IP Library › Granted Patent US 12,624,204
Granted Patent B2
US 12,624,204 · App. 17/898,545 · Granted May 12, 2026

Ultra-high molecular weight polymers and methods of using the same

Inventors: Cullen L. Davidson (Gainesville, FL); Wallace G. Sawyer (Gainesville, FL); Brent S. Sumerlin (Gainesville, FL); Juan M. Urueña Vargas (Gainesville, FL)
Assignee: University of Florida Research Foundation, INC.
C08L33/24A61K9/006A61K47/54A61K47/542A61K47/6903C08F220/54C08L43/00C08L53/00
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Quick Facts
Patent No.
US 12,624,204
App. No.
17/898,545
Granted
May 12, 2026
Kind
B2
Abstract

The present disclosure provides for compositions including at least one type of water-soluble polymer, methods of making the water-soluble polymer, structures having the water-soluble polymer disposed thereof, and methods of use thereof.

Claims (54)

1 . A composition comprising: an ophthalmic aqueous solution including a first water-soluble polymer, wherein the first water-soluble polymer includes a plurality of backbone units and at least one first type of a mucin-binding unit, wherein the backbone units comprise greater than 50% of the first water-soluble polymer based on molecular weight, wherein the first type of mucin-binding unit comprises of 1 unit up to 50% of the first water-soluble polymer based on molecular weight, wherein the first type of mucin-binding unit comprises monomer units, copolymers that include the monomer units, or both, wherein the monomer unit includes a boronic acid group,

wherein the first water-soluble polymer includes a second type of mucin-binding unit, wherein the second type of mucin-binding unit comprises monomer units, copolymers that include the monomer units, or both, wherein the monomer unit is selected from the group consisting of: acrylic acid, methacrylic acid, 4-vinylbenzoic acid, 4-(acrylamido)phenylboronic acid, 3-(acrylamido)phenylboronic acid, (2-(3-acrylamidopropanamido)phenyl) boronic acid (APAPBA), 2-(acrylamido)phenylboronic acid, 4-vinylphenylboronic acid, 3-vinylphenylboronic acid, 2-vinylphenylboronic acid, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, pyridyl disulfide ethyl acrylate, pyridyl disulfide ethyl acrylamido, pyridyl disulfide alkyl (e.g. ethyl) methacrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl acrylate, 2-(pyridin-2-yldisulfaneyl)ethyl acrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, or 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, N-(2-(tritylthio)ethyl) acrylamide, a monomer including one or more boronic acid groups, a monomer containing one or more disulfide-forming groups, a halogenated versions of each of these, or a derivative of any one of these or copolymer of anyone of these, wherein the first type of mucin-binding unit is different than the second type of mucin-binding unit;

wherein the first type of mucin binding unit comprises 1 functional unit to about 5% of the first water-soluble polymer based on molecular weight; wherein the second type of mucin binding unit comprises 1 functional unit to about 5% of the first water-soluble polymer based on molecular weight.

2 . The composition of claim 1 , wherein the backbone unit comprises monomer units, copolymers including the monomer units, or both the monomer units and the copolymers, wherein the monomer unit is selected from the group consisting of: an acrylamide monomer, a methacrylamide monomer, an acrylate monomer, a methacrylate monomer, a styrenic monomer, a vinyl pyridine monomer, a maleimide monomer, a maleic anhydride-derived monomer, a vinyl ester monomer, a vinyl ether monomer, a vinyl amide monomer, a vinyl amine monomer, a vinyl halide monomer, or a derivative of anyone of these.

3 . The composition of claim 1 , wherein the backbone unit comprises a monomer unit, a copolymer including the monomer unit or both, wherein the monomer unit is selected from the group consisting of: acrylamide, N,N-dimethylacrylamide, N,N-dialkylacrylamides, N-alkylacrylamides, N,N-dialkyl methacrylamides, N-alkyl methacrylamides, poly(ethlylene glycol) acrylate, poly(ethylene glycol) methacrylate, poly(ethylene glycol) acrylamide, and poly(ethylene glycol) methacrylamide.

4 . The composition of claim 1 , wherein the backbone unit is N,N-dimethylacrylamide.

5 . The composition of claim 1 , wherein the first water-soluble polymer includes a second type of mucin-binding unit, wherein the second type of mucin-binding unit comprises monomer units, copolymers that include the monomer units, or both, wherein the monomer unit is selected from the group consisting of: acrylic acid, methacrylic acid, 4-vinylbenzoic acid, 4-(acrylamido)phenylboronic acid, 3-(acrylamido)phenylboronic acid, (2-(3-acrylamidopropanamido)phenyl) boronic acid (APAPBA), 2-(acrylamido)phenylboronic acid, 4-vinylphenylboronic acid, 3-vinylphenylboronic acid, 2-vinylphenylboronic acid, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, pyridyl disulfide ethyl acrylate, pyridyl disulfide ethyl acrylamido, pyridyl disulfide alkyl (e.g. ethyl) methacrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl acrylate, 2-(pyridin-2-yldisulfaneyl)ethyl acrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, or 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, N-(2-(tritylthio)ethyl) acrylamide, a monomer including one or more boronic acid groups, a monomer containing one or more disulfide-forming groups, a halogenated versions of each of these, or a derivative of any one of these or copolymer of anyone of these, wherein the first type of mucin-binding unit is different than the second type of mucin-binding unit.

6 . The composition of claim 5 , wherein the first water-soluble polymer includes a third type of mucin-binding unit, wherein the third type of mucin-binding unit comprises monomer units, copolymers that include the monomer units, or both, wherein the monomer unit is selected from the group consisting of: acrylic acid, methacrylic acid, 4-vinylbenzoic acid, 4-(acrylamido)phenylboronic acid, 3-(acrylamido)phenylboronic acid, (2-(3-acrylamidopropanamido)phenyl) boronic acid (APAPBA), 2-(acrylamido)phenylboronic acid, 4-vinylphenylboronic acid, 3-vinylphenylboronic acid, 2-vinylphenylboronic acid, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, pyridyl disulfide ethyl acrylate, pyridyl disulfide ethyl acrylamido, pyridyl disulfide alkyl (e.g. ethyl) methacrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl acrylate, 2-(pyridin-2-yldisulfaneyl)ethyl acrylamido, 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, or 2-(pyridin-2-yldisulfaneyl)ethyl methacrylate, N-(2-(tritylthio)ethyl) acrylamide, a monomer including one or more boronic acid groups, a monomer containing one or more disulfide-forming groups, a halogenated versions of each of these, or a derivative of any one of these or copolymer of anyone of these, wherein the first type of mucin-binding unit is different than the second type of mucin-binding unit, wherein the second type of mucin-binding unit is different than the third type of mucin-binding unit monomer including one or more pyridyl disulfide groups, or a derivative of any one of these.

7 . The composition of claim 6 , wherein the first type of mucin binding unit comprises 1 functional unit to about 5% of the first water-soluble polymer based on molecular weight; wherein the second type of mucin binding unit comprises 1 functional unit to about 5% of the first water-soluble polymer based on molecular weight; wherein the third type of mucin binding unit comprises 1 functional unit to about 5% of the first water-soluble polymer based on molecular weight.

8 . The composition of claim 1 , wherein the first water-soluble polymer has a structure that is linear or non-linear, wherein the non-linear structure is selected from the group consisting of star-like, branched, hyperbranched, cyclic, graph copolymer, or bottle brush-like.

9 . The composition of claim 1 , wherein the first type of mucin binding unit is located solely at one or both terminal ends of the first water-soluble polymer.

10 . The composition of claim 1 , wherein the first water-soluble polymer is selected from the group consisting of: a block copolymer, a random copolymer, a statistical copolymer, an alternative copolymer, or a gradient copolymer.

11 . The composition of claim 10 , wherein the block copolymer is an AB diblock copolymer or an ABA triblock copolymer, optionally wherein the mucin-binding units are isolated on the A block of the AB diblock copolymer or A block of the ABA triblock copolymer.

12 . The composition of claim 1 , wherein the first water-soluble polymer has the following chemical structure:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight,

wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , and R b4 , independently of one another, are selected from: H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 ) (R 2 )(R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or a linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 , —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 )CH 2 SO 3 , —C(O)N(H)C((CH 3 ) 2 )CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, and wherein Y is C.

13 . The composition of claim 1 , wherein the first water-soluble polymer has the following chemical structure:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit c is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , R b4 , R c1 , R c2 , R c3 , and R c4 , independently of one another, can be H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 )(R 2 )(R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 —, —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 —, —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, wherein Y is C, and wherein Z is C.

14 . The composition of claim 13 , wherein unit a, unit b, and unit c are different from one another.

15 . The composition of claim 1 , wherein the first water-soluble polymer has chemical structure as shown below:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit c is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit d is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , R b4 , R c1 , R c2 , R c3 , R c4 , R d1 , R d2 , R d3 , and R d4 , independently of one another, can be H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 ) (R 2 ) (R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 —, —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 , —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, wherein Y is C, wherein Z is C, and wherein Q is C.

16 . The composition of claim 15 , wherein unit a, unit b, unit c, and unit d are different from one another.

17 . A synthetic method of making the first water-soluble polymer of claim 1 , comprising: polymerizing a backbone unit and at least one mucin-binding unit to form the first water-soluble polymer of claim 1 .

18 . A composition comprising: an ophthalmic aqueous solution including a first water-soluble polymer, wherein the first water-soluble polymer includes a plurality of backbone units and at least one first type of a mucin-binding unit, wherein the backbone units comprise greater than 50% of the first water-soluble polymer based on molecular weight, wherein the first type of mucin-binding unit comprises of 1 unit up to 50% of the first water-soluble polymer based on molecular weight, wherein the first type of mucin-binding unit comprises monomer units, copolymers that include the monomer units, or both, wherein the monomer unit includes a boronic acid group, wherein the first type of mucin binding unit is located solely at one or both terminal ends of the first water-soluble polymer.

19 . The composition of claim 18 , wherein the backbone unit comprises monomer units, copolymers including the monomer units, or both the monomer units and the copolymers, wherein the monomer unit is selected from the group consisting of: an acrylamide monomer, a methacrylamide monomer, an acrylate monomer, a methacrylate monomer, a styrenic monomer, a vinyl pyridine monomer, a maleimide monomer, a maleic anhydride-derived monomer, a vinyl ester monomer, a vinyl ether monomer, a vinyl amide monomer, a vinyl amine monomer, a vinyl halide monomer, or a derivative of anyone of these.

20 . The composition of claim 18 , wherein the backbone unit comprises a monomer unit, a copolymer including the monomer unit or both, wherein the monomer unit is selected from the group consisting of: acrylamide, N,N-dimethylacrylamide, N,N-dialkylacrylamides, N-alkylacrylamides, N,N-dialkyl methacrylamides, N-alkyl methacrylamides, poly(ethlylene glycol) acrylate, poly(ethylene glycol) methacrylate, poly(ethylene glycol) acrylamide, and poly(ethylene glycol) methacrylamide.

21 . The composition of claim 18 , wherein the backbone unit is N,N-dimethylacrylamide.

22 . The composition of claim 18 , wherein the first water-soluble polymer has the following chemical structure:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight,

wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , and R b4 , independently of one another, are selected from: H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 ) (R 2 ) (R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or a linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 —, —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 —, —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, and wherein Y is C.

23 . The composition of claim 18 , wherein the first water-soluble polymer has the following chemical structure:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit c is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , R b4 , R c1 , R c2 , R c3 , and R c4 , independently of one another, can be H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 ) (R 2 ) (R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 , —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 —, —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, wherein Y is C, and wherein Z is C.

24 . The composition of claim 23 , wherein unit a, unit b, and unit c are different from one another.

25 . The composition of claim 18 , wherein the first water-soluble polymer has chemical structure as shown below:

wherein unit a is the backbone unit and m is greater than 50% of the first water-soluble polymer based on molecular weight, wherein unit b is the first type of mucin binding unit and n is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit c is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit d is the second type of mucin binding unit and o is 1 unit to about 50% of the first water-soluble polymer based on molecular weight, wherein unit a and unit b are different from one another,

R a1 , R a2 , R a3 , R a4 , R b1 , R b2 , R b3 , R b4 , R c1 , R c2 , R c3 , R c4 , R d1 , R a2 , R a3 , and R d4 , independently of one another, can be H, —OR 1 , —NR 1 R 2 , —N + (R 1 ) 3 , —N + (R 1 ) 2 (R 2 ), —N + (R 1 ) (R 2 ) (R 3 ), —S(O) 2 R 1 , —S(O) 2 OR 1 , —S(O) 2 NR 1 R 2 , —NR 1 S(O) 2 R 2 , —NR 1 C(O)R 2 , —C(O)R 1 , —C(O)OR 1 , —C(O)NR 1 R 2 , —NR 1 C(O)OR 2 , —NR 1 C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —NR 1 S(O) 2 NR 1 R 2 , —C(O)NR 1 S(O) 2 NR 1 R 2 , catechol, a boronic acid group, and a pyridyl disulfide group, where each R 1 , R 2 , and R 3 is independently H or linear or branched C 1-18 alkyl as well as —C(O)OCH 2 CH 2 —OH, —C(O)OCH 2 CH 2 —N(CH 3 ) 2 , —C(O)OCH 2 CH 2 —N + (CH 3 ) 3 , —C(O)OCH 2 CH 2 —OSO 3 —, —C(O)OCH 2 CH 2 —OSO 3 H, —C(O)OCH 2 CH 2 —SO 3 —, —C(O)OCH 2 CH 2 —SO 3 H, and —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 , —C(O)N(H)C((CH 3 ) 2 ) CH 2 SO 3 H,

wherein one of R b1 , R b2 , R b3 , R b4 , is a boronic acid group,

wherein X is C, wherein Y is C, wherein Z is C, and wherein Q is C.

26 . The composition of claim 25 , wherein unit a, unit b, unit c, and unit d are different from one another.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2025
From: SAWYER, WALLACE GREGORY; SUMERLIN, BRENT S.; URUEÑA VARGAS, JUAN MANUEL; DAVIDSON, CULLEN LEE GARRETT
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 071373/0553 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2023
From: DAVIDSON, CULLEN L.; SAWYER, WALLACE G.; SUMERLIN, BRENT S.; VARGAS, JUAN M. UREAÑA
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
Reel/Frame 065069/0563 →
Continuity (2)
Provisional Application 63239027 · Aug 31, 2021
Related Publication 20230076717A1 · Mar 9, 2023
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