Transl Clin Pharmacol.  2015 Jun;23(1):26-30. 10.12793/tcp.2015.23.1.26.

Bioequivalence study of Donepezil hydrochloride in healthy Korean volunteers

Affiliations
  • 1Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, Seoul 110-744, Korea.
  • 2Department of Clinical Pharmacology and Therapeutics, Kyung Hee University College of Medicine and Hospital, Seoul 130-872, Korea. bhkim98@khu.ac.kr

Abstract

Donepezil is a centrally acting, reversible acetylcholinesterase inhibitor that is widely used for treating Alzheimer's disease. This study aimed to compare the pharmacokinetics of Bastia(R), a test tablet formulation of donepezil hydrochloride 10 mg, with those of Aricept(R), the reference tablet formulation of donepezil hydrochloride 10 mg, in healthy Korean male volunteers. A randomized, single-dose, two-way crossover study was conducted in 32 subjects. Subjects received a single dose of either test or reference compound and the alternate drug after a 4-week washout period. Serial blood samples for pharmacokinetic analysis were collected prior to dosing and periodically for 288 h after dosing for measurement of the plasma concentrations of donepezil. A non-compartmental method was used to estimate the pharmacokinetic parameters. The maximum concentration (C(max)) and the area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC(288h)) for the two formulations were compared to evaluate bioequivalence. The C(max) of the test and reference drugs were 27.58+/-7.46 and 26.35+/-6.51 microg/L (mean+/-SD), respectively, while AUC(288h) was 1080.14+/-229.77 and 1043.07+/-242.28 microg.h/L (mean+/-SD), respectively. The geometric mean ratios (90% confidence interval) of the C(max) and AUC(288h) of the two tablets were 1.043 (0.990-1.099) and 1.039 (1.013-1.065). In conclusion, the newly formulated tablet of donepezil hydrochloride 10 mg is bioequivalent to the currently marketed 10 mg tablet.

Keyword

Bioequivalence; Pharmacokinetics; Donepezil

MeSH Terms

Acetylcholinesterase
Alzheimer Disease
Cross-Over Studies
Humans
Male
Pharmacokinetics
Plasma
Tablets
Therapeutic Equivalency*
Volunteers*
Acetylcholinesterase
Tablets

Figure

  • Figure 1. Mean plasma concentration-time profiles of donepezil after single oral administration of reference formulation (filled circles) and test formulation (open circles). Bars represent standard deviations. (Left, linear; right, log-linear)

  • Figure 2. Individual subject's Cmax and AUC288h values for donepezil reference formulation and test formulation (Left: AUC288h, Right: Cmax)


Reference

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