IP Library Granted Patent US 7,417,077
Granted Patent B2
US 7,417,077 · App. 10/333,026 · Granted Aug 26, 2008

Composition for an injectable bone mineral substitute material

Assignee: Bone Support AB
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Quick Facts
Patent No.
US 7,417,077
App. No.
10/333,026
Granted
Aug 26, 2008
Kind
B2
Abstract

The invention refers to an injectable composition for a bone mineral substitute material, which comprises a dry powder mixed with an aqueous liquid. The powder comprises a first reaction component comprising a calcium sulphate hemihydrate with the capability of being hardened to calcium sulphate dihydrate when reacting with said aqueous liquid; a second reaction component, which comprise a calcium phosphate with the capability of being hardened to a calcium phosphate cement when reacting with said aqueous liquid; and at least one accelerator for the reaction of said first and/or second reaction component with said aqueous liquid. A method of producing an injectable bone mineral substitute material is also provided, wherein the composition is mixed in a closed mixing and delivery system for delivery.

Claims (59)

1. A composition for a bone mineral substitute material comprising a dry powder, the dry powder comprising a first setting reaction component, which is a calcium sulphate hemihydrate;

a second setting reaction component, which is a calcium phosphate; and

at least one particulate accelerator for the setting reaction of both the first and the second setting reaction components, wherein the at least one accelerator for the reaction of the first setting reaction component is particulate calcium sulphate dihydrate, and the at least one accelerator for the reaction of the second setting reaction component is hardened particulate calcium phosphate cement.

2. The composition of claim 1 , wherein the calcium sulphate hemihydrate is an α-calcium sulphate hemihydrate.

3. The composition of claim 1 , wherein the calcium phosphate is a tricalcium phosphate.

4. The composition of claim 1 , wherein the particulate calcium phosphate cement has a Ca/P ratio between 1.5 and 2.

5. The composition of claim 1 , wherein the particulate calcium phosphate cement is hydroxylapatite (HA), tricalcium phosphate (TCP), or a mixture thereof.

6. The composition of claim 5 , wherein the hydroxylapatite is precipitated hydroxylapatite (PHA).

7. The composition of claim 1 , wherein the particulate calcium phosphate cement has a particle size which is less than 20 μm.

8. The composition of claim 7 , wherein the particulate calcium phosphate cement has a particle size which is less than 10 μm.

9. The composition of claim 1 , wherein the particulate calcium phosphate cement comprises 0.1 wt % to 10 wt % of the calcium phosphate.

10. The composition of claim 9 , wherein the particulate calcium phosphate cement comprises 0.5 wt % to 5 wt % of the calcium phosphate.

11. The composition of claim 1 , wherein at least one of the calcium sulfate hemihydrate or the calcium phosphate reaction component is in particulate form with a particle size of 1 μm to 100 μm.

12. The composition of claim 11 , wherein the particle size is 1 μm to 10 μm.

13. The composition of claim 3 , wherein the tricalcium phosphate is α-tricalcium phosphate.

14. The composition claim 1 , wherein the particulate calcium sulphate dihydrate is α-calcium sulphate dihydrate.

15. The composition of claim 14 , wherein the particulate calcium sulphate dihydrate has a particle size less than 1 mm.

16. The composition of claim 15 , wherein the particulate calcium sulphate dihydrate has a particle size less than 150 μm.

17. The composition of claim 16 , wherein the particulate calcium sulphate dihydrate has a particle size less than 50 μm.

18. The composition of claim 1 , wherein the particulate calcium sulphate dihydrate comprises 0.1 wt % to 10 wt % of the first reaction component.

19. The composition of claim 18 , wherein the particulate calcium sulphate dihydrate comprises 0.1 wt % to 2 wt % of the first reaction component.

20. The composition of claim 1 , wherein the calcium sulfate hemihydrate comprises 2 wt % to 80 wt % of the dry powder.

21. The composition of claim 20 , wherein the calcium sulfate hemihydrate comprises 10 wt % to 30 wt % of the dry powder.

22. The composition of claim 1 , wherein the calcium phosphate reaction component comprises 10 wt % to 98 wt % of the dry powder.

23. The composition of claim 22 , wherein the calcium phosphate reaction component comprises 70 wt % to 90 wt % of the dry powder.

24. The composition of claim 1 , further comprising a biologically active substance.

25. The composition of claim 24 , wherein the biologically active substance comprises a growth factor, an anti-cancer substance, an antibiotic, and an antioxidant, and mixtures thereof.

26. A composition for a bone mineral substitute material comprising a dry powder, the dry powder comprising

a first setting reaction component, which is a calcium sulphate hemihydrate;

a second setting reaction component, which is a calcium phosphate;

at least one accelerator for the setting reaction of the first or second setting reaction component, or both the first and the second setting reaction components, wherein the at least one accelerator is chosen from at least one accelerator for the reaction of the first setting reaction component, wherein the accelerator is particulate calcium sulphate dihydrate, and the at least one accelerator for the reaction of the second setting reaction component, wherein the accelerator is hardened particulate calcium phosphate cement; and

a biologically compatible oil to improve the injectability of the composition.

27. The composition of claim 26 , wherein the calcium sulphate hemihydrate is an α-calcium sulphate hemihydrate.

28. The composition according to claim 26 , wherein the calcium phosphate is a tricalcium phosphate.

29. The composition according to claim 26 , wherein the biologically compatible oil is vitamin E.

30. The composition according to claim 26 , wherein the biologically compatible oil comprises 0.1 wt % to 5 wt % of the composition.

31. The composition according to claim 30 , wherein the biologically compatible oil comprises 0.5 wt % to 2 wt % of the composition.

32. A composition for a bone mineral substitute material comprising

a dry powder, the dry powder comprising a first setting reaction component, which is a calcium sulphate hemihydrate;

a second setting reaction component, which is a calcium phosphate;

at least one accelerator for the setting reaction of the first or the second setting reaction component, or both the first and the second setting reaction components, wherein the at least one accelerator is chosen from at least one accelerator for the reaction of the first setting reaction component, the accelerator being a particulate calcium sulphate dihydrate, and at least one accelerator for the reaction of the second setting reaction component, the accelerator being a hardened particulate calcium phosphate cement; and

a pH reducing component to improve the injectability of the composition.

33. The composition of claim 32 , wherein the calcium sulphate hemihydrate is an α-calcium sulphate hemihydrate.

34. The composition of claim 32 , wherein the calcium phosphate is a tricalcium phosphate.

35. The composition of claim 32 , wherein the pH reducing component is ascorbic acid or citric acid.

36. The composition of claim 32 , wherein the pH reducing component comprises 0.1 wt % to 5 wt % of the composition.

37. The composition of claim 36 , wherein the pH reducing component comprises 0.5 wt % to 2 wt % of the composition.

38. A kit for use in preparing a composition for a bone mineral substitute material, said kit comprising:

(1) the composition according to claim 1 ; and

(2) optionally an aqueous liquid.

39. The composition of claim 1 , wherein the composition further comprises an aqueous liquid.

40. The composition of claim 39 , wherein the aqueous liquid comprises between 0.1 ml and 2 ml per gram of the dry powder.

41. The composition of claim 40 , wherein the aqueous liquid comprises between 0.5 ml and 1 ml per gram of the dry powder.

42. The composition according to claim 39 , wherein the aqueous liquid comprises distilled water or a balanced salt solution.

43. The composition of claim 39 , wherein the composition is contacted with the aqueous liquid and is capable of being hardened in a body fluid in vivo to a bi-phasic cement implant that with time obtains a porous structure for bone ingrowth.

44. A composition for a bone mineral substitute material comprising a dry powder, the dry powder comprising a first setting reaction component, which is a calcium sulphate hemihydrate;

a second setting reaction component, which is a calcium phosphate; and

at least one particulate accelerator for the setting reaction of both the first and the second setting reaction components, wherein the at least one accelerator for the reaction of the first setting reaction component is particulate calcium sulphate dihydrate, and the at least one accelerator for the reaction of the second setting reaction component is hardened particulate calcium phosphate cement, wherein the calcium sulphate dihydrate comprises 0.1 wt % to 10 wt % of the first reaction component.

45. A composition for a bone mineral substitute material according to claim 44 , wherein the calcium sulphate dihydrate comprises 0.1 wt % to 2 wt % of the first reaction component.

Assignments (4)
CHANGE OF NAME Recorded Sep 16, 2010
From: BONE SUPPORT NYA AB
To: BONE SUPPORT AB
Reel/Frame 025000/0076 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF ASSIGNOR FROM "BONESUPPORT AB" TO "BONE SUPPORT AB" AND ASSIGNEE FROM "BONESUPPORT NYA AB" TO "BONE SUPPORT NYA AB" PREVIOUSLY RECORDED ON REEL 024879 FRAME 0744. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNOR'S INTEREST. Recorded Sep 14, 2010
From: BONE SUPPORT AB
To: BONE SUPPORT NYA AB
Reel/Frame 024973/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2010
From: BONESUPPORT AB
To: BONESUPPORT NYA AB
Reel/Frame 024879/0744 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2003
From: LIDGREN, LARS; NILSSON, MALIN
To: BONE SUPPORT AB
Reel/Frame 014619/0562 →
Priority Claims (1)
SE 0002676 · Jul 17, 2000 · national
Continuity (1)
Related Publication 20040048947A1 · Mar 11, 2004