Diagnostic imaging agents for Alzheimer's disease: copper radiopharmaceuticals that target Aβ plaques
Version 2 2024-06-04, 08:06Version 2 2024-06-04, 08:06
Version 1 2017-08-04, 10:51Version 1 2017-08-04, 10:51
journal contribution
posted on 2024-06-04, 08:06authored byJL Hickey, S Lim, David HayneDavid Hayne, BM Paterson, JM White, VL Villemagne, P Roselt, D Binns, C Cullinane, CM Jeffery, RI Price, KJ Barnham, PS Donnelly
One of the pathological hallmarks of Alzheimer's disease is the presence of amyloid-β plaques in the brain and the major constituent of these plaques is aggregated amyloid-β peptide. New thiosemicarbazone-pyridylhydrazine based ligands that incorporate functional groups designed to bind amyloid-β plaques have been synthesized. The new ligands form stable four coordinate complexes with a positron-emitting radioactive isotope of copper, (64)Cu. Two of the new Cu(II) complexes include a functionalized styrylpyridine group and these complexes bind to amyloid-β plaques in samples of post-mortem human brain tissue. Strategies to increase brain uptake by functional group manipulation have led to a (64)Cu complex that effectively crosses the blood-brain barrier in wild-type mice. The new complexes described in this manuscript provide insight into strategies to deliver metal complexes to amyloid-β plaques.