Urso R, Segre G, Bianchi E, Bruni G, Dal Pra P, Fiaschi A I
Instituro di Farmacologia, Universita di Siena, Italia.
Eur J Drug Metab Pharmacokinet. 1991;Spec No 3:111-5.
Plasma kinetics of atropine and ipratropium was assessed in rat after i.v. (10 mg/kg), oral and i.p. (50 mg/kg) administration by a radioreceptor assay (RRA). The volume of the central compartment and the clearance of both drugs were very similar (about 3 L/kg and 3.5 L/h/kg respectively) while the steady state volume of distribution and the terminal half-life of atropine were higher than those of ipratropium. After i.p. administration the kinetics of ipratropium was very different from what was expected after the i.v. experiment.
通过放射受体分析法(RRA)评估了大鼠静脉注射(10毫克/千克)、口服和腹腔注射(50毫克/千克)后阿托品和异丙托溴铵的血浆动力学。两种药物的中央室容积和清除率非常相似(分别约为3升/千克和3.5升/小时/千克),而阿托品的稳态分布容积和终末半衰期高于异丙托溴铵。腹腔注射后,异丙托溴铵的动力学与静脉注射实验后的预期情况非常不同。