The investigation of the pharmacokinetics of two enrofloxacin preparations following parenteral administration in calves
Bideci, Gül Banu ÇiçekKaya, Sezai
Background: Enrofloxacin is a bactericidal antimicrobial drug in the fluoroquinolone group, developed for use only in the veterinary field. It is effective against gram negative and gram positive bacteria, Mikoplazma, Rickettsia, Ehrlichia ve Chlamydia. Enrofloxacin is converted to several effective and ineffective metabolites including ciprofloxacin. Ten to fifty percent of the drug is eliminated via urine and bile in unmetabolized form. Enrofloxacin is used in all domestic animal including ruminant and winged animals. In calves, enrofloxacin finds utilization in the respiratory system infections, septicemia caused by colibacillosis and in cases of intestinal inflammation by oral and parenteral ways. There are around 1920 enrofloxacin preparations with different formulations in Turkey. Eight hundred fifty-five of these preparations are in the form of parenteral solutions that are ready for use. In this study, the pharmacokinetics of two enrofloxacin preparations that are used in calves were investigated.Materials, Methods & Results: Ten female calves (Jersey strain, 46-50 day-old) were included. The animals were taken to a separate environment 15 days in advance, and medication administration was restrained. Throughout the trial, the animals were fed with unmedicated feed. Calf growing feed, water, and hay were given freely as feed. They continued to be fed by 3 liters of milk twice a day. The study was reviewed by Ankara University Animal Trials Local Ethics Committee and approved with decision number 2007-7-17 and file number 2007-56. The calves were divided into two groups including five calves each. Reference drug and test drug were administered intramuscularly at a dose of 2.5 mg per kg to group 1 and group 2, respectively. Blood samples were taken before (0.0 min) and after the drug administration at 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24 and 36th h. The method used by Anadon et al. was used for plasma enrofloxacin extraction and concentration.[...](AU)
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