Literature DB >> 21943887

Donepezil dosing strategies: pharmacokinetic considerations.

Irving H Gomolin1, Candace Smith2, Thomas M Jeitner3.   

Abstract

Donepezil (Aricept) is a cholinesterase inhibitor approved for the treatment of Alzheimer's disease. Immediate release formulations of 5- and 10-mg tablets were approved by the Food and Drug Administration in the United States in 1996. In July 2010, the Food and Drug Administration approved a 23-mg sustained release (SR) formulation. The SR formulation may provide additional benefit to patients receiving 10 mg daily but the incidence of adverse reactions is increased. We derived plasma concentration profiles for higher dose immediate-release formulations (15 mg once daily, 10 mg twice daily, and 20 mg once daily) and for the profile anticipated to result from the 23-mg SR formulation. Our model predicts similar steady-state concentration profiles for 10 mg twice daily, 20 mg once daily, and 23 mg SR once daily. This provides the theoretical basis for incremental immediate release dose escalation to minimize the emergence of adverse reactions and the potential to offer a cost-effective alternative to the SR formulation with currently approved generic immediate release formulations.
Copyright © 2011 American Medical Directors Association. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21943887     DOI: 10.1016/j.jamda.2011.02.004

Source DB:  PubMed          Journal:  J Am Med Dir Assoc        ISSN: 1525-8610            Impact factor:   4.669


  3 in total

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3.  PLGA Microspheres with Alginate-Coated Large Pores for the Formulation of an Injectable Depot of Donepezil Hydrochloride.

Authors:  Dohyun Kim; Tae Hee Han; Seong-Chul Hong; Sun Jae Park; Yong Hak Lee; Hyeongmin Kim; Minwoo Park; Jaehwi Lee
Journal:  Pharmaceutics       Date:  2020-04-01       Impact factor: 6.321

  3 in total

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