Roy C, Foz A, Segura C, Tirado M, Teixell M, Teruel D
Infection. 1983 Nov-Dec;11(6):326-8. doi: 10.1007/BF01641358.
We studied the in vitro activity of ciprofloxacin against 570 strains of ampicillin-resistant Enterobacteriaceae and 286 Pseudomonas aeruginosa strains. 95.26% of the Enterobacteriaceae and 53.45% of the P. aeruginosa were inhibited by 0.1 mg/l of ciprofloxacin. 2 mg/l of ciprofloxacin inhibited all of the Enterobacteriaceae strains and 4 mg/l all of the P. aeruginosa. We compared the activity of ciprofloxacin with that of temocillin in the Enterobacteriaceae strains. In the P. aeruginosa strains, classified according to their susceptibility to carbenicillin and gentamicin, we compared the activity of ciprofloxacin with that of ceftazidime. In the strains studied, the in vitro activity of ciprofloxacin is superior to that of temocillin against the Enterobacteriaceae and to that of ceftazidime against the P. aeruginosa strains.
我们研究了环丙沙星对570株耐氨苄西林肠杆菌科细菌和286株铜绿假单胞菌的体外活性。0.1mg/l的环丙沙星可抑制95.26%的肠杆菌科细菌和53.45%的铜绿假单胞菌。2mg/l的环丙沙星可抑制所有肠杆菌科菌株,4mg/l可抑制所有铜绿假单胞菌。我们比较了环丙沙星与替莫西林在肠杆菌科菌株中的活性。在根据对羧苄西林和庆大霉素的敏感性分类的铜绿假单胞菌菌株中,我们比较了环丙沙星与头孢他啶的活性。在所研究的菌株中,环丙沙星对肠杆菌科细菌的体外活性优于替莫西林,对铜绿假单胞菌菌株的体外活性优于头孢他啶。