Intraocular drug delivery and filter device and methods of using same
US-10518002-B2 · Dec 31, 2019 · US
US11160908B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11160908-B2 |
| Application number | US-201916705989-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 6, 2019 |
| Priority date | Sep 6, 2013 |
| Publication date | Nov 2, 2021 |
| Grant date | Nov 2, 2021 |
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The present disclosure provides an implantable device comprising a substrate capable of capturing an intraocular target molecule and to methods of use thereof.
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The invention claimed is: 1. A method of treating an ocular disorder in a subject, the method comprising the steps of: implanting into an eye of the subject, and in contact with a fluid of the eye, a device comprising a substrate having a high affinity for a target molecule present in the eye; the substrate capturing the target molecule from the fluid; leaving the device in the eye for a period of time to reduce or alleviate one or more symptoms of the ocular disorder; and regenerating the device in situ by exposing the device to an energy source sufficient to denature and release a captured amount of the target molecule, wherein the device has a higher affinity for the target molecule compared to a corresponding denatured target molecule. 2. The method of claim 1 , wherein the substrate comprises a hollow tube. 3. The method of claim 2 , wherein the substrate comprises a plurality of hollow tubes bundled together. 4. The method of claim 1 , wherein the substrate is a solid, a porous matrix, a gel, a sheet, a membrane, a colloid, a microparticle, or a nanoparticle. 5. The method of claim 1 , wherein the substrate is incorporated into one of a glaucoma drainage device, an aqueous shunting device, an intraocular lens, and a drug delivery device. 6. The method of claim 1 , further comprising the steps of anchoring the device to a tissue of the eye. 7. The method of claim 1 , further comprising the steps of securing the substrate in one of an anterior chamber and a vitreous cavity of the eye. 8. The method of claim 1 , wherein the period of time is at least 6 months. 9. The method of claim 1 , further comprising the step of regenerating the device in situ at least twice. 10. The method of claim 1 , further comprising the step of regenerating the device in situ at least 4 times. 11. The method of claim 1 , wherein the device is coated with an antibody specific to the target molecule. 12. The method of claim 1 , wherein the substrate is treated with a chemical moiety such that the amount of the target molecule adsorbed to the surface is visible by color change. 13. The method of claim 1 , wherein the substrate does not include a polyethylene glycol-conjugated oligonucleotide.
Ocular inserts or implants · CPC title
implantable in, or in contact with, the eye, e.g. ocular inserts · CPC title
Phosphorus-containing compounds, e.g. phosphates, phosphonates · CPC title
Ceramic or ceramic-like structures, e.g. glasses · CPC title
for photoablation · CPC title
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