Blood-brain barrier permeable carbon nano-assemblies for amyloid-β clearance and neurotoxic attenuation

被引:1
|
作者
Hou, Tongtong [1 ]
Yang, Qian [2 ]
Ding, Minling [1 ]
Wang, Xin [1 ]
Mei, Kun [1 ]
Guan, Ping [1 ]
Wang, Chaoli [2 ]
Hu, Xiaoling [1 ]
机构
[1] Northwestern Polytech Univ, Sch Chem & Chem Engn, Dept Chem, Xian 710072, Peoples R China
[2] Air Force Med Univ, Sch Pharm, Dept Pharmaceut Anal, Xian 710032, Peoples R China
基金
美国国家科学基金会;
关键词
Nano-assemblies; beta-amyloid; Blood-brain barrier; GRAPHENE QUANTUM DOTS; PHOTOTHERMAL THERAPY; AGGREGATION; PHOTOOXYGENATION; NANOPARTICLES; DISSOCIATION; PEPTIDES; DESIGN;
D O I
10.1016/j.colsurfb.2024.114182
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Abnormal amyloid /3-protein (A/342) fibrillation is a key event in Alzheimer's disease (AD), and photodynamic therapy (PDT) possesses great potential in modulating A/342 self-assembly. However, the poor blood-brain barrier (BBB) penetration, low biocompatibility, and limited tissue penetration depth of existing photosensitizers limit the progress of photo-oxidation strategies. In this paper, novel indocyanine green-modified graphene quantum dot nano-assemblies (NBGQDs-ICGs) were synthesized based on a molecular assembly strategy of electrostatic interactions for PDT inhibition of A/342 self-assembly process and decomposition of preformed fibrils under nearinfrared light. Combining the small-size structure of graphene quantum dots and the near-infrared lightresponsive properties of ICGs, the NBGQDs-ICGs could achieve BBB penetration under 808 nm irradiation. More importantly, the neuroprotective mechanism of NBGQDs-ICG was studied for the first time by AFM, which effectively weakened the adhesion of A/342 aggregates to the cell surface by blocking the interaction between A/342 and the cell membrane, and restored the mechanical stability and adhesion of the neuron membrane. Meanwhile, NBGQDs-ICG promoted phagocytosis of A/342 by microglia. In addition, the good biocompatibility and stability ensured the biosafety of NBGQDs-ICG in future clinical applications. We anticipate that such multifunctional nanocomponents may provide promising avenues for the development of novel AD inhibitors.
引用
收藏
页数:12
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