Affiliation:
1. Department of Internal Medicine, University of Texas Medical School, Houston 77030.
Abstract
The in vitro activity of DU-6859a (DU), a new fluoroquinolone agent, was evaluated against 233 gram-positive cocci and was compared with those of ciprofloxacin, vancomycin, nafcillin, and ampicillin. The MICs of DU for 90% of the staphylococci tested were < or = 0.06 microgram/ml. All of the groups A and B and viridans group streptococci were inhibited by < or = 0.125 microgram of DU per ml, which was 32-fold more active than ciprofloxacin. On the basis of MICs for 90% of the strains tested, DU was 32- and 16-fold more active than ciprofloxacin against Enterococcus faecalis and Enterococcus faecium, respectively. The bactericidal activity of DU was demonstrated by time-kill techniques against all ciprofloxacin-susceptible enterococci. DU shows promise for the treatment of infections with gram-positive cocci and warrants further evaluation by in vitro and in vivo studies.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference29 articles.
1. In vitro activities of sparfloxacin, tosufloxacin, ciprofloxacin, and fleroxacin;Barry A. L.;Antimicrob. Agents Chemother.,1991
2. Rapid development of ciprofloxacin resistance in methicillin-susceptible and -resistant Staphylococcus aureus;Blumberg H. M.;J. Infect. Dis.,1991
3. In vitro activity of sparfloxacin compared with those of five other quinolones;Canton E.;Antimicrob. Agents Chemother.,1992
4. In vitro activity of CI-934, a quinolone carboxylic acid active against gram-positive and -negative bacteria;Cohen M. A.;Antimicrob. Agents Chemother.,1985
5. In vitro antibacterial activities of the fluoroquinolones PD 117596;Cohen M. A.;PD 124816, and PD 127391. Diagn. Microbiol. Infect. Dis.,1991
Cited by
28 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献