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Single-dose pharmacokinetics of the monobactam azthreonam (SQ 26,776) in healthy subjects.健康受试者中单环β-内酰胺类氨曲南(SQ 26,776)的单剂量药代动力学。
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High-pressure liquid chromatographic analysis of aztreonam in sera and urine.血清和尿液中氨曲南的高效液相色谱分析
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Multiple-dose pharmacokinetics of the monobactam azthreonam (SQ 26,776) in healthy subjects.单环β-内酰胺类药物氨曲南(SQ 26,776)在健康受试者中的多剂量药代动力学。
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氨曲南在革兰氏阴性菌感染患者中的药代动力学。

Pharmacokinetics of aztreonam in patients with gram-negative infections.

作者信息

Janicke D M, Cafarell R F, Parker S W, Apicella M A, Jusko W J

出版信息

Antimicrob Agents Chemother. 1985 Jan;27(1):16-20. doi: 10.1128/AAC.27.1.16.

DOI:10.1128/AAC.27.1.16
PMID:4039117
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC176197/
Abstract

Aztreonam pharmacokinetics were assessed in seven patients treated for urinary (n = 6) or lower respiratory (n = 1) tract infections. Each patient was studied twice, at the beginning and end of therapy (7 to 10 days). The patients enrolled had normal to moderately impaired renal function; a good correlation (r2 = 0.90) between serum aztreonam clearance (CL) and creatinine clearance (CLCR) was observed (mean CL/CLCR ratio = 1.11). CL ranged from 21.6 to 121 ml/min per 70 kg, and the half-life ranged from 1.6 to 8.9 h. The mean steady-state volume of distribution (0.16 +/- 0.05 [standard deviation] liter/kg) approximated the extracellular fluid volume. Protein binding of aztreonam in serum (mean, 30%) was lower than that reported in healthy adults. CL increased significantly from the first to the last day of the study, probably reflecting increasing renal function. After multiple dosing (1 g every 8 h), no significant accumulation of aztreonam was observed. Overall, the disposition of aztreonam is comparable in infected and noninfected subjects, and dosing adjustments in patients with renal impairment should be facilitated by the good correlation between CL and CLCR.

摘要

对7例因泌尿系统感染(n = 6)或下呼吸道感染(n = 1)接受治疗的患者进行了氨曲南的药代动力学评估。每位患者在治疗开始和结束时(7至10天)各进行了两次研究。入选患者的肾功能正常至中度受损;观察到血清氨曲南清除率(CL)与肌酐清除率(CLCR)之间具有良好的相关性(r2 = 0.90)(平均CL/CLCR比值 = 1.11)。CL范围为每70 kg体重21.6至121 ml/分钟,半衰期范围为1.6至8.9小时。平均稳态分布容积(0.16 +/- 0.05 [标准差]升/千克)接近细胞外液容积。氨曲南在血清中的蛋白结合率(平均为30%)低于健康成年人的报道值。从研究的第一天到最后一天,CL显著增加,这可能反映了肾功能的改善。多次给药(每8小时1 g)后,未观察到氨曲南有明显蓄积。总体而言,感染和未感染受试者中氨曲南的处置情况相当,CL与CLCR之间的良好相关性应有助于指导肾功能受损患者的剂量调整。