基于树突分子的药物传递系统:一种治疗帕金森病的新方法

Michaella B. Ordonio, R. Zaki, A. Elkordy
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引用次数: 2

摘要

帕金森病(PD)是一种进行性神经退行性疾病,其特征是多巴胺的丧失。由于多巴胺难以进入血脑屏障,因此考虑利用树突和其他纳米材料偶联神经递质和其他PD药物。树状大分子是三维的、超分支的结构,分为几代。α -突触核蛋白(ASN)是参与调节多巴胺能功能的蛋白质,是路易小体内发现的主要聚集体。不同类型的树状大分子在破坏ASN和纤颤的不稳定β结构的形成方面显示出功效。PD药物与纳米材料的结合引起了药物在血脑屏障内的持续作用和持续释放。本研究的目的是回顾基于树突的药物递送系统在解决帕金森病的根本原因中的应用,并强调使用口服和静脉注射以外的给药途径递送抗帕金森药物,如罗替戈汀,普拉克索和多巴胺。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dendrimers-Based Drug Delivery System: A Novel Approach in Addressing Parkinson’s Disease
Parkinson’s disease (PD) is a progressive neurodegenerative disease that is characterized by the loss of dopamine. Since dopamine has trouble entering the blood–brain barrier, the utilization of dendrimers and other nanomaterials is considered for conjugating the neurotransmitter and other PD drugs. Dendrimers are three-dimensional, hyper-branched structures that are categorized into several generations. Alpha-synuclein (ASN) is the protein involved in regulating dopaminergic functions and is the main aggregate found inside Lewy bodies. Different types of dendrimers have shown efficacy in disrupting the formation of unstable beta structures of ASN and fibrillation. The conjugation of PD drugs into nanomaterials has elicited a prolonged duration of action and sustained release of the drugs inside the BBB. The objectives of this study are to review the applications of a dendrimer-based drug delivery system in addressing the root cause of Parkinson’s disease and to emphasize the delivery of anti-Parkinson’s drugs such as rotigotine, pramipexole and dopamine using routes of administration other than oral and intravenous.
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