Antibacterial Activity of Cinoxacin In Vitro

Author:

Giamarellou Helen1,Jackson George G.1

Affiliation:

1. Department of Medicine, Abraham Lincoln School of Medicine, University of Illinois, Chicago, Illinois 60680

Abstract

Cinoxacin is a new synthetic compound similar chemically and in antimicrobial activity to oxolonic acid and nalidixic acid. It is most effective against Escherichia coli and Proteus mirabilis , but at concentrations expected in the urine it is inhibitory for all species of Enterobacteriaceae . Relative to nalidixic acid, cinoxacin has slightly greater inhibitory and bactericidal activity, less inoculum effect probably due to less heterogeneity in the susceptibility of bacterial cells, and less inhibition by high concentrations of serum protein. Both drugs are more active in an acid than an alkaline medium. Glucose can specifically antagonize the inhibitory effect against P. mirabilis . In urine the bactericidal rate and effect are decreased. Resistance to cinoxacin can be developed quickly by serial transfers in vitro. Some nonresistant organisms remained viable in bactericidal drug concentrations. The in vivo importance of the favorable features of cinoxacin must be determined by clinical trials.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference6 articles.

1. Cinoxacin: effectiveness against experimental pyelonephritis in rats;Holmes D. H.;Antimicrob. Agents Chemother.,1974

2. Lilly Research Laboratories. 1974. Clinical pharmacology of cinoxacin. Lilly Research Laboratory Indianapolis.

3. Cinoxacin: in vitro antibacterial studies of a new synthetic organic acid;Lumish R M;Antimicrob. Agents Chemother.,1975

4. Treatment of pyelonephritis: bacterial, drug and host factors in success or failure among 252 patients;McCabe W. R.;N. Engl. J. Med.,1965

5. Serum versus urinary antimicrobial concentrations and urinary tract infections;Stamey T. A.;N. Engl. J. Med.,1974

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