Synthesis and evaluation of curcumin-based near-infrared fluorescent probes for detection of amyloid β; peptide in Alzheimer mouse models

被引:5
作者
Li, Li [1 ,2 ]
Xiang, Fengting [1 ]
Yao, Luyang [1 ]
Zhang, Chuang [1 ]
Jia, Xirong [1 ]
Chen, Anqi [1 ]
Liu, Yu [1 ,3 ]
机构
[1] Liaoning Univ, Sch Pharm, Shenyang 110036, Peoples R China
[2] Liaoning Key Lab New Drug Res & Dev, Shenyang 110036, Peoples R China
[3] Liaoning Univ, Judicial Expertise Ctr, Shenyang 110036, Peoples R China
关键词
Alzheimer's disease; Fluorescence probe; Near-infrared fluorescence; Amyloid-beta plagues; Curcumin; In vivo imaging; CROSS-LINKING; A-BETA; DISEASE; DERIVATIVES; DEPOSITS; PLAQUES; DESIGN; BRAIN;
D O I
10.1016/j.bmc.2023.117410
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The abnormal accumulation of amyloid beta protein (A beta) is one of the most important causes of Alzheimer's disease (AD) and is usually a detecting biomarker. Curcumin and its derivatives have potential A beta aggregate targeting ability; we synthesized a series of curcumin-based near-infrared fluorescence probes in this study. By characterizing the excitation wavelength and emission wavelength, the imaging characteristics of the investigation in the near-infrared light region were determined; with an increase in the concentration of the probe compounds, the fluorescence intensity showed an upward trend, demonstrating ideal optical characteristics. In vivo, imaging results showed that the synthesized probe compounds could penetrate the blood-brain barrier (BBB) and specifically bind to A beta in the brain of APP/PS1 mice. Especially for compound 3b, the maximum emission wavelength was around 667 nm, and the fluorescence signal intensity in the brain of the APP/PS1 mice model was more than twice that of the wild control group at 120 min after administration, which could display A beta pathological changes. The fluorescent probes designed in this study can become an effective tool for early AD diagnosis and visual detection.
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页数:9
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