Hohl P, Felber A M
Pharma Research Department, Hoffmann-La Roche, Basel, Switzerland.
Chemotherapy. 1990;36(6):403-6. doi: 10.1159/000238796.
Fleroxacin (Ro 23-6240, AM-833), a new fluoro-4-quinolone, was tested in vitro against 273 gram-positive clinical isolates. Norfloxacin, a quinolone mostly used in urinary tract infections, was included as a standard. Overall, in vitro activities of fleroxacin and norfloxacin were superposable, but interestingly, fleroxacin was two- to fourfold more active against Staphylococcus aureus, and 1 mg/l of fleroxacin inhibited all 5 multiply resistant Corynebacterium jeikeium tested. While both quinolones were similarly active weight by weight, fleroxacin with its more favorable pharmacokinetic properties harbors the added promise of clinical usefulness in systemic infections against susceptible isolates.
氟罗沙星(Ro 23 - 6240,AM - 833),一种新型氟喹诺酮类药物,针对273株革兰氏阳性临床分离菌株进行了体外测试。将主要用于尿路感染的喹诺酮类药物诺氟沙星作为对照标准。总体而言,氟罗沙星和诺氟沙星的体外活性相当,但有趣的是,氟罗沙星对金黄色葡萄球菌的活性比诺氟沙星高两到四倍,并且1mg/L的氟罗沙星能抑制所有测试的5株多重耐药杰氏棒状杆菌。虽然两种喹诺酮类药物按重量计活性相似,但氟罗沙星具有更有利的药代动力学特性,有望在针对易感菌株的全身感染中发挥临床作用。