Issue 50, 2016

Radiolabeled pyridinyl analogues of dibenzylideneacetone as β-amyloid imaging probes

Abstract

In continuation of our investigation of the dibenzylideneacetone scaffold as Aβ imaging probes, a series of derivatives containing pyridine rings with lower lipophilicity was synthesized and evaluated. Some of these probes displayed high affinities to Aβ1–42 aggregates, which ranged from 18.0 to 8.2 nM. The high and specific binding of the radiolabeled tracers was further confirmed by in vitro autoradiography on brain sections from AD patients and transgenic mouse. In biodistribution experiments, two 18F-labeled tracers [18F]17a and [18F]18 displayed high initial brain uptake (5.05 and 6.24% ID g−1, respectively, at 2 min postinjection) and fast clearance from the brain with brain2 min/brain60 min ratios of 6.08 and 8.00. These results demonstrate that the probes [18F]17a and [18F]18 with a dibenzylideneacetone structure containing pyridine rings have great strength in imaging Aβ plaques in the brain.

Graphical abstract: Radiolabeled pyridinyl analogues of dibenzylideneacetone as β-amyloid imaging probes

Supplementary files

Article information

Article type
Paper
Submitted
27 Febr. 2016
Accepted
18 Apr. 2016
First published
20 Apr. 2016

RSC Adv., 2016,6, 44646-44654

Radiolabeled pyridinyl analogues of dibenzylideneacetone as β-amyloid imaging probes

X. Cui, X. Zhang, C. Peng, J. Dai, B. Liu and M. Cui, RSC Adv., 2016, 6, 44646 DOI: 10.1039/C6RA05168E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements