Dual-Carbon Dots Composite: A Multifunctional Photo-Propelled Nanomotor Against Alzheimer's β-Amyloid

被引:1
|
作者
Lin, Xiaoding [1 ,2 ]
Dong, Xiaoyan [1 ,2 ]
Sun, Yan [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Biochem Engn, Key Lab Syst Bioengn, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Frontiers Sci Ctr Synthet Biol, Minist Educ, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; beta-amyloid protein; carbon dots; multifunctionality; nanomotor; photooxygenation; DISEASE; NANOPARTICLES; HYPOTHESIS; A-BETA-42;
D O I
10.1002/smll.202407154
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The abnormal accumulation of beta-amyloid protein (A beta) is considered as the main pathological hallmark of Alzheimer's disease (AD). The design of potent multifunctional theranostic agents targeting A beta is one of the effective strategies for AD prevention and treatment. Nanomotors as intelligent, advanced, and multifunctional nanoplatforms can perform many complex tasks, but their application in AD theranostics is rare. Herein, sub-10nm multifunctional dual-carbon dots composites (ERCD) with photo-propelled nanomotor behavior are fabricated by conjugating near-infrared (NIR) carbon dots (RCD) of thermogenic and photodynamic capability with the previously reported epigallocatechin gallate-derived carbonized polymer dots (ECD). ERCD-1 (ECD:RCD = 1:2.5) showed potent inhibitory capability similar to ECD in the absence of NIR light, and exhibited photooxygenation activity and nanomotor behavior powered by "self-thermophoretic force" under NIR irradiation, significantly enhancing the inhibition, disaggregation, and photooxygenation capabilities. The nanomotor suppressed A beta fibrillization and rapidly disaggregated mature A beta fibrils at very low concentrations (0.5 mu g mL(-1)). Moreover, the NIR-activated ERCD-1 imaged A beta plaques in vivo and prolonged nematode lifespan by 6 d at 2 mu g mL(-1). As a proof-of-concept, this work opened a new avenue to the design of multifunctional sub-10nm nanomotors targeting A beta for AD theranostics.
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页数:15
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