Method and device for treating and managing diseased ocular tissue
Abstract
A method of treating and managing diseased ocular tissue in the bulbar conjunctiva comprises providing a device comprising a plurality of microneedles arranged on a substrate contacting the device with a diseased ocular tissue region formed in the bulbar conjunctiva stroma to form a plurality of micro-injury sites therein. A device comprises a contact lens substrate comprising a substantially elliptical corneal portion and a limbus portion located radially about the corneal portion. A scleral portion is located radially about the substrate. The device is at least partially degradable and comprises a therapeutic compound. At least a portion of the scleral portion is configured to overlay, and deliver the therapeutic compound to, a diseased ocular tissue located adjacent to the cornea of a patient.
Claims
exact text as granted — not AI-modified1 . A device for treating and managing diseased ocular tissue in a patient's bulbar conjunctiva, comprising:
a substrate having a top side and an opposing underside: a plurality of microneedles positioned on the top side of the substrate; and a connector element, connected to the underside of the substrate; wherein the microneedles comprise a first material and the connector element comprises a second material, the first material being different from and degrading at a faster rate than the second material upon contact with the patient's eye; and wherein the microneedles are arranged and dimensioned such that when the substrate is brought into contact with the diseased tissue, the microneedles penetrate a diseased ocular tissue region formed in the bulbar conjunctival stroma, to produce a plurality of micro-injury sites within the diseased bulbar conjunctival stroma region, and cause release of growth factors and formation of new collagen fibrils.
2 . The device of claim 1 , wherein the substrate comprises an open central portion.
3 . The device of claim 1 , wherein the connector element comprises an elongate member allowing a user to manually bring the device into contact with the patient's eye.
4 . The device of claim 1 , wherein the first material comprises collagen.
5 . The device of claim 1 , wherein the substrate comprises a hydrogel.
6 . The device of claim 1 , wherein the substrate and the plurality of microneedles comprise different materials.
7 . A device for treating and managing diseased ocular tissue in a patient's bulbar conjunctiva, comprising:
a substrate comprising a top side and an opposing under side; a connector element connected to the underside of the substrate; a non-degraded device configuration comprising:
a plurality of a plurality of microneedles positioned on the top side of the substrate; and
a degraded device configuration comprising:
at least a portion of the plurality of the microneedles being degraded;
wherein the device is configured to transition from the non-degraded configuration to the degraded configuration after contacting the patient's eye.
8 . The device of claim 7 , wherein the plurality microneedles comprise a first material and the connector element comprises a second material, said first and second materials being different from each other.
9 . The device of claim 8 , wherein the first material degrades at a faster rate than the second material upon contacting the patient's eye.
10 . The device of claim 10 , wherein the connector element comprises an elongate member allowing a user to manually bring the device into contact with the patient's eye.
11 . The device of claim 10 , wherein the first material comprises collagen.
12 . The device of claim 7 , wherein the substrate comprises a hydrogel.
13 . The device of claim 7 , wherein the substrate and the plurality of microneedles comprise different materials.
14 . A device for treating and managing diseased ocular tissue in a patient's bulbar conjunctiva, comprising:
a substrate having a top side and an opposing underside: a plurality of microneedles positioned on the top side of the substrate; and a connector element releasably connected to the underside of the substrate.
15 . The device of claim 14 , wherein at least a portion of the plurality of microneedles comprise a material which changes shape upon contacting and absorbing patient tears.
16 . The device of claim 14 , wherein at least a portion of the plurality of microneedles comprise a material which changes size upon contacting and absorbing patient tears.
17 . The device of claim 14 , wherein at least a portion of the plurality of microneedles comprise a material which dissolves upon contacting and absorbing patient tears.Join the waitlist — get patent alerts
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