Comparative Pharmacokinetics and Metabolism of Cephapirin in Laboratory Animals and Humans

Author:

Cabana B. E.1,Harken D. R. Van1,Hottendorf G. H.1

Affiliation:

1. Research Division, Bristol Laboratories, Syracuse, New York 13201

Abstract

Comparative drug disposition studies in mice, rats, dogs, and humans indicate that cephapirin, a new semisynthetic cephalosporin antibiotic that exhibits broad-spectrum antimicrobial activity, is metabolized to desacetylcephapirin in these species. Pharmacokinetic analyses of the concentrations of cephapirin and desacetylcephapirin in plasma and urine reveal that the rate and extent of deacetylation decreases from rodents to dogs to humans. The kinetic analyses also suggest that the kidney performs a role not only in the excretion but also in the metabolism of cephapirin to desacetylcephapirin.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference23 articles.

1. Cephapirin: pharmacology in normal human volunteers;Axelrod J.;J. Clin. Pharmacol.,1972

2. Clinical and in vitro evaluation of cephapirin: a new parenteral cephalosporin;Bodner S. J.;Am. J. Med. Sci.,1972

3. Clinical and in vitro evaluation of cephapirin, a new cephalosporin antibiotic;Bran J. L.;Antimicrob. Agents Chemother.,1972

4. The role of the kidney in the elimination of cephapirin in man;Cabana B. E.;J. Pharmacokinet. Biopharm.,1975

5. Chisholm D. R. F. Leitner M. Misiek G. E. Wright and K. E. Price. 1970. Laboratory studies with a new cephalosporanic acid derivative p. 244-246. Antimicrob. Agents Chemother. 1969.

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