DENDRIMER COMPOSITIONS AND METHODS FOR DRUG DELIVERY TO THE EYE
Dendrimer compositions and methods for the treatment of one or more inflammatory and/or angiogenic diseases and/or disorders of the eye include hydroxyl-terminated dendrimers complexed or conjugated with one or more active agents for the treatment or alleviation of one or more symptoms of the diseases of the eye, and/or for diagnosing the diseases and/or disorders of the eye. The dendrimers may include one or more ethylene diamine-core poly(amidoamine) (PAMAM) hydroxyl-terminated generation-4, 5, 6, 7, 8, 9, or 10 dendrimers. The active agents may be VEGFR tyrosine kinase inhibitors including sunitinib or analogues thereof. Preferably, the compositions are suitable for administration via a systemic route to target activated microglia/macrophages in retina/choroid.
1 - 33 . (canceled)
34 . A dendrimer-conjugate comprising a dendrimer conjugated to one or more receptor tyrosine kinase inhibitors,
wherein the dendrimer comprises a plurality of terminal hydroxyl groups and at least one terminal group forming an ether bond between the dendrimer and a linker,
wherein the linker is conjugated to a receptor tyrosine kinase inhibitor of the formula:
35 . The dendrimer-conjugate of claim 34 , wherein the one or more receptor tyrosine kinase inhibitors are at a concentration of between about 5% and about 20% by weight of the dendrimer-conjugate.
36 . The dendrimer-conjugate of claim 35 comprising a ratio of dendrimer to receptor tyrosine kinase inhibitor of 1:7.
37 . The dendrimer-conjugate of claim 34 , wherein the one or more receptor tyrosine kinase inhibitors are conjugated to less than 20% of all terminal hydroxyl groups on the dendrimer.
38 . The dendrimer-conjugate of claim 34 , wherein the dendrimer is a poly(amidoamine) dendrimer.
39 . The dendrimer-conjugate of claim 34 , wherein the dendrimer is a generation 4, generation 5, or generation 6 poly(amidoamine) dendrimer.
40 . The dendrimer-conjugate of claim 39 , wherein the dendrimer is a generation 4 poly(amidoamine) dendrimer.
41 . The dendrimer-conjugate of claim 34 , wherein the linker comprises polyethylene glycol.
42 . The dendrimer-conjugate of claim 34 , wherein the linker comprises triazole.
43 . The dendrimer-conjugate of claim 34 , wherein the linker comprises polyethylene glycol and triazole.
44 . The dendrimer-conjugate of claim 34 , wherein an amide bond is formed between the linker and the receptor tyrosine kinase inhibitor.
45 . The dendrimer-conjugate of claim 34 , wherein the linker-receptor tyrosine kinase inhibitor comprises a structure of the formula:
46 . The dendrimer-conjugate of claim 34 , wherein the dendrimer-conjugate is of the formula:
wherein:
D is the dendrimer;
m is an integer from 16 to 4096; and
n is an integer from 1 to 100.
47 . The dendrimer-conjugate of claim 46 , wherein:
m is an integer from 49 to 59;
n is an integer from 5 to 15; and
the sum of m and n is 64.
48 . A method of treating a disease or disorder of the eye in a subject in need thereof, the method comprising administering to the subject an effective amount of the dendrimer-conjugate of claim 34 .
49 . The method of claim 48 , wherein the disease or disorder of the eye is selected from the group consisting of age-related macular degeneration (AMD), retinitis pigmentosa, optic neuritis, uveitis, retinal detachment, temporal arteritis, retinal ischemia, arteriosclerotic retinopathy, hypertensive retinopathy, retinal artery blockage, retinal vein blockage, diabetic retinopathy, macular edema, retinal neovascularization, and choroidal neovascularization.
50 . The method of claim 48 , wherein the disease or disorder of the eye is wet AMD.
51 . The method of claim 48 , wherein the disease or disorder of the eye is diabetic macular edema.
52 . The method of claim 48 , wherein the dendrimer-conjugate is administered to the subject intravenously, subcutaneously, or orally.
53 . The method of claim 52 , wherein the dendrimer-conjugate is administered to the subject subcutaneously in an amount of about 0.5 to 100 milligrams of the dendrimer-conjugate per kilogram body weight (mg/kg) of the subject.