Akademik Veri Yönetim Sistemi
VETERINARY RESEARCH COMMUNICATIONS, cilt.31, sa.1, ss.67-75, 2007 (SCI-Expanded)
The effect of experimentally induced fever on the pharmacokinetics of cefepime administered intravenously at a dose of 75 mg/kg bw was studied in six healthy rabbits. The study was conducted in two consecutive phases, separated by a washout period of 2 weeks. Infection was induced by the intravenous inoculation of 5 x 10(8) cfu of Escherichia coli 24 h before the pharmacokinetic investigation was carried out. Serial blood samples for cefepime concentration determination were obtained for 48 It following drug administration. The concentrations of cefepime in the plasma were determined by a quantitative microbiological assay using an agargel diffusion method employing Bacillus subtilis ATCC 6633 as the test organism, with a level of delectability of approximately 0.10 mu g/ml. Cefepime plasma concentrations versus time were evaluated by non-compartmental methods using WinNonLin. Cefepime was well tolerated and no serious adverse events were observed. Rectal temperature increased 1 degrees C 24 h post injection in infected animals. Highly significant differences in the blood plasma concentrations of cefepime were observed between febrile and healthy animals at all the sampling times. This could explain the greater area under the plasma level-time curve of the drug in febrile compared with healthy animals. The results from pharmacokinetic calculations showed that both the distribution volume at steady state (V-dss) and body clearance (CLtot) were affected in febrile as compared to healthy animals. The mean values of V-dss and CLtot of cefepinne in healthy rabbits were 1.168 L/kg and 0.303 L/kg/h, respectively. As compared with healthy animals, the mean estimates of V-dss (0.917 L/kg) and CLtot (0.205 L/kg per h) of cefepime were significantly lower, whereas t1/2 lambda, MRT and AUMC were significantly higher in febrile rabbits. It is concluded that, although experimental infection had an effect on the disposition kinetics of cefepime in healthy and febrile rabbits, this was not sufficiently pronounced to require alteration of the dosage during disease.