Montanari M P, Prenna M, Mingoia M, Ripa S, Varaldo P E
Institute of Microbiology, University of Ancona Medical School, Italy.
Chemotherapy. 1998 Mar-Apr;44(2):85-93. doi: 10.1159/000007097.
The in vitro inhibitory and bactericidal activities of the investigational fluoroquinolone trovafloxacin were studied and compared with those of five other fluoroquinolones (ciprofloxacin, ofloxacin, pefloxacin, rufloxacin and sparfloxacin) against a wide range of clinical isolates from Italian hospitals. Against gram-positive bacteria, trovafloxacin was overall more active than the other antibiotics tested, including sparfloxacin, another gram-positive-oriented fluoroquinolone, and was active against all ciprofloxacin-resistant streptococci, enterococci, and listeriae, all ciprofloxacin-resistant Staphylococcus aureus isolates and most ciprofloxacin-resistant coagulase-negative staphylococci. Its antistaphylococcal activity was not affected by oxacillin resistance or susceptibility of the isolates, nor was its antipneumococcal activity affected by whether isolates were susceptible or resistant to penicillin. Against gram-negative bacteria, trovafloxacin retained a high potency mostly comparable with that of ciprofloxacin. Rufloxacin and pefloxacin were less active than the other fluoroquinolones against most test strains of both gram-positive and gram-negative organisms. Trovafloxacin minimal bactericidal concentrations usually equalled or exceeded by 2-4 times the minimal inhibitory concentration values, indicating that the compound is overall highly bactericidal.
对研究用氟喹诺酮类药物曲伐沙星的体外抑制和杀菌活性进行了研究,并与其他五种氟喹诺酮类药物(环丙沙星、氧氟沙星、培氟沙星、芦氟沙星和司帕沙星)针对来自意大利医院的多种临床分离菌株的活性进行了比较。针对革兰氏阳性菌,曲伐沙星总体上比其他受试抗生素更具活性,包括另一种以革兰氏阳性菌为靶向的氟喹诺酮类药物司帕沙星,并且对所有耐环丙沙星的链球菌、肠球菌和李斯特菌、所有耐环丙沙星的金黄色葡萄球菌分离株以及大多数耐环丙沙星的凝固酶阴性葡萄球菌均有活性。其抗葡萄球菌活性不受分离株对苯唑西林的耐药性或敏感性影响,其抗肺炎球菌活性也不受分离株对青霉素敏感或耐药情况的影响。针对革兰氏阴性菌,曲伐沙星大多保持与环丙沙星相当的高效能。芦氟沙星和培氟沙星对大多数革兰氏阳性和革兰氏阴性受试菌株的活性低于其他氟喹诺酮类药物。曲伐沙星的最小杀菌浓度通常等于或超过最小抑菌浓度值2至4倍,表明该化合物总体上具有高度杀菌作用。