ABSTRACT
The pharmacokinetics of 4-methylimidazole (4MI), a toxin found in ammoniated forage, was studied after i.v. infusion or oral administration of a single dose of 20 mg 4MI/kg BW to sheep. A two-compartment open model was used to describe i.v. infusion data. Oral data were described by a one-compartment open model. A rapid distribution phase (t1/2 alpha = 28 min) was observed after i.v. infusion. The biological half-lives obtained after i.v. infusion (t1/2 beta = 9.72 h) and oral dosing (t1/2 beta = 9.37 h) were similar. The bioavailability of oral 4MI was .69, with a relatively rapid absorption phase (t1/2abs = 1.52 h). The relatively large volume of distribution (61.6 and 65.8 liters for i.v. infusion and oral dosage, respectively) indicates that 4MI is distributed in the extravascular compartment. A dose of 20 mg/kg BW did not cause any apparent ill effects to the animals.
Subject(s)
Imidazoles/pharmacokinetics , Sheep/metabolism , Absorption , Administration, Oral , Animals , Biological Availability , Female , Imidazoles/administration & dosage , Infusions, Intravenous/veterinary , Intestinal Absorption , Tissue DistributionABSTRACT
A method for 4-methylimidazole (4MI) extraction and quantitation in body fluids and forage samples was developed. The procedures involve ion-pair extraction of the compound with the quantitation done by ion-pair liquid chromatography. The results indicate that this high-performance liquid chromatographic method is sensitive, reproducible and more rapid than others that have been previously used. The mean recovery of 4MI from plasma and tall fescue (Festuca arundinacea) hay samples were above 95 and 85%, respectively. The versatility of the procedure makes it suitable for the determination of 4MI in body fluids and in forage samples.
