| Literature DB >> 26262759 |
Hualong Fu1, Mengchao Cui1, Liu Zhao1, Peiyu Tu1, Kaixiang Zhou1, Jiapei Dai2, Boli Liu1.
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26262759 DOI: 10.1021/acs.jmedchem.5b00861
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446