Abstract
The in vitro activity of ciprofloxacin against a wide range of bacterial isolates was assessed in comparison with norfloxacin, enoxacin, co-trimoxazole and penicillin (or ampicillin) where appropriate. Minimal inhibitory concentrations (MICs) indicated that ciprofloxacin was highly active against gram-negative bacilli of the Enterobacteriaceae and Pseudomonas groups, notably against strains resistant to gentamicin. Similarly, Staphylococcus aureus (including methicillin-resistant strains) and Haemophilus influenzae were susceptible, regardless of penicillinase production. Norfloxacin and enoxacin were less active than ciprofloxacin against the majority of species tested, although enoxacin blood levels were generally higher. Most co-trimoxazole-resistant strains were susceptible to the quinoline group of drugs.
MeSH Terms
Anti-Bacterial Agents/pharmacology
Bacteria/drug effects
Ciprofloxacin
Dose-Response Relationship, Drug
Drug Combinations/pharmacology
Drug Resistance, Microbial
Enoxacin
Humans
Microbial Sensitivity Tests
Nalidixic Acid/analogs & derivatives,pharmacology
Naphthyridines/pharmacology
Norfloxacin
Quinolines/pharmacology
Sulfamethoxazole/pharmacology
Trimethoprim/pharmacology
Trimethoprim, Sulfamethoxazole Drug Combination
Chemicals
Anti-Bacterial Agents
Drug Combinations
Naphthyridines
Quinolines
Enoxacin
Nalidixic Acid
Ciprofloxacin
Trimethoprim, Sulfamethoxazole Drug Combination
Trimethoprim
Sulfamethoxazole
Norfloxacin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shrire L
Saunders J
Traynor R
Koornhof H J
References (8)
8 references, click to expand
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