J. Landuyt et al., THE INTRAMUSCULAR BIOAVAILABILITY OF A PHENYLBUTAZONE PREPARATION IN THE HORSE, Journal of veterinary pharmacology and therapeutics, 16(4), 1993, pp. 494-500
The plasma concentrations of phenylbutazone (PBZ) and its major metabo
lites, oxyphenbutazone (OPBZ) and gamma-OH-phenylbutazone (OHPBZ) were
determined for up to 72 h in six horses, following intravenous (i.v.)
and intramuscular (i.m.) administration of 4 g phenylbutazone, 20 ml
Phenylarthrite(R) Ventoquinol (Vetoquinol Specialites Pharmaceutiques
Veterinaires, Magny-Vernois, 70200 Lure, France). After i.v. dosing th
e plasma disposition was best described by a two-compartment open mode
l. The hydroxylated metabolites OPBZ and OHPBZ were present in detecta
ble concentrations for 72 h and 48 h, respectively. After 36 h the OPB
Z concentrations exceeded plasma PBZ concentrations. The plasma dispos
ition following i.m. injection could be described by a one-compartment
open model. The hydroxylated metabolites OPBZ and OHPBZ were present
in detectable concentrations For 72 h and 36 h, respectively. Only aft
er 72 h was the concentration of OPBZ in plasma higher than the concen
tration of PBZ. The mean i.m. bioavailability of phenylbutazone was ca
lculated to be 91.7 +/- 10.1%.