IP Library › Granted Patent US 9,561,248
Granted Patent B2
US 9,561,248 · App. 14/324,889 · Granted Feb 7, 2017

Method for rehydrating polysaccharide particles

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,561,248
App. No.
14/324,889
Granted
Feb 7, 2017
Kind
B2
Abstract

Tissue and other body structures may be protected using a hydrated composition made from free-flowing substantially collagen-free rehydratable polysaccharide particles and rehydratable polysaccharide sponges. Rehydration of the particles without clumping may be carried out be dispersing the particles in a biocompatible water-miscible polar dispersant such as ethanol and combining the dispersion with sufficient aqueous solvent for the particles to convert them to a cohesive hydrogel. The hydrated composition may assist in returning an injured, inflamed or surgically repaired surface to a normal state, e.g., through one or more healing mechanisms such as modulation of an inflammatory response, phagocytosis, mucosal remodeling, reciliation or other full or partial restoration of normal function.

Claims (29)

1. A method for converting a dry powdered composition to a gel, which method comprises:

a) dispersing free-flowing polysaccharide particles in a biocompatible water-miscible polar dispersant that is a sufficiently poor solvent for the particles so that the mixture of particles and dispersant will not form a true solution, and

b) combining the resulting dispersion with sufficient aqueous solvent for the particles to convert them to a cohesive hydrogel,

wherein the water-miscible polar dispersant comprises water, ethanol, isopropanol or acetone.

2. A method according to claim 1 wherein the water-miscible polar dispersant is water and the aqueous solvent for the particles is acidified water.

3. A method according to claim 1 wherein the water-miscible polar dispersant comprises ethanol.

4. A method according to claim 1 wherein the water-miscible polar dispersant comprises isopropanol or acetone.

5. A method according to claim 1 wherein the polysaccharide particles have been crosslinked.

6. A method according to claim 1 wherein the polysaccharide particles have been crosslinked using a separate crosslinking agent.

7. A method according to claim 1 wherein the polysaccharide particles are uncrosslinked.

8. A method according to claim 1 wherein the polysaccharide particles are substantially collagen-free.

9. A method according to claim 1 wherein the polysaccharide particles are substantially a single polysaccharide.

10. A method according to claim 1 wherein the polysaccharide particles are a blend of two or more polysaccharides.

11. A method according to claim 1 wherein the polysaccharide comprises cellulose, chitosan, agar, alginate, carrageenan, chitin, chondroitin sulfate, dextran, galactomannan, glycogen, hyaluronic acid, starch or mixture thereof.

12. A method according to claim 1 wherein the polysaccharide comprises an oxidized polysaccharide or salt.

13. A method according to claim 1 wherein the polysaccharide comprises carboxymethylcellulose.

14. A method according to claim 1 wherein the polysaccharide is substantially only carboxymethylcellulose.

15. A method according to claim 1 wherein the polysaccharide comprises chitosan.

16. A method according to claim 15 wherein the chitosan is unmodified.

17. A method according to claim 1 wherein the polysaccharide comprises a mixture of chitosan and another polysaccharide.

18. A method according to claim 1 wherein the polysaccharide comprises a mixture of carboxymethylcellulose and chitosan.

19. A method according to claim 1 comprising forming the cohesive hydrogel without visible clumps of unhydrated polysaccharide.

20. A method according to claim 1 further comprising injecting or spraying a layer of the cohesive hydrogel onto mucosal tissue.

21. A method according to claim 1 further comprising injecting or spraying the cohesive hydrogel into an opening, recess, passageway or joint in a limb.

22. A method according to claim 1 further comprising injecting or spraying the cohesive hydrogel into an opening, recess, passageway or joint in a spinal column.

23. A method for converting a dry powdered composition to a gel, which method comprises:

a) dispersing free-flowing polysaccharide particles in a biocompatible water-miscible polar dispersant, and

b) combining the resulting dispersion with sufficient aqueous solvent for the particles to convert them to a cohesive hydrogel,

wherein the polysaccharide particles have been dehydrothermally crosslinked.