Berdeaux A, Roche A, Labaille T, Giroux B, Edouard A, Giudicelli J F
Br J Clin Pharmacol. 1984 Nov;18(5):759-63. doi: 10.1111/j.1365-2125.1984.tb02539.x.
The hepatic extraction of amiodarone and N-desethylamiodarone has been investigated in seven patients following catheterization of the portal and hepatic veins under general anaesthesia. Amiodarone (600 mg) was administered orally 4 h before regional blood sampling. Concentrations of amiodarone and N-desethylamiodarone, determined by h.p.l.c., were about twice as high in the portal vein compared with those in the hepatic vein, the calculated hepatic extraction ratios of both compounds being 0.39 +/- 0.07 and 0.34 +/- 0.03, respectively. The presence of N-desethylamiodarone in the portal vein in higher concentrations than in the hepatic vein strongly suggests that N-dealkylation of amiodarone occurs in the gut wall or lumen, a finding which might account for the low and highly variable intersubject amiodarone bioavailability.
在全身麻醉下对7例患者进行门静脉和肝静脉插管后,研究了胺碘酮和N-去乙基胺碘酮的肝摄取情况。在区域血样采集前4小时口服胺碘酮(600毫克)。通过高效液相色谱法测定,门静脉中胺碘酮和N-去乙基胺碘酮的浓度约为肝静脉中的两倍,两种化合物的计算肝摄取率分别为0.39±0.07和0.34±0.03。门静脉中N-去乙基胺碘酮的浓度高于肝静脉,这强烈表明胺碘酮的N-脱烷基化发生在肠壁或肠腔内,这一发现可能解释了胺碘酮个体间生物利用度低且高度可变的原因。