Pharmacokinetics after intravenous and oral administration of enrofloxacin in sheep
Bermingham, E. C., & Papich, M. G. (2002, July). AMERICAN JOURNAL OF VETERINARY RESEARCH, Vol. 63, pp. 1012–1017.
MeSH headings : Administration, Oral; Animals; Anti-Infective Agents / administration & dosage; Anti-Infective Agents / blood; Anti-Infective Agents / pharmacokinetics; Area Under Curve; Biological Availability; Ciprofloxacin / administration & dosage; Ciprofloxacin / blood; Ciprofloxacin / pharmacokinetics; Cross-Over Studies; Enrofloxacin; Female; Fluoroquinolones; Half-Life; Injections, Intravenous / veterinary; Quinolones / administration & dosage; Quinolones / blood; Quinolones / pharmacokinetics; Sheep / blood; Sheep / metabolism
TL;DR:
Enrofloxacin administered orally to sheep has a prolonged half-life and high oral bioavailability and was sufficient to achieve a plasma concentration of 8 to 10 times the minimum inhibitory concentration of any microorganism with an MIC < or = 0.29 microg/ml.
(via
Semantic Scholar)
UN Sustainable Development Goal Categories
Sources: Web Of Science, NC State University Libraries