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阿奇霉素单独及与阿托伐醌联合给药在人类免疫缺陷病毒感染儿童中的药代动力学。美国国立过敏与传染病研究所艾滋病临床试验组254团队。

Pharmacokinetics of azithromycin administered alone and with atovaquone in human immunodeficiency virus-infected children. The ACTG 254 Team.

作者信息

Ngo L Y, Yogev R, Dankner W M, Hughes W T, Burchett S, Xu J, Sadler B, Unadkat J D

机构信息

Department of Pharmaceutics, University of Washington, Seattle, Washington 98195, USA.

出版信息

Antimicrob Agents Chemother. 1999 Jun;43(6):1516-9. doi: 10.1128/AAC.43.6.1516.

Abstract

To evaluate if atovaquone (ATQ) interacts pharmacokinetically with azithromycin (AZ) in human immunodeficiency virus-infected children, 10 subjects (ages, 4 to 13 years) were randomized in a crossover study to receive AZ (5 mg/kg/day) alone (ALONE) or AZ (5 mg/kg/day) and ATQ (30 mg/kg/day) simultaneously (SIM) prior to receiving AZ and ATQ staggered by 12 h. Despite a lack of significant difference in the mean AZ pharmacokinetic parameters, the steady-state values of AZ's area under the concentration-time curve from 0 to 24 h and maximum concentration in serum were consistently lower (n = 7 of 7) for the SIM regimen than they were for the ALONE regimen. A larger study will be required to determine if ATQ affects AZ pharmacokinetics and efficacy in a clinically significant manner.

摘要

为评估阿托伐醌(ATQ)与阿奇霉素(AZ)在感染人类免疫缺陷病毒的儿童体内是否存在药代动力学相互作用,10名受试者(年龄4至13岁)参与了一项交叉研究,随机分组后,在接受AZ(5mg/kg/天)和ATQ(30mg/kg/天)错开12小时给药之前,分别单独接受AZ(5mg/kg/天)(单独给药组)或同时接受AZ(5mg/kg/天)和ATQ(30mg/kg/天)(联合给药组)。尽管AZ的平均药代动力学参数无显著差异,但联合给药组0至24小时的浓度-时间曲线下面积及血清中的最大浓度的稳态值始终低于单独给药组(7例中有7例)。需要开展更大规模的研究,以确定ATQ是否会以具有临床意义的方式影响AZ的药代动力学和疗效。

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本文引用的文献

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Disposition of oral azithromycin in humans.口服阿奇霉素在人体内的处置。
Clin Pharmacol Ther. 1997 Jun;61(6):641-8. doi: 10.1016/S0009-9236(97)90098-9.
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Survival in children with perinatally acquired human immunodeficiency virus type 1 infection.
N Engl J Med. 1989 Dec 28;321(26):1791-6. doi: 10.1056/NEJM198912283212604.
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Perinatally acquired human immunodeficiency virus infection.
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