Population pharmacokinetics of eniporide and its metabolite in healthy subjects and patients with acute myocardial infarction

被引:2
作者
Bhattaram, VA
Nagaraja, NV
Peters, T
Machnig, T
Kroesser, S
Kovar, A
Derendorf, H
机构
[1] Univ Florida, Dept Pharmaceut, Gainesville, FL 32610 USA
[2] Merck KGaA, Dept Clin Pharmacokinet, Darmstadt, Germany
[3] Merck KGaA, Dept Clin Sci, Darmstadt, Germany
[4] Merck KGaA, Dept Clin Pharmacol, Darmstadt, Germany
关键词
eniporide; pharmacokinetics; acute myocardial infarction;
D O I
10.1177/0091270004274431
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eniporide ( EMD 96 875) is a novel and selective inhibitor of the Na+- H+ exchange ( NHE-1) inhibitor. The study objectives were to identify a structural model for population pharmacokinetic analysis of eniporide and its metabolite ( EMD 112 843) using nonlinear mixed-effects modeling after short-term infusion ( dose: 2.5-400 mg) in healthy subjects and patients undergoing myocardial reperfusion therapy. Pooled concentrations of eniporide and its metabolite from healthy subjects (n = 153; 4815 observations) and patients ( n = 304; 1465 observations) were included in the pharmacokinetic analysis. Population estimates of clearance and volume of distribution of eniporide were 29.2 L/h ( 24.1% coefficient of variation [CV], healthy), 20.8 L/h ( 28.0% CV, patients) and 20.4 L ( 13.1% CV, healthy), 16.9 L ( 24.9% CV, patients), respectively. Statistical significance was achieved for the effect of age on clearance and creatinine clearance on volume of distribution of eniporide. The impact of the covariates on eniporide pharmacokinetics is minimal to warrant any dosage adjustments in patient population.
引用
收藏
页码:631 / 639
页数:9
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