Pioglitazone Loaded-PLGA-PEG Nanoparticles: Drug Release and Interactions

RAN Pub Date : 2016-04-01 DOI:10.11159/NDDTE16.106
M. Abreu, M. A. Egea, A. Calpena, M. Espina, Maria L. García
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引用次数: 0

Abstract

Extended Abstract Introduction The main obstacle to transport drugs to the brain, for neurodegenerative diseases treatment, is the blood-brain barrier (BBB), acting as an immune and metabolic barrier [1]. Pioglitazone (PGZ) is an oral anti-diabetic from thiazolidinediones, agonist of the peroxisome proliferator-activated receptors (PPARs), which could play an important role on mechanisms of neurodegenerative diseases [2, 3]. The main goal of this work was the PGZ association nanostructured systems, to nanoparticles (NPs) from poly (D,L-lactide-co-glycolide) poly(ethylene glycol) (PLGA-PEG) that are able to pass BBB.
吡格列酮负载plga - peg纳米颗粒:药物释放和相互作用
在神经退行性疾病的治疗中,将药物输送到大脑的主要障碍是血脑屏障(BBB),它是一种免疫和代谢屏障[1]。吡格列酮(PGZ)是噻唑烷二酮类口服抗糖尿病药物,是过氧化物酶体增殖物激活受体(ppar)的激动剂,在神经退行性疾病的机制中发挥重要作用[2,3]。这项工作的主要目标是PGZ结合纳米结构系统,从聚(D, l -丙交酯-共乙二醇酯)聚(乙二醇)(PLGA-PEG)到能够通过血脑屏障的纳米颗粒(NPs)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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