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环孢素与多剂量双氯芬酸合用时的药代动力学。

Pharmacokinetics of cyclosporine and multiple-dose diclofenac during coadministration.

作者信息

Mueller E A, Kovarik J M, Koelle E U, Merdjan H, Johnston A, Hitzenberger G

机构信息

Department of Human Pharmacology, Sandoz Pharma, Ltd., Basle, Switzerland.

出版信息

J Clin Pharmacol. 1993 Oct;33(10):936-43. doi: 10.1002/j.1552-4604.1993.tb01926.x.

Abstract

Pursuant to anecdotal case reports of a possible drug-drug interaction between cyclosporine and diclofenac, an open, two-period crossover study in 24 healthy male volunteers was undertaken in which a single oral dose of 300 mg cyclosporine was administered alone and on day 8 of multiple oral dosing of 50 mg diclofenac every 8 hours. Serial blood samples were obtained over 48 hours after each cyclosporine dose and over a dosing interval for diclofenac on day 7 (diclofenac alone) and day 8 (coadministration of diclofenac with cyclosporine). The mean pharmacokinetic characteristics of cyclosporine were unchanged during coadministration with diclofenac. Based on area under the curve comparison, lack of a pharmacokinetic interaction was conclusively demonstrated for the extent of cyclosporine absorption. The diclofenac maximum plasma concentration and area under the curve over a dosing interval were significantly increased during coadministration; however, a straightforward interpretation of the statistical results was confounded by pronounced variability in diclofenac pharmacokinetics. The results underscore the need for continued caution when cyclosporine and diclofenac are coadministered.

摘要

根据环孢素与双氯芬酸之间可能存在药物相互作用的轶事性病例报告,对24名健康男性志愿者进行了一项开放、两阶段交叉研究,其中单次口服300毫克环孢素,分别在单独给药时以及每8小时多次口服50毫克双氯芬酸第8天时给药。在每次环孢素给药后48小时内以及第7天(仅双氯芬酸)和第8天(双氯芬酸与环孢素合用)双氯芬酸的一个给药间隔内采集系列血样。与双氯芬酸合用时,环孢素的平均药代动力学特征未发生变化。基于曲线下面积比较,环孢素吸收程度方面未发现药代动力学相互作用。合用期间,双氯芬酸的最大血浆浓度和给药间隔内的曲线下面积显著增加;然而,双氯芬酸药代动力学的显著变异性使统计结果的直接解释变得复杂。结果强调,环孢素与双氯芬酸合用时仍需持续谨慎。

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