Population pharmacokinetics of a single intramuscular administration of tulathromycin in adult desert tortoises (Gopherus agassizii )
Autor: | Lisa A. Tell, M. E. Kinney, R. Gehring, N. Lamberski, Michael Neely, R. Foster, Raymund F. Wack |
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Rok vydání: | 2014 |
Předmět: |
Pharmacology
education.field_of_study Pathology medicine.medical_specialty Veterinary medicine General Veterinary medicine.drug_class Population Antibiotics Cmax Population pharmacokinetics Biology Disaccharides Injections Intramuscular Anti-Bacterial Agents Turtles Pharmacokinetics Heterocyclic Compounds medicine Population data Animals Parent Form Tulathromycin education |
Zdroj: | Journal of Veterinary Pharmacology and Therapeutics. 37:500-507 |
ISSN: | 0140-7783 |
DOI: | 10.1111/jvp.12118 |
Popis: | Tulathromycin, a long acting macrolide antibiotic, has demonstrated efficacy against respiratory pathogens including Mycoplasma bovis and M. hyopneumoniae. A pharmacokinetic study was performed to evaluate the clinical applicability of tulathromycin in desert tortoises following a single intramuscular dose of 5 mg/kg. A single blood sample was collected from 110 different desert tortoises at 0.25, 0.5, 1, 4, 8, 24, 48, 72, 120, and 240 h following drug administration. Plasma concentrations of the parent form of tulathromycin were measured using liquid chromatography/mass spectrometry. As each tortoise was only bled once, pharmacokinetic parameters were initially estimated using a naïve pooled data approach. Given the variability in the data, population-based compartmental modeling was also performed. Using nonparametric population compartmental modeling, a two-compartment model with first-order absorption and elimination best fit the data. An observed Cmax of 36.2 ± 29.7 μg/mL was detected at 0.25 h (observed Tmax ). The elimination half-life (T½el ) was long (77.1 h) resulting in detectable plasma concentrations 240 h postadministration. This study represents a preliminary step in evaluating the utility of tulathromycin in chelonian species and demonstrates that population data modeling offers advantages for estimating pharmacokinetic parameters where sparse data sampling occurs and there is substantial variability in the data. |
Databáze: | OpenAIRE |
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