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Abstract
Toxic amyloid-beta (Aβ) plaque and harmful inflammation are two leading symptoms of Alzheimer's disease (AD). This research designs a near-infrared-II aggregation-induced emission (AIE) nanotheranostic for precise AD therapy. The nanotheranostic's in vivo BBB penetration and specific plaque binding are monitored, and ROS triggers the release of two AIE molecules to inhibit Aβ fibril formation, degrade Aβ fibrils, prevent reaggregation, scavenge ROS, and alleviate inflammation. This leads to behavioral and cognitive improvements in a female AD mouse model.
Publisher
Nature Communications
Published On
Jan 24, 2024
Authors
Jiefei Wang, Ping Shangguan, Xiaoyu Chen, Yong Zhong, Ming Lin, Mu He, Yisheng Liu, Yuan Zhou, Xiaobin Pang, Lulu Han, Mengya Lu, Xiao Wang, Yang Liu, Huiqing Yang, Jingyun Chen, Chenhui Song, Jing Zhang, Xin Wang, Bingyang Shi, Ben Zhong Tang
Tags
Alzheimer's disease
amyloid-beta
nanotheranostic
aggregation-induced emission
blood-brain barrier
cognitive improvement
reactive oxygen species
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