Eason C T, Usansky J I, Henry G P, Powles P, Bonner F W
Sterling-Winthrop Research Centre, Alnwick, Northumberland, U.K.
Eur J Drug Metab Pharmacokinet. 1988 Apr-Jun;13(2):129-33. doi: 10.1007/BF03191314.
The pharmacokinetic characteristics of amrinone have been studied in six female marmosets following oral administration of 1, 12.5, 25, 50 and 75 mg.kg-1 and an intravenous dose of 1mg.kg-1. The mean plasma AUC0 infinity was determined at each dose level; the values obtained were 2.5, 18.7, 33.9, 103 and 312 micrograms.h.ml-1 for the oral doses of 1, 12.5, 25, 50 and 75 mg.kg-1 respectively and 1.9 micrograms.h.ml-1 for the intravenous dose of 1mg.kg-1. Mean maximum observed plasma concentrations were 0.6, 7.1, 11.7, 23.7 and 40.0 micrograms.ml-1 respectively following oral doses. Over the range 1 to 50 mg.kg-1 the AUC0 infinity was linear; at 75 mg.kg-1 the AUC0 infinity was disproportionately greater. Elimination appeared to be first order over the dose range 1 to 50 mg.kg-1 and the t1/2 in the marmoset was approximately 1 to 3 hours over this dose range. The plasma levels achieved are discussed in relation to the observed effects on the platelet population in this species following chronic administration at high dose levels.
在六只雌性狨猴口服1、12.5、25、50和75毫克·千克⁻¹以及静脉注射1毫克·千克⁻¹剂量的氨力农后,对其药代动力学特征进行了研究。在每个剂量水平测定了平均血浆AUC₀至无穷大;口服1、12.5、25、50和75毫克·千克⁻¹剂量时获得的值分别为2.5、18.7、33.9、103和312微克·小时·毫升⁻¹,静脉注射1毫克·千克⁻¹剂量时为1.9微克·小时·毫升⁻¹。口服给药后,平均最大观察到的血浆浓度分别为0.6、7.1、11.7、23.7和40.0微克·毫升⁻¹。在1至50毫克·千克⁻¹范围内,AUC₀至无穷大呈线性;在75毫克·千克⁻¹时,AUC₀至无穷大不成比例地更大。在1至50毫克·千克⁻¹剂量范围内,消除似乎为一级,在此剂量范围内狨猴的t1/2约为1至3小时。讨论了在该物种中高剂量长期给药后达到的血浆水平与对血小板群体观察到的影响之间的关系。