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新型单环β-内酰胺类药物卡芦莫南的体外抗菌活性比较

Comparative in vitro antimicrobial activity of carumonam, a new monocyclic beta-lactam.

作者信息

Smith B R, LeFrock J L, McCloskey R V, Donato J B, Weber S J, Joseph W S

出版信息

Antimicrob Agents Chemother. 1986 Feb;29(2):346-9. doi: 10.1128/AAC.29.2.346.

Abstract

The antimicrobial activity of carumonam (formerly RO-17-2301), a monocyclic beta-lactam antibiotic, was compared with those of aztreonam, cefotaxime, cefoperazone, ceftazidime, piperacillin, and gentamicin against 455 bacterial isolates. Carumonam did not possess activity against gram-positive cocci and was generally comparable to aztreonam and ceftazidime for most gram-negative bacilli. However, carumonam was the most active beta-lactam against gentamicin-resistant Pseudomonas aeruginosa strains (90% MIC, 8 micrograms/ml).

摘要

将单环β-内酰胺类抗生素卡芦莫南(曾用名RO-17-2301)的抗菌活性与氨曲南、头孢噻肟、头孢哌酮、头孢他啶、哌拉西林和庆大霉素针对455株细菌分离株的抗菌活性进行了比较。卡芦莫南对革兰氏阳性球菌无活性,对于大多数革兰氏阴性杆菌,其活性总体上与氨曲南和头孢他啶相当。然而,对于耐庆大霉素的铜绿假单胞菌菌株,卡芦莫南是活性最强的β-内酰胺类抗生素(90% MIC为8微克/毫升)。

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Carumonam versus ceftazidime for urinary tract infections.卡芦莫南与头孢他啶治疗尿路感染的比较。
Antimicrob Agents Chemother. 1988 Jul;32(7):1031-3. doi: 10.1128/AAC.32.7.1031.

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