Findlay J W, Fowle A S, Butz R F, Jones E C, Weatherley B C, Welch R M, Posner J
Br J Clin Pharmacol. 1986 Jul;22(1):61-71. doi: 10.1111/j.1365-2125.1986.tb02881.x.
Four healthy male subjects received single oral doses of 15, 30 and 60 mg of codeine and pholcodine according to a balanced cross-over design with an interval of 7 days between the six treatments. Blood samples were collected for 8 h after each drug administration. In phase 2 of the study six different male volunteers received single oral doses of 60 mg of codeine and pholcodine with a 14 day interval between successive drug treatments. Blood was sampled for 12 h after codeine and 121 h after pholcodine administration. Plasma concentrations of free (unconjugated) and total (unconjugated plus conjugated) codeine, pholcodine and morphine were determined by radioimmunoassay and selected pharmacokinetic parameters were derived from these data. Pharmacokinetics of both drugs were independent of dose. Codeine was absorbed and eliminated relatively rapidly [elimination t1/2 = 2.3 +/- 0.4 h (mean +/- s.d.)]. While codeine kinetics were adequately described by a one-compartment open model with first-order absorption, a two-compartment model was required to describe pholcodine elimination from plasma (t1/2,z = 37.0 +/- 4.2 h). Plasma concentrations of conjugated codeine were much greater than those of the unconjugated alkaloid. By contrast, pholcodine appeared to undergo little conjugation. Biotransformation of codeine to morphine was evident in all subjects, although the extent of this metabolic conversion varied considerably between subjects. Morphine was not detectable in the plasma of any subject after pholcodine administration.
四名健康男性受试者按照平衡交叉设计,单次口服15毫克、30毫克和60毫克的可待因和福尔可定,六种治疗之间间隔7天。每次给药后采集8小时的血样。在研究的第二阶段,六名不同的男性志愿者单次口服60毫克的可待因和福尔可定,连续药物治疗之间间隔14天。可待因给药后采集12小时血样,福尔可定给药后采集121小时血样。通过放射免疫测定法测定游离(未结合)和总(未结合加结合)可待因、福尔可定和吗啡的血浆浓度,并从这些数据中得出选定的药代动力学参数。两种药物的药代动力学均与剂量无关。可待因吸收和消除相对较快[消除半衰期=2.3±0.4小时(平均值±标准差)]。虽然可待因动力学可以用具有一级吸收的单室开放模型充分描述,但需要用双室模型来描述福尔可定从血浆中的消除(终末半衰期=37.0±4.2小时)。结合型可待因的血浆浓度远高于未结合生物碱的浓度。相比之下,福尔可定似乎很少发生结合。在所有受试者中,可待因向吗啡的生物转化都很明显,尽管这种代谢转化的程度在受试者之间有很大差异。福尔可定给药后,任何受试者的血浆中均未检测到吗啡。