Composition of orthopedic knee implant and the method for manufacture thereof

• US 20170071744A1
• Filed: 09/14/2016
• Published: 03/16/2017
• Est. Priority Date: 09/15/2015
• Status: Abandoned Application

• Current Assignee: Lalitha Kuppuswamy, Sulzhan Bali
• Original Assignee: Lalitha Kuppuswamy, Sulzhan Bali
• Inventors: Bali, Sulzhan, Kuppuswamy, Lalitha
• Application Number:
  US15/265,566
• Publication Number:
  US 20170071744A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61F 2/30771 applied in original prostheses, e.g. holes or grooves
• CPC Class Codes: A61F 2/30942 for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques
• CPC Class Codes: A61F 2/38 for elbows or knees
• CPC Class Codes: A61F 2002/30962 using stereolithography
• CPC Class Codes: A61F 2002/3097 using laser
• CPC Class Codes: A61F 2310/00023 Titanium or titanium-based alloys, e.g. Ti-Ni alloys
• CPC Class Codes: A61F 2310/00089 Zirconium or Zr-based alloys
• CPC Class Codes: A61F 2310/00095 Niobium or Nb-based alloys
• CPC Class Codes: A61L 2400/12 Nanosized materials, e.g. nanofibres, nanoparticles, nanowires, nanotubes; Nanostructured surfaces
• CPC Class Codes: A61L 2400/18 Modification of implant surfaces in order to improve biocompatibility, cell growth, fixation of biomolecules, e.g. plasma treatment
• CPC Class Codes: A61L 2430/02 for reconstruction of bones; weight-bearing implants
• CPC Class Codes: A61L 27/047 Other specific metals or alloys not covered by A61L27/042 - A61L27/045 or A61L27/06
• CPC Class Codes: A61L 27/06 Titanium or titanium alloys
• 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 27/56 Porous materials, e.g. foams or sponges

Abstract

The present invention discloses a composition of a knee implant comprising biomaterials such as combination of Ti—Nb—Zr alloy and tantalum to support osseointegration. The present invention further discloses a method of manufacturing customized patient-specific knee implant using 3D printing technology to suit the patient. The method involves the use of high energy source such as fiber laser or electron-beam. The base plate is mounted on the CNC. The energy source creates a melt pool on the base plate and the energy source is fed with a biomaterial in the form of wire or powder. The biomaterial is deposited on the base plate layer by layer, which solidifies in the melt pool of the base plate. The knee implant thus fabricated suits the elastic modulus of the bone and is useful as customized implant in patient undergoing replacement surgery.

Claims

1. A composition of a knee implant for a patient undergoing replacement surgery, the knee implant comprising:

a. tantalum at a concentration of 30% to 60%; and

b. a Ti—

Nb—

Zr alloy at the concentration of 40% to 70%.

2. The composition as claimed in claim 1, wherein the surface of the implant in contact with a bone is made of tantalum and the surface of the implant not in contact with the bone is made of Ti—

Nb—

Zr alloy.

3. A method for manufacture of a knee implant, wherein the method uses an additive manufacturing technology or 3-Dimentional (3D) printing technology, the method comprises the steps of:

a. mounting a base plate on a Computer Numerical Control (CNC) table in a vacuum chamber;

b. mounting a high energy source such as a micro-plasma torch or a laser beam on a vertical Z axis of the CNC table such that the energy source creates a melt pool on the base plate;

c. feeding the energy source with a biomaterial in the form of a wire or a powder or a combination of both;

d. allowing the biomaterial to melt from the energy source and depositing the melted biomaterial on the base plate layer by layer and allowing the layers to solidify in the melt pool of the base plate;

e. continuing the movement of melt pool and deposition by simultaneously moving the vertical energy source and the CNC table to obtain an optimum configuration of the knee implant;

f. stopping the deposition of the biomaterial when about 500 to 750 microns of the bearing surface is yet to be deposited in case of femoral component; and

g. in-situ surface hardening by initiating the deposition again after triggering the flow of a gas or ion source such as oxygen and/or nitrogen into the melt pool and also after applying a suitable bias, where necessary, to an implant being deposited.

4. The method as claimed in claim 3, wherein the vacuum chamber is evacuated to ensure that the oxygen content is less than 1 ppm (parts per million) so as to eliminate oxidation of the biomaterial.

5. The method as claimed in claim 3, wherein the energy source is flexible in movement within the axis and the capacity of the energy source is maintained at 1 to 2 kW (Kilo Watt) for plasma torch or 500 W for cw fiber laser or 20 kW peak for pulsed laser.

6. The method as claimed in claim 3, wherein in-situ surface hardening of the implant is achieved by introducing nanopowder selected from a group comprising titanium dioxide (TiO2), titanium nitride (TiN), titanium carbide (TiC), tantalum pentoxide (Ta2O5), or tantalum nitride (TaN) into the melt pool.

7. The method as claimed in claim 3, wherein the biomaterial is a combination of Ti—

Nb—

Zr alloy and tantalum.

8. The method as claimed in claim 3, wherein the rate of deposition of the biomaterial varies between 50 gms per hour to 500 gms per hour.

9. The method as claimed in claim 3, wherein the surface of the implant in contact with a bone is electrochemically oxidized to create multiple oxide nanotubes such that increasing the porosity and promoting osseointegration by traversing or scanning of laser beam on one or more porous parts of the implant prior to electrochemical oxidation.

10. The method as claimed in claim 3, wherein the porosity of the implant is altered through space-holder-technique by adding sodium chloride or ceramic oxide to the melt pool of the base plate such that porosity of the implant achieved is 100 to 700 microns.

11. The method as claimed in claim 3, wherein the elastic modulus of the implant is matched with that of the bone by varying the porosity of the implant and the biomaterial.

12. A method for selection of customized and patient-specific knee implant, the method comprises the steps of:

a. subjecting a damaged knee of a patient to a Computer Tomography (CT) scanning;

b. converting the CT scan data to a Standard Template Library (STL) file of the knee and designing a knee implant based on this data to fit the damaged knee with minimal bone chipping;

c. checking the physical model of the knee implant for approval by a surgeon with respect to size and configuration of the knee implant;

d. manufacturing a metal knee implant for the approved physical model by using additive manufacturing technology; and

e. fixing the metal knee implant into the patient along with one or more patient-specific instruments manufactured along with the implant.

13. The method as claimed in claim 12, wherein the physical model of the knee implant is prepared using acrylonitrile butadiene styrene plastic.

14. The method as claimed in claim 12, wherein the knee implant is patient specific resulting in accurate fixation with minimal bone chipping.