R. Goldstein et al., PHARMACOKINETICS OF AMPICILLIN ADMINISTERED INTRAVENOUSLY AND INTRAOSSEOUSLY TO KITTENS, Research in Veterinary Science, 59(2), 1995, pp. 186-187
An aqueous solution of ampicillin sodium (100 mg ml(-1)) was administe
red intravenously and intraosseously to six kitten at 50 mg kg(-1) in
a crossover study. Jugular vein blood samples were taken at intervals
up to eight hours after treatment and the serum ampicillin concentrati
on-time data, derived from a microbiological assay, were analysed phar
macokinetically. The disposition kinetics of ampicillin administered b
y the two routes were very similar. The mean elimination half-life (t(
1/2 beta)), the area-derived volume of distribution (V-area) and the t
otal body clearance (Cl-B) values after the intravenous and intraosseo
us treatment were 86.3 and 79.0 minutes, 0.9 and 0.8 litre kg(-1) and
7.3 and 7.6 ml min(-1) kg(-1), respectively. No side-effects related t
o the intraosseous administration of the drug were observed.