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新型二氟喹诺酮衍生物Ro 23 - 6240与其他抗菌剂相比的体外活性。

In vitro activity of Ro 23-6240, a new difluoroquinolone derivative, compared with that of other antimicrobial agents.

作者信息

Manek N, Andrews J M, Wise R

出版信息

Antimicrob Agents Chemother. 1986 Aug;30(2):330-2. doi: 10.1128/AAC.30.2.330.

Abstract

Ro 23-6240 is a new difluorinated quinolone antimicrobial agent. Its in vitro activity against a wide range of bacteria was compared with those of other quinolones and beta-lactams. Generally, members of the family Enterobacteriaceae were inhibited by low concentrations of Ro 23-6240 (MIC90 [MIC for 90% of isolates tested], less than or equal to 1 microgram/ml). Ninety percent of Staphylococcus aureus (including methicillin-resistant strains) and Neisseria gonorrhoeae isolates were inhibited by 0.5 microgram/ml. Pseudomonas aeruginosa (MIC90, 2 micrograms/ml) and Bacteroides fragilis (MIC90, 4 micrograms/ml) showed intermediate susceptibility, and Streptococcus pneumoniae (MIC90, 8 micrograms/ml) was less susceptible. Strains resistant to nalidixic acid were less susceptible to all the quinolones tested. The protein binding of Ro 23-6240 (5 micrograms/ml) was 27%.

摘要

Ro 23-6240是一种新型二氟喹诺酮类抗菌剂。将其对多种细菌的体外活性与其他喹诺酮类药物和β-内酰胺类药物进行了比较。一般来说,肠杆菌科成员对低浓度的Ro 23-6240敏感(MIC90[对90%受试分离株的MIC],小于或等于1微克/毫升)。90%的金黄色葡萄球菌(包括耐甲氧西林菌株)和淋病奈瑟菌分离株被0.5微克/毫升的药物抑制。铜绿假单胞菌(MIC90,2微克/毫升)和脆弱拟杆菌(MIC90,4微克/毫升)表现出中度敏感性,而肺炎链球菌(MIC90,8微克/毫升)敏感性较低。对萘啶酸耐药的菌株对所有受试喹诺酮类药物的敏感性较低。Ro 23-6240(5微克/毫升)的蛋白结合率为27%。

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