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Time dependent influence of diazepam on the pharmacokinetics of ibuprofen in man.

机译:地西epa对布洛芬在人体内药代动力学的时间依赖性影响。

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Circadian variation in the disease activity of rheumatoid arthritis has been established. Several nonsteroidal anti-inflammatory drugs have been studied for their chronokinetic behaviour. Time dependent influence of diazepam on the pharmacokinetics of diclofenac and naproxen has been reported. We report the time dependent influence of diazepam on the pharmacokinetics of ibuprofen in healthy subjects. Either ibuprofen or ibuprofen with diazepam was administered at 10.00 or 22.00 hours to eight healthy volunteers in a randomized crossover study. Serum ibuprofen levels were estimated by high performance liquid chromatography. There was a significant (p < 0.05) increase in mean elimination half life (2.39 +/- 0.42 to 3.59 +/- 0.35 h) following ibuprofen and diazepam administration compared to ibuprofen alone administered at 22.00 hours. The mean clearance of ibuprofen was therefore lowered from 62.7 +/- 8.9 to 41.7 +/- 2.6 ml/h/kg under the influence of diazepam during the night. Such a time dependent influence of diazepam on the pharmacokinetics of ibuprofen may be due to circadian variation in the pattern of protein production in the liver and/or competitive protein binding of the two drugs during the dark period.
机译:已经建立了类风湿关节炎疾病活动的昼夜节律变化。已经研究了几种非甾体抗炎药的计时动力学行为。地西epa对双氯芬酸和萘普生的药代动力学具有时间依赖性影响。我们报告了地西epa对布洛芬在健康受试者体内药代动力学的时间依赖性影响。在随机交叉研究中,布洛芬或布洛芬与地西epa分别于10.00或22.00小时施用于八名健康志愿者。通过高效液相色谱法评估血清布洛芬水平。与在22.00小时单独使用布洛芬相比,在布洛芬和地西epa给药后,平均消除半衰期(2.39 +/- 0.42至3.59 +/- 0.35小时)显着(p <0.05)增加。因此,在夜间地西epa的影响下,布洛芬的平均清除率从62.7 +/- 8.9降至41.7 +/- 2.6 ml / h / kg。地西epa对布洛芬药代动力学的这种时间依赖性影响可能是由于在黑暗期肝脏中蛋白质生产模式的昼夜节律变化和/或两种药物的竞争性蛋白质结合所致。

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