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Cu2+‐Chelatable and ROS‐Scavenging MXenzyme as NIR‐II‐Triggered Blood–Brain Barrier‐Crossing Nanocatalyst against Alzheimer's Disease

Transition‐metal dyshomeostasis has been identified as a critical pathogenic factor for the aggregates of amyloid‐beta (Aβ) peptide, which is associated with the onset and progression of Alzheimer's disease (AD). Excessive transition‐metal ions, especially copper ion (Cu2+), catalyze the format...

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Published in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2022-09, Vol.18 (39), p.n/a
Main Authors: Du, Chengjuan, Feng, Wei, Dai, Xinyue, Wang, Jianhong, Geng, Daoying, Li, Xiaodan, Chen, Yu, Zhang, Jun
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container_title Small (Weinheim an der Bergstrasse, Germany)
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Feng, Wei
Dai, Xinyue
Wang, Jianhong
Geng, Daoying
Li, Xiaodan
Chen, Yu
Zhang, Jun
description Transition‐metal dyshomeostasis has been identified as a critical pathogenic factor for the aggregates of amyloid‐beta (Aβ) peptide, which is associated with the onset and progression of Alzheimer's disease (AD). Excessive transition‐metal ions, especially copper ion (Cu2+), catalyze the formation of reactive oxygen species (ROS), triggering neuroinflammation and neuronal cell apoptosis. Therefore, developing a robust chelating agent can not only efficiently bind toxic Cu2+, but also simultaneously scavenge the over‐generated ROS that is urgently needed for AD treatment. In this work, a 2D niobium carbide (Nb2C) MXene‐based nano‐chelator is constructed and its performance in suppressing Cu2+‐induced accumulation of aggregated Aβ peptide and acting as a nanozyme (MXenzyme) with powerful antioxidant property to scavenge excess cellular ROS is explored, and the intrinsic mechanism is revealed by computational simulation. Importantly, the benign photothermal effect of Nb2C MXenzyme demonstrates the facilitated permeability of the blood–brain barrier under near‐infrared laser irradiation, conquering limitations of the most conventional anti‐AD therapeutic agents. This work not only demonstrates a favorable strategy for combating AD by engineering Nb2C MXenzyme‐based neuroprotective nano‐chelator, but also paves a distinct insight for extending the biomedical applications of MXenes in treating transition‐metal dyshomeostasis‐and ROS‐mediated central nervous system diseases. An integrated nano‐chelator with cascade nanozyme based on 2D niobium carbide (Nb2C) MXene is developed to selectively capture Cu2+ and eliminate excessive reactive oxygen species against neurodegenerative diseases. This work demonstrates that Nb2C MXenzyme features the desirable clinical translation potential, largely based on the facile formulation, antioxidant enzyme‐mimicking performance, and effective blood‐brain barrier penetration under near infrared laser stimulus.
doi_str_mv 10.1002/smll.202203031
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subjects Alzheimer's disease
Apoptosis
Biocompatibility
Biomedical materials
Blood-brain barrier
Central nervous system
Chelating agents
Chelation
Chemical compounds
Copper
copper ions chelating therapy
Infrared lasers
MXenzymes
Nanotechnology
nanozymes
Nb 2C MXenes
Niobium carbide
Peptides
Pharmacology
reactive oxygen species scavenging
Scavenging
title Cu2+‐Chelatable and ROS‐Scavenging MXenzyme as NIR‐II‐Triggered Blood–Brain Barrier‐Crossing Nanocatalyst against Alzheimer's Disease
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