IP Library Granted Patent US 12685800
Granted Patent B2
US 12685800 · App. 17/914,502 · Granted Jul 21, 2026

Hydrogel compositions and preparation thereof

Inventors: Victor Ramos Perez (Llica de Vall, ES); Mario Lopez Moya (Llica de Vall, ES)
Assignee: IBERHOSPITEX, S.A.
A61L26/008A61L26/0014A61L26/0066A61L2300/206A61L2300/404
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Quick Facts
Patent No.
US 12685800
App. No.
17/914,502
Granted
Jul 21, 2026
Kind
B2
Abstract

The present invention refers to a composition comprising: a) a crosslinked hydrophilic polymer containing amino functional groups, and b) a swelling agent, wherein the crosslinked hydrophilic polymer a) is obtainable by reacting a hydrophilic polymer containing amino functional groups with a crosslinking agent which contains at least two epoxide functional groups. The invention also refers to a method for preparing said composition and uses thereof in medical applications.

Claims (51)

1 . A composition comprising:

a) a crosslinked hydrophilic polymer obtained by reacting a hydrophilic polymer containing secondary or tertiary amino functional groups with a crosslinking agent which contains at least two epoxide functional groups, wherein the hydrophilic polymer containing secondary or tertiary amino functional groups is a random copolymer of Formula I,

wherein

n and m are independently selected from an integer from 100 to 50,000;

R 1 , R 2 , R 4 , R 5 , R 6 and R 8 are each independently selected from —H, —OH and C 1 -C 6 alkyl optionally substituted by at least one hydroxyl group;

R 3 is selected from:

(i) —OH,

(ii) N-lactam,

(iii) —COOR 9 , wherein R 9 is selected from —H, C 1 -C 6 alkyl optionally substituted by at least one group selected from a hydroxyl group and —(CH 2 —CH 2 —O) p —H wherein p is an integer from 1 to 10,

(iv) —CONR 10 R 11 , wherein R 10 and R 11 are independently selected from —H, C 1 -C 6 alkyl optionally substituted by at least one group selected from a hydroxyl group and (CH 2 —CH 2 —O) p —H wherein p is an integer from 1 to 10,

(v) —NHCOR 12 , wherein R 12 is selected from C 1 -C 6 alkyl optionally substituted by at least one group selected from a hydroxyl group and —(CH 2 —CH 2 —O) p —H wherein p is an integer from 1 to 10, and

(vi) —(CH 2 —CH 2 —O) p —H wherein p=1-10; and

R 7 is selected from:

(i) —COOR 13 , wherein R 13 is C 1 -C 6 alkyl substituted by at least one amino functional group,

(ii) —CONR 14 R 15 , wherein R 14 is C 1 -C 6 alkyl substituted by at least one amino functional group and R 15 is selected from —H, C 1 -C 6 alkyl optionally substituted by at least one group selected from a hydroxyl group, an amino functional group and —(CH 2 —CH 2 —O) p —H wherein p=1-10, and

(iii) —NHCOR 14 , wherein R 14 is selected from C 1 -C 6 alkyl optionally substituted by at least one group selected from a hydroxyl group and —(CH 2 —CH 2 —O) p —H wherein p is an integer from 1 to 10; and

b) a swelling agent.

2 . The composition according to claim 1 , wherein the molar percentage of the monomers in the hydrophilic polymer that contain an amino functional group is from 1% to 60%.

3 . The composition according to claim 1 , wherein the hydrophilic polymer containing amino functional groups is selected from poly(2-hydroxyethyl methacrylate-co-2-aminoethyl methacrylate), poly(acrylamide-co-2-aminoethyl methacrylate), poly(2-hydroxyethyl methacrylate-co-2-dimethylaminoethyl methacrylate), poly(1-vinylpyrrolidone-co-2-dimethylaminoethyl methacrylate), poly(acrylamide-co-2-dimethylaminoethyl methacrylate), poly(vinyl alcohol-co-n-[3-(dimethylamino)propyl] methacrylamide), and poly(acrylamide-co-3-dimethylaminopropyl methacrylamide).

4 . The composition according to claim 1 , wherein the crosslinking agent is selected from C 4 -C 12 alkyl diepoxides, di-glycidyl ethers, tri-glycidyl ethers, poly-glycidyl ethers, and tris(2,3-epoxypropyl) isocyanurate.

5 . The composition according to claim 4 , wherein the crosslinking agent is selected from the group consisting of ethyleneglycol diglycidyl ether, glycerol diglycidyl ether, butanediol diglycidyl ether, diethylene glycol diglycidyl ether, hexanediol diglycidyl ether, neopentyl glycol diglycidyl ether, glycerol triglycidyl ether, glycerol polyglycidyl ether, trimethololpropane polyglycidyl ether, pentaerythritol polyglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, and combinations thereof.

6 . The composition according to claim 1 , wherein the swelling agent is selected from the group consisting of water, monohydric alcohols, polyhydric alcohols, ethoxylated polyhydric alcohols, methyl ethers of ethoxylated polyhydric alcohols, and combinations thereof.

7 . The composition according to claim 1 , wherein the swelling agent is selected from the group consisting of propylene glycol, dipropylene glycol, polyethylene glycol of molecular weight between 200 and 600, glycerol, diglycerol, triglycerol, tetraglycerol, and combinations thereof.

8 . The composition according to claim 1 , further comprising at least one compound selected from:

c) a modifying polymer compatible with the swelling agent, and

d) an active pharmaceutical ingredient.

9 . The composition according to claim 8 , comprising:

a) from 5% to 50% by weight of cross-linked hydrophilic polymer containing amino functional groups,

b) from 40% to 70% by weight of swelling agent, and optionally at least one further compound selected from

c) from 1% to 10% by weight of modifying polymer compatible with the swelling agent, and

d) from 0.5% to 25% by weight of active agent.

10 . The composition according to claim 8 , comprising an antimicrobial.

11 . The composition according to claim 1 , wherein the composition is a hydrogel.

12 . The composition according to claim 1 , wherein the composition is transparent and, optionally, colorless.

13 . The composition according claim 1 , wherein the composition is adhesive.

14 . The composition according to claim 1 , wherein:

the hydrophilic polymer containing amino functional groups is selected from poly(2-hydroxyethyl methacrylate-co-2-aminoethyl methacrylate), poly(acrylamide-co-2-aminoethyl methacrylate), poly(2-hydroxyethyl methacrylate-co-2-dimethylaminoethyl methacrylate), poly(1-vinylpyrrolidone-co-2-dimethylaminoethyl methacrylate), poly(acrylamide-co-2-dimethylaminoethyl methacrylate), poly(vinyl alcohol-co-n-[3-(dimethylamino)propyl] methacrylamide) and poly(acrylamide-co-3-dimethylaminopropyl methacrylamide);

the crosslinking agent is selected from C 4 -C 12 alkyl diepoxides, di-glycidyl ethers, tri-glycidyl ethers, poly-glycidyl ethers, and tris(2,3-epoxypropyl) isocyanurate; and

the swelling agent is selected from the group consisting of water, monohydric alcohols, polyhydric alcohols, ethoxylated polyhydric alcohols, methyl ethers of ethoxylated polyhydric alcohols, and combinations thereof.

15 . The composition according to claim 14 , wherein the composition is an adhesive, transparent and, optionally, colorless, hydrogel.

16 . The composition according to claim 10 , wherein the antimicrobial is chlorhexidine gluconate.

17 . A skin-contact medical article selected from the group consisting of a wound-dressing, a securement dressing, a sealant, a plaster and a patch, the article comprising the composition according to claim 1 .

18 . A method for obtaining a composition according to claim 1 , the method comprising:

(i) mixing in the presence of a volatile solvent: a) a hydrophilic polymer containing secondary or tertiary amino functional groups, b) a swelling agent, c) a crosslinking agent which contains at least two epoxide functional groups,

(ii) subjecting the mixture at a temperature from 40 to 100° C. during 1 to 24 h, and optionally

(iii) placing in an aqueous solution for swelling.

19 . A skin-contact medical article selected from the group consisting of a wound-dressing, a securement dressing, a sealant, a plaster and a patch, comprising the composition according to claim 14 .

20 . A method for obtaining a composition according to claim 8 , the method comprising:

(i) mixing in the presence of a volatile solvent: a) a hydrophilic polymer containing secondary or tertiary amino functional groups, b) a swelling agent, c) a crosslinking agent which contains at least two epoxide functional groups, and optionally at least one further compound selected from d) a modifying polymer compatible with the swelling agent, and e) an active pharmaceutical ingredient,

(ii) subjecting the mixture at a temperature from 40 to 100° C. during 1 to 24 h, and optionally

(iii) placing in an aqueous solution for swelling.