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新型氯氟喹诺酮BAY y 3118与环丙沙星、司帕沙星及其他抗菌药物相比,对厌氧菌的活性增强。

Increased activity of a new chlorofluoroquinolone, BAY y 3118, compared with activities of ciprofloxacin, sparfloxacin, and other antimicrobial agents against anaerobic bacteria.

作者信息

Aldridge K E

机构信息

Department of Medicine, Louisiana State University Medical Center, New Orleans 70112.

出版信息

Antimicrob Agents Chemother. 1994 Jul;38(7):1671-4. doi: 10.1128/AAC.38.7.1671.

Abstract

A total of 435 clinical isolates of anaerobes were tested with a broth microdilution method to determine the activity of BAY y 3118 compared with those of other agents against anaerobic bacteria. All strains of Bacteroides capillosus, Prevotella spp., Porphyromonas spp., Fusobacterium spp., Clostridium spp., Eubacterium spp., Peptostreptococcus spp., and Veillonella parvula were susceptible (MICs of < or = 2 micrograms/ml) to BAY y 3118. Against the 315 strains of the Bacteroides fragilis group, five strains required elevated MICs (> or = 4 micrograms/ml) of BAY y 3118. Only imipenem and metronidazole were active against all anaerobes. Overall, BAY y 3118 was more active than ciprofloxacin, sparfloxacin, piperacillin, cefotaxime, and clindamycin against the test isolates.

摘要

采用肉汤微量稀释法对总共435株厌氧菌临床分离株进行检测,以确定BAY y 3118相对于其他药物对厌氧菌的活性。所有毛螺菌属、普雷沃菌属、卟啉单胞菌属、梭杆菌属、梭菌属、真杆菌属、消化链球菌属和小韦荣球菌菌株对BAY y

3118敏感(MIC≤2微克/毫升)。对于315株脆弱拟杆菌群菌株,5株对BAY y 3118的MIC升高(≥4微克/毫升)。只有亚胺培南和甲硝唑对所有厌氧菌有活性。总体而言,BAY y 3118对受试分离株的活性高于环丙沙星、司帕沙星、哌拉西林、头孢噻肟和克林霉素。

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本文引用的文献

1
In vitro activity of Bay Y3118 against anaerobic bacteria.Bay Y3118对厌氧菌的体外活性。
Antimicrob Agents Chemother. 1993 Nov;37(11):2509-13. doi: 10.1128/AAC.37.11.2509.
2
In vitro activity of Bay y 3118, a new quinolone.新型喹诺酮类药物Bay y 3118的体外活性
Antimicrob Agents Chemother. 1993 Nov;37(11):2348-57. doi: 10.1128/AAC.37.11.2348.
7
Comparative activity of ciprofloxacin against anaerobic bacteria.
Antimicrob Agents Chemother. 1985 Mar;27(3):427-8. doi: 10.1128/AAC.27.3.427.
8
Comparative in vitro activity of lomefloxacin, a new difluoroquinolone.
Eur J Clin Microbiol Infect Dis. 1989 Feb;8(2):164-8. doi: 10.1007/BF01963905.

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