Investigation of PK-PD drug-drug interaction between acenocoumarol and amoxicillin plus clavulanic acid

被引:8
作者
Delavenne, X. [1 ,2 ]
Laporte, S. [1 ,2 ]
Demasles, S. [3 ]
Mallouk, N. [1 ,2 ]
Basset, T. [4 ]
Tod, M. [5 ]
Girard, P. [5 ]
Mismetti, P. [1 ,2 ,6 ]
机构
[1] Univ St Etienne, EA3065, Fac Med, St Etienne, France
[2] Hosp St Etienne, Dept Clin Pharmacol, St Etienne, France
[3] Univ Hosp St Etienne, Dept Neurol, St Etienne, France
[4] Univ Hosp St Etienne, Pharmacol Lab, St Etienne, France
[5] Univ Lyon 1, Fac Med, EA3738, CTO, F-69000 Oullins, France
[6] Univ Hosp St Etienne, CIE3, Dept Internal Med & Therapeut, St Etienne, France
关键词
acenocoumarol; amoxicillin; drug-drug interaction; indirect response model; pharmacokinetic-pharmacodynamic; MODELS; VARIABILITY; KINETICS; WARFARIN;
D O I
10.1111/j.1472-8206.2008.00642.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A pharmacokinetic-pharmacodynamic (PK-PD) drug-drug interaction between acenocoumarol and amoxicillin + clavulanic acid antibiotic was assessed in eight healthy volunteers, using a population PK-PD) model. Each subject received at day 1 a single dose of 8 mg of acenocoumarol. Then 1 g of amoxicillin + 250 mg of clavulanic acid was given from days 3 to 9. On day 8, each subject received a single dose of 8 mg of acenocoumarol concomitantly with the antibiotic combination. Eleven blood samples were taken during 48 h following each acenocoumarol administration. Acenocoumarol plasma concentrations and prothrombin time were measured at each sampling time. We first identified the structural PK model by pooling data from this trial with individual data from other acenocoumarol PK trials. An indirect response model was used to fit PD data. Models were built using a nonlinear mixed effect modelling approach with NONMEM software. Covariates were tested on PK and PD parameters, including antibiotic treatment. Acenocoumarol PK data were fitted by a two-compartment, first-order input model with log normal inter-individual variability. Weight and antibiotic treatment were found to improve significantly the fit of PK data with a 15% decrease in acenocoumarol clearance with concomitant antibiotics (P < 0.05). An indirect response model was successfully applied to the PK-PD data of acenocoumarol. No covariate, including antibiotic treatment effect, significantly affected PT. Drug-drug interaction was demonstrated at the PK level, without any PD corollary.
引用
收藏
页码:127 / 135
页数:9
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