Population Pharmacokinetic/Pharmacodynamic Analysis of Nociceptive Pain Models Following an Oral Pregabalin Dose Administration to Healthy Subjects

被引:2
|
作者
van Esdonk, Michiel J. [1 ,2 ]
Lindeman, Ian [1 ]
Okkerse, Pieter [1 ]
de Kam, Marieke L. [1 ]
Groeneveld, Geert J. [1 ]
Stevens, Jasper [3 ]
机构
[1] Ctr Human Drug Res, Leiden, Netherlands
[2] Leiden Univ, Div Syst Biomed & Pharmacol, Leiden Acad Ctr Drug Res, Leiden, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
来源
关键词
CLINICAL PHARMACOKINETICS;
D O I
10.1002/psp4.12318
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A battery of pain models can be used in clinical trials to investigate the efficacy and to establish the concentration-effect relationship of novel analgesics. This study quantified the pharmacokinetics (PK) of pregabalin after a single oral dose of 300mg and the pharmacodynamics (PD) on the pain tolerance threshold (PTT) of the cold pressor, electrical stimulation, the pressure pain model, and on the pain detection threshold of a contact heat pain model. The PK were best described using a one-compartment model with lag time, linear absorption, and linear elimination. The PTT of the cold pressor showed a negative linear decrease over time without pregabalin. A linear drug effect was identified on the PTT of the cold pressor test and an on/off effect for the electrical stimulation PTT. No PK/PD relationship could be identified on the pressure pain and heat pain test. Citation:
引用
收藏
页码:573 / 580
页数:8
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