The pharmacokinetics of enrofloxacin (ENR) and cipro-floxacin (CIP) in
newborn and young rabbits were studied, Rabbits of different ages (1-
, 8-, 16-, and 30-day-old) were administered, by the intraperitoneal r
oute (IP), a dose of 7.5 mg of either drug/kg, In 1-, 8-, and 16-day-o
ld rabbits, broad samples were drawn by cardiac puncture, under light
ether anaesthesia, at predetermined times after drug administration, I
re 30-day-old rabbits, serial blood samples were drawn through an arte
rial catheter. Plasma was immediately obtained and analysed using an H
PLC method, ENR and CIP plasma protein binding was also determined, Th
e plasma pharmacokinetic profiles of ENR and CIP obtained for 30-day-o
ld rabbits agreed truth those reported in the literature for healthy a
dult rabbits, Nevertheless, significant differences were observed for
the body clearance, the slope of the terminal phase, the volume of dis
tribution, and the area under the curve when compared with those for y
ounger animals (1-, 8-, and 16-day-old rabbits), indicating a Limited
capacity of neonatal rabbits to eliminate ENR and CIP, No differences
were found when we compared the calculated values for ENR or CIP plasm
a protein binding as a function of the postnatal age, indicating that
development does not seem to alter the free fraction of these drugs in
the rabbit, Taking into account that extensive placental and milli tr
ansfer has been reported for these drugs after administration to pregn
ant or nursing rabbits, a cautious attitude regarding their use in the
se animals must be adopted.