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改善多奈哌齐鼻脑递送的制剂策略。

Formulation Strategies to Improve Nose-to-Brain Delivery of Donepezil.

作者信息

Espinoza Lupe Carolina, Silva-Abreu Marcelle, Clares Beatriz, Rodríguez-Lagunas María José, Halbaut Lyda, Cañas María-Alexandra, Calpena Ana Cristina

机构信息

Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, 08028 Barcelona, Spain.

Departamento de Química y Ciencias Exactas, Universidad Técnica Particular de Loja, Loja 1101608, Ecuador.

出版信息

Pharmaceutics. 2019 Feb 1;11(2):64. doi: 10.3390/pharmaceutics11020064.

Abstract

Donepezil (DPZ) is widely used in the treatment of Alzheimer's disease in tablet form for oral administration. The pharmacological efficacy of this drug can be enhanced by the use of intranasal administration because this route makes bypassing the blood⁻brain barrier (BBB) possible. The aim of this study was to develop a nanoemulsion (NE) as well as a nanoemulsion with a combination of bioadhesion and penetration enhancing properties (PNE) in order to facilitate the transport of DPZ from nose-to-brain. Composition of NE was established using three pseudo-ternary diagrams and PNE was developed by incorporating Pluronic F-127 to the aqueous phase. Parameters such as physical properties, stability, in vitro release profile, and ex vivo permeation were determined for both formulations. The tolerability was evaluated by in vitro and in vivo models. DPZ-NE and DPZ-PNE were transparent, monophasic, homogeneous, and physically stable with droplets of nanometric size and spherical shape. DPZ-NE showed Newtonian behavior whereas a shear thinning (pseudoplastic) behavior was observed for DPZ-PNE. The release profile of both formulations followed a hyperbolic kinetic. The permeation and prediction parameters were significantly higher for DPZ-PNE, suggesting the use of polymers to be an effective strategy to improve the bioadhesion and penetration of the drug through nasal mucosa, which consequently increase its bioavailability.

摘要

多奈哌齐(DPZ)以片剂形式口服广泛用于治疗阿尔茨海默病。该药物的药理功效可通过鼻内给药来增强,因为这种给药途径使绕过血脑屏障(BBB)成为可能。本研究的目的是开发一种纳米乳剂(NE)以及一种具有生物黏附性和渗透促进特性相结合的纳米乳剂(PNE),以促进DPZ从鼻腔到脑的转运。使用三个伪三元相图确定NE的组成,并通过将泊洛沙姆F - 127加入水相来开发PNE。对两种制剂测定了物理性质、稳定性、体外释放曲线和离体渗透等参数。通过体外和体内模型评估耐受性。DPZ - NE和DPZ - PNE均为透明、单相、均匀且物理稳定的制剂,具有纳米级大小的球形液滴。DPZ - NE表现出牛顿流体行为,而DPZ - PNE观察到剪切变稀(假塑性)行为。两种制剂的释放曲线均遵循双曲线动力学。DPZ - PNE的渗透和预测参数显著更高,表明使用聚合物是提高药物通过鼻黏膜的生物黏附性和渗透性的有效策略,从而提高其生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f8d/6410084/f07a4c70cd55/pharmaceutics-11-00064-g001.jpg

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