The pharmacokinetics of xylazine hydrochloride: an interspecific study
Tóm tắt
The pharmacokinetic disposition of xylazine hydrochloride is described after both intravenous and intramuscular injection of a single dose, in four domestic species: horse, cattle, sheep and dog, by an original high performance liquid chromatographic technique. Remarkably small interspecific differences are reported. After intravenous administration, systemic half‐life (
Từ khóa
Tài liệu tham khảo
Alvinerie M., 1980, Determination of xylazine in plasma using high performance liquid chromatography, Journal of Chromatography.
Baggot J.D., 1977, The Basis of Veterinary Clinical Pharmacology
Duhm B., 1969, Unfersuchungen mit radiaktiv markierten Bay Va 1470 An Ratten, Berliner und Münchener Tierärztliche wochen-schrift, 82, 104
Eichner R.D., 1979, Xylazine induced hyperglycemia in beef cattle, American Journal of veterinary Research, 40, 127
Hoffman P.E., 1974, Clinical evaluation of xylazine as a chemical restraining agent, sedative and analgesic in horses, Journal of American veterinary Medicine Association, 164, 42
McCashin F.B.&Gabel A.A.(1971)Rompun. A new sedative with analgesic properties.Proceedings of 17th Annual Convention of the American Association of Equine Practitioners 111–116.
Newkirk H.L., 1974, Xylazine as a sedative analgesic for dogs and cats, Modern veterinary Practice, 55, 677
Putter J., 1973, Chemical studies to detect residues of xylazine hydrochloride, Veterinary Medicine Reviews, 73, 145
Sams R., 1978, Equine pharmacology, 17