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新喹啉衍生物依诺沙星(CL-919)的体外活性与其他抗菌剂的比较。

In-vitro activity of enoxacin (CL-919), a new quinoline derivative, compared with that of other antimicrobial agents.

作者信息

Wise R, Andrews J M, Danks G

出版信息

J Antimicrob Chemother. 1984 Mar;13(3):237-44. doi: 10.1093/jac/13.3.237.

DOI:10.1093/jac/13.3.237
PMID:6586712
Abstract

The in-vitro activity of enoxacin (CI-919), a new synthetic quinoline derivative was compared with that of three other quinolines ofloxacin, norfloxacin and nalidixic acid. In addition beta-lactams and gentamicin were also included when appropriate. The MICs of enoxacin for 90% of Escherichia coli, Klebsiella spp., Enterobacter spp., Proteus spp., Providencia stuartii, Pseudomonas aeruginosa and Staphylococcus aureus were less than 4 mg/l, for Haemophilus influenzae less than 0.25 mg/l and Neisseria gonorrhoeae less than 0.03 mg/l. Bacteroides fragilis and streptococci (including Streptococcus pneumoniae) were less susceptible, MIC90 16 mg/l. Against many of the common Enterobacteriaceae enoxacin displayed a similar degree of activity as gentamicin. Gentamicin-resistant strains of common bacterial pathogens were susceptible to enoxacin as were methicillin-resistant Staph. aureus. The protein binding of enoxacin (concentration 5 mg/l) was 18%.

摘要

对新型合成喹啉衍生物依诺沙星(CI - 919)的体外活性与其他三种喹啉类药物氧氟沙星、诺氟沙星和萘啶酸进行了比较。此外,还在适当情况下纳入了β - 内酰胺类药物和庆大霉素。依诺沙星对90%的大肠杆菌、克雷伯菌属、肠杆菌属、变形杆菌属、斯氏普罗威登斯菌、铜绿假单胞菌和金黄色葡萄球菌的最低抑菌浓度(MIC)低于4mg/L,对流感嗜血杆菌低于0.25mg/L,对淋病奈瑟菌低于0.03mg/L。脆弱拟杆菌和链球菌(包括肺炎链球菌)的敏感性较低,MIC90为16mg/L。依诺沙星对许多常见肠杆菌科细菌的活性程度与庆大霉素相似。常见细菌病原体的庆大霉素耐药菌株对依诺沙星敏感,耐甲氧西林金黄色葡萄球菌也对依诺沙星敏感。依诺沙星(浓度5mg/L)的蛋白结合率为18%。

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