Dual-functional AIE fluorescent probes for imaging β-amyloid plaques and lipid droplets

被引:51
|
作者
Wang, Yuxuan [1 ]
Qiu, Yutai [1 ]
Sun, Anyang [2 ,3 ]
Xiong, Yinghong [1 ]
Tan, Huiya [1 ]
Shi, Yuqi [2 ,3 ,4 ]
Yu, Pan [1 ]
Roy, Gaurab [1 ]
Zhang, Lei [1 ]
Yan, Jinwu [1 ]
机构
[1] South China Univ Technol, Sch Biol & Biol Engn, MOE Int Joint Res Lab Synthet Biol & Med, Guangzhou 510006, Peoples R China
[2] Shanghai Univ Med & Hlth Sci, Shanghai Zhoupu Hosp, Dept Neurol, Shanghai 201318, Peoples R China
[3] Shanghai Univ Med & Hlth Sci, Lab Neurogenerat Dis & Mol Imaging, Shanghai 201318, Peoples R China
[4] Univ Shanghai Sci & Technol, Sch Med Instrument & Food Engn, Shanghai 200093, Peoples R China
关键词
AIE; Alzheimer's disease; Dual-functional; Beta-amyloid; Lipid droplets; Fluorescent probe; AGGREGATION-INDUCED EMISSION; ALZHEIMERS-DISEASE; LUMINOGENS; VISCOSITY; DESIGN; RED;
D O I
10.1016/j.aca.2020.07.073
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Alzheimer's disease (AD) is a chronic neurodegenerative disease. Better imaging and early diagnosis of biomarkers of AD is extremely important for therapeutic interventions. The amyloid cascade hypothesis and its revised version identify insoluble beta-amyloid deposition as a good diagnostic biomarker for AD. Moreover, lipid droplets may also act as an auxiliary biomarker related to AD pathology based on recent studies. Herein, two quinoline-based AIE probes were designed and synthesized for the imaging of A beta plaques and lipid droplets. The probes exhibited remarkable turn-on fluorescence enhancements with the A beta aggregates. The lipid droplets-targeting probe FB exhibited high selectivity and binding affinity towards the A beta aggregates with a detection limit as low as 26.9 nM. Furthermore, FB was capable of readily imaging A beta plaques and lipid droplets at the cellular level and in brain sections of transgenic AD mice. The probe FB can serve as a promising tool for developing early diagnosis and innovative therapeutics of AD. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 118
页数:10
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