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Publication : Biological evaluation of the radioiodinated imidazo[1,2-a]pyridine derivative DRK092 for amyloid-β imaging in mouse model of Alzheimer's disease.

First Author  Chen CJ Year  2014
Journal  Neurosci Lett Volume  581
Pages  103-8 PubMed ID  25172571
Mgi Jnum  J:215372 Mgi Id  MGI:5605195
Doi  10.1016/j.neulet.2014.08.036 Citation  Chen CJ, et al. (2014) Biological evaluation of the radioiodinated imidazo[1,2-a]pyridine derivative DRK092 for amyloid-beta imaging in mouse model of Alzheimer's disease. Neurosci Lett 581:103-8
abstractText  Non-invasive determination of amyloid-beta peptide (Abeta) deposition has important significance for early diagnosis and medical intervention in Alzheimer's disease (AD). In this study, we investigated the availability of a radioiodinated imidazo[1,2-a]pyridine derivative, termed (125)I-DRK092, as single photon emission computed tomography (SPECT) ligand for in vivo detection of Abeta deposition. DRK092 showed high binding affinity for either synthetic human Abeta fibrils or brain homogenates from amyloid precursor protein transgenic (Tg) mouse (PS1-ki/JU-Tg2576) and AD patient with a dissociation constant (Kd) of one-digit nM, and excellent brain permeability (peak value of uptake: approximately 0.9% of injection dose/g rat brain). Ex vivo autoradiographic analysis showed that measurement with (125)I-DRK092 has higher sensibility for detecting Abeta accumulation than with (125)I-IMPY, a well-known amyloid SPECT ligand, in Tg mice. In vitro autoradiography with (125)I-DRK092 also confirmed higher accumulation of radioactivity in the cortical area, enriched with Abeta plaques, of Tg mouse and AD patient brains, as compared with the corresponding areas in non-Tg mouse and healthy control brains. All the data presented above lead us to draw the conclusion that radioiodinated DRK092 is a potential SPECT ligand for amyloid imaging in AD.
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