Kannan R, Ikeda N, Wagner R, Drachenberg M, Singh B N
J Pharm Sci. 1984 Sep;73(9):1208-11. doi: 10.1002/jps.2600730906.
The serum kinetics of amiodarone and its major metabolite the deethyl analogue were studied in rabbits after intravenous administration. The elimination of the drug and the metabolite from serum occurred as a biexponential function. Both compounds exhibited a rapid distribution phase (6.5 and 4.4 min, respectively) and had elimination half-lives of 136 and 235 min, respectively. There was a rapid uptake of both drugs by the myocardium, with maximal concentrations at 5 and 15 min. The myocardial concentrations were higher than the respective serum concentrations and declined with time. There was a wide scatter in myocardium-serum ratios, which ranged from 1 to 11 for amiodarone and 12 to 29 for the metabolite. Neither the drug nor the metabolite produced significant changes in the surface electrocardiogram after intravenous administration. These data suggest that accumulation of the metabolite does not account for the slow onset of action of amiodarone.
静脉注射后,在兔体内研究了胺碘酮及其主要代谢产物去乙基类似物的血清动力学。药物及其代谢产物从血清中的消除呈双指数函数。两种化合物均表现出快速分布相(分别为6.5分钟和4.4分钟),消除半衰期分别为136分钟和235分钟。心肌对两种药物的摄取均很快,在5分钟和15分钟时达到最大浓度。心肌浓度高于各自的血清浓度,并随时间下降。心肌与血清浓度之比差异很大,胺碘酮为1至11,代谢产物为12至29。静脉注射后,药物和代谢产物均未引起体表心电图的显著变化。这些数据表明,代谢产物的蓄积不能解释胺碘酮起效缓慢的原因。