IP Library Granted Patent US 7,709,631
Granted Patent B2
US 7,709,631 · App. 11/700,241 · Granted May 4, 2010

Oxidized microbial cellulose and use thereof

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Quick Facts
Patent No.
US 7,709,631
App. No.
11/700,241
Granted
May 4, 2010
Kind
B2
Abstract

This application describes a bioresorbable biocellulose suitable for medical and surgical applications. In particular, the invention describes periodate oxidized microbial cellulose that can be produced to have any mechanical and degradation profile, depending on the desired application of the oxidized cellulose.

Claims (19)

1. A method of making a bioresorbable oxidized biocellulose comprising (i) producing microbial cellulose, (ii) pre-soaking the biocellulose in an aqueous solution containing an electrolyte at a concentration is in the range of 0.001 M to 1.0 M for 30 minutes to 24 hours, and (iii) oxidizing the microbial cellulose with a solution of sodium meta-periodate in the presence of the solution of step (ii); wherein the electrolye is NaCl.

2. The method of claim 1 , wherein the microbial cellulose is produced by Acetobacter xylinum .

3. The method of claim 1 , wherein the desired degree of oxidation is achieved by varying a factor selected from the group consisting of periodate concentration, periodate solution volume, periodate:cellulose ratio, reaction temperature, reaction duration, and a combination thereof.

4. The method of claim 3 wherein the molarity of periodate ranges from 0.005M to 1.0M.

5. The method of claim 3 wherein the ratio of periodate to cellulose ranges from 0.05 to 10.

6. The method of claim 3 wherein the temperature is between 5° C. and 50° C.

7. The method of claim 3 wherein the oxidation of step (iii) is reacted for 30 minutes to 24 hours.

8. The method of claim 1 , wherein the oxidized biocellulose is dried by a method selected from the group consisting of at least one of air-drying, oven drying, manually dehydration, solvent dehydration, drying over a desiccant, drying under vacuum, lyophilization, and supercritical fluid drying.

9. The method of claim 8 wherein the oxidized biocellulose is solvent dehydrated with acetone, methanol, ethanol, 1-propanol, iso-propanol, 1-butanol, 2-butanol, tetrahydrofuran, or glycerol.

10. The method of claim 8 wherein the oxidized biocellulose is solvent dehydrated with methanol or acetone followed by exchange with supercritical CO 2 .

11. The method of claim 8 wherein the material is placed in a chamber at a temperature ranging from 20° C. to 100° C.

12. A method for making a bioresorbable medical material comprising (i) producing a microbial cellulose, (ii) pre-soaking the microbial cellulose in an aqueous solution containing NaCl in a concentration in the range of 0.001 M to 1.0 M for 30 minutes to 24 hours, and (iii) oxidizing the microbial cellulose with a solution of sodium meta-periodate in the presence of the solution of step (ii), whereby a bioresorbable medical material is made.

13. The method of claim 12 , wherein the medical material is selected from the group consisting of sutures, hemostats, wound coverings, implantable tissue substitutes, tissue engineering matrices, or adhesion prevention devices.

14. The method of claim 12 , wherein the medical material is used for repair and/or regeneration of a musculoskeletal tissue, a neurological tissue; cardiovascular tissue, abdominal tissue, bladder neck suspension, gastroplasty, hernia repair, gastrointestinal closure, guided tissue regeneration for a dental application, or a bulking agent for plastic or reconstructive surgery.

15. The method of claim 14 , wherein the neurological tissue comprises dura.

16. The method of claim 1 , wherein the biocellulose is pre-soaked for 3 hours.

17. The method of claim 1 , wherein the biocellulose after the step of oxidizing has a suture pull-out strength of 5.31±0.44 N.

18. The method of claim 1 , wherein the electrolyte concentration is in the Range of 0.1 to 0.5 M.

19. The method of claim 1 , wherein the biocellulose is pre-soaked for 6 hours.

Assignments (6)
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF ASSIGNOR PREVIOUSLY RECORDED ON REEL 039177 FRAME 0235. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNORS INTEREST. Recorded Sep 7, 2016
From: SYNTHES USA PRODUCTS, LLC
To: DEPUY SYNTHES PRODUCTS, INC.
Reel/Frame 039937/0696 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2016
From: SYNTHES USA, LLC
To: DEPUY SYNTHES PRODUCTS, INC.
Reel/Frame 039177/0235 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2014
From: ELLIOT CAPITAL INVESTMENTS III, LTD.
To: SYNTHES USA PRODUCTS, LLC
Reel/Frame 033227/0223 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2012
From: XYLOS CORPORATION
To: ELLIOT CAPITAL INVESTMENTS III, LTD.
Reel/Frame 029120/0401 →
SECURITY AGREEMENT Recorded Jul 26, 2011
From: XYLOS CORPORATION
To: ARGENT CAPITAL INVESTMENTS III, LTD.; FCA INVESTMENT COMPANY; JANSHEN, JOHN; MERCURIUS BELEGGINGSMAATSCHAPPIJ BV; PARTICIPATIEMAATSCHAPPIJ AVANTI LIMBURG BV; STIMEX PARTICIPATIEMAATSCHAPPIJ BV; VROMEN, FRITS F.; ROEST, C.A.W.; JONGEN, C.; WANG, JONAS C.T.; DUTHIE, ANGUS M.; PIETRUSKI, JOHN M.; MCNULTY, MARK S.
Reel/Frame 026653/0650 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2007
From: HARRIS, JEREMY J.; SERAFICA, GONZALO; DAMIEN, CHRISTOPHER J.; NONNENMANN, HEATHER R.
To: XYLOS CORPORATION
Reel/Frame 019087/0291 →