IP Library › Granted Patent US 9,186,190
Granted Patent B2
US 9,186,190 · App. 13/498,436 · Granted Nov 17, 2015

Functionalized nanodiamond reinforced biopolymers

Inventors: Gongyao Zhou (Wilmington, DE); Peter I. Lelkes (Cherry Hill, NJ); Yury Gogotsi (Ivyland, PA); Vadym Mochalin (Philadelphia, PA)
Assignee: Drexel University
A61B17/866A61L31/125A61L31/128A61B17/864A61L2400/12
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Quick Facts
Patent No.
US 9,186,190
App. No.
13/498,436
Granted
Nov 17, 2015
Kind
B2
Abstract

The present invention includes a composition for implantation in a patient, comprising surface-functionalized nanodiamonds and at least one biodegradable biocompatible polymer. The present invention also includes a surgical fixation device for use in a patient.

Claims (29)

1. A nanocomposite material comprising poly-L-lactic acid (PLLA) and 1-10% by weight of octadecylamine-surface-functionalized nanodiamonds (ND-ODA), wherein ND-ODA has the formula of

and wherein the Young's modulus of the nanocomposite material is between 5.1 and 8.0 GPa.

2. The nanocomposite material of claim 1 , wherein the ND-ODA are prepared by peptide bond formation between octadecylamine and a carboxylate group on the surface-functionalized nanodiamonds.

3. The nanocomposite material of claim 1 , further comprising a composition comprising at least one bioactive agent selected from the group consisting of a bone healing drug, growth factor, bone cell, bone stem cell, antibiotic, and anti-inflammatory drug.

4. The nanocomposite material of claim 1 , wherein the Meyer's hardness of the nanocomposite material is between 0.20 and 0.51 GPa.

5. The nanocomposite material of claim 1 , wherein there is no phase separation of ND-ODA and PLLA.

6. A surgical fixation screw, comprising:

an interconnective porous shell, wherein said shell comprises a nanocomposite material comprising poly-L-lactic acid (PLLA) and 1-10% by weight of octadecylamine-surface-functionalized nanodiamonds (ND-ODA), wherein ND-ODA has the formula of

and wherein the Young's modulus of the nanocomposite material is between 5.1 and 8.0 GPa, and

a hollow core within said shell, wherein said hollow core is closed on the posterior end of said screw and open on the anterior end of said screw.

7. The surgical fixation screw of claim 6 , wherein said hollow core is optionally filled with a composition comprising at least one bioactive agent selected from the group consisting of a bone healing drug, growth factor, bone cell, bone stem cell, antibiotic, and anti-inflammatory drug.

8. The surgical fixation screw of claim 6 , wherein said posterior end is tapered with respect to said anterior end.

9. The surgical fixation screw of claim 8 , wherein said screw has full-length taper.

10. The surgical fixation screw of claim 6 , wherein said anterior end is without head.

11. The surgical fixation screw of claim 6 , wherein said posterior end is rounded and blunt.

12. The surgical fixation screw of claim 6 , wherein said shell has controllable varying coarseness, whereby phase of said nanocomposite material around said hollow core is coarser than phase of said nanocomposite material on outside surface of said screw.

13. The surgical fixation screw of claim 12 , wherein said controllable varying coarseness is achieved through injection molding.

14. A method of performing an orthopedic surgery procedure in a patient, comprising the steps of:

inserting a surgical fixation screw in at least one orifice of a bone or tissue of said patient, wherein said screw comprises:

an interconnective porous shell, wherein said shell comprises a nanocomposite material comprising poly-L-lactic acid (PLLA) and 1-10% by weight of octadecylamine-surface-functionalized nanodiamonds (ND-ODA), wherein ND-ODA has the formula of

and wherein the Young's modulus of the nanocomposite material is between 5.1 and 8.0 GPa, and

a hollow core within said shell, wherein said hollow core is closed on the posterior end of said screw and open on the anterior end of said screw, and

filling said hollow core of said screw with a composition comprising at least one bioactive agent selected from the group consisting of a bone healing drug, growth factor, bone cell, bone stem cell, antibiotic, and anti-inflammatory drug.

15. The method of claim 14 , wherein said posterior end is tapered with respect to said anterior end.

16. The method of claim 15 , wherein said screw has full-length taper.

17. The method of claim 14 , wherein said anterior end is without head.

18. The method of claim 14 , wherein said posterior end is rounded and blunt.

19. The method of claim 14 , wherein said shell has controllable varying coarseness, whereby phase of said nanocomposite material around said hollow core is coarser than phase of said nanocomposite material on outside surface of said screw.

20. The method of claim 19 , wherein said controllable varying coarseness is achieved through injection molding.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 5, 2012
From: ZHOU, GONGYAO; LELKES, PETER I.; GOGOTSI, YURY; MOCHALIN, VADYM
To: DREXEL UNIVERSITY
Reel/Frame 028493/0662 →
Continuity (2)
Provisional Application 61248202 · Oct 2, 2009
Related Publication 20120271361A1 · Oct 25, 2012