Guimaraes M A, Noone P
J Antimicrob Chemother. 1986 Jan;17(1):63-7. doi: 10.1093/jac/17.1.63.
The in-vitro activities of four quinolone carboxylic acids against 423 clinical isolates of Gram-negative rods and staphylococci from infected hospitalised patients were compared. The antibiotics included nalidixic acid and the newer compounds, norfloxacin (MK-0366), ciprofloxacin (Bay 09867) and enoxacin (AT 2266 or CI919). Norfloxacin showed slightly more activity than enoxacin, but both agents had markedly greater potencies and broader antibacterial spectrums than nalidixic acid. Ciprofloxacin was the most active quinolone tested against both gentamicin-susceptible and gentamicin-resistant stains, having an MIC90 equal or less than 1 mg/l for all species studied.
比较了四种喹诺酮羧酸对423株来自住院感染患者的革兰氏阴性杆菌和葡萄球菌临床分离株的体外活性。抗生素包括萘啶酸和较新的化合物,诺氟沙星(MK - 0366)、环丙沙星(Bay 09867)和依诺沙星(AT 2266或CI919)。诺氟沙星的活性略高于依诺沙星,但这两种药物的效力均明显高于萘啶酸,且抗菌谱更广。环丙沙星是针对庆大霉素敏感和庆大霉素耐药菌株测试的最具活性的喹诺酮类药物,对所有研究的菌种,其MIC90等于或小于1mg/L。