McKiernan B C, Neff-Davis C A, Koritz G D, Davis L E, Pheris D R
J Vet Pharmacol Ther. 1981 Jun;4(2):103-10. doi: 10.1111/j.1365-2885.1981.tb00718.x.
The pharmacokinetics of theophylline were investigated in dogs following intravenous, single oral, and multiple oral doses of aminophylline. Mean half-life (t1/2) of theophylline following single intravenous administration was 5.7 h and the apparent specific volume of distribution (V'd area) was 0.82 litre/kg. The bioavailability of theophylline was high (91%) following oral administration of aminophylline tablets and the absorption half-life (t1/2ab) was 0.4 h. Theophylline plasma concentrations observed following repeated oral administration of aminophylline tablets were somewhat greater than predicted. This suggests that theophylline plasma concentrations should be monitored and the dosage regimen individually adjusted in critically ill animals.
在犬类动物中,对静脉注射、单次口服和多次口服氨茶碱后的茶碱药代动力学进行了研究。单次静脉给药后,茶碱的平均半衰期(t1/2)为5.7小时,表观分布容积(V'd area)为0.82升/千克。口服氨茶碱片后,茶碱的生物利用度较高(91%),吸收半衰期(t1/2ab)为0.4小时。多次口服氨茶碱片后观察到的茶碱血浆浓度略高于预测值。这表明,对于危重病动物,应监测茶碱血浆浓度并根据个体情况调整给药方案。