Latini R, Connolly S J, Kates R E
J Pharmacol Exp Ther. 1983 Mar;224(3):603-8.
The time course of myocardial uptake and disposition of amiodarone was studied after both acute i.v. and chronic oral administration. In addition, the myocardial disposition of a metabolite, N-desethylamiodarone, was studied after chronic oral amiodarone administration. After i.v. administration, the plasma concentrations of amiodarone fell rapidly; however, peak myocardial concentrations were not observed until 10 to 30 min after administration. Amiodarone was highly concentrated in the myocardium; the average (+/- S.D.) myocardial/plasma concentration ratio between 2 and 6 hr after administration was 89 +/- 32. Although there was significant interanimal variability, there was relative consistency over time in the ratio for each dog during this time period. Although no metabolite (N-desethylamiodarone) was detected in the plasma after the single i.v. dose, it was present in both plasma and myocardial samples after chronic oral therapy. Mean steady-state plasma concentrations of amiodarone and N-desethylamiodarone ranged from 0.62 to 1.63 micrograms/ml and 0.19 to 0.43 micrograms/ml, respectively. These studies show that the myocardial disposition kinetics of amiodarone are different from other drugs studied and both amiodarone and its N-desethyl metabolite accumulate extensively in the myocardium.
在急性静脉注射和慢性口服给药后,研究了胺碘酮在心肌中的摄取和分布的时间过程。此外,在慢性口服胺碘酮给药后,研究了一种代谢物N-去乙基胺碘酮在心肌中的分布。静脉注射后,胺碘酮的血浆浓度迅速下降;然而,给药后10至30分钟才观察到心肌浓度峰值。胺碘酮在心肌中高度浓缩;给药后2至6小时的平均(±标准差)心肌/血浆浓度比为89±32。尽管动物之间存在显著差异,但在此时间段内每只狗的该比值随时间相对一致。虽然单次静脉注射剂量后血浆中未检测到代谢物(N-去乙基胺碘酮),但在慢性口服治疗后的血浆和心肌样本中均有存在。胺碘酮和N-去乙基胺碘酮的平均稳态血浆浓度分别为0.62至1.63微克/毫升和0.19至0.43微克/毫升。这些研究表明,胺碘酮的心肌分布动力学与其他研究的药物不同,胺碘酮及其N-去乙基代谢物在心肌中广泛蓄积。