DENDRIMER COMPOSITIONS AND METHODS FOR DRUG DELIVERY
Dendrimer compositions and methods for the treatment of cancer or autoimmune diseases are described. The compositions include dendrimers complexed or conjugated with one or more active agents for the treatment or alleviation of one or more symptoms of cancer or autoimmune diseases. 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 immunomodulatory agents such as STING agonists, CSF1R inhibitors, PARP inhibitors, VEGFR tyrosine kinase inhibitors, MEK inhibitors, glutaminase inhibitors, TIE II antagonists, and CXCR2 inhibitors, and STING antagonists. Methods of using the dendrimer compositions to treat cancer, bone disease or inflammatory diseases are also provided.
1 - 73 . (canceled)
74 . A composition comprising a hydroxyl-terminated dendrimer conjugated to a receptor tyrosine kinase inhibitor through a linker, wherein an ether bond is formed between the linker and a terminal hydroxyl group of the dendrimer.
75 . The composition of claim 74 , wherein the receptor tyrosine kinase inhibitor is a VEGFR tyrosine kinase inhibitor or a CSF1R tyrosine kinase inhibitor.
76 . The composition of claim 75 , wherein the receptor tyrosine kinase inhibitor is a VEGFR tyrosine kinase inhibitor selected from the group consisting of sorafenib, sunitinib, pazopanib, vandetanib, axitinib, cediranib, vatalanib, dasatinib, nintedanib, and motesanib.
77 . The composition of claim 76 , wherein the receptor tyrosine kinase inhibitor is sorafenib.
78 . The composition of claim 75 , wherein the receptor tyrosine kinase inhibitor is a CSF1R tyrosine kinase inhibitor selected from the group consisting of PLX3397, PLX108-01, ARRY-382, PLX7486, BLZ945, JNJ-40346527, and GW-2580.
79 . The composition of claim 74 , wherein the hydroxyl-terminated dendrimer is a generation 4, generation 5, or generation 6 poly(amidoamine) (PAMAM) dendrimer.
80 . The composition of claim 79 , wherein the hydroxyl-terminated dendrimer is a generation 6 PAMAM dendrimer.
81 . The composition of claim 74 , wherein the linker comprises polyethylene glycol.
82 . The composition of claim 74 , wherein an amide bond is formed between the linker and the receptor tyrosine kinase inhibitor.
83 . The composition of claim 74 , wherein the dendrimer comprises the receptor tyrosine kinase inhibitor at a concentration of between 5% and 20% by weight of the dendrimer conjugate.
84 . The composition of claim 74 , wherein the hydroxyl-terminated dendrimer is a dendrimer of Formula (I):
wherein:
D is a generation 4, generation 5, or generation 6 PAMAM dendrimer;
L is one or more linking moieties or spacers;
Y is a linkage group selected from secondary amides (—CONH—), tertiary amides (—CONR—), sulfonamide (—S(O) 2 —NR—), secondary carbamates (—OCONH—, —NHCOO—), tertiary carbamates (—OCONR—, —NRCOO—), carbonate (—O—C(O)—O—), ureas (—NHCONH—, —NRCONH—, —NHCONR—, —NRCONR—), carbinols (—CHOH—, —CROH—), disulfide groups, hydrazones, hydrazides, and ethers (—O—), wherein R is an alkyl group, an aryl group, or a heterocyclic group;
X is the receptor tyrosine kinase inhibitor;
m is an integer from 16 to 4096; and
n is an integer from 1 to 100.
85 . The composition of claim 84 , wherein the one or more linking moieties or spacers comprise polyethylene glycol.
86 . The composition of claim 84 , wherein Y is a secondary amide (—CONH—).
87 . The composition of claim 84 , wherein X is a VEGFR tyrosine kinase inhibitor or a CSF1R tyrosine kinase inhibitor.
88 . The composition of claim 87 , wherein X is a VEGFR tyrosine kinase inhibitor selected from the group consisting of sorafenib, sunitinib, pazopanib, vandetanib, axitinib, cediranib, vatalanib, dasatinib, nintedanib, and motesanib.
89 . The composition of claim 88 , wherein X is sorafenib.
90 . A method of treating a cancer comprising administering to a subject in need thereof an effective amount of the composition of claim 74 .
91 . The method of claim 90 , wherein the cancer is liver cancer, breast cancer, ovarian cancer, uterine cancer, prostate cancer, testicular germ cell tumor, brain cancer, gastric cancer, esophageal cancer, lung cancer, renal cell cancer, or colon cancer.
92 . The method of claim 90 , wherein the cancer is a hepatocellular carcinoma or hepatoblastoma.
93 . A method for enhancing tumor-specific cytotoxic T cell responses in a subject having a tumor, the method comprising administering to the subject an effective amount of the composition of claim 74 .