Penetration of parenterally administered ceftiofur into sterile vs. Pasteurella haemolytica-infected tissue chambers in cattle

• Published in: Journal of veterinary pharmacology and therapeutics Vol. 19; no. 5; p. 376
• Main Authors: Clarke, C R, Brown, S A, Streeter, R N, Clarke, J M, Hamlow, P J, Callahan, J K, Hubbard, V L, Speedy, A K, Burrows, G E
• Format: Journal Article
• Language: English
• Published: England 01.10.1996
• Subjects: Animals; Cattle; Cattle Diseases; Cephalosporins - administration & dosage; Cephalosporins - blood; Cephalosporins - pharmacokinetics; Chromatography, High Pressure Liquid - veterinary; Diffusion Chambers, Culture; Dose-Response Relationship, Drug; Injections, Intravenous - veterinary; Pasteurella Infections - metabolism; Pasteurella Infections - physiopathology; Protein Binding; Software
• ISSN: 0140-7783
• DOI: 10.1111/j.1365-2885.1996.tb00067.x

The effect of bacterial infection on antibiotic activity and penetration of parenterally administered ceftiofur into implanted tissue chambers was studied in cattle. Tissue chambers were implanted subcutaneously in the paralumbar fossae of eight calves (256-290 kg body weight). Approximately 80 days after implantation, the two chambers on one side of each animal were inoculated with Pasteurella haemolytica (10(6) CFU/chamber). Eighteen hours after inoculation, ceftiofur sodium was administered intravenously (5 mg/kg) to each of the calves. Non-infected chamber fluid, infected chamber fluid and heparinized blood samples were collected immediately before and at 1, 3, 6, 12 and 24 h after drug administration. Concentrations of ceftiofur and desfuroylceftiofur metabolites and ceftiofur-equivalent microbiological activity were measured by high-pressure liquid chromatography and microbiological assay respectively. Concentrations of ceftiofur and desfuroylceftiofur metabolites and anti-microbial activity in P. haemolytica-infected tissue chambers were significantly higher than those in non-infected tissue chambers at all sampling times, indicating that ceftiofur, regardless of the method used for analysis, localizes at higher concentrations at tissue sites infected with P. haemolytica. Antibiotic activity-concentration ratios were lower in plasma and infected chamber fluid compared with non-infected chamber fluid, suggesting that antibiotic was bound to proteins. However, higher antimicrobial activity in the infected chamber fluid compared with the non-infected chamber fluid, suggests that active drug is reversibly bound to proteins. Protein-bound desfuroylceftiofur may represent a reservoir for release of active drug at the site of infection in the animal.