Blood-brain barrier Permeable nanoparticles for Alzheimer's disease treatment by selective mitophagy of microglia. (September 2022)

• Record Type: Journal Article
• Authors: Zhong, Gang; Long, Huiping; Zhou, Tian; Liu, Yisi; Zhao, Jianping; Han, Jinyu; Yang, Xiaohu; Yu, Yin; Chen, Fei; Shi, Shengliang
• Is Part Of: Biomaterials. Volume 288(2022)
• Publication Date: 2022-09
• Subjects: Alzheimer's disease -- Prussian blue -- Polyamidoamine dendrimer -- Nanoparticles -- Microglia modulation -- Mitophagy; Biomedical materials -- Periodicals; Biocompatible Materials -- Periodicals; Biomatériaux -- Périodiques; 610.28
• DOI: 10.1016/j.biomaterials.2022.121690
• Languages: English
• ISSNs: 0142-9612

Abstract

Abstract: Current treatments for Alzheimer's disease (AD) that focus on inhibition of Aβ aggregation failed to show effectiveness in people who already had Alzheimer's symptoms. Strategies that synergistically exert neuroprotection and alleviation of oxidative stress could be a promising approach to correct the pathological brain microenvironment. Based on the key roles of microglia in modulation of AD microenvironment, we describe here the development of Prussian blue/polyamidoamine (PAMAM) dendrimer/Angiopep-2 (PPA) nanoparticles that can regulate the mitophagy of microglia as a potential AD treatment. PPA nanoparticles exhibit superior blood-brain barrier (BBB) permeability and exert synergistic effects of ROS scavenging and restoration of mitochondrial function of microglia. PPA nanoparticles effectively reduce neurotoxic Aβ aggregate and rescue the cognitive functions in APP/PS1 model mice. Together, our data suggest that these multifunctional dendrimer nanoparticles exhibit efficient neuroprotection and microglia modulation and can be exploited as a promising approach for the treatment of AD. Graphical abstract: A hybrid nanoparticle platform with high blood-brain-barrier (BBB) transport efficacy is developed for treatment of Alzheimer's disease (AD). This unique nanoparticle platform exerts synergistic effects of reactive oxygen species scavenging and restoration of mitochondrial function of microglia, thus exhibits efficient neuroprotection and rescue the cognitive functions of AD model mice. Image 1