The effect of nateglinide on the pharmacokinetics and pharmacodynamics of acenocoumarol
| Autor: | James F. McLeod, Harold T. Smith, Pratapa Prasad, Hilde Bigler, Gangadhar Sunkara, Yibin Wang, Monica Ligueros-Saylan |
|---|---|
| Rok vydání: | 2004 |
| Předmět: |
Adult
Male Phenylalanine Nateglinide Pharmacology Placebo Double-Blind Method Pharmacokinetics Cyclohexanes medicine Humans Hypoglycemic Agents Drug Interactions Prothrombin time Acenocoumarol Cross-Over Studies medicine.diagnostic_test business.industry Anticoagulants Drug Tolerance General Medicine Drug interaction Crossover study Area Under Curve Pharmacodynamics Prothrombin Time Female Safety business medicine.drug |
| Zdroj: | Current Medical Research and Opinion. 20:41-48 |
| ISSN: | 1473-4877 0300-7995 |
| DOI: | 10.1185/030079903125002685 |
| Popis: | The potential for a drug interaction was investigated between nateglinide, an oral antidiabetic agent, and acenocoumarol, an oral anticoagulant, as these drugs are primarily metabolized via CYP2C9.A two-period, randomized, double-blind, two-way crossover study design was employed to evaluate the effect of nateglinide on the pharmacokinetics and pharmacodynamics of acenocoumarol in 11 healthy male or female subjects. All subjects received either nateglinide 120 mg t.i.d. or placebo for 5 days in a crossover fashion and a single 10-mg dose of acenocoumarol on day 3. Plasma concentrations of R- and S-acenocoumarol and the anticoagulation parameters [prothrombin time (PT) and international normalized ratio of PT (PTINR)] were determined for 72 h following acenocoumarol administration. The pharmacokinetic and pharmacodynamic parameters of acenocoumarol were determined by noncompartmental analysis.The mean (coefficient of variation (CV%)) area under the concentration-time curve (AUC(0-t)) of R-acenocoumarol in the presence and absence of nateglinide was 4217 (23%) and 3831 (24%) ng.h/ml, respectively. The corresponding values for S-acenocoumarol were 397 (20%) and 382 (23%), respectively. The mean (CV%) C(max) of R-acenocoumarol in the presence and absence of nateglinide was 304 (16%) and 316 (16%), respectively and the corresponding values for S-acenocoumarol were 142 (36%) and 141 (34%), respectively. The 90% confidence intervals indicated that exposure parameters, AUC(0-t) and C(max), of both R- and S-acenocoumarol were within the acceptable limits of 0.8-1.25. The mean (CV%) of area under the concentration-time curve of PT (AUC(PT)) following acenocoumarol administration in the presence and absence of nateglinide was 1170 (10%) and 1136 (8%), respectively. The corresponding AUC(INR) values were 104 (13%) and 99 (10%), respectively. Nateglinide co-administration has no influence on the PT or PTINR of acenocoumarol (p0.05).Co-administration of nateglinide does not influence either the pharmacokinetics or the anticoagulant activity of R- and S-acenocoumarol in healthy subjects. This suggests that no dosage adjustments will be required when nateglinide and acenocoumarol are coadministered in clinical practice. |
| Databáze: | OpenAIRE |
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