Comparative in vitro activity of lomefloxacin, a new difluoroquinolone

Eur J Clin Microbiol Infect Dis. 1989 Feb;8(2):164-8. doi: 10.1007/BF01963905.

Abstract

The in vitro activity of lomefloxacin, a new difluoroquinolone, was compared with that of norfloxacin, ciprofloxacin, gentamicin and ceftazidime against a total of 577 recent clinical isolates. MICs were determined by a standard agar dilution procedure, and two inocula (10(4) and 10(6) CFU) were used throughout. Lomefloxacin inhibited most species of the Enterobacteriaceae, Staphylococcus aureus (including methicillin-resistant strains) and Haemophilus influenzae at less than or equal to 1 mg/l. Pseudomonas aeruginosa (MIC 90, 4 mg/l) was somewhat more resistant, and Pseudomonas maltophilia (MIC 90, 16 mg/l) and the Bacteroides fragilis group (MIC 90, 32 mg/l) were considerably more resistant. Overall, lomefloxacin was as active as norfloxacin, but was two- to eightfold less active than ciprofloxacin against most species tested.

Publication types

  • Comparative Study

MeSH terms

  • Anti-Infective Agents / administration & dosage
  • Anti-Infective Agents / pharmacokinetics*
  • Bacteria, Aerobic / drug effects*
  • Bacteria, Anaerobic / drug effects*
  • Ceftazidime / administration & dosage
  • Ceftazidime / pharmacokinetics
  • Ciprofloxacin / administration & dosage
  • Ciprofloxacin / pharmacokinetics
  • Drug Evaluation, Preclinical
  • Fluoroquinolones*
  • Gentamicins / administration & dosage
  • Gentamicins / pharmacokinetics
  • Microbial Sensitivity Tests
  • Norfloxacin / administration & dosage
  • Norfloxacin / pharmacokinetics
  • Quinolones*

Substances

  • Anti-Infective Agents
  • Fluoroquinolones
  • Gentamicins
  • Quinolones
  • Ciprofloxacin
  • Ceftazidime
  • lomefloxacin
  • Norfloxacin