Jon Jiyoon, Jeong Jieun, Jung Joohee, Cho Hyosun, Song Kyoung, Kim Eun-Sook, Lee Sang Hyup, Han Eunyoung, Chung Woo-Hyun, Moon Aree, Kang Kyu-Tae, Kim Min-Soo, Park Heejun
College of Pharmacy, Duksung Women's University, Samyangro 144-gil, Dobong-gu, Seoul 01369, Republic of Korea.
College of Pharmacy and Research Institute for Drug Development, Pusan National University, Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.
Pharmaceutics. 2025 Jul 24;17(8):958. doi: 10.3390/pharmaceutics17080958.
Donepezil (DPZ) is an Alzheimer's disease (AD) drug that promotes cholinergic neurotransmission and exhibits excellent acetylcholinesterase (AChE) selectivity. The current oral formulations of DPZ demonstrate decreased bioavailability, attributed to limited drug permeability across the blood-brain barrier (BBB). In order to overcome these limitations, various dosage forms aimed at delivering DPZ have been explored. This discussion will focus on the nose-to-brain (N2B) delivery system, which represents the most promising approach for brain drug delivery. Intranasal (IN) drug delivery is a suitable system for directly delivering drugs to the brain, as it bypasses the BBB and avoids the first-pass effect, thereby targeting the central nervous system (CNS). Currently developed formulations include lipid-based, solid particle-based, solution-based, gel-based, and film-based types, and a systematic review of the N2B research related to these formulations has been conducted. According to the in vivo results, the brain drug concentration 15 min after IN administration was more than twice as high those from other routes of administration, and the direct delivery ratio of the N2B system improved to 80.32%. The research findings collectively suggest low toxicity and high therapeutic efficacy for AD. This review examines drug formulations and delivery methods optimized for the N2B delivery of DPZ, focusing on technologies that enhance mucosal residence time and bioavailability while discussing recent advancements in the field.
多奈哌齐(DPZ)是一种用于治疗阿尔茨海默病(AD)的药物,它可促进胆碱能神经传递,并且对乙酰胆碱酯酶(AChE)具有出色的选择性。DPZ目前的口服制剂生物利用度较低,这归因于药物透过血脑屏障(BBB)的通透性有限。为了克服这些限制,人们探索了各种旨在递送DPZ的剂型。本讨论将聚焦于鼻脑(N2B)递送系统,它是脑内药物递送最具前景的方法。鼻腔给药是一种将药物直接递送至脑内的合适系统,因为它绕过了血脑屏障,避免了首过效应,从而靶向中枢神经系统(CNS)。目前开发的剂型包括脂质型、固体颗粒型、溶液型、凝胶型和薄膜型,并且已经对与这些剂型相关的N2B研究进行了系统综述。根据体内实验结果,鼻腔给药后15分钟时脑内药物浓度比其他给药途径高出两倍多,N2B系统的直接递送率提高到了80.32%。这些研究结果共同表明其对AD具有低毒性和高治疗效果。本综述考察了针对DPZ的N2B递送优化的药物剂型和递送方法,重点关注提高黏膜滞留时间和生物利用度的技术,同时讨论该领域的最新进展。