Sader H S, Jones R N, Allen S D, Gerlach E H, Murray P R, Washington J A
Department of Pathology, University of Iowa Hospital & Clinics, Iowa City 52242.
J Chemother. 1993 Oct;5(5):283-8. doi: 10.1080/1120009x.1993.11739245.
The in vitro activity of OPC-17116, a new fluoroquinolone, was compared with those of ciprofloxacin, ofloxacin and cefixime. A total of 5,231 fresh clinical isolates from five geographically separate US medical centers were tested. The primary results of this study are: 1. OPC-17116 is very active against Enterobacteriaceae [MIC90s, 0.015-1 microgram/ml, except Providencia rettgeri (MIC90, > 8 micrograms/ml)], 2. among nonenteric Gram-negative bacilli (e.g. Xanthomonas maltophilia, MIC90, 2 micrograms/ml) and Gram-positive cocci (e.g. oxacillin-susceptible staphylococci, MIC90s, 0.12-0.5 microgram/ml) OPC-17116 demonstrated higher activity than ciprofloxacin or ofloxacin, 3. the quinolones were more active than cefixime against most of the species tested, especially against Gram-positive and non-enteric Gram-negative organisms. The results of this study, associated with prior documented favorable qualities, support continued investigation of OPC-17116 for clinical use.
将新型氟喹诺酮类药物OPC - 17116的体外活性与环丙沙星、氧氟沙星和头孢克肟进行了比较。共对来自美国五个地理位置分散的医疗中心的5231株新鲜临床分离株进行了检测。本研究的主要结果如下:1. OPC - 17116对肠杆菌科细菌具有很强的活性[MIC90为0.015 - 1微克/毫升,除雷氏普罗威登斯菌(MIC90,> 8微克/毫升)外];2. 在非肠道革兰氏阴性杆菌(如嗜麦芽窄食单胞菌,MIC90为2微克/毫升)和革兰氏阳性球菌(如对苯唑西林敏感的葡萄球菌,MIC90为0.12 - 0.5微克/毫升)中,OPC - 17116表现出比环丙沙星或氧氟沙星更高的活性;3. 喹诺酮类药物对大多数受试菌种的活性高于头孢克肟,尤其是对革兰氏阳性菌和非肠道革兰氏阴性菌。本研究结果与先前记录的良好特性相结合,支持对OPC - 17116继续进行临床应用研究。