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盐酸多奈哌齐单次口服给药后的药代动力学和药效学特征

Pharmacokinetic and pharmacodynamic profile of donepezil HCl following single oral doses.

作者信息

Rogers S L, Friedhoff L T

机构信息

Eisai Inc., Glenpointe Centre West, Teaneck, NJ 07666-6741, USA.

出版信息

Br J Clin Pharmacol. 1998 Nov;46 Suppl 1(Suppl 1):1-6. doi: 10.1046/j.1365-2125.1998.0460s1001.x.

Abstract

AIM

The aim of this study was to characterize the pharmacokinetic and pharmacodynamic profile of donepezil HCl, a chemically distinct and specific acetylcholinesterase (AChE) inhibitor for the treatment of Alzheimer's disease, following administration of single oral doses.

METHODS

This was a double-blind, randomized, single-dose, placebo-controlled, sequential-group, ascending-dose study in healthy male volunteers (n = 48). Six dose levels were investigated, ranging from 0.3 to 6.0 mg. Donepezil concentrations in plasma were determined by HPLC with UV detection. Pharmacodynamic activity was determined by the radioenzymatic measurement of erythrocyte membrane acetylcholinesterase (rbc-AChE) inhibition.

RESULTS

The pharmacokinetic disposition of donepezil was observed to be both linear and dose proportional following single-dose administration. The mean peak plasma concentration (Cmax) of donepezil was observed at 4.1+/-1.5 h. The mean terminal disposition half-life was 81.5+/-22.0 h. The post-absorption phase of the plasma concentration-time curves for the 4.0 mg and 6.0 mg doses appeared to be biphasic, but the rate of donepezil clearance was independent of dose. Plasma concentrations for the 0.3, 0.6 and 0.9 mg dose groups were generally below the level of HPLC detection (2.0 ng ml(-1)), preventing accurate characterization of these doses. A direct correlation was observed between plasma donepezil concentrations and extent of AChE inhibition. For the 4.0 and 6.0 mg donepezil dose groups, maximal AChE inhibition (Emax) ranged from 33% to 35% and there was significant correlation between AChE inhibition and donepezil plasma concentration (P<0.005).

CONCLUSIONS

The pharmacokinetics of donepezil were found to be linear and dose proportional following the administration of single doses to healthy volunteers. A direct correlation was also observed between plasma donepezil concentrations and AChE inhibition. The extended half-life of donepezil makes it suitable for once-daily dosing.

摘要

目的

本研究旨在描述盐酸多奈哌齐(一种化学结构独特且特异性的乙酰胆碱酯酶(AChE)抑制剂,用于治疗阿尔茨海默病)单次口服给药后的药代动力学和药效学特征。

方法

这是一项针对健康男性志愿者(n = 48)的双盲、随机、单剂量、安慰剂对照、序贯分组、递增剂量研究。研究了六个剂量水平,范围从0.3至6.0毫克。采用高效液相色谱-紫外检测法测定血浆中多奈哌齐的浓度。通过放射酶法测定红细胞膜乙酰胆碱酯酶(rbc-AChE)抑制作用来确定药效学活性。

结果

单次给药后,观察到多奈哌齐的药代动力学处置呈线性且与剂量成比例。多奈哌齐的平均血浆峰浓度(Cmax)在4.1±1.5小时出现。平均终末处置半衰期为81.5±22.0小时。4.0毫克和6.0毫克剂量组的血浆浓度-时间曲线的吸收后阶段似乎呈双相,但多奈哌齐的清除率与剂量无关。0.3、0.6和0.9毫克剂量组的血浆浓度通常低于高效液相色谱检测水平(2.0纳克/毫升),妨碍了对这些剂量的准确表征。观察到血浆多奈哌齐浓度与AChE抑制程度之间存在直接相关性。对于4.0毫克和6.0毫克多奈哌齐剂量组,最大AChE抑制(Emax)范围为33%至35%,且AChE抑制与多奈哌齐血浆浓度之间存在显著相关性(P<0.005)。

结论

在健康志愿者单次给药后,发现多奈哌齐的药代动力学呈线性且与剂量成比例。还观察到血浆多奈哌齐浓度与AChE抑制之间存在直接相关性。多奈哌齐的半衰期延长使其适合每日一次给药。

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