Bassey C M, Baltch A L, Smith R P
J Antimicrob Chemother. 1986 May;17(5):623-8. doi: 10.1093/jac/17.5.623.
The in-vitro antimicrobial activity of five new quinolones, enoxacin (CI-919, AT-2266), ciprofloxacin (Bay o 9867), amifloxacin (WIN 49375) norfloxacin (MK 0366), and ofloxacin (ORF 18489), was compared against 104 strains of Enterobacteriaceae, 51 Pseudomonas species, 7 Acinetobacter calcoaceticus var. anitratus, and 15 enterococci. In general the quinolones tested were active against most bacterial strains. Ciprofloxacin was the most active with MIC90 for all genera tested ranging from 0.03 to 4.0 mg/l. The range of MIC90 for enoxacin and amifloxacin was 0.06 to 16.0 mg/l, for ofloxacin 0.25 to 8.0 mg/l, and for norfloxacin 0.06 to 32.0 mg/l. All strains of P. aeruginosa tested were resistant to amikacin (MIC greater than or equal to 16 mg/l); those resistant by virtue of inactivating enzyme production were less susceptible to ciprofloxacin, ofloxacin, and norfloxacin than those strains exhibiting decreased uptake of amikacin. Susceptibility to enoxacin and amifloxacin was not affected by the mechanism of aminoglycoside resistance. Of 65 strains tested with four quinolones using log and lag phase bacterial growth, the MICs in log phase growth were one to two dilutions higher for 42% of strains tested with amifloxacin, 33% of those tested with norfloxacin, and 23% for those tested with enoxacin and ciprofloxacin.
比较了五种新型喹诺酮类药物依诺沙星(CI-919,AT-2266)、环丙沙星(Bay o 9867)、阿米氟沙星(WIN 49375)、诺氟沙星(MK 0366)和氧氟沙星(ORF 18489)对104株肠杆菌科细菌、51株假单胞菌属细菌、7株醋酸钙不动杆菌无硝变种及15株肠球菌的体外抗菌活性。总体而言,所测试的喹诺酮类药物对大多数菌株具有活性。环丙沙星活性最强,对所有测试菌属的MIC90范围为0.03至4.0毫克/升。依诺沙星和阿米氟沙星的MIC90范围为0.06至16.0毫克/升,氧氟沙星为0.25至8.0毫克/升,诺氟沙星为0.06至32.0毫克/升。所有测试的铜绿假单胞菌菌株对阿米卡星耐药(MIC大于或等于16毫克/升);因产生灭活酶而耐药的菌株比那些表现出对阿米卡星摄取减少的菌株对环丙沙星、氧氟沙星和诺氟沙星的敏感性更低。对依诺沙星和阿米氟沙星的敏感性不受氨基糖苷类耐药机制的影响。在用对数期和迟缓期细菌生长对65株菌株进行四种喹诺酮类药物测试时,对于42%用阿米氟沙星测试的菌株、33%用诺氟沙星测试的菌株以及23%用依诺沙星和环丙沙星测试的菌株,其对数期生长时的MIC比相应时期高1至2个稀释度。