IP Library › Granted Patent US 10,765,523
Granted Patent B2
US 10,765,523 · App. 15/749,918 · Granted Sep 8, 2020

Prosthesis component and method for the production thereof

Inventors: Augusto Mayer Pujadas (Parets Del Valles, ES); Guillem Dominguez Santalo (Parets Del Valles, ES); Jose Sanahuja Clot (Parets Del Valles, ES); Francesc Xavier Gil Mur (Barcelona, ES); Miguel Punset Fuste (Barcelona, ES); Cristina Maria Caparros Vazquez (Barcelona, ES); Meritxell Molmeneu Trias (Barcelona, ES); Monica Ortiz Hernandez (Barcelona, ES)
Assignee: Zanini Auto Grup, S.A.
A61F2/3609A61F2/30A61F2/30965A61L27/06A61L27/14A61L27/16A61L27/306A61F2/3094A61F2/3662A61L2420/08A61L2430/24
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Quick Facts
Patent No.
US 10,765,523
App. No.
15/749,918
Granted
Sep 8, 2020
Kind
B2
Abstract

The prosthesis component ( 10 ), comprising a substrate ( 11 ) made of a polymeric material and a coating ( 12 ), characterized in that said coating ( 12 ) comprises titanium. The method for manufacturing the prosthesis component ( 10 ) comprising the stages of forming a polymeric substrate ( 11 ) and depositing a coating ( 12 ) on said polymeric substrate ( 11 ) comprising titanium by means of physical vapor deposition sputtering. It enables providing a prosthesis component that improves the fixation thereof, based on the formation of a bioactive layer to improve the degree of osseointegration and, therefore, the fixation thereof to the bone.

Claims (22)

1. A prosthesis component comprising a substrate made of a polymeric material and a coating, wherein said coating comprises an anchoring layer in contact with the substrate, an outer surface layer comprising titanium, and a transition layer arranged between the anchoring layer and the outer surface layer, said transition layer being made of chromium and titanium mixture.

2. The prosthesis component according to claim 1 , wherein said anchoring layer of the coating is made of chromium.

3. The prosthesis component according to claim 1 , wherein said anchoring layer has a thickness of between 10 nm and 100 nm.

4. The prosthesis component according to claim 1 , wherein said outer surface layer has a thickness of between 400 nm and 1000 nm.

5. The prosthesis component according to claim 1 , wherein said transition layer has a thickness of between 10 nm and 50 nm.

6. The prosthesis component according to claim 1 , wherein said coating has an outer roughness of between 2 and 6 μm.

7. The prosthesis component according to claim 1 , wherein said coating is deposited on the substrate by means of physical vapor deposition (PVD) sputtering.

8. The prosthesis component according to claim 1 , wherein said polymeric substrate comprises ultra high molecular weight polyethylene (UHMWPE), highly crosslinked polyethylenes (HXLPE), high density polyethylene (HDP), polyether ether ketone (PEEK), polymethylmethacrylate (PMMA), polyethylene (PE), or combinations thereof.

9. The prosthesis component according to claim 1 , wherein said polymeric substrate further comprises vitamin E.

10. A method for manufacturing said prosthesis component according to claim 1 , comprising the stages of:

forming said polymeric substrate; and

depositing said coating on said polymeric substrate by means of physical vapor deposition (PVD) sputtering, and

forming a transition layer arranged between an anchoring layer and an outer surface layer of the prosthesis component, said transition layer being made of a chromium and titanium mixture.

11. The method for manufacturing a prosthesis component according to claim 10 , further comprising a surface bioactivation treatment stage subsequent to forming and polymeric substrate.

12. The method for manufacturing a prosthesis component according to claim 11 , wherein said surface bioactivation treatment stage comprises:

chemical treatment of the component to create a layer of sodium titanate gel on the coating;

drying of said sodium titanate gel layer; and

heat treatment of the component.

13. The method for manufacturing a prosthesis component according to claim 12 , wherein said chemical treatment comprises immersing the component in a NaOH solution at a temperature of between 40° C. and 140° C. for a period of time of between 6 hours and 72 hours.

14. The method for manufacturing a prosthesis component according to claim 13 , wherein said chemical treatment further comprises immersing the component in ultra pure water after immersing the component in the NaOH solution.

15. The method for manufacturing a prosthesis component according to claim 12 , wherein said drying is carried out at a temperature of between 40° C. and 140° C. for a period of time of between 6 hours and 72 hours.

16. The method for manufacturing a prosthesis component according to claim 12 , wherein said chemical treatment is carried out for a period of time of between 60 and 300 minutes at a temperature of between 40° C. and 140° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2018
From: PUJADAS, AUGUSTO MAYER; SANTALO, GUILLEM DOMINGUEZ; CLOT, JOSE SANAHUJA; GIL MUR, FRANCES XAVIER; FUSTE, MIGUEL PUNSET; CAPARROS VAZQUEZ, CHRISTINA MARIA; TRIAS, MERITXELL MOLMENEU; HERNANDEZ, MONICA ORTIZ
To: ZANINI AUTO GRUP, S.A.
Reel/Frame 045460/0772 →
Continuity (1)
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