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新型二氟喹诺酮替马沙星(A-62254)对癌症患者分离出的细菌的体外活性比较

Comparative in vitro activity of the new difluoro-quinolone temafloxacin (A-62254) against bacterial isolates from cancer patients.

作者信息

Rolston K V, Ho D H, LeBlanc B, Gooch G, Bodey G P

机构信息

Department of Medical Specialties, University of Texas System Cancer Center, Houston 77030.

出版信息

Eur J Clin Microbiol Infect Dis. 1988 Oct;7(5):684-6. doi: 10.1007/BF01964255.

Abstract

The in vitro activity of temafloxacin, a new difluoro quinolone agent, against 725 bacterial isolates representing 32 species was evaluated in comparison with that of ciprofloxacin. Temafloxacin inhibited the majority of Enterobacteriaceae isolates at a concentration of less than or equal to 0.5 microgram/ml. It was also extremely active against Acinetobacter spp. and Aeromonas hydrophila. Its activity was 2-8 fold less than that of ciprofloxacin against most gram-negative isolates. Methicillin-susceptible and methicillin-resistant Staphylococcus aureus, coagulase-negative Staphylococcus spp., Streptococcus spp., Listeria monocytogenes, Bacillus spp. and group JK corynebacteria were inhibited at concentrations equal to that of ciprofloxacin.

摘要

将新型二氟喹诺酮类药物替马沙星与环丙沙星相比较,评估了其对代表32个菌种的725株细菌分离株的体外活性。替马沙星在浓度小于或等于0.5微克/毫升时可抑制大多数肠杆菌科分离株。它对不动杆菌属和嗜水气单胞菌也极具活性。其对大多数革兰氏阴性分离株的活性比对环丙沙星低2至8倍。甲氧西林敏感和耐甲氧西林金黄色葡萄球菌、凝固酶阴性葡萄球菌属、链球菌属、单核细胞增生李斯特菌、芽孢杆菌属和JK群棒状杆菌在与环丙沙星相同的浓度下被抑制。

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