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基于胰岛素的纳米载体的研究进展

Ionizing radiation-engineered nanogels as insulin nanocarriers for the development of a new strategy for the treatment of Alzheimer's disease.

机构信息

Istituto di Biomedicina e Immunologia Molecolare "A. Monroy" (IBIM), Consiglio Nazionale delle Ricerche, Via U. La Malfa, 153, 90146 Palermo (PA), Italy.

Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, Università di Palermo, Viale delle Scienze, Building 6, 90128 Palermo (PA), Italy.

出版信息

Biomaterials. 2016 Feb;80:179-194. doi: 10.1016/j.biomaterials.2015.11.057. Epub 2015 Dec 2.

Abstract

A growing body of evidence shows the protective role of insulin in Alzheimer's disease (AD). A nanogel system (NG) to deliver insulin to the brain, as a tool for the development of a new therapy for Alzheimer's Disease (AD), is designed and synthetized. A carboxyl-functionalized poly(N-vinyl pyrrolidone) nanogel system produced by ionizing radiation is chosen as substrate for the covalent attachment of insulin or fluorescent molecules relevant for its characterization. Biocompatibility and hemocompatibility of the naked carrier is demonstrated. The insulin conjugated to the NG (NG-In) is protected by protease degradation and able to bind to insulin receptor (IR), as demonstrated by immunofluorescence measurements showing colocalization of NG-In(FITC) with IR. Moreover, after binding to the receptor, NG-In is able to trigger insulin signaling via AKT activation. Neuroprotection of NG-In against dysfunction induced by amyloid β (Aβ), a peptide mainly involved in AD, is verified. Finally, the potential of NG-In to be efficiently transported across the Blood Brain Barrier (BBB) is demonstrated. All together these results indicate that the synthesized NG-In is a suitable vehicle system for insulin deliver in biomedicine and a very promising tool to develop new therapies for neurodegenerative diseases.

摘要

越来越多的证据表明胰岛素在阿尔茨海默病(AD)中具有保护作用。设计并合成了一种将胰岛素递送到大脑的纳米凝胶系统(NG),作为开发阿尔茨海默病(AD)新疗法的工具。选择羧基功能化的聚(N-乙烯基吡咯烷酮)纳米凝胶系统作为共价连接胰岛素或与其特征相关的荧光分子的基底。证明了裸载体的生物相容性和血液相容性。通过免疫荧光测量证明,与 NG 结合的胰岛素(NG-In)可抵抗蛋白酶降解并能与胰岛素受体(IR)结合,表明 NG-In(FITC)与 IR 共定位。此外,与受体结合后,NG-In 能够通过 AKT 激活触发胰岛素信号。验证了 NG-In 对淀粉样蛋白β(Aβ)引起的功能障碍的神经保护作用,Aβ是主要涉及 AD 的肽。最后,证明了 NG-In 具有穿过血脑屏障(BBB)的有效转运能力。所有这些结果表明,合成的 NG-In 是一种适用于生物医学中胰岛素传递的载体系统,也是开发神经退行性疾病新疗法的非常有前途的工具。

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