Pharmacokinetics and inflammatory fluid penetration of sparfloxacin

Antimicrob Agents Chemother. 1992 Nov;36(11):2444-6. doi: 10.1128/AAC.36.11.2444.

Abstract

A single 400-mg oral dose of sparfloxacin was given to each of six healthy male volunteers, and the concentrations of the drug were measured in plasma, cantharides-induced inflammatory fluid, and urine over the subsequent 52 h. The mean peak concentration in plasma of 1.6 micrograms/ml was attained at a mean time of 2.7 h postdose. The mean peak concentration in inflammatory fluid of 1.3 micrograms/ml was attained at a mean time of 5 h postdose. The mean elimination half-life in plasma was 17.6 h, and that in inflammatory fluid was 19.7 h. The overall penetration into inflammatory fluid was 117%. Urinary recovery within the first 52 h postdose was 8.8% of the administered dose. Our results indicate that a once-daily dosage of sparfloxacin should be adequate to treat systemic infections caused by most common bacterial pathogens.

MeSH terms

  • Administration, Oral
  • Adult
  • Blister / blood
  • Blister / chemically induced
  • Blister / metabolism*
  • Exudates and Transudates / metabolism*
  • Fluoroquinolones*
  • Humans
  • Inflammation / blood
  • Inflammation / metabolism*
  • Intestinal Absorption
  • Male
  • Quinolones / blood
  • Quinolones / pharmacokinetics*

Substances

  • Fluoroquinolones
  • Quinolones
  • sparfloxacin