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布洛芬和舒林酸在酒精性肝病中的动力学

Ibuprofen and sulindac kinetics in alcoholic liver disease.

作者信息

Juhl R P, Van Thiel D H, Dittert L W, Albert K S, Smith R B

出版信息

Clin Pharmacol Ther. 1983 Jul;34(1):104-9. doi: 10.1038/clpt.1983.137.

Abstract

Ibuprofen and sulindac kinetics after oral doses were compared in 15 patients with alcoholic liver disease and 29 normal subjects. The patients with alcoholic liver disease were divided into a group with fair hepatic function (FHF) and a group with poor hepatic function (PHF) based on elimination rates of indocyanine green. The effects of alcoholic liver disease on the ibuprofen kinetics were minimal. The absorption of the drug appeared to be delayed in some of the PHF patients, and slight differences were noted in the serum AUC and the elimination rate constant for ibuprofen. The absorption of sulindac was delayed in both PHF and FHF groups of patients, as was the appearance of the active metabolite, sulindac sulfide, and the inactive metabolite, sulindac sulfone. The plasma AUC for sulindac sulfide in patients with poor hepatic function was four times that in normal subjects. The kinetics of sulindac, a pro-drug that relies on the liver for conversion to an active metabolite, were markedly affected by alcoholic liver disease.

摘要

在15例酒精性肝病患者和29名正常受试者中比较了口服剂量后布洛芬和舒林酸的动力学。根据吲哚菁绿的消除率,将酒精性肝病患者分为肝功能良好组(FHF)和肝功能不良组(PHF)。酒精性肝病对布洛芬动力学的影响极小。在一些PHF患者中,药物的吸收似乎延迟,并且在血清AUC和布洛芬的消除速率常数方面存在细微差异。舒林酸在PHF组和FHF组患者中的吸收均延迟,活性代谢物舒林酸硫化物和非活性代谢物舒林酸砜的出现也延迟。肝功能不良患者中舒林酸硫化物的血浆AUC是正常受试者的四倍。舒林酸是一种前体药物,依赖肝脏转化为活性代谢物,其动力学受到酒精性肝病的显著影响。

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