Literature DB >> 8587150

Effect of water deprivation on the disposition kinetics of enrofloxacin in camels.

R Gavrielli1, R Yagil, G Ziv, C V Creveld, A Glickman.   

Abstract

Concentrations of enrofloxacin equivalent activity were determined (by microbiological assay) in the serum of normal camels and camels at the end of a 14-day water-deprivation period following single intravenous (i.v.), intramuscular (i.m.) and subcutaneous (s.c.) administrations at 2.5 mg/kg. Also, normal camels were given an oral drench of the drug at 5 mg/kg. Pharmacokinetic variables were determined using compartmental and non-compartmental analytical methods. Camels lost on average 12.5% of body weight at the end of the water-deprivation period. The disposition kinetics of i.v. administered drug in normal and water-deprived camels were very similar. The t1/2 beta was 3.0-3.5 h; MRT was 4.0-4.5 h; Vc was 0.3 L/kg; Vss was 1.0 L/kg and ClB was 4.0-4.6 mL/min/kg. The effect of water deprivation on the rate of drug absorption and elimination after i.m. administration was inconsistent, and there was also a large degree of variability in the normal animals that precluded statistical significance. After s.c. administration, the mean absorption half-life (t1/2abs) in the water-deprived camels was significantly longer than in the normal camels. Systemic availability (F) was similar in both normal and water-deprived camels after i.m. dosing but was significantly greater (P < 0.05) in normal camels (0.92 compared with 0.65 in water-deprived camels) after s.c. treatment. In normal camels, urinary recovery at 12 h after i.v. and s.c. dosing was 25% and 15%, respectively, and the extent of serum protein binding ranged between 1.7% at 1.8 micrograms/mL and 24% at 0.33 microgram/mL. The drug was not detected in serum after oral administration. Serum and milk enrofloxacin equivalent activities were determined after i.v. (one camel) and i.m. (one camel) drug administration. Serum drug concentrations were consistently higher than in the milk. The AUCmilk/AUCserum ratios were 0.27 and 0.39 after i.v. and i.m. drug administration, respectively. An i.m. or s.c. treatment regimen of 2.5 mg/kg q.12 h is suggested for clinical and bacteriological efficacy trials with enrofloxacin in normally hydrated and dehydrated camels.

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Year:  1995        PMID: 8587150     DOI: 10.1111/j.1365-2885.1995.tb00600.x

Source DB:  PubMed          Journal:  J Vet Pharmacol Ther        ISSN: 0140-7783            Impact factor:   1.786


  5 in total

1.  Pharmacokinetic disposition of subcutaneously administered enrofloxacin in goats.

Authors:  S Ramesh; G S Rao; J K Malik
Journal:  Vet Res Commun       Date:  2002-10       Impact factor: 2.459

2.  The effect of water deprivation on the pharmacokinetics of antipyrine and sulphadimidine following intravenous administration in Nubian goats.

Authors:  H A Elsheikh; I A Osman; A S Abdullah
Journal:  Vet Res Commun       Date:  1997-11       Impact factor: 2.459

3.  Pharmacokinetics of enrofloxacin and its metabolite ciprofloxacin after intramuscular administration of enrofloxacin in goats.

Authors:  G S Rao; S Ramesh; A H Ahmad; H C Tripathi; L D Sharma; J K Malik
Journal:  Vet Res Commun       Date:  2001-04       Impact factor: 2.459

4.  Disposition kinetics of difloxacin in rabbit after intravenous and intramuscular injection of Dicural.

Authors:  A M Abd El-Aty; A Goudah; M Ismail; M Shimoda
Journal:  Vet Res Commun       Date:  2005-05       Impact factor: 2.459

5.  Pharmacokinetic-pharmacodynamic integration of enrofloxacin and its metabolite ciprofloxacin in buffalo calves.

Authors:  Prashant S Daundkar; Bhaskar Vemu; Vinod K Dumka; Suresh K Sharma
Journal:  Vet Med Sci       Date:  2015-11-26
  5 in total

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