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Cross-over study of the pharmacokinetics of cefonicid administered intravenously or intramuscularly to healthy adult humans

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Summary

The pharmacokinetics of cefonicid were investigated in eight healthy adults. A one-gram dose was administered either intramuscularly or intravenously in a cross-over design study. Mean peak cefonicid plasma concentrations of 186 to 204 mcg/ml and 88 to 123 mcg/ml were achieved after intravenous and intramuscular injection, respectively, with elimination half-lives of 4.9 h and 5.3 h. Cefonicid concentrations were measured by both microbiological (M.A.) and high-performance liquid chromatography (HPLC) assays. Results were quite similar with the two techniques, except for the urinary recovery of cefonicid in the first 24 hours (83% of the dose with MA — vs 53% with HPLC method).

The apparent volume of distribution (Vd area) was 0.18 1/kg; the total body clearance (CT) and the renal clearance (CR) were 24–26 ml/min and 15–19 ml/min, respectively. The kinetic data of cefonicid were not significantly different for the two routes of administration.

A one-gram i.v. or i.m. cefonicid dose produced high and prolonged plasma concentrations with a longer half-life than obtained with commonly used cephalosporins.

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References

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Correspondence to J. P. Fillastre.

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Fourtillan, J.B., Leroy, A., Lefebvre, M.A. et al. Cross-over study of the pharmacokinetics of cefonicid administered intravenously or intramuscularly to healthy adult humans. European Journal of Drug Metabolism and Pharmacokinetics 10, 225–230 (1985). https://doi.org/10.1007/BF03189746

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Key-words

  • Pharmacokinetics
  • Cefonicid
  • Healthy adults