Modified alginates for anti-fibrotic materials and applications
Covalently modified alginate polymers, possessing enhanced biocompatibility and tailored physiochemical properties, as well as methods of making and use thereof, are disclosed herein. The covalently modified alginates are useful as a matrix for coating of any material where reduced fibrosis is desired, such as encapsulated cells for transplantation and medical devices implanted or used in the body.
1. A method of treating a disease or disorder in a human or animal patient, comprising:
implanting or transplanting into a human or animal patient a composition comprising capsules having a mean diameter between 1 mm and 8 mm, inclusive, wherein the capsules comprise a biological material encapsulated in an ionically crosslinked singularly modified alginate polymer of Formula I:
wherein,
X is oxygen, sulfur, or NR 4 ,
R 1 is
wherein z is an integer from 0 to 5, n is an integer from 1 to 12, m is an integer from 3 to 16, R a is independently selected from alkoxy, amino, alkylamino, dialkylamino, hydroxy, or substituted alkyl,
wherein
Y 1 and Y 2 independently are hydrogen or —PO(OR 5 ) 2 , or
Y 2 is absent, and Y 1 , together with the two oxygen atoms to which Y 1 and Y 2 are attached form a cyclic structure as shown in Formula II
wherein
R 2 and R 3 are, independently, hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, alkylthio, substituted alkylthio, arylthio, substituted arylthio, carbonyl, substituted carbonyl, carboxyl, substituted carboxyl, amino, substituted amino, amido, substituted amido, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, substituted heterocyclic, amino acid, poly(ethylene glycol), peptide, or polypeptide group, or
R 2 and R 3 , together with the carbon atom to which they are attached, form a 3- to 8-membered unsubstituted or substituted carbocyclic or heterocyclic ring, and
R 4 and R 5 are, independently, hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, alkylthio, substituted alkylthio, arylthio, substituted arylthio, carbonyl, substituted carbonyl, carboxyl, substituted carboxyl, amino, substituted amino, amido, substituted amido, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, substituted heterocyclic, amino acid, poly(ethylene glycol), peptide, or polypeptide group.
2. The method of claim 1 , wherein X is O.
3. The method of claim 1 , wherein R 1 is selected from the group consisting of:
wherein, R a is hydroxy.
4. The method of claim 1 , wherein R 1 is selected from the group consisting of:
5. The method of claim 1 , wherein Y 1 and Y 2 are hydrogen.
6. The method of claim 1 , wherein the mean diameter of the capsules is between 1.5 mm to 8 mm.
7. The method of claim 6 , wherein the mean diameter of the capsules is between 1.5 mm to 6 mm.
8. The method of claim 1 , wherein the biological material is cells.
9. The method of claim 8 , wherein the cells comprise pancreatic islet cells.
10. The method of claim 1 , wherein the disease or disorder is diabetes.
11. The method of claim 1 , wherein the disease or disorder is diabetes and the biological material is pancreatic islet cells.
12. The method of claim 1 , wherein R 1 is
13. The method of claim 1 , wherein R 1 is
14. The method of claim 1 , wherein R 1 is
15. The method of claim 1 , wherein R 1 is
16. The method of claim 1 , wherein R 1 is
17. The method of claim 1 , wherein R 1 is