材料科学
共价键
肽
磁共振成像
生物物理学
纤维
纳米颗粒
共价有机骨架
氢键
纳米技术
金属有机骨架
衰减
膜
纳米医学
活性氧
核磁共振
淀粉样变性
淀粉样纤维
膜透性
磁导率
氧化物
氧化铁纳米粒子
淀粉样蛋白(真菌学)
超顺磁性
氢
肽键
功能(生物学)
化学工程
作者
Zhuo Zhang,Mingchen Lv,Wei Hu,Jiaxi Xu,Shangpeng Liu,Biao Yang,Fan Zhang,Zhen Fan
标识
DOI:10.1002/adfm.202529220
摘要
ABSTRACT The abnormal amyloid‐ β (A β ) aggregation is critical in the progression of Alzheimer's disease pathology, yet clinical therapeutics to alleviate amyloidosis in the patients is hindered due to low efficiency and side effects. Here, a multifunctional nanoplatform (Pep‐COF@E/P/S), where A β targeting peptide KLVFFA, small‐molecule EGCG and superparamagnetic iron oxide nanoparticles (SPIONs) were combined together upon the covalent organic framework to attenuate A β fibrils, alleviate A β fibrils‐induced cytotoxicity, and function as an MRI probe, is reported. Specifically, Pep‐COF@E/P/S enables A β targeting through the hydrogen bond of the KLVFFA component. Meanwhile, A β fibrils were attenuated by hydrogen bond and electrostatic interactions, thereby alleviating A β fibrils‐induced reactive oxygen species (ROS) and mitochondrial dysfunction as well as membrane damage further. In addition, Pep‐COF@E/P/S also exhibited favorable blood compatibility, biosafety as well as BBB permeability in vivo. Of note, the combination of SPIONs enables Pep‐COF@E/P/S as a potential MRI probe. It is expected that multifunctional Pep‐COF@E/P/S provides an attractive avenue to promote the development of precise and efficacious treatment of Alzheimer's disease.
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