Effect of voriconazole on the pharmacokinetics and pharmacodynamics of zolpidem in healthy subjects

被引:18
|
作者
Saari, Teijo I.
Laine, Kari
Leino, Kari
Valtonen, Mika
Neuvonen, Pertti J.
Olkkola, Klaus T.
机构
[1] Turku Univ, Dept Anaesthesiol & Intens Care, FIN-20520 Turku, Finland
[2] Turku Univ, Dept Pharmacol & Clin Pharmacol, FIN-20520 Turku, Finland
[3] Univ Helsinki, Dept Clin Pharmacol, FIN-00014 Helsinki, Finland
关键词
CYP3A4; cytochrome P450; drug interaction; voriconazole; zolpidem;
D O I
10.1111/j.1365-2125.2006.02707.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: To assess the effect of voriconazole on the pharmacokinetics and pharmacodynamics of zolpidem. Methods: In a randomized cross-over study with two phases, 10 healthy subjects ingested 10 mg of zolpidem with or without oral voriconazole pretreatment. The concentrations of zolpidem were measured in plasma up to 24 h and pharmacodynamic variables were monitored for 12 h. Results: Voriconazole increased the peak plasma concentration of zolpidem by 1.23-fold [P < 0.05; 90% confidence interval (CI) 1.05, 1.45] and the area under the plasma zolpidem concentration-time curve by 1.48-fold (P < 0.001; 90% CI 1.29, 1.74). The time to peak plasma zolpidem concentration was unchanged by voriconazole but the half-life was prolonged from 3.2 to 4.1 h (P < 0.01; 95% CI on the difference 0.27, 1.45). The pharmacodynamics of zolpidem were unaffected by voriconazole. Conclusion: Voriconazole caused a moderate increase in exposure to zolpidem in healthy young subjects but no clear pharmacodynamic changes were observed between the groups.
引用
收藏
页码:116 / 120
页数:5
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