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空腹状态下、与食物同服以及与抗酸剂同服时乙胺丁醇的药代动力学。

Pharmacokinetics of ethambutol under fasting conditions, with food, and with antacids.

作者信息

Peloquin C A, Bulpitt A E, Jaresko G S, Jelliffe R W, Childs J M, Nix D E

机构信息

Department of Medicine, National Jewish Medical and Research Center, Denver, Colorado 80206, USA.

出版信息

Antimicrob Agents Chemother. 1999 Mar;43(3):568-72. doi: 10.1128/AAC.43.3.568.

Abstract

Ethambutol (EMB) is the most frequent "fourth drug" used for the empiric treatment of Mycobacterium tuberculosis and a frequently used drug for infections caused by Mycobacterium avium complex. The pharmacokinetics of EMB in serum were studied with 14 healthy males and females in a randomized, four-period crossover study. Subjects ingested single doses of EMB of 25 mg/kg of body weight under fasting conditions twice, with a high-fat meal, and with aluminum-magnesium antacid. Serum was collected for 48 h and assayed by gas chromatography-mass spectrometry. Data were analyzed by noncompartmental methods and by a two-compartment pharmacokinetic model with zero-order absorption and first-order elimination. Both fasting conditions produced similar results: a mean (+/- standard deviation) EMB maximum concentration of drug in serum (Cmax) of 4.5 +/- 1.0 micrograms/ml, time to maximum concentration of drug in serum (Tmax) of 2.5 +/- 0.9 h, and area under the concentration-time curve from 0 h to infinity (AUC0-infinity) of 28.9 +/- 4.7 micrograms.h/ml. In the presence of antacids, subjects had a mean Cmax of 3.3 +/- 0.5 micrograms/ml, Tmax of 2.9 +/- 1.2 h, and AUC0-infinity of 27.5 +/- 5.9 micrograms.h/ml. In the presence of the Food and Drug Administration high-fat meal, subjects had a mean Cmax of 3.8 +/- 0.8 micrograms/ml, Tmax of 3.2 +/- 1.3 h, and AUC0-infinity of 29.6 +/- 4.7 micrograms.h/ml. These reductions in Cmax, delays in Tmax, and modest reductions in AUC0-infinity can be avoided by giving EMB on an empty stomach whenever possible.

摘要

乙胺丁醇(EMB)是经验性治疗结核分枝杆菌最常用的“第四种药物”,也是治疗鸟分枝杆菌复合体感染常用的药物。在一项随机、四周期交叉研究中,对14名健康男性和女性进行了乙胺丁醇在血清中的药代动力学研究。受试者在禁食条件下两次口服单剂量25mg/kg体重的乙胺丁醇,一次同时进食高脂餐,一次同时服用铝镁抗酸剂。采集血清48小时,采用气相色谱-质谱法进行检测。数据采用非房室模型方法以及零级吸收和一级消除的二房室药代动力学模型进行分析。两种禁食条件下结果相似:血清中药物的平均(±标准差)最大浓度(Cmax)为4.5±1.0μg/ml,血清中药物达到最大浓度的时间(Tmax)为2.5±0.9小时,0小时至无穷大的浓度-时间曲线下面积(AUC0-∞)为28.9±4.7μg·h/ml。在服用抗酸剂的情况下,受试者的平均Cmax为3.3±0.5μg/ml,Tmax为2.9±1.2小时,AUC0-∞为27.5±5.9μg·h/ml。在进食美国食品药品监督管理局规定的高脂餐的情况下,受试者的平均Cmax为3.8±0.8μg/ml,Tmax为3.2±1.3小时,AUC0-∞为29.6±4.7μg·h/ml。只要有可能,空腹服用乙胺丁醇可避免这些Cmax降低、Tmax延迟以及AUC0-∞适度降低的情况。

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