SUSTAINED RELEASE SILICA HYDROGEL COMPOSITES FOR TREATING OPHTHALMOLOGICAL CONDITIONS AND METHODS OF USING SAME
Some embodiments relate to a sustained release silica hydrogel composite comprising an anti-complement agent and methods of using same to treat ophthalmological conditions. The anti-complement agent may be an anti-C5 agent comprising a C5-specific aptamer.
1 . A sustained release silica hydrogel composite, the composite comprising: silica content in the range of 5-35% and anti-C5 agent in the range of 1-40%, wherein the anti-C5 agent comprises a C5-specific aptamer, in which the aptamer comprises a nucleotide sequence of fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCf CfUmGfCmG-3T (SEQ ID NO: 1), in which fC and fU=2′ fluoro nucleotides, mG and mA=2′-OMe nucleotides, all other nucleotides are 2′-OH, and 3T indicates an inverted deoxythymidine.
2 . The sustained release silica hydrogel composite of claim 1 , wherein the composite comprises silica content in the range of 5-35% and anti-C5 agent in the range of 5-40%.
3 . The sustained release silica hydrogel composite of claim 1 , wherein the composite comprises silica content in the range of 5-30% and anti-C5 agent in the range of 1-5%, 5-10%, 10-15%, 15-20%, 20-25%, or 25-30%.
4 . The sustained release silica hydrogel composite of claim 1 , wherein the composite comprises silica content in the range of 25-30% and anti-C5 agent in the range of 5-10%.
5 . The sustained release silica hydrogel composite of claim 1 , wherein the composite comprises silica content of about 27.4% and anti-C5 agent of about 8%.
6 . The sustained release silica hydrogel composite of claim 1 , wherein the composite comprises silica microparticles dispersed in silica-sol hydrogel.
7 . The sustained release silica hydrogel composite of claim 1 , wherein the composite has a 2:1 ratio, 1:1 ratio, or 1:2 ratio of silica dissolution rate to anti-C5 agent dissolution rate.
8 . The sustained release silica hydrogel composite of claim 1 , wherein the anti-C5 agent is pegylated.
9 . The sustained release silica hydrogel composite of claim 1 , wherein the anti-C5 agent is unpegylated.
10 . A syringe comprising the sustained release silica hydrogel composite of claim 1 .
11 . A method for ameliorating, treating or reducing the severity of a symptom of an ophthalmological condition in a subject in need thereof, the method comprising administering to the subject the sustained release silica hydrogel composite of claim 1 .
12 . A method for preventing or delaying the progression of an ophthalmological condition in a subject in need thereof, the method comprising administering to the subject the sustained release silica hydrogel composite of claim 1 .
13 . A method for treating or reducing the severity of an ophthalmological condition in a subject in need thereof, the method comprising administering to the subject the sustained release silica hydrogel composite of claim 1 .
14 . The method of claim 11 , wherein the ophthalmological condition is incomplete retinal pigment epithelial (RPE) and outer retinal atrophy, complete RPE and outer retinal atrophy, nascent geographic atrophy, geographic atrophy, or wet age-related macular degeneration.
15 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject by subconjunctival, retrobulbar, intracameral, sub-tenon, sub-retinal, suprachoroidal, or intravitreal injection.
16 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject by intravitreal injection.
17 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject by suprachoroidal injection.
18 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject at a dose of from about 0.3 mg/eye to about 5 mg/eye.
19 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject at a dose of about 2 mg/eye.
20 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject at a frequency in which the duration between doses is at least about three months.
21 . The method of claim 11 , wherein the sustained release silica hydrogel composite is administered to the subject at a frequency in which the duration between doses is about four months, about five months, or about six months.
22 . A formulation comprising a population of microparticles, the microparticles comprising: silica content in the range of 10-70% and anti-C5 agent in the range of 5-50%, wherein the anti-C5 agent comprises a C5-specific aptamer, in which the aptamer comprises a nucleotide sequence of fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCf CfUmGfCmG-3T (SEQ ID NO: 1), in which fC and fU=2′ fluoro nucleotides, mG and mA=2′-OMe nucleotides, all other nucleotides are 2′-OH, and 3T indicates an inverted deoxythymidine.
23 . The formulation of claim 22 , wherein the microparticles comprise silica content in the range of 60-75% and anti-C5 agent in the range of 2.5-5.0%, 5-10%, 10-15%, 15-20%, 20-25%, or 25-30%.
24 . The formulation of claim 22 , wherein the microparticles comprise silica content in the range of 60-72% and anti-C5 agent in the range of 2.5-25%.
25 . The formulation of claim 22 , wherein the microparticles comprise silica content in the range of 64-68% and anti-C5 agent in the range of 15-19%.
26 . The formulation of claim 22 , wherein the anti-C5 agent is pegylated.
27 . The formulation of claim 22 , wherein the anti-C5 agent is unpegylated.