| Literature DB >> 27639367 |
Jianhua Jia1, Kaixiang Zhou1, Jiapei Dai2, Boli Liu1, Mengchao Cui3.
Abstract
An array of complexes, 99mTc/Re-labeled cyclopentadienyl tricarbonyl and 2-phenyl/pyridylbenzothiazoles, conjugated through an ester linkage were tested as potential β-amyloid (Aβ) probes for SPECT imaging. The [CpRe/99mTc(CO)3] complexes were prepared by double ligand transfer reactions from ferrocene precursors, and the X-ray structure of one rhenium surrogate revealed a classical "piano stool" like geometry. Several of the rhenium complexes displayed high affinity for Aβ1-42 aggregates in in vitro inhibition assays, and they could intensely stain Aβ deposits on brain sections from transgenic mice and Alzheimer's disease (AD) patients. Complex [99mTc]4h strongly binds to Aβ deposits in blood vessels of the brain section of AD patients in in vitro autoradiography. Biodistribution experiments in normal mice revealed that 99mTc-labeled tracers exhibited moderate degree of initial brain uptake (0.54%-1.06% ID/g at 2 min). These tracers targeting Aβ plaques of AD patients warrant further structure optimization to improve their ability to penetrate blood-brain barrier, moreover, they may be suitable for developing imaging probes for targeting amyloid aggregates outside of the brain.Entities:
Keywords: Affinity; Alzheimer's disease; SPECT imaging; β-amyloid
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Year: 2016 PMID: 27639367 DOI: 10.1016/j.ejmech.2016.09.001
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514