IP Library Granted Patent US 9,422,373
Granted Patent B2
US 9,422,373 · App. 13/487,524 · Granted Aug 23, 2016

Modified alginates for cell encapsulation and cell therapy

Inventors: Arturo J. Vegas (Cambridge, MA); Minglin Ma (Cambridge, MA); Kaitlin M. Bratlie (Ames, MA); Daniel G. Anderson (Sudbury, MA); Robert S. Langer (Newton, MA)
Assignee: Massachusetts Institute of Technology
C08B37/0084A61K9/0024A61K9/5161
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Quick Facts
Patent No.
US 9,422,373
App. No.
13/487,524
Granted
Aug 23, 2016
Kind
B2
Abstract

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 the encapsulation and transplantation of cells. Also disclosed are high throughput methods for the characterizing the biocompatibility and physiochemical properties of modified alginate polymers.

Claims (97)

1. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein:

X is NR;

R 1 is substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, substituted heterocyclic, or poly(ethylene glycol); and

Y 1 and Y 2 independently are hydrogen or —PO(OR) 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 below

wherein, when R 1 is substituted alkyl, and the substituted alkyl comprises poly(ethylene glycol), the poly(ethylene glycol) comprises a substituted heteroaryl group;

wherein R is, independently for each occurrence, hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, or substituted heterocyclic;

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, an 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;

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, and wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification, and wherein the modified alginate has a contact angle of more than 90°.

2. The modified alginate of claim 1 , wherein the modified alginate is a singularly modified alginate polymer.

3. The modified alginate of claim 1 , wherein the modified alginate is a multiply modified alginate polymer.

4. A modified alginate polymer, wherein the modified alginate is one of the following

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification.

5. The modified alginate of claim 1 , wherein more than 15% of the monomers in the modified alginate polymer are covalently modified monomers.

6. The modified alginate of claim 1 , where the modified alginate is capable of being ionically crosslinked using Ca 2+ , Ba 2+ , or Sr 2+ to form a hydrogel.

7. The modified alginate of claim 1 , wherein the modified alginate has a contact angle of more than 95°.

8. The modified alginate of claim 1 , wherein the modified alginate induces a lower foreign body response than an unmodified alginate polymer.

9. A mixture comprising the modified alginate of claim 1 and an unmodified alginate.

10. The mixture of claim 9 , wherein the modified alginate and unmodified alginate form a hydrogel, wherein the hydrogel induces a lower foreign body response than a hydrogel formed from an unmodified alginate.

11. The modified alginate of claim 1 , wherein the alginate induces a lower foreign body response in an assay comprising:

injecting the modified alginate into a laboratory animal; and

measuring the cathepsin activity induced by the modified alginate using fluorescent animal imaging.

12. The modified alginate of claim 1 , comprising one or more covalently modified monomers selected from the group consisting of

13. The modified alginate of claim 12 , comprising two or more different covalently modified monomers.

14. A hydrogel comprising a modified alginate according to claim 1 .

15. The hydrogel of claim 14 , comprising Ca 2+ , Ba 2+ , or Sr 2+ crosslinking the modified alginate.

16. A capsule comprising a hydrogel according to claim 14 and having a biological material encapsulated therein.

17. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein X is NH;

wherein Y 1 is hydrogen; wherein Y 2 is hydrogen;

wherein R 1 is —CH 2 —CH 2 —O—CH 2 —CH 2 —OH,

wherein R 8 is hydrogen and R 4 is

or

wherein R 4 is hydrogen and R 8 is

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification.

18. The modified alginate of claim 17

wherein R 8 is hydrogen, and R 4 is

or

wherein R 4 is hydrogen, and R 8 is

19. The modified alginate of claim 18 , wherein R 1 is

wherein R 4 is

20. The modified alginate of claim 19 , wherein R 1 is

wherein R 4 is

21. The modified alginate of claim 19 , wherein R 1 is

wherein R 4 is

22. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein X is oxygen;

wherein Y 1 is hydrogen; wherein Y 2 is hydrogen;

wherein R 1 is

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, and wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification.

23. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein X is N-Me;

wherein Y 1 is hydrogen; wherein Y 2 is hydrogen;

wherein R 1 is —(CH 2 —CH 2 ) 3 —NH—CH 3 ,

or

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, and wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification.

24. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein X is NH;

wherein R 1 is

wherein R 4 and R 8 are independently selected from the pairs of substituents consisting of:

(i)

(ii) both

(iii) both methyl; and

(iv)

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, and wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification.

25. The modified alginate of claim 1 , wherein the one or more covalently modified monomers comprise one or more covalently modified mannuronate monomers and one or more covalently modified guluronate monomers.

26. The modified alginate of claim 1 , wherein the modified alginate was produced from alginate isolated from an organism.

27. The modified alginate of claim 26 , wherein the organism is marine brown algae, Pseudomonas, Azotobacter, Laminaria, Macrocystis pyrifera , or Ascophyllum nodosum.

28. The hydrogel of claim 14 , wherein the hydrogel induces a lower foreign body response than a hydrogel formed from an unmodified alginate polymer.

29. The capsule of claim 16 , wherein the biological material is cells.

30. The capsule of claim 29 , wherein the cells are islet cells.

31. The capsule of claim 29 , wherein the cells are from an established cell culture line.

32. The capsule of claim 29 , wherein the cells are heterologous.

33. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein X is NH, Y 1 is hydrogen, Y 2 is hydrogen, R 1 is

and

R 4 is

34. The modified alginate of claim 33 , wherein R 1 is

35. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein:

X is NR;

R 1 is substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, or substituted heterocyclic;

Y 1 and Y 2 independently are hydrogen or —PO(OR) 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 below

wherein R 1 does not include a poly(ethylene glycol) chain;

wherein R is, independently for each occurrence, hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, or substituted heterocyclic;

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, an 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;

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification, and wherein the modified alginate has a contact angle of more than 90°.

36. A modified alginate comprising one or more covalently modified monomers defined by Formula I

wherein:

X is NR;

R 1 is substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, substituted heterocyclic, or poly(ethylene glycol);

Y 1 and Y 2 independently are hydrogen or —PO(OR) 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 below

wherein R 1 does not include a substituted phosphonyl group or an azide group;

wherein R is, independently for each occurrence, hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, aroxy, substituted aroxy, polyaryl, substituted polyaryl, C 3 -C 20 cyclic, substituted C 3 -C 20 cyclic, heterocyclic, or substituted heterocyclic;

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, an 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;

wherein the modified alginate is purified after chemical modification, wherein the purity of the modified alginate polymer as determined by 1 H NMR is at least 90%, wherein the modified alginate after purification induces a lower foreign body response than the chemically modified alginate prior to purification, and wherein the modified alginate has a contact angle of more than 90°.

37. The modified alginate of claim 1 , wherein R 1 is substituted alkyl, wherein the substituted alkyl comprises a poly(ethylene glycol), and wherein the poly(ethylene glycol) comprises a substituted heteroaryl group.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2018
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY; THE CHILDREN'S MEDICAL CENTER CORPORATION
Reel/Frame 046822/0056 →
CONFIRMATORY LICENSE Recorded Sep 27, 2012
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029045/0716 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2012
From: VEGAS, ARTURO J.; MA, MINGLIN; BRATLIE, KAITLIN M.; ANDERSON, DANIEL G.; LANGER, ROBERT S.
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 028766/0581 →
Continuity (2)
Provisional Application 61492705 · Jun 2, 2011
Related Publication 20120308650A1 · Dec 6, 2012