Caccia S, Conforti I, Duchier J, Garattini S
Eur J Clin Pharmacol. 1985;29(2):221-4. doi: 10.1007/BF00547426.
The kinetics of accumulation and elimination of d- and l-fenfluramine (F) and norfenfluramine (NF) have been studied in 8 young healthy volunteers given daily doses of 60 mg of sugar-coated tablets of 20 mg dl-F hydrochloride (dl-F) t.i.d. and capsules of 15 mg d-F hydrochloride (d-F) b.i.d. for 15 days. Repeated doses of d-F plus l-F gave the same values for the parameters measured as did d-F administered alone. Steady-state concentrations of all compounds were achieved within 4-8 days. The predicted mean steady-state concentrations of d-F and elimination half-lives calculated from the results of a previous single dose study were similar to those measured at steady state in this study, confirming the lack of effect of the drug on hepatic microsomal enzymes and on kinetics after repeated dosing. d-NF concentrations were approximately half those of the parent drug and the half-life was almost twice as long. Steady state concentrations both of L-f and l-NF were consistently about 40-50% higher than of the d-isomers and there was a comparable in the half-life.
在8名年轻健康志愿者中研究了右旋和左旋芬氟拉明(F)及去甲芬氟拉明(NF)的蓄积和消除动力学。这些志愿者每日服用60毫克含20毫克盐酸消旋芬氟拉明(消旋F)的糖衣片,每日三次,以及15毫克盐酸右旋芬氟拉明(右旋F)胶囊,每日两次,共15天。重复给予右旋F加左旋F所测得的参数值与单独给予右旋F时相同。所有化合物在4 - 8天内达到稳态浓度。根据先前单剂量研究结果计算出的右旋F预测平均稳态浓度和消除半衰期与本研究中稳态时测得的结果相似,证实了该药物对肝微粒体酶及重复给药后动力学无影响。右旋去甲芬氟拉明(d-NF)浓度约为母体药物的一半,半衰期几乎长一倍。左旋芬氟拉明(L-f)和左旋去甲芬氟拉明(l-NF)的稳态浓度始终比右旋异构体高约40 - 50%,半衰期也有类似情况。