Heterocyclic molecules for biomedical imaging and therapeutic applications
Probes which target diffuse and fibrillar forms of amyloid beta (Aβ) are described. These probes demonstrate high initial brain penetration and facile clearance from non-targeted regions. The agents can be used to image amyloid quantitatively for monitoring efficacy of Aβ-modifying therapeutics and assist in premortem diagnosis of Alzheimer's disease (AD). Disclosed probes can bind Aβ aggregates of preformed Aβ 1-42 fibrils in vitro and can be used to image fibrillar and diffuse plaques ex vivo in brain sections. Disclosed probes can be used to determine Aβ burden in early stages of AD. These probes can be used for multimodality imaging of Aβ. F-AI-187 (1 μM) can detect Aβ plaques in brain sections of APP/PS1 mice. F-AI-187 (10 μM) can detect Aβ plaques in the frontal lobe in a brain section of a patient with confirmed AD. Some probes can be used for fluorescence imaging of plaque.
1. A compound or a pharmaceutically acceptable salt thereof selected from the group consisting of
or a pharmaceutically acceptable salt thereof.
2. A gold nanoparticle conjugated to the compound according to claim 1 .
3. A method of imaging distribution of amyloid beta in a sample or a subject, comprising:
administering the compound or a pharmaceutically acceptable salt thereof according to claim 1 to the sample or subject wherein the compound or pharmaceutically acceptable salt thereof comprises a radionuclide; and
subjecting the sample or subject to PET or SPECT scanning.
4. A method of imaging cardiac systemic amyloidosis in a subject, comprising administering an imaging effective amount of the compound or a pharmaceutically acceptable salt thereof according to claim 1 to the subject, and imaging systemic amyloidosis in the subject by PET or SPECT scanning.
5. A complex comprising:
the compound or a pharmaceutically acceptable salt thereof according to claim 1 ; and
a gold nanoparticle.
6. The compound or a pharmaceutically acceptable salt thereof according to claim 1 , Wherein the compound is
7. The compound or a pharmaceutically acceptable salt thereof according to claim 6 , wherein the F is 18 F.
8. The compound or a pharmaceutically acceptable salt thereof according to claim 1 , wherein the F is 18 F.