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新型氟喹诺酮类药物A-80556的体外和体内评价

In vitro and in vivo evaluations of A-80556, a new fluoroquinolone.

作者信息

Clement J J, Tanaka S K, Alder J, Vojtko C, Beyer J, Hensey D, Ramer N, McDaniel D, Chu D T

机构信息

Abbott Laboratories, Abbott Park, Illinois 60064-3500.

出版信息

Antimicrob Agents Chemother. 1994 May;38(5):1071-8. doi: 10.1128/AAC.38.5.1071.

Abstract

A-80556 is a novel fluoroquinolone with potent antibacterial activity against gram-positive, gram-negative, and anaerobic organisms. A-80556 was more active than ciprofloxacin, ofloxacin, lomefloxacin, and sparfloxacin against gram-positive bacteria. A-80556 was particularly active against Staphylococcus aureus (MIC for 90% of isolates [MIC90], 0.12 microgram/ml, relative to fluoroquinolone-susceptible strains) and Streptococcus pneumoniae (MIC90, 0.12 microgram/ml). A-80556 was also the most active of the quinolones tested against ciprofloxacin-resistant S. aureus, with an MIC90 of 4.0 micrograms/ml; that of ciprofloxacin was > 128 micrograms/ml. However, the significance of this activity is not known. A-80556 was slightly less active against Escherichia coli (MIC90, 0.06 microgram/ml) and other enteric organisms than ciprofloxacin (MIC90 for E. coli, < or = 0.03 microgram/ml). A-80556 was slightly less active against Pseudomonas aeruginosa (MIC90, 4.0 micrograms/ml) than ciprofloxacin (MIC90, 2.0 micrograms/ml) and more active against Acinetobacter spp. (respective MIC90s, 0.12 and 0.5 microgram/ml). A-80556 was also the most active compound against anaerobes. Against Bacteroides fragilis, the MIC90 of A-80556 was 2.0 micrograms/ml; that of ciprofloxacin was 16 micrograms/ml. The in vivo efficacy of A-80556 in experimental models with both gram-positive and gram-negative infections was consistent with the in vitro activity and pharmacokinetics and oral absorption in mice.

摘要

A - 80556是一种新型氟喹诺酮类药物,对革兰氏阳性菌、革兰氏阴性菌及厌氧菌具有强大的抗菌活性。A - 80556对革兰氏阳性菌的活性比环丙沙星、氧氟沙星、洛美沙星和司帕沙星更强。A - 80556对金黄色葡萄球菌(90%分离株的最低抑菌浓度[MIC90],0.12微克/毫升,相对于氟喹诺酮敏感菌株)和肺炎链球菌(MIC90,0.12微克/毫升)特别有效。A - 80556也是所测试的喹诺酮类药物中对环丙沙星耐药的金黄色葡萄球菌活性最强的,其MIC90为4.0微克/毫升;环丙沙星的MIC90大于128微克/毫升。然而,这种活性的意义尚不清楚。A - 80556对大肠杆菌(MIC90,0.06微克/毫升)和其他肠道菌的活性略低于环丙沙星(大肠杆菌的MIC90,≤0.03微克/毫升)。A - 80556对铜绿假单胞菌(MIC90,4.0微克/毫升)的活性略低于环丙沙星(MIC90,2.0微克/毫升),而对不动杆菌属的活性更强(各自的MIC90分别为0.12和0.5微克/毫升)。A - 80556也是对厌氧菌活性最强的化合物。对脆弱拟杆菌,A - 80556的MIC90为2.0微克/毫升;环丙沙星的MIC90为16微克/毫升。A - 80556在革兰氏阳性菌和革兰氏阴性菌感染实验模型中的体内疗效与体外活性、药代动力学及在小鼠体内的口服吸收情况一致。

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