Evaluation of potential losartan-phenytoin drug interactions in healthy volunteers

被引:28
作者
Fischer, TL
Pieper, JA
Graff, DW
Rodgers, JE
Fischer, JD
Parnell, KJ
Goldstein, JA
Greenwood, R
Patterson, JH
机构
[1] Univ N Carolina, Div Pharmacotherapy, Sch Pharm, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Chapel Hill, NC 27599 USA
[3] Pharsight Corp, Mountain View, CA USA
[4] Natl Inst Environm Hlth Sci, Res Triangle Pk, NC USA
关键词
D O I
10.1067/mcp.2002.127945
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Phenytoin, a cytochrome P450 (CYP) 2C9 substrate, has a narrow therapeutic index and nonlinear pharmacokinetics. Therefore there is the potential for significant concentration-related adverse effects when phenytoin is coadministered with other CYP2C9 substrates. Losartan, an antihypertensive agent, is also a substrate for CYP2C9. Objective: Our objective was to assess the effects of losartan on the pharmacokinetics of phenytoin and the effects of phenytoin on the pharmacokinetics of losartan in a healthy population of volunteers. Methods: A prospective, randomized, 3-period crossover study was conducted in 16 healthy volunteers with phenytoin alone, phenytoin in combination with losartan, and losartan alone. Each treatment was given for 10 days with a 3-week washout period between treatments. On day 10, plasma concentrations of phenytoin and plasma and urine concentrations of losartan and its active carboxylic-acid metabolite E3174 were measured to determine steady-state pharmacokinetic parameters. Results: Coadministration of losartan had no effect on the pharmacokinetics of phenytoin. Coadministration of phenytoin increased the mean area under the concentration-time curve from time zero to 24 hours [AUC(0-24)] of losartan by 17% (355 +/- 220 ng . h/mL versus 427 +/- 177 ng . h/mL; P = .1), but this difference was not statistically significant. In the 14 CYP2C9*1/*1 subjects, the mean AUC(0-24) of losartan was increased by 29% (284 +/- 84 rig . h/mL versus 402 +/- 128 rig . h/mL; P = .008). Coadministration of phenytoin significantly reduced the AUC(0-24) of E3174 by 63% (1254 +/- 256 rig . h/mL versus 466 +/- 174 rig . h/mL; P = .0001) and the formation clearance of losartan to E3174 (1.91 +/- 0.8 mL/h per kilogram versus 0.62 +/- 0.4 mL/h per kilogram; P = .0001). Conclusions: Losartan, a CYP2C9 substrate, had no effect on the pharmacokinetics of phenytoin. However, phenytoin inhibited the CYP2C9-mediated conversion of losartan to E3174.
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页码:238 / 246
页数:9
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