pravastatin is very susceptible to interaction with the CYP3A4 inhibitor itraconazole. Clin Pharmacol Ther 1998;63:332-41.
    • (1998) Clin Pharmacol Ther , vol.63 , pp. 332-341
    • Neuvonen, P.J.1    Kantola, T.2    Kivistö, K.T.3
  • 5
    • 0031803373 scopus 로고    scopus 로고
    • Different effects of itraconazole on the pharmacokinetics of fluvastatin and lovastatin
    • Kivistö KT, Kantola T, Neuvonen PJ. Different effects of itraconazole on the pharmacokinetics of fluvastatin and lovastatin. Br J Clin Pharmacol 1998;46:49-53.
    • (1998) Br J Clin Pharmacol , vol.46 , pp. 49-53
    • Kivistö, K.T.1    Kantola, T.2    Neuvonen, P.J.3
  • 6
    • 0029758869 scopus 로고    scopus 로고
    • Itraconazole drastically increases plasma concentrations of lovastatin and lovastatin acid
    • Neuvonen PJ, Jalava KM. Itraconazole drastically increases plasma concentrations of lovastatin and lovastatin acid. Clin Pharmacol Ther 1996;60:54-61.
    • (1996) Clin Pharmacol Ther , vol.60 , pp. 54-61
    • Neuvonen, P.J.1    Jalava, K.M.2
  • 7
    • 0030935086 scopus 로고    scopus 로고
    • Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions
    • Bertz RJ, Granneman GR. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997;32:210-58.
    • (1997) Clin Pharmacokinet , vol.32 , pp. 210-258
    • Bertz, R.J.1    Granneman, G.R.2
  • 9
    • 0030812885 scopus 로고    scopus 로고
    • In vitro metabolism of simvastatin in humans (SBT) identification of metabolizing enzymes and effect of the drug on hepatic P450s
    • Prueksaritanont T, Gorham LM, Ma B, Liu L, Yu X, Zhao JJ, et al. In vitro metabolism of simvastatin in humans (SBT) identification of metabolizing enzymes and effect of the drug on hepatic P450s. Drug Metab Dispos 1997;25:1191-9.
    • (1997) Drug Metab Dispos , vol.25 , pp. 1191-1199
    • Prueksaritanont, T.1    Gorham, L.M.2    Ma, B.3    Liu, L.4    Yu, X.5    Zhao, J.J.6
  • 10
    • 0032911163 scopus 로고    scopus 로고
    • Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors lovastatin and pravastatin in the liver
    • Jacobsen W, Kirchner G, Hallensleben K, Mancinelli L, Deters M, Hackbarth I, et al. Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors lovastatin and pravastatin in the liver. Drug Metab Dispos 1999;27:173-9.
    • (1999) Drug Metab Dispos , vol.27 , pp. 173-179
    • Jacobsen, W.1    Kirchner, G.2    Hallensleben, K.3    Mancinelli, L.4    Deters, M.5    Hackbarth, I.6
  • 12
    • 0036786383 scopus 로고    scopus 로고
    • No effect of age or gender on the pharmacokinetics of rosuvastatin: A new HMG-CoA reductase inhibitor
    • Martin PD, Dane AL, Nwose OM, Schneck DW, Warwick MJ. No effect of age or gender on the pharmacokinetics of rosuvastatin: a new HMG-CoA reductase inhibitor. J Clin Pharmacol 2002;42:1116-21.
    • (2002) J Clin Pharmacol , vol.42 , pp. 1116-1121
    • Martin, P.D.1    Dane, A.L.2    Nwose, O.M.3    Schneck, D.W.4    Warwick, M.J.5
  • 13
    • 0001452963 scopus 로고    scopus 로고
    • Disposition of new HMG-CoA reductase inhibitor ZD4522 following dosing in healthy subjects
    • Martin PD, Dane AL, Schneck DW, Warwick MJ. Disposition of new HMG-CoA reductase inhibitor ZD4522 following dosing in healthy subjects [abstract]. J Clin Pharmacol 2000;40:1056.
    • (2000) J Clin Pharmacol , vol.40 , pp. 1056
    • Martin, P.D.1    Dane, A.L.2    Schneck, D.W.3    Warwick, M.J.4
  • 14
    • 0000626919 scopus 로고    scopus 로고
    • ZD4522 - An HMG-CoA reductase inhibitor free of metabolically mediated drug interactions: Metabolic studies in human in vitro systems
    • McCormick AD, McKillop D, Butters CJ, Miles GS, Baba T, Touchi A, et al. ZD4522 - an HMG-CoA reductase inhibitor free of metabolically mediated drug interactions: metabolic studies in human in vitro systems [abstract]. J Clin Pharmacol 2000;40:1055.
    • (2000) J Clin Pharmacol , vol.40 , pp. 1055
    • McCormick, A.D.1    McKillop, D.2    Butters, C.J.3    Miles, G.S.4    Baba, T.5    Touchi, A.6
  • 15
    • 4244147940 scopus 로고    scopus 로고
    • Tissue specific distribution of S-4522, a novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, to the liver in rats
    • Nezasa K, Takeuchi M, Yukawa T, Kawahara M, Inazawa K, Hasegawa H, et al. Tissue specific distribution of S-4522, a novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, to the liver in rats [abstract]. Xenobiotic Metab Dispos 1998;13(Suppl):S226.
    • (1998) Xenobiotic Metab Dispos , vol.13 , Issue.SUPPL.
    • Nezasa, K.1    Takeuchi, M.2    Yukawa, T.3    Kawahara, M.4    Inazawa, K.5    Hasegawa, H.6
  • 16
    • 0002186061 scopus 로고    scopus 로고
    • Rosuvastatin is a high affinity substrate of hepatic organic anion transporter OATP-C
    • Brown CDA, Windass A, Bleasby K, Lauffart B. Rosuvastatin is a high affinity substrate of hepatic organic anion transporter OATP-C [abstract]. Atheroscl Suppl 2001;2:90.
    • (2001) Atheroscl Suppl , vol.2 , pp. 90
    • Brown, C.D.A.1    Windass, A.2    Bleasby, K.3    Lauffart, B.4
  • 17
    • 0037024131 scopus 로고    scopus 로고
    • Quantification of rosuvastatin in human plasma by automated solid-phase extraction using tandem mass-spectrometric detection
    • Hull CK, Penman AD, Smith CK, Martin PD. Quantification of rosuvastatin in human plasma by automated solid-phase extraction using tandem mass-spectrometric detection. J Chromatogr B Analyt Technol Biomed Life Sci 2002;772:219-28.
    • (2002) J Chromatogr B Analyt Technol Biomed Life Sci , vol.772 , pp. 219-228
    • Hull, C.K.1    Penman, A.D.2    Smith, C.K.3    Martin, P.D.4
  • 18
    • 0034883375 scopus 로고    scopus 로고
    • Optimizing drug development: Strategies to assess drug metabolism/transporter interaction potential - Toward a consensus
    • Tucker GT, Houston JB, Huang S-M. Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential - toward a consensus. Clin Pharmacol Ther 2001;70:103-14.
    • (2001) Clin Pharmacol Ther , vol.70 , pp. 103-114
    • Tucker, G.T.1    Houston, J.B.2    Huang, S.-M.3
  • 20
    • 0036891228 scopus 로고    scopus 로고
    • No effect of rosuvastatin on the pharmacokinetics of digoxin in healthy volunteers
    • Martin PD, Kemp JV, Dane AL, Warwick MJ, Schneck DW. No effect of rosuvastatin on the pharmacokinetics of digoxin in healthy volunteers. J Clin Pharmacol 2002;42:1352-7.
    • (2002) J Clin Pharmacol , vol.42 , pp. 1352-1357
    • Martin, P.D.1    Kemp, J.V.2    Dane, A.L.3    Warwick, M.J.4    Schneck, D.W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.