IP Library Granted Patent US 8,093,365
Granted Patent B2
US 8,093,365 · App. 12/372,598 · Granted Jan 10, 2012

Biocompatible materials containing stable complexes method of TSG-6 and hyaluronan and method of using same

Assignees: New York University; Polytechnic Institute of NYU
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Quick Facts
Patent No.
US 8,093,365
App. No.
12/372,598
Granted
Jan 10, 2012
Kind
B2
Abstract

The present invention provides a biocompatible material in the form of a solid, a water insoluble cross-linked gel or a liposome, which contains a stable complexes of TNF-stimulated gene protein (TSG-6) and hyaluronan.

Claims (25)

1. A biocompatible material in the form of a water insoluble covalently cross-linked gel, comprising:

hyaluronan (HA), as a water insoluble covalently cross-linked HA gel or mutually cross-linked with at least one other polymer in a water insoluble covalently cross-linked gel; and

TNF-stimulated gene 6 protein (TSG-6) in a stable complex with said HA, wherein said TSG-6 in said stable complex is capable of transferring heavy chains (HCs) of inter-α-inhibitor (IαI) to bound or free HA.

2. The biocompatible material of claim 1 , wherein said HA is the water insoluble covalently cross-linked HA gel to which TSG-6 is complexed.

3. The biocompatible material of claim 1 , wherein the stable complex of TSG-6 and HA is resistant to treatment with 6M guanidine HCl containing 8% lauryl sulfobetain (3-(Dodecyldimethylammonio)propanesulfonate, ZWITTERGENT®) for 30 minutes at ambient temperature or is resistant to boiling in reducing SDS-PAGE sample buffer of 0.25 M Tris pH 6.8, 2% sodium dodecylsulfate, 5% 2-mercapto ethanol, and 10% glycerol.

4. The biocompatible material of claim 1 , which is present on the surface of a solid medical device that is implantable or in-dwelling in a patient or is transiently introduced into a patient during the course of a medical procedure.

5. The biocompatible material of claim 1 , wherein said HA is mutually cross-linked with at least one other polymer in a water insoluble covalently cross-linked gel.

6. The biocompatible material of claim 1 , which is biodegradable.

7. The biocompatible material of claim 1 , wherein said stable complex of TSG-6 and HA is capable of being released in a soluble form.

8. A soluble stable complex of TSG-6 and HA that is released from the biocompatible material of claim 7 .

9. A biocompatible material in the form of a solid, comprising:

hyaluronan (HA) bound to the surface of a water insoluble solid biocompatible or pharmaceutically acceptable carrier, but not to a liposome or a water insoluble covalently cross-linked gel; and

TNF-stimulated gene 6 protein (TSG-6) in a stable complex with said HA, wherein said TSG-6 in said stable complex is capable of transferring heavy chains (HCs) of inter-α-inhibitor (IαI) to bound or free HA.

10. The biocompatible material of claim 9 , wherein said water insoluble solid biocompatible or pharmaceutically acceptable carrier is a nanoparticle.

11. The biocompatible material of claim 9 , wherein HA is bound to the surface of a solid medical device that is implantable or in-dwelling in a patient or is transiently introduced into a patient during the course of a medical procedure.

12. The biocompatible material of claim 9 , which is biodegradable.

13. The biocompatible material of claim 9 , wherein said stable complex of TSG-6 and HA is capable of being released in a soluble form.

14. The biocompatible material of claim 9 , wherein the stable complex of TSG-6 and HA is resistant to treatment with 6M guanidine HCl containing 8% lauryl sulfobetain (3-(Dodecyldimethylammonio)propanesulfonate, ZWITTERGENT®) for 30 minutes at ambient temperature or is resistant to boiling in reducing SDS-PAGE sample buffer of 0.25 M Tris pH 6.8, 2% sodium dodecylsulfate, 5% 2-mercapto ethanol, and 10% glycerol.

15. A biocompatible material in the form of a liposome, comprising:

hyaluronan (HA) bound to the surface of a liposome; and

TNF-stimulated gene 6 protein (TSG-6) in a stable complex with said HA, wherein said TSG-6 in said stable complex is capable of transferring heavy chains (HCs) of inter-α-inhibitor (IαI) to bound or free HA.

16. The biocompatible material of claim 15 , which is present on the surface of a solid medical device that is implantable or in-dwelling in a patient or is transiently introduced into a patient during the course of a medical procedure.

17. The biocompatible material of claim 15 , which is biodegradable.

18. The biocompatible material of claim 15 , wherein said stable complex of TSG-6 and HA is capable of being released in a soluble form.

19. The biocompatible material of claim 15 , wherein the stable complex of TSG-6 and HA is resistant to treatment with 6M guanidine HCl containing 8% lauryl sulfobetain (3-(Dodecyldimethylammonio)propanesulfonate, ZWITTERGENT®) for 30 minutes at ambient temperature or is resistant to boiling in reducing SDS-PAGE sample buffer of 0.25 M Tris pH 6.8, 2% sodium dodecylsulfate, 5% 2-mercapto ethanol, and 10% glycerol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2009
From: WISNIEWSKI, HANS-GEORG; BAND, PHILIP
To: NEW YORK UNIVERSITY
Reel/Frame 022697/0221 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2009
From: COWMAN, MARY K.
To: POLYTECHNIC INSTITUTE OF NYU
Reel/Frame 022702/0426 →
Continuity (2)
Provisional Application 61033204 · Mar 3, 2008
Related Publication 20090226499A1 · Sep 10, 2009