Periti P, Mazzei T, Nicoletti P
Chemioterapia. 1987 Apr;6(2):75-8.
The in-vitro antimicrobial activity of three new quinolones, ciprofloxacin, ofloxacin and pefloxacin, was compared against 194 recent clinical isolates, 50 S. aureus, 50 E. coli, 45 E. cloacae and 49 P. aeruginosa. About half of the strains were resistant to a standard reference antibiotic like oxacillin (S. aureus), ampicillin (E. coli), gentamicin (E. cloacae) and amikacin (P. aeruginosa). The resistant selected strains were less susceptible to the three fluoroquinolones tested than the parent isolates, but, except for pefloxacin against E. cloacae and P. aeruginosa, the decrease in susceptibility was relatively low and MICs remained below the resistance break-point.
比较了三种新型喹诺酮类药物环丙沙星、氧氟沙星和培氟沙星对194株近期临床分离菌的体外抗菌活性,这些分离菌包括50株金黄色葡萄球菌、50株大肠杆菌、45株阴沟肠杆菌和49株铜绿假单胞菌。约一半的菌株对标准参考抗生素耐药,如对金黄色葡萄球菌的苯唑西林、对大肠杆菌的氨苄西林、对阴沟肠杆菌的庆大霉素和对铜绿假单胞菌的阿米卡星。与亲本分离株相比,耐药选择株对所测试的三种氟喹诺酮类药物的敏感性较低,但是,除了培氟沙星对阴沟肠杆菌和铜绿假单胞菌外,敏感性降低相对较小,且最低抑菌浓度仍低于耐药断点。