Abstract
Alzheimer's disease (AD) is pathologically characterized by the accumulation of β-amyloid (Aβ) deposits in the parenchymal and cortical brain. In this work, we designed, synthesized, and evaluated a series of near-infrared (NIR) probes with electron donor-acceptor end groups interacting through a π-conjugated system for the detection of Aβ deposits in the brain. Among these probes, 3b and 3c had excellent fluorescent properties (emission maxima > 650 nm and high quantum yields) and displayed high sensitivity and high affinities to Aβ aggregates (3b, Kd = 8.8 nM; 3c, Kd = 1.9 nM). Both 3b and 3c could readily penetrate the blood-brain barrier with high initial brain uptake and fast to moderate washout from the brain. In vivo NIR imaging revealed that 3b and 3c could efficiently differentiate transgenic and wild-type mice. In summary, our research provides new hints for developing smarter and more activatable NIR probes targeting Aβ.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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2-Naphthylamine / analogs & derivatives*
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2-Naphthylamine / chemical synthesis
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2-Naphthylamine / chemistry
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2-Naphthylamine / pharmacokinetics
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Aged
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Aged, 80 and over
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Alzheimer Disease / diagnosis
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Alzheimer Disease / metabolism
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Alzheimer Disease / pathology*
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Amyloid beta-Peptides / metabolism*
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Animals
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Blood-Brain Barrier / metabolism
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Brain / metabolism
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Brain / pathology*
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Female
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Fluorescent Dyes / chemical synthesis
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Fluorescent Dyes / chemistry*
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Fluorescent Dyes / pharmacokinetics
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Humans
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Male
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Mice, Inbred ICR
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Mice, Transgenic
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Middle Aged
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Molecular Docking Simulation
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Nitriles / chemical synthesis
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Nitriles / chemistry*
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Nitriles / pharmacokinetics
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Plaque, Amyloid / metabolism
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Plaque, Amyloid / pathology*
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Protein Binding
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Spectroscopy, Near-Infrared
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Stereoisomerism
Substances
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2-(3-(6-(dimethylamino)naphthalen-2-yl)allylidene)malononitrile
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Amyloid beta-Peptides
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Fluorescent Dyes
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Nitriles
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2-Naphthylamine