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阿明洛芬渗透入滑液的群体药代动力学研究。

A population pharmacokinetic study of alminoprofen penetration into synovial fluid.

作者信息

Tod M, Pobel C, Le Gros V, Louchahi K, Petitjean O, Brion N, Garcia-Mace J L

机构信息

Département de Pharmacotoxicologie, Hôpital Avicenne, Bobigny, France.

出版信息

Biopharm Drug Dispos. 1995 Nov;16(8):627-34. doi: 10.1002/bdd.2510160803.

DOI:10.1002/bdd.2510160803
PMID:8573683
Abstract

The pharmacokinetics of alminoprofen in plasma and synovial fluid (SF) at steady state (300 mg t.i.d.) was studied in 45 patients with knee effusion. Plasma and SF samples, one each per patient, were obtained. Six groups were made according to the time of sampling after ingestion of the 13th dose: 1 h (n = 7), 2 h (n = 7), 4 h (n = 7), 6 h (n = 10), 8 h (n = 6), 12 h (n = 8). A three-compartment model was used to describe alminoprofen kinetics in plasma and SF, with two parameterizations, a 'classical' and a 'physiological' one. The non-linear mixed effect model approach was used to estimate the mean and variance of the pharmacokinetic parameters. The mean +/- SE of the estimates (coefficient of variation of interindividual variability as a percentage) were volume of distribution, 11.0 +/- 1.711 (12%); elimination rate constant, 0.236 +/- 0.025 h-1 (18%); absorption rate constant 2.80 +/- 0.31 h-1 (464%), clearance of influx into SF, 0.29 +/- 0.14 mL min-1; clearance of efflux into plasma, 0.56 +/- 0.25 mL min-1. These two clearances were not significantly different, which indicates that passive diffusion occurs in both directions. The mean +/- SD alminoprofen concentration versus time curve in plasma and SF at steady state was simulated and showed that the mean +/- SD maximal concentration in SF was 8.1 +/- 6.3 mg L-1 and was obtained 4 h after dose administration.

摘要

在45例膝关节积液患者中研究了稳态(每日3次,每次300 mg)下阿明洛芬在血浆和滑液(SF)中的药代动力学。采集了每位患者的一份血浆和SF样本。根据第13剂摄入后的采样时间分为6组:1小时(n = 7)、2小时(n = 7)、4小时(n = 7)、6小时(n = 10)、8小时(n = 6)、12小时(n = 8)。采用三室模型描述阿明洛芬在血浆和SF中的动力学,有两种参数化方式,即“经典”和“生理”参数化。使用非线性混合效应模型方法估计药代动力学参数的均值和方差。估计值的均值±标准误(个体间变异性的变异系数百分比)分别为分布容积11.0±1.711(12%);消除速率常数0.236±0.025 h-1(18%);吸收速率常数2.80±0.31 h-1(464%);流入SF的清除率0.29±0.14 mL min-1;流出到血浆的清除率0.56±0.25 mL min-1。这两种清除率无显著差异,表明双向均发生被动扩散。模拟了稳态下血浆和SF中阿明洛芬浓度随时间变化的均值±标准差曲线,结果显示SF中的均值±标准差最大浓度为8.1±6.3 mg L-1,在给药后4小时获得。

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引用本文的文献

1
Pharmacokinetics of nonsteroidal anti-inflammatory drugs in synovial fluid.非甾体抗炎药在滑液中的药代动力学
Clin Pharmacokinet. 1999 Mar;36(3):191-210. doi: 10.2165/00003088-199936030-00002.
2
Role of population pharmacokinetics in drug development. A pharmaceutical industry perspective.群体药代动力学在药物研发中的作用。制药行业视角。
Clin Pharmacokinet. 1997 Apr;32(4):294-312. doi: 10.2165/00003088-199732040-00003.