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Tissue penetration and pharmacokinetics of lomefloxacin following multiple doses

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Abstract

The pharmacokinetics of lomefloxacin were studied after three days of oral administration of 400 mg/day lomefloxacin. Following the final dose the concentrations in serum, urine and cantharidin-induced inflammatory fluid were measured by a microbiological assay. The mean peak serum level was 4.9 mg/l at a mean time of 0.8 h. The mean serum elimination half-life was 6.2 h. The mean maximum inflammatory fluid level attained was 3.2 mg/l at 2.7 h. Urinary recovery accounted for the greater part of lome-floxacin's elimination.

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Kavi, J., Stone, J., Andrews, J.M. et al. Tissue penetration and pharmacokinetics of lomefloxacin following multiple doses. Eur. J. Clin. Microbiol. Infect. Dis. 8, 168–170 (1989). https://doi.org/10.1007/BF01963906

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