Abstract
The in vitro activity of seven quinolone derivatives against 100 clinical isolates of Clostridium difficile was determined. CI934 was the most active, inhibiting 90% of the strains at 4 micrograms/ml and 100% at 8 micrograms/ml. Ofloxacin and ciprofloxacin had moderate activity (16 and 32 micrograms/ml) whereas enoxacin, pefloxacin, norfloxacin, and nalidixic acid had poor activity (128 micrograms/ml).
MeSH Terms
Anti-Bacterial Agents/pharmacology
Child
Ciprofloxacin
Clostridium/classification,drug effects
Enoxacin
Fluoroquinolones
Humans
Infant, Newborn
Microbial Sensitivity Tests
Nalidixic Acid/pharmacology
Naphthyridines/pharmacology
Norfloxacin/analogs & derivatives,pharmacology
Ofloxacin
Oxazines/pharmacology
Pefloxacin
Quinolines/pharmacology
Chemicals
Anti-Bacterial Agents
Fluoroquinolones
Naphthyridines
Oxazines
Quinolines
Pefloxacin
Enoxacin
Nalidixic Acid
Ciprofloxacin
CI 934
Ofloxacin
Norfloxacin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Delmee M
Avesani V
References (10)
10 references, click to expand
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