Koritz G D, Bourne D W, Hunt J P, Prasad V I, Bevill R F, Gautam S R
J Vet Pharmacol Ther. 1981 Sep;4(3):233-9. doi: 10.1111/j.1365-2885.1981.tb00735.x.
The pharmacokinetics of theophylline in swine were investigated following the oral and intravascular administration of single doses of theophylline free base. The mean half-life of theophylline following intravascular administration was 11.0 h, and the apparent specific volume of distribution was 0.61 liter/kg. Following oral administration, theophylline in solution was absorbed quite rapidly with a bioavailability of 79%. The similarity of the pharmacokinetics of theophylline in swine and humans suggests that swine may provide a useful model for the study of the bioequivalency of theophylline dosage forms intended for human use. The pharmacokinetic characteristics of theophylline also favor its consideration for usage as a therapeutic agent in swine.
在单次静脉注射和口服茶碱游离碱后,对猪体内茶碱的药代动力学进行了研究。静脉注射后,茶碱的平均半衰期为11.0小时,表观分布比容为0.61升/千克。口服后,溶液中的茶碱吸收相当迅速,生物利用度为79%。猪与人茶碱药代动力学的相似性表明,猪可能为研究人用茶碱剂型的生物等效性提供有用的模型。茶碱的药代动力学特征也有利于将其考虑用作猪的治疗药物。