Your browser doesn't support javascript.
loading
Biofilm-camouflaged Prussian blue synergistic mitochondrial mass enhancement for Alzheimer's disease based on Cu2+ chelation and photothermal therapy.
Li, Lianxin; Xiong, Yu; Zhang, Yuewen; Yan, Yujiao; Zhao, Ruixin; Yang, Fengmei; Xie, Meng.
Afiliación
  • Li L; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Xiong Y; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Zhang Y; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Yan Y; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Zhao R; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Yang F; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
  • Xie M; School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China. Electronic address: xiemeng@ujs.edu.cn.
J Control Release ; 375: 269-284, 2024 Sep 13.
Article en En | MEDLINE | ID: mdl-39245418
ABSTRACT
Alzheimer's disease (AD) is one of the most common neurodegenerative diseases characterized by cognitive and memory impairment. Metal ion imbalance and Mitochondrial dysfunction, leading to abnormal aggregation of ß-amyloid protein (Aß), are key factors in the pathogenesis of AD. Therefore, we designed a composite nanometer system of red blood cell (RBC) membranes-encapsulated Prussian blue nanoparticles (PB/RBC). Prussian blue nanoparticles (PBNPs) can chelate Cu2+ and reduce reactive oxygen species (ROS). The RBC membranes are a kind of natural long-lasting circulating carrier. At the same time, through NIR irradiation, the excellent photothermal ability of PBNPs can also temporarily open the blood-brain barrier (BBB), enhance the transmission efficiency of PB/RBC across the BBB, and depolymerize the formed Aß deposits, thereby achieving the optimal therapeutic effect. In vitro and in vivo studies demonstrated that PB/RBC could inhibit Cu2+-induced Aß monomers aggregation, eliminate the deposition of Aß plaques, improve the quality of mitochondria, restore the phagocytic function of microglia, alleviate neuroinflammation in APP/PS1 mice, and repair memory damage. In conclusion, our biofilm-camouflaged nano-delivery system provides significant neuroprotection by inhibiting Cu2+-induced Aß monomers aggregation, photothermally depolymerizing Aß fibrils and reducing the level of ROS, thus effectively ameliorating and treating AD.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Control Release Asunto de la revista: FARMACOLOGIA Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Control Release Asunto de la revista: FARMACOLOGIA Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos