The pharmacokinetics of amoxicillin were studied in five Desert sheep and f
ive Nubian goats after intravenous (i.v.) or intramuscular (i.m.) administr
ation of a single dose of 10 mg/kg body weight. Following i.v. injection, t
he plasma concentration-versus-time data were best described by a two-compa
rtment open model. The kinetic variables were similar in both species excep
t for the volume of the central compartment (V-c), which was larger in shee
p (p < 0.05). Following i.m. injection, except for the longer half-life tim
e of absorption in goats (p < 0.05), there were no significant differences
in other pharmacokinetic parameters between sheep and goats. The route of a
moxicillin administration had no significant effect on the terminal elimina
tion half-life in either species. The bioavailability of the drug (F) after
i.m. administration was high (> 0.90) in both species. These results indic
ate that the pharmacokinetics of amoxicillin did not differ between sheep a
nd goats; furthermore, because of the high availability and short half-life
of absorption, the i.m. route gives similar results to the i.v. route. The
refore, identical intramuscular and intravenous dose regimens should be app
licable to both species.