García-Garrote F, Cercenado E, Alcalá L, Bouza E
Servicio de Microbiología, Hospital General Universitario "Gregorio Marañón," Madrid, Spain.
Antimicrob Agents Chemother. 1998 Sep;42(9):2452-5. doi: 10.1128/AAC.42.9.2452.
The in vitro activity of LY333328 was compared with those of vancomycin and teicoplanin against 425 gram-positive clinical isolates, including a variety of multiply resistant strains. LY333328 at </=4 microgram/ml inhibited all microorganisms tested, including methicillin- and teicoplanin-resistant staphylococci, glycopeptide-resistant enterococci, penicillin- and multiply resistant pneumococci, and viridans and beta-hemolytic streptococci.
将LY333328的体外活性与万古霉素和替考拉宁针对425株革兰氏阳性临床分离菌(包括多种多重耐药菌株)的活性进行了比较。浓度≤4微克/毫升的LY333328抑制了所有测试的微生物,包括耐甲氧西林和耐替考拉宁的葡萄球菌、耐糖肽的肠球菌、耐青霉素和多重耐药的肺炎球菌以及草绿色链球菌和β-溶血性链球菌。