Abstract
The in vitro activity of OPC-17116 was compared to that of five similar fluoroquinolones (ciprofloxacin, enoxacin, norfloxacin, ofloxacin and temafloxacin). A total of 700 isolates from recent cases of clinical bacteremia were tested. Fifty additional stock strains with well-characterized resistance mechanisms were also processed. The minimal concentrations inhibiting 90% of strains (MIC90) of Enterobacteriaceae species were for OPC-17116 0.015-0.5 micrograms/ml and for ciprofloxacin 0.015-0.25 micrograms/ml. Moraxella catarrhalis, Haemophilus influenzae and Neisseria gonorrhoeae were very susceptible to OPC-17116 (MIC90 0.015 micrograms/ml) thus being fourfold more active than ciprofloxacin. For all beta-hemolytic streptococci and pneumococci OPC-17116 MICs were less than or equal to 0.5 micrograms/ml. The most resistant enteric bacilli were among the Citrobacter freundii and Providencia rettgeri strains (MIC90 0.5 micrograms/ml). Pseudomonas aeruginosa strains were comparably susceptible to OPC-17116 (MIC90 0.5 micrograms/ml). Low pH and CO2 incubation had an adverse effect on OPC-17116 MICs, and resistance development was documented among current clinical isolates of staphylococci, pseudomonas and some Enterobacteriaceae.
MeSH Terms
Anti-Infective Agents/pharmacology
Drug Evaluation, Preclinical
Drug Resistance, Microbial
Fluoroquinolones
Gram-Negative Bacteria/drug effects
Gram-Positive Bacteria/drug effects
Microbial Sensitivity Tests
Mutation/genetics
Piperazines/pharmacology
Quinolones/pharmacology
Chemicals
Anti-Infective Agents
Fluoroquinolones
Piperazines
Quinolones
grepafloxacin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sader H S
Department of Pathology, University of Iowa College of Medicine, Iowa City 52242.
Erwin M E
Jones R N
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