Shrire L, Saunders J, Traynor R, Koornhof H J
Eur J Clin Microbiol. 1984 Aug;3(4):328-32. doi: 10.1007/BF01977488.
The in vitro activity of ciprofloxacin against a wide range of bacterial isolates was assessed in comparison with norfloxacin, enoxacin, co-trimoxazole and penicillin (or ampicillin) where appropriate. Minimal inhibitory concentrations (MICs) indicated that ciprofloxacin was highly active against gram-negative bacilli of the Enterobacteriaceae and Pseudomonas groups, notably against strains resistant to gentamicin. Similarly, Staphylococcus aureus (including methicillin-resistant strains) and Haemophilus influenzae were susceptible, regardless of penicillinase production. Norfloxacin and enoxacin were less active than ciprofloxacin against the majority of species tested, although enoxacin blood levels were generally higher. Most co-trimoxazole-resistant strains were susceptible to the quinoline group of drugs.
在适当情况下,将环丙沙星对多种细菌分离株的体外活性与诺氟沙星、依诺沙星、复方新诺明和青霉素(或氨苄青霉素)进行了比较评估。最低抑菌浓度(MIC)表明,环丙沙星对肠杆菌科和假单胞菌属的革兰氏阴性杆菌具有高度活性,特别是对庆大霉素耐药的菌株。同样,金黄色葡萄球菌(包括耐甲氧西林菌株)和流感嗜血杆菌也敏感,无论其是否产生青霉素酶。诺氟沙星和依诺沙星对大多数测试菌种的活性低于环丙沙星,尽管依诺沙星的血药浓度通常较高。大多数耐复方新诺明的菌株对喹啉类药物敏感。