Hydrogel drug delivery implants

Patent metadata

Field	Value
Publication number	US-2026060921-A1
Application number	US-202519258825-A
Country	US
Kind code	A1
Filing date	Jul 2, 2025
Priority date	Dec 10, 2014
Publication date	Mar 5, 2026
Grant date	—

Abstract

Materials and methods for treating a patient, optionally a patient with an eye disease, comprising providing a collection of particles that comprise a first biodegradable material that is a hydrogel or a xerogel and a therapeutic agent, with the first material, before biodegradation, having a rate of release for the therapeutic agent as measured in physiological solution, and forming a second hydrogel ex vivo or in situ on a tissue of the patient at a site of intended use, optionally at or near an eye, that at least partially coats the collection of particles. The agent is released to treat the patient.

First claim

1 . A hydrogel formed by in situ polymerization around hydrogel and/or xerogel particles, with the particles containing a therapeutic agent, said in-situ formed hydrogel enveloping and/or encapsulating the particles, wherein precursors react with each other to form the hydrogel enveloping the particles, wherein the precursors comprise two or more electrophilic functional groups or two or more nucleophilic functional groups, such that a nucleophilic functional group on one precursor may react with an electrophilic functional group on another precursor to form a covalent bond, wherein the electrophilic functional groups comprise succimide, succinimide ester, N-hydroxysuccinimide, maleimide, succinate, nitrophenyl carbonate, aldehyde, vinylsulfone, azide, hydrazide, isocyanate, diisocyanate, tosyl, tresyl, or carbonyldiimidazole and wherein the nucleophilic functional groups comprises a primary amine or a primary thiol, wherein the hydrogel and/or xerogel particles, before degradation, have a first rate of release for the therapeutic agent as measured in physiological solution, and wherein the enveloping hydrogel delays the rate of release of the therapeutic agent by no more than 20% as measured at the 50% w/w release of the therapeutic agent.

2 . The hydrogel of claim 1 wherein the particles are placed at a site in a patient and the precursors are subsequently applied to the site or wherein the particles and the precursors are mixed and the mixture is injected into a site in a patient.

3 . The hydrogel of claim 2 wherein the site is at or near an eye and wherein the therapeutic agent is controllably released from a resulting in situ hydrogel drug delivery implant for about one to about three months.

4 . The hydrogel of claim 2 wherein the applying is through a needle or cannula and wherein the particles have a diameter from about 1 to about 100 microns.

5 . The hydrogel of claim 2 wherein the precursors form an absorbable hydrogel that adheres to the site and wherein the enveloping hydrogel is biodegradable.

6 . The hydrogel of claim 2 wherein the site comprises the anterior chamber, the posterior chamber, the vitreous, the episcleral, the subconjunctival, on a surface of a cornea or a conjunctiva, on a sclera, in a sclera, beneath a sclera, or between a sclera and subconjunctiva in a site under and contacting the conjunctiva, on or under the palpebral or tarsal conjunctivam, in an eyelid, superior fornix, inferior fornix, bulbar conjunctiva, fornix conjunctiva, in the choroid, between the choroid and sclera, between the retina and choroid, or a combination of the same.

7 . The hydrogel of claim 2 wherein the mixture is applied to a site in a patient using a needle, a microneedle, a cannula, a catheter, a hollow wire, a trocar, a sprayer, and/or a syringe.

8 . The hydrogel of claim 2 wherein the hydrogel and/or xerogel particles have a first diffusivity for the therapeutic agent and wherein the enveloping hydrogel has a second diffusivity for the therapeutic agent.

9 . The hydrogel of claim 8 wherein the first diffusivity has a first rate and the second diffusivity has a second rate, wherein the second rate is from 4 times to 20 times the first rate.

10 . The hydrogel of claim 1 wherein the enveloping hydrogel is free of the therapeutic agent until such time as the therapeutic agent diffuses from the particles into the enveloping hydrogel.

11 . The hydrogel of claim 1 wherein the electrophilic precursor and/or the nucleophilic precursor comprise a polymer selected from the group consisting of polyethylene glycol, polyacrylic acid, polyvinylpyrrolidone, and block copolymers thereof, alginate, gellan, collagen, and polysaccharide.

12 . The hydrogel of claim 1 wherein the electrophilic functional groups comprise N-hydroxysuccinimidyl adipate, N-hydroxysuccinimidyl glutarate, N-hydroxysuccinimidyl succinate, N-hydroxysuccinimidyl azelate, or N-hydroxysuccinimidyl carbonate and wherein the nucleophilic functional groups comprises a primary amine.

13 . The hydrogel of claim 1 wherein the therapeutic agent has a molecular weight in a range from about 200 Da to about 400 kDa or wherein the therapeutic agent is a protein that has a molecular mass of at least about 10,000 Daltons and a sugar is associated with the protein.

14 . The hydrogel of claim 1 wherein the therapeutic agent is selected from the group consisting of a fluoroquinolone, moxifloxacin, travoprost, dexamethasone, or a vestibulotoxin.

15 . The hydrogel of any of claim 1 wherein therapeutic agent comprises a protein of at least about 1000 Da.

16 . The hydrogel of claim 1 wherein the therapeutic agent has a molecular weight in a range from about 10 kDa to about 180 kDa.

Assignees

• Incept Llc

Inventors

• Jarrett Peter
• El-Hayek Rami
• Sawhney Amarpreet S

Classifications

• A61K39/3955

  against proteinaceous materials, e.g. enzymes, hormones, lymphokines · CPC title

• A61K9/50

  Microcapsules {having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals (A61K9/2081 takes precedence; particles with a single coating comprising drug A61K9/167)} · CPC title

• A61K47/10

  Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers · CPC title

• A61K9/06 Primary

  Ointments; Bases therefor; {Other semi-solid forms, e.g. creams, sticks, gels (composition of ointments, creams or gels A61K47/00)} · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title