Filler composition for soft tissue augmentation and reconstructive surgery

• US 20040047892A1
• Filed: 10/23/2003
• Published: 03/11/2004
• Est. Priority Date: 11/15/2000
• Status: Abandoned Application

• Current Assignee: Abdellatif Chenite, Cyril Chaput, Eric Andre Desrosiers, Matthew Shive
• Original Assignee: Abdellatif Chenite, Cyril Chaput, Eric Andre Desrosiers, Matthew Shive
• Inventors: Desrosiers, Eric Andre, Shive, Matthew, Chaput, Cyril, Chenite, Abdellatif
• Application Number:
  US10/416,942
• Publication Number:
  US 20040047892A1
• Time in Patent Office: Days
• US Class Current: 424/423
• CPC Class Codes: A61L 27/20 Polysaccharides
• CPC Class Codes: A61L 27/24 Collagen
• CPC Class Codes: A61L 27/50 Materials characterised by their function or physical properties , e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
• CPC Class Codes: A61L 27/52 Hydrogels or hydrocolloids
• CPC Class Codes: C08L 5/08 Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof

Abstract

The present invention relates to a filler composition for soft-tissue augmentation and reconstructive surgery comprising an effective amount of an injectable thermo-gelling solution comprising 0.1 to 5.0% by weight of chitosan or collagen or a derivative thereof; and 1.0 to 20% by weight of a salt of polyol or sugar selected from the group consisting of mono-phosphate dibasic salt, mono-sulfate salt and a mono-carboxylic acid salt of polyol or sugar. The solution is stable and turns into a gel within a tem-perature range from 20 to 70° C. The gel has a cosmetically acceptable consistency for providing a mechanical support to surrounding soft tissues once injected therein. The composition can thus be used as filler for soft tissue augmentation and reconstructive surgery.

Claims

1. A filler composition for soft-tissue augmentation and reconstructive surgery comprising an injectable thermoforming solution comprising:

a) 0.1 to 5.0% by weight of chitosan or collagen or a derivative thereof; and

b) 1.0 to 20% by weight of a salt of polyol or sugar selected from the group consisting of mono-phosphate dibasic salt, mono-sulfate salt and a mono-carboxylic acid salt of polyol or sugar;

wherein said solution is stable and turns into a solid gel within a temperature range from 20 to 70°

C., said gel having a acceptable consistency for providing a mechanical support or a volume or thickness increase to surrounding soft tissues once injected therein.

2. The composition of claim 1, wherein said salt is a mono-phosphate dibasic salt of glycerol selected from the group consisting of glycerol-2-phosphate, sn-glycerol 3-phosphate and L-glycerol-3-phosphate salts.

3. The composition of claim 1, wherein said salt is a mono-phosphate dibasic salt and said polyol is selected from the group consisting of histidinol, acetol, diethylstilbestrol, indole-glycerol, sorbitol, ribitol, xylitol, arabinitol, erythritol, inositol, mannitol, and glucitol or a mixture thereof.

4. The composition of claim 1, wherein said salt is a mono-phosphate dibasic salt and said sugar is selected from the group consisting of fructose, galactose, ribose, glucose, xylose, rhamnulose, sorbose, erythrulose, deoxy-ribose, ketose, mannose, arabinose, fuculose, fructopyranose, ketoglucose, sedoheptulose, trehalose, tagatose, sucrose, allose, threose, xylulose, hexose, methylthio-ribose, methylthio-deoxy-ribulose, and a mixture thereof.

5. The composition of claim 1, wherein said salt is a mono-phosphate dibasic salt and said polyol is selected from the group consisting of palmitoyl-glycerol, linoleoyl-glycerol, oleoyl-glycerol, and arachidonoyl-glycerol, or a mixture thereof.

6. The composition of claim 1, wherein said solution is selected from the group consisting of chitosan-β

-glycerophosphate, chitosan-α

-glycerophosphate, chitosan-glucose-1-glycerophosphate, and chitosan-fructose-6-glycerophosphate.

7. The composition of claim 1, wherein said gel is formed in situ sub-cutaneously, intra-peritoneally, intramuscularly or within the substance of biological connective tissues, organ walls or parts, body conduits or cavities, eye cul-de-sac.

8. The composition of claim 1, wherein said solution comprises an additional polymer selected in a group consisting of cellulose, methyl cellulose or a derivative thereof, hydroxyalkyl cellulose or a derivative thereof, a water-soluble vinyl polymer, a poly(alkylene glycol) and a copolymer thereof, a poly(alkylene oxide) and a copolymer thereof, and a mono-functional poly(ethylene glycol), or a mixture thereof.

9. The composition of claim 1, wherein said solution comprises a water-soluble chemical agent having a pKa between 6.0 and 8.2.

10. The composition of claim 1, wherein said solution comprises a water-soluble phosphate or carbonate salt.

11. A method for producing a composition as defined in claim 1, which comprises the steps of:

a) dissolving a chitosan, collagen or a derivative thereof within an aqueous acidic solution of a pH from about 2.0 to about 5.0 to obtain an aqueous solution having a concentration of 0.1 to 5.0% by weight of a chitosan, collagen or a derivative thereof;

b) dissolving 1.0 to 20% by weight of a salt of polyol or sugar into the aqueous solution of step a) to obtain an injectable thermo-gelling solution, wherein said salt is selected from the group consisting of mono-phosphate dibasic salt, mono-sulfate salt and a mono-carboxylic acid salt, wherein said an injectable thermo-gelling solution has a concentration of 0.1 to 5.0% by weight of a chitosan, collagen or a derivative thereof, and a concentration of 1.0 to 20% by weight of a salt of a polyol or sugar, and has a pH from about 6.4 to about 7.4.

12. The method of claim 11, which further comprises after step b), a step of:

c) heating the injectable thermo-gelling solution of step b) at a solidifying temperature ranging from about 20°

C. to about 80°

C. until formation of a gel.

13. The method of claim 11, wherein a pharmaceutical agent is added to the injectable thermo-gelling solution of step b).

14. The method of claim 11, wherein said aqueous solution is prepared from at least one organic or inorganic acid selected from the group consisting of acetic acid, ascorbic acid, salicylic acid, phosphoric acid, hydrochloric acid, propionic acid, and formic acid, or a mixture thereof.

15. The method of claim 11, wherein said salt is a mono-phosphate dibasic salt of glycerol is selected from the group consisting of glycerol-2-phosphate, sn-glycerol 3-phosphate and L-glycerol-3-phosphate salts.

16. The method of claim 11, wherein said salt is a glycerophosphate salt selected from the group consisting of glycerophosphate disodium, glycerophosphate dipotassium, glycerophosphate calcium, glycerophosphate barium and glycerophosphate strontium.

17. The method of claim 11, wherein said salt is a mono-phosphate dibasic salt of a polyol, and said polyol is selected from a group consisting of histidinol, acetol, diethylstilbestrol, indoleglycerol, sorbitol, ribitol, xylitol, arabinitol, erythritol, inositol, mannitol, and glucitol, or a mixture thereof.

18. The method of claim 15, 16 or 17, wherein said salt is a mono-phosphate dibasic salt of a sugar, and said sugar is selected from a group consisting of fructose, galactose, ribose, glucose, xylose, rhamnulose, sorbose, erythrulose, deoxy-ribose, ketose, mannose, arabinose, fuculose, fructopyranose, ketoglucose, sedoheptulose, trehalose, tagatose, sucrose, allose, threose, xylulose, hexose, methylthio-ribose, methylthio-deoxy-and ribulose, or a mixture thereof.

19. The method of claim 11, wherein said salt is a mono-phosphate dibasic salt of a polyol, and said polyol is selected from the group consisting of palmitoyl-glycerol, linoleoyl-glycerol, oleoyl-glycerol, and arachidonoyl-glycerol, or a mixture thereof.

20. The method of claim 11, wherein said salt is a mono-phosphate dibasic salt and said phosphate is selected from the group consisting of a phosphate disodium, phosphate dipotassium, phosphate calcium, phosphate barium and phosphate strontium.

21. The method of claim 11, wherein said injectable thermogelling solution is kept in a stable ungelled liquid form at a temperature ranging from about 0°

C. to about 20°

C.

22. The method of claim 12, wherein the gel is a thermo-irreversible gel when the pH of said injectable thermo-gelling solution is >

6.9.

23. Use of a composition as defined in claim 1 as a filler for soft tissue augmentation and reconstructive surgery.

24. Use of a cosmetic composition as defined in claim 1 for producing biocompatible degradable materials.

31. The composition of any one of claims 1 to 10 and 25 to 30, wherein said composition is injected through a needle, catheter or trocar.

32. The composition of any one of claims 1 to 10 and 25 to 30, wherein said composition is injected during the course of an endoscopic procedure.

33. The composition of any one of claims 1 to 10 and 25 to 30, wherein said composition is injected percutaneously.

34. The composition of any one of claims 1 to 10 and 25 to 30, wherein said composition is pre-heated at a temperature between 20 and 45°

C. before being injected.

35. A method for treating urinary incontinence comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into an area of the urethral sphincter, said composition having a bulking action into said sphincter, thus treating urinary incontinence.

36. A method for breast augmentation comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a breast, said composition increasing the tissue volume of the breast.

37. A method of cosmetic treatment of wrinkles comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a soft tissue in or around the face of a patient, said composition having a cosmetically acceptable consistency for providing a mechanical support or a volume or thickness increase to surrounding soft tissues of the patient.

38. A method of load bearing tissue augmentation comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 between said load bearing tissue and a load-exerting medium.

39. A method for treating acne scars or viral pock marks comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a soft tissue underlying said scar or pock mark of a patient for increasing the volume of the soft tissue masking the scars or the pock marks.

40. A method for changing the contour of a nose of a patient comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into the soft tissue on the contour of the nose for increasing the volume of the soft tissue, thus changing the contour of the nose.

41. A method for augmenting the volume or thickness of soft-tissues comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a soft tissue.

42. A method for operating plastic corrections comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a soft tissue or a tissue cavity to create the plastic corrections.

43. A method for operating reconstructive or restorative surgeries comprising the step of injecting a composition as defined in any one of claims 1 to 10 and 25 to 30 into a soft tissue, a body cavity or conduit, an organ wall or a part thereof to create a reconstructive or restorative action.

25. A filler composition for soft-tissue augmentation and reconstructive surgery comprising an injectable thermo-forming solution comprising at least one fatty acid.

26. The filler composition of claim 25, wherein the fatty acid is selected from the group consisting of palmitate, stearate, myristate, palmitoleate, oleate, vaccenate and linoleate, or the like, and their acyclic, cyclic, heterocyclic, aromatic ester derivatives containing at least one moiety selected from the group consisting of hydroxy, acyloxy, aryloxy, amino, sulfhydryl, sulfonate, sulfate, phosphonate, phosphate, bis-, tris- and poly-phosphonates and phosphates, phosphatidyl, nucleosides, oligosaccharides, polysaccharides, and polyols, or the like.

27. The composition of claim 25, wherein said fatty acid is mixed with an appropriate metabolically absorbable liquid vehicle, to reduce viscosity and allow injectability at room temperature.

28. The composition of claim 25, wherein said fatty acid is mixed with a liquid vehicle selected from the group consisting of water, alcoholic solvents, alkylene glycols, and poly-alcohols, or the like.

29. The composition of claim 25, wherein said fatty acid is mixed with liquid vehicle selected from the group consisting of ethanol, isopropyl alcohol, ethylene glycol, and glycerol, or the like, or a mixture thereof.

30. The composition of claim 25, wherein said solution comprises at least palmitate and oleoate.