IP Library Granted Patent US 6,987,136
Granted Patent B2
US 6,987,136 · App. 10/127,947 · Granted Jan 17, 2006

Bioactive spinal implant material and method of manufacture thereof

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 6,987,136
App. No.
10/127,947
Granted
Jan 17, 2006
Kind
B2
Abstract

Bioactive spinal implant materials having optimized radiopacity, stiffness, and bioactivity properties for formulation of shaped bodies capable of withstanding large dynamic, compressive loads are provided. The invention also provides methods of making the optimized implant materials.

Claims (24)

1. An implant comprising a synthetic, bioactive spinal implant material formed from a one-paste, 0% by weight bisphenol-A-glycidyl methacrylate polymerized resin matrix comprising about 10% by weight to about 60% by weight of the total composition of the implant material, the polymerized resin matrix comprising diurethane dimethacrylate and tri-ethylene glycol dimethacrylate resins, the resin matrix further comprising silane treated borosilicate filler, the implant material having a range of radiopacity from about 30 to about 55 and a range of stiffness from about 6 GPa to about 20 GPa.

2. The implant of claim 1 wherein said filler is bioactive.

3. The implant of claim 2 wherein said filler comprises combeite.

4. The implant of claim 1 wherein the polymerized resin matrix comprises about 20% by weight to about 40% by weight of the total composition of the implant material.

5. The implant of claim 2 wherein there is about 60% by weight to about 80% by weight filler comprising the total composition of the implant material.

6. The implant of claim 1 having a range of radiopacity from about 38 to about 50 and a stiffness from about 8 GPa to about 17 GPa.

7. A synthetic spinal implant material comprising 0% by weight bisphenol-A-glycidyl methacrylate, polymerizable resin matrix comprising at least diurethane dimethacrylate and tri-ethylene glycol dimethacrylate resins and silane treated borosilicate filler, said material, when polymerized, exhibiting a radiopacity from about 30 to about 55 and a stiffness of about 6 GPa to about 20 GPa.

8. The synthetic spinal implant material of claim 7 wherein the polymerizable resin matrix comprises about 10% by weight to about 90% by weight of the total composition of the implant material.

9. The synthetic spinal implant material of claim 7 wherein the polymerizable resin matrix comprises about 20% by weight to about 40% by weight of the total composition of the implant material.

10. The synthetic spinal implant material of claim 7 wherein said filler comprises about 60% to about 80% of the total composition of the implant material.

11. The synthetic spinal implant material of claim 7 further comprising combeite.

12. A method of making a one paste synthetic spinal implant material having 0% by weight bisphenol-A-glycidyl methacrylate, comprising:

providing a blend of diurethane dimethacrylate and tri-ethylene glycol dimethacrylate;

mixing said blend with at least one filler comprising silane treated borosilicate comprising from about 22% by weight to about 24% by weight of the material, the blend of diurethane dimethacrylate and tri-ethylene glycol dimethacrylate comprising from about 30% by weight to about 40% by weight of the material; and

agitating the resultant mixture to form said implant material having, when polymerized, a radiopacity from about 30 to about 55 and a stiffness of about 6 GPa to about 20 GPa.

13. The method of claim 12 further comprising combeite.

14. The method of claim 12 wherein the filler comprises about 60% by weight to about 80% by weight of the total composition of the implant material.

15. The method of claim 12 wherein the material has a range of radiopacity of about 38 to about 50 and a range of stiffness from about 8 GPa to about 17 GPa.

16. A synthetic, bioactive spinal implant material formed from a one-paste, 0% by weight bisphenol-A-glycidyl methacrylate polymerized resin matrix comprising about 24-percent to about 28 percent by weight diurethane dimethacrylate and about 7 percent to about 9 percent by weight and tri-ethylene glycol dimethacrylate resins, about 22 percent to about 24 percent by weight silane treated borosilicate filler, and said material having a range of radiopacity from about 30 to about 55 and a range of stiffness from about 6 GPa to about 20 GPa.

17. The synthetic spinal implant material of claim 7 comprising 22% to 24% by weight of silane treated borosilicate.

18. The spinal implant material of claim 7 comprising 24% to about 28% by weight diurethane dimethacrylate and 7% to about 9% by weight tri-ethylene glycol dimethacrylate.

19. The spinal material of claim 7 comprising a one-paste system.

20. The spinal material of claim 7 having a radiopacity between about 38 to about 50 and a range of stiffness from about 8 GPa to about 17 GPa.

21. The spinal material of claim 7 wherein said polymerized material forms calcium phosphate on its surface when contacted with bodily fluid.

Assignments (10)
RELEASE OF LIEN IN INTELLECTUAL PROPERTY Recorded Jul 26, 2011
From: LB I GROUP INC.
To: ORTHOVITA, INC. (FOR ITSELF AND AS SUCCESSOR BY MERGER TO VITA LICENSING, INC. AND PARTISYN CORP.); ORTHOVITA INTERNATIONAL SERVICES, INC.; VITA SPECIAL PURPOSE CORP.
Reel/Frame 026648/0422 →
MERGER Recorded Dec 1, 2008
From: VITA LICENSING, INC.
To: ORTHOVITA, INC.
Reel/Frame 021901/0354 →
MERGER Recorded Nov 20, 2008
From: VITA SPECIAL PURPOSE CORP
To: VITA LICENSING, INC.
Reel/Frame 021890/0490 →
SECURITY AGREEMENT Recorded Aug 3, 2007
From: VITA SPECIAL PURPOSE CORP.
To: LB I GROUP INC.
Reel/Frame 019649/0291 →
RELEASE AND TERMINATION OF SECURITY INTEREST RECORDED AT REEL/FRAME NOS: 014754/0452; 014757/0714; 015398/0167; 015402/0518; 015596/0177; 015580/0887; 015603/0752; 015577/0341; 015603/0896 AND 015584/0474 (SEE DOCUMENT FOR DETAILS) Recorded Jul 30, 2007
From: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS INDENTURE TRUSTEE
To: VITA SPECIAL PURPOSE CORPORATION
Reel/Frame 019605/0382 →
TRANSFER OF GRANTEE'S (DEBTOR'S) RIGHTS UNDER CERTAIN SECURITY INTEREST AGREEMENTS TO NEW GRANTEE (SECURED PARTY) Recorded Jan 12, 2005
From: ROYALTY SECURITIZATION TRUST I
To: DEUTSCHE BANK TRUST COMPANY AMERICAS (AS INDENTURE TRUSTEE)
Reel/Frame 015584/0474 →
TRANSFER FOR GRANTEE'S (DEBTOR'S) RIGHTS UNDER CERTAIN SECURITY INTEREST AGREEMENTS TO NEW GRANTEE (SECURED PARTY) Recorded Jan 11, 2005
From: ROYALTY FINANCIAL COMPANY LLC
To: ROYALTY SECURITIZATION TRUST I
Reel/Frame 015577/0341 →
TRANSFER OF GRANTEE'S (DEBTOR'S) RIGHTS UNDER CERTAIN SECURITY INTEREST AGREEMENTS TO NEW GRANTEE (SECURED PARTY) Recorded Jan 10, 2005
From: PAUL ROYALTY FUND, L.P.
To: ROYALTY FINANCIAL COMPANY LLC
Reel/Frame 015580/0887 →
CHANGE OF NAME Recorded Nov 23, 2004
From: PAUL CAPITAL ROYALTY ACQUISITION FUND, L.P.
To: PAUL ROYALTY FUND, L.P.
Reel/Frame 015409/0413 →
SECURITY INTEREST Recorded Jun 18, 2004
From: VITA SPECIAL PURPOSE CORPORATION
To: PAUL CAPITAL ROYALTY ACQUISITION FUND, L.P.
Reel/Frame 014757/0714 →