Pourbaix S, Berger Y, Desager J P, Pacco M, Harvengt C
Clin Pharmacol Ther. 1985 Feb;37(2):118-23. doi: 10.1038/clpt.1985.22.
The relative and absolute bioavailability of different oral forms of amiodarone was examined in 12 subjects. The doses were 5 mg/kg iv, two 200-mg commercial tablets by mouth, two 200-mg tablets (new formulation) by mouth, and 400 mg in a drinkable solution. Plasma levels of amiodarone and its N-desethylated metabolite were determined by HPLC. Statistical analysis indicated bioequivalence of the oral forms for all the kinetic parameters examined. After oral dosing, amiodarone was slowly absorbed and the maximum plasma level (0.55 +/- 0.20 mg/l) was reached in 4.5 hr. The absolute bioavailability of oral amiodarone was calculated by comparison of AUCs after oral dosing with those after intravenous injection. A mean oral bioavailability of 65% +/- 22% was indicated. Since the tablets were bioequivalent to the drinkable solution, incomplete absorption seems not be a result of the dissolution characteristics of the commercial formulation but rather of a first-pass effect.
在12名受试者中检测了不同口服剂型胺碘酮的相对生物利用度和绝对生物利用度。给药剂量分别为:静脉注射5mg/kg;口服两片200mg的市售片剂;口服两片200mg的片剂(新剂型);口服400mg可饮用溶液。采用高效液相色谱法测定血浆中胺碘酮及其N-去乙基代谢物的水平。统计分析表明,所检测的所有动力学参数的口服剂型具有生物等效性。口服给药后,胺碘酮吸收缓慢,4.5小时达到血浆最高水平(0.55±0.20mg/L)。通过比较口服给药后与静脉注射后的药时曲线下面积(AUC)来计算口服胺碘酮的绝对生物利用度。结果表明平均口服生物利用度为65%±22%。由于片剂与可饮用溶液具有生物等效性,吸收不完全似乎不是市售制剂溶解特性的结果,而是首过效应的结果。