DENDRIMER COMPOSITIONS AND USE IN TREATMENT OF NEUROLOGICAL AND CNS DISORDERS
A dendrimer formulation, such as a PAMAM dendrimer or a multiarm PEG polymeric formulation has been developed for systemic administration to the brain or central nervous system. In the preferred embodiment, the dendrimers are in the form of dendrimer nanoparticles comprising poly(amidoamine)(PAMAM) hydroxyl-terminated dendrimers covalently linked to at least one therapeutic, prophylactic or diagnostic agent for treatment of one or more symptoms of neurodegenerative, neurodevelopmental or neurological disorders such as Rett syndrome of autism spectrum disorders. D6 generation dendrimers provide significantly enhanced uptake into areas of brain injury, providing a means for diagnosis as well as drug delivery.
1 - 23 . (canceled)
24 . A method of detecting neuroinflammation in a subject, the method comprising:
administering to the subject a composition comprising a hydroxyl-terminated poly(amidoamine)(PAMAM) dendrimer conjugated to an imaging agent,
wherein the imaging agent comprises fluorine-18 (F-18); and
detecting the imaging agent in a tissue of the central nervous system in the subject,
wherein the detected imaging agent is indicative of neuroinflammation in the subject.
25 . The method of claim 24 , wherein the PAMAM dendrimer is a generation 4, generation 5, or generation 6 dendrimer.
26 . The method of claim 25 , wherein the PAMAM dendrimer is a generation 4 dendrimer.
27 . The method of claim 24 , wherein the composition does not comprise a targeting agent.
28 . The method of claim 24 , wherein the PAMAM dendrimer is conjugated to the imaging agent via a linker comprising polyethylene glycol.
29 . The method of claim 24 , wherein the tissue of the central nervous system in the subject comprises brain tissue.
30 . The method of claim 24 , wherein the subject has a neurological or neurodegenerative disorder.
31 . The method of claim 24 , wherein the subject has a disease or disorder selected from the group consisting of multiple sclerosis, amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, and Huntington's disease.
32 . The method of claim 24 , wherein the composition is administered to the subject systemically.
33 . The method of claim 32 , wherein the composition is administered to the subject intravenously.
34 . A method of detecting neuroinflammation in a subject, the method comprising:
administering to the subject a composition comprising a hydroxyl-terminated poly(amidoamine)(PAMAM) dendrimer conjugated to an imaging agent,
wherein the imaging agent comprises a chelator and copper-64 (64Cu); and
detecting the imaging agent in a tissue of the central nervous system in the subject,
wherein the detected imaging agent is indicative of neuroinflammation in the subject.
35 . The method of claim 34 , wherein the PAMAM dendrimer is a generation 4, generation 5, or generation 6 dendrimer.
36 . The method of claim 35 , wherein the PAMAM dendrimer is a generation 4 dendrimer.
37 . The method of claim 34 , wherein the PAMAM dendrimer is conjugated to the imaging agent via a linker comprising polyethylene glycol.
38 . The method of claim 34 , wherein the chelator is selected from the group consisting of di-ethylene tri-amine penta-acetic acid (DTPA), 1,4,7,10-tetra-azacyclododecane-1,4,7,10-tetraacetic acid (DOTA), di-amine dithiol, activated mercaptoacetyl-glycyl-glycyl-glycine (MAG3), and hydrazidonicotinamide (HYNIC).
39 . The method of claim 34 , wherein the tissue of the central nervous system in the subject comprises brain tissue.
40 . The method of claim 34 , wherein the subject has a neurological or neurodegenerative disorder.
41 . The method of claim 34 , wherein the subject has a disease or disorder selected from the group consisting of multiple sclerosis, amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, and Huntington's disease.
42 . The method of claim 34 , wherein the composition is administered to the subject systemically.
43 . The method of claim 42 , wherein the composition is administered to the subject intravenously.