Digranes A, Benonisen E, Salveson A, Zahm F
Department of Microbiology and Immunology, Gade Institute, Haukeland Hospital, Bergen, Norway.
Chemotherapy. 1988;34(5):401-10. doi: 10.1159/000238599.
The in vitro activity of fleroxacin (Ro 23-6240) against 441 bacterial isolates was compared with those of ciprofloxacin, ofloxacin, amoxycillin, cefadroxil, cefuroxime and tobramycin. An agar dilution method was used for the determination of minimal inhibitory concentrations (MICs). Ciprofloxacin showed the highest activity against the Enterobacteriaceae, 95% of the isolates were inhibited by 0.06 mg/l, but fleroxacin and ofloxacin were also highly active (MIC 90% = 0.5 and 0.25 mg/l, respectively). Ciprofloxacin was the most active agent against Pseudomonas aeruginosa (MIC 90% = 0.12 mg/l), whereas the activities of fleroxacin and ofloxacin were more variable. Tobramycin was highly active against P. aeruginosa, 75% of the isolates were inhibited by 0.5 mg/l or less. The quinolones and tobramycin exhibited high activity against Acinetobacter calcoaceticus, the great majority of the isolates being susceptible to 0.5 mg/l or less of any agent. All the quinolones showed high activity against Staphylococcus aureus, but fleroxacin was less active against Staphylococcus epidermidis and Staphylococcus saprophyticus than were the other derivatives. The pneumococcal and streptococcal isolates were markedly less susceptible to fleroxacin than to the other quinolones tested (MIC range 4-32 mg/l). All isolates of Haemophilus influenzae and Neisseria gonorrhoeae were inhibited by the lowest concentration of the quinolones employed in the study (0.03 mg/l). Cefuroxime was also highly active against N. gonorrhoeae, whether the strains were beta-lactamase-producing or not, but was somewhat less active against H. influenzae. The quinolones displayed moderate and similar activity against Bacteroides fragilis isolates (MIC range 1-16 mg/l). The MICs of fleroxacin against gram-negative rods were generally 4-16 times higher at pH 8.8 than those obtained at pH 5.8 and 7.3. The activity against gram-positive cocci was not markedly influenced by changes in pH.
将氟罗沙星(Ro 23 - 6240)对441株细菌分离株的体外活性与环丙沙星、氧氟沙星、阿莫西林、头孢羟氨苄、头孢呋辛和妥布霉素进行了比较。采用琼脂稀释法测定最低抑菌浓度(MIC)。环丙沙星对肠杆菌科细菌显示出最高活性,95%的分离株被0.06mg/l抑制,但氟罗沙星和氧氟沙星也具有高活性(MIC 90%分别为0.5和0.25mg/l)。环丙沙星是对铜绿假单胞菌最具活性的药物(MIC 90% = 0.12mg/l),而氟罗沙星和氧氟沙星的活性则更具变异性。妥布霉素对铜绿假单胞菌具有高活性,75%的分离株被0.5mg/l或更低浓度抑制。喹诺酮类药物和妥布霉素对乙酸钙不动杆菌表现出高活性,绝大多数分离株对任何一种药物0.5mg/l或更低浓度敏感。所有喹诺酮类药物对金黄色葡萄球菌均显示出高活性,但氟罗沙星对表皮葡萄球菌和腐生葡萄球菌的活性低于其他衍生物。肺炎球菌和链球菌分离株对氟罗沙星的敏感性明显低于所测试的其他喹诺酮类药物(MIC范围为4 - 32mg/l)。所有流感嗜血杆菌和淋病奈瑟菌分离株均被研究中使用的最低浓度喹诺酮类药物(0.03mg/l)抑制。头孢呋辛对淋病奈瑟菌也具有高活性,无论菌株是否产β-内酰胺酶,但对流感嗜血杆菌的活性略低。喹诺酮类药物对脆弱拟杆菌分离株表现出中等且相似的活性(MIC范围为1 - 16mg/l)。氟罗沙星在pH 8.8时对革兰氏阴性杆菌的MIC通常比在pH 5.8和7.3时高4 - 16倍。对革兰氏阳性球菌的活性不受pH变化的明显影响。