Near-Infrared Activated Black Phosphorus as a Nontoxic Photo-Oxidant for Alzheimer's Amyloid-β Peptide

被引:78
作者
Li, Yang [1 ,2 ]
Du, Zhi [1 ,2 ]
Liu, Xinping [1 ,2 ]
Ma, Mengmeng [1 ,2 ]
Yu, Dongqin [1 ,2 ]
Lu, Yao [3 ]
Ren, Jinsong [1 ,2 ]
Qu, Xiaogang [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Lab Chem Biol, Changchun 130022, Jilin, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Jilin, Peoples R China
[3] Changchun Univ Sci & Technol, Sch Chem & Environm Engn, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; amyloid-beta; black phosphorus; nontoxic photo-oxidants; photo-oxygenation; singlet oxygen; COMMON MECHANISM; AGGREGATION; NANOPARTICLES; PHOTOSENSITIZERS; NEUROTOXICITY; INHIBITION; NANOSHEETS; TOXICITY; DISEASE; IMPLIES;
D O I
10.1002/smll.201901116
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The inhibition of amyloid-beta (A beta) aggregation by photo-oxygenation has become an effective way of treating Alzheimer's disease (AD). New near-infrared (NIR) activated treatment agents, which not only possess high photo-oxygenation efficiency, but also show low biotoxicity, are urgently needed. Herein, for the first time, it is demonstrated that NIR activated black phosphorus (BP) could serve as an effective nontoxic photo-oxidant for amyloid-beta peptide in vitro and in vivo. The nanoplatform BP@BTA (BTA: one of thioflavin-T derivatives) possesses high affinity to the A beta peptide due to specific amyloid selectivity of BTA. Importantly, under NIR light, BP@BTA can significantly generate a high quantum yield of singlet oxygen (O-1(2)) to oxygenate A beta, thereby resulting in inhibiting the aggregation and attenuating A beta-induced cytotoxicity. In addition, BP could finally degrade into nontoxic phosphate, which guarantees the biosafety. Using transgenic Caenorhabditis elegans CL2006 as AD model, the results demonstrate that the O-1(2)-generation system could dramatically promote life-span extension of CL2006 strain by decreasing the neurotoxicity of A beta.
引用
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页数:6
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