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替吉莫南(一种新型口服单环β-内酰胺类抗生素)的体外抗菌活性

In vitro antimicrobial activity of tigemonam, a new orally administered monobactam.

作者信息

Fuchs P C, Jones R N, Barry A L

机构信息

St. Vincent Hospital and Medical Center, Portland, Oregon 97225.

出版信息

Antimicrob Agents Chemother. 1988 Mar;32(3):346-9. doi: 10.1128/AAC.32.3.346.

Abstract

At five geographically separate medical centers, over 6,000 clinical bacterial isolates were tested for their susceptibility to tigemonam by the broth microdilution method. The antimicrobial spectrum of tigemonam was similar to that of aztreonam, but with two differences. Aztreonam was more active against Pseudomonas spp., and tigemonam was more active against some streptococci. Tigemonam was highly resistant to hydrolysis by the eight beta-lactamase enzymes tested. A significant (greater than a fourfold increase in the MICs of tigemonam) inoculum effect occurred when 3 of 13 isolates were tested with inocula of 5 X 10(5) and 1 X 10(7) CFU/ml. Tigemonam was bactericidal for all but 1 of the 13 isolates. Of the four quality-control strains recommended by the National Committee for Clinical Laboratory Standards, only Escherichia coli ATCC 25922 provided on-scale results. The proposed MIC quality-control range of tigemonam for E. coli ATCC 25922 is 0.13 to 0.5 micrograms/ml.

摘要

在五个地理位置分散的医学中心,采用肉汤微量稀释法对6000多株临床分离的细菌进行了替吉莫南敏感性检测。替吉莫南的抗菌谱与氨曲南相似,但有两点不同。氨曲南对假单胞菌属更具活性,而替吉莫南对某些链球菌更具活性。替吉莫南对所检测的8种β-内酰胺酶具有高度的水解抗性。当用5×10⁵和1×10⁷CFU/ml的接种量对13株分离菌中的3株进行检测时,出现了显著的(替吉莫南的MIC增加四倍以上)接种量效应。替吉莫南对13株分离菌中除1株外的所有菌株均具有杀菌作用。在国家临床实验室标准委员会推荐的四种质量控制菌株中,只有大肠埃希菌ATCC 25922给出了在范围内的结果。替吉莫南对大肠埃希菌ATCC 25922的建议MIC质量控制范围为0.13至0.5微克/毫升。

相似文献

2
Tigemonam, an oral monobactam.替吉莫南,一种口服单环β-内酰胺类抗生素。
Antimicrob Agents Chemother. 1988 Jan;32(1):84-91. doi: 10.1128/AAC.32.1.84.

本文引用的文献

2
In vitro activity of azthreonam, a monobactam antibiotic.单环β-内酰胺类抗生素氨曲南的体外活性
Antimicrob Agents Chemother. 1982 Nov;22(5):832-8. doi: 10.1128/AAC.22.5.832.

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