Pharmacokinetics of ceftazidime given alone and combination with probenecid to unweaned calves
Soback, S.; Ziv, G.
American Journal of Veterinary Research 50(9): 1566-1569
1989
ISSN/ISBN: 0002-9645 PMID: 2679252 Document Number: 331695
Ceftazidime pharmacokinetic values were studied in unweaned calves given the antibiotic alone or in combination with probenecid. Ceftazidime was administered IV to 9 calves at a dosage of 10 mg/kg of body weight and IM (10 mg/kg) to 8 calves, to 7 calves (10 mg/kg plus probenecid [40 mg/kg]), and to 9 calves (10 mg/kg plus probenecid [80 mg/kg]). Serum concentration-vs-time data were analyzed, using noncompartmental methods based on statistical moment theory. The data for IV ceftazidime administration also were fitted by use of a linear, open 2-compartment model. The mean (.+-. SD) terminal half-life was 138.7 .+-. 23.6 minutes and 126.3 .+-. 10.5 minutes after IV and IM administrations, respectively. The mean residence time was 167.3 .+-. 21.1 minutes and 201.4 .+-. 16.8 minutes after IV and IM administrations, respectively. Coadministration of probenecid did not affect the terminal half-life or mean residence time values. The total body clearance was 1.75 .+-. 0.26 ml/min/kg, and the volume of distribution at steady state was 0.294 .+-. 0.064 L/kg. The estimated mean absorption time was 34.1 minutes. There were no significant differences between the mean residence time calculated by statiscal moment theory or by compartmental analysis, indicating central compartment output of ceftazidime. The 90% minimal inhibitory concentration values of ceftazidime determined for Escherichia coli, Salmonella spp. Pasteurella multocida, and P. haemolytica isolates ranged from < 0.01 to 0.1 .mu.g/ml.