Acutephase Response Alters the Disposition Kineti

Authors: A M Abd ElAty A Goudah S M Mouneir Y E Sunwoo J H Jang J G Shin J H Shim M Shimoda

Publish Date: 2006/12/20

Volume: 31, Issue: 1, Pages: 67-75

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Abstract

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 × 108 cfu of Escherichia coli 24 h before the pharmacokinetic investigation was carried out Serial blood samples for cefepime concentration determination were obtained for 48 h 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 detectability of approximately 010 μg/ml Cefepime plasma concentrations versus time were evaluated by noncompartmental methods using WinNonLin Cefepime was well tolerated and no serious adverse events were observed Rectal temperature increased 1°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 cefepime in healthy rabbits were 1168 L/kg and 0303 L/kg/h respectively As compared with healthy animals the mean estimates of V dss 0917 L/kg and CLtot 0205 L/kg per h of cefepime were significantly lower whereas t 1/2λ 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

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