共 29 条
COMPARATIVE IN-VITRO ACTIVITY OF DU-6859A, A NEW FLUOROQUINOLONE AGENT, AGAINST GRAM-POSITIVE COCCI
被引:23
作者:

KORTEN, V
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SCH MED,CTR INFECT DIS,DEPT INTERNAL MED,HOUSTON,TX 77030

TOMAYKO, JF
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SCH MED,CTR INFECT DIS,DEPT INTERNAL MED,HOUSTON,TX 77030

MURRAY, BE
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SCH MED,CTR INFECT DIS,DEPT INTERNAL MED,HOUSTON,TX 77030
机构:
[1] UNIV TEXAS,SCH MED,CTR INFECT DIS,DEPT INTERNAL MED,HOUSTON,TX 77030
[2] UNIV TEXAS,SCH MED,DEPT MICROBIOL & MOLEC GENET,HOUSTON,TX 77030
关键词:
D O I:
10.1128/AAC.38.3.611
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
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 less than or equal to 0.06 mu g/ml. All of the groups A and B and viridans group streptococci were inhibited by less than or equal to 0.125 mu g of DU per mi, 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.
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页码:611 / 615
页数:5
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