Pharmacokinetics and tissue penetration of orally administered pefloxacin

Eur J Clin Microbiol. 1987 Oct;6(5):521-4. doi: 10.1007/BF02014239.

Abstract

The pharmacokinetics of the quinolone pefloxacin were determined following a 400 mg oral dose given to each of six male volunteers. Concentrations were determined in serum and urine by high-performance liquid chromatography, and in cantharidin-induced inflammatory fluid by a microbiological assay. The mean peak serum level of 6.6 micrograms/ml was attained rapidly 0.8 h after administration. The mean serum elimination half-life was 11.6 h. Inflammatory fluid was penetrated quickly with a mean peak level of 3.9 micrograms/ml occurring at 2.4 h. Pefloxacin was excreted in the urine as the parent compound and its two metabolites, norfloxacin and pefloxacin N-oxide (24 h urinary recovery being 8.0%, 12.0% and 13.1% respectively of the dose). This study suggests that a twice or possibly once daily dosage may be sufficient to treat systemic infections caused by susceptible pathogens. Once daily dosing should be sufficient for urinary tract infections.

MeSH terms

  • Administration, Oral
  • Adult
  • Anti-Infective Agents / pharmacokinetics*
  • Blister / metabolism
  • Half-Life
  • Humans
  • Male
  • Norfloxacin / administration & dosage
  • Norfloxacin / analogs & derivatives*
  • Norfloxacin / pharmacokinetics
  • Pefloxacin
  • Tissue Distribution

Substances

  • Anti-Infective Agents
  • Pefloxacin
  • Norfloxacin