Method of forming a nitinol stent

Patent metadata

Field	Value
Publication number	US-9849009-B2
Application number	US-201615047683-A
Country	US
Kind code	B2
Filing date	Feb 19, 2016
Priority date	Feb 23, 2012
Publication date	Dec 26, 2017
Grant date	Dec 26, 2017

Abstract

A method of a forming a hollow, drug-eluting nitinol stent includes shaping a composite wire into a stent pattern, wherein the composite wire includes an inner member, a nitinol intermediate member, and an outer member. After the composite wire is shaped into the stent pattern, the composite wire is heat treated to set the nitinol intermediate member in the stent pattern. After heat treatment, the composite wire is processed to remove the outer member and the inner member without adversely affecting the intermediate member. Openings may be provided through the intermediate member and the lumen of the intermediate member may be filled with a substance to be eluted through the openings.

First claim

What is claimed is:

1. A method of forming a stent comprising the steps of:
receiving a composite wire, wherein the composite wire comprises an inner member disposed within a lumen of an outer member, wherein the inner member is a solid Nitinol material;
after receiving the composite wire, shaping the composite wire into a stent pattern;
heat treating the composite wire in the stent pattern;
after the heat treating step, processing the composite wire such that the outer member is completely removed from around the inner member while preserving the solid inner member and the stent pattern.

2. The method of claim 1 , wherein the outer member is selected from the group consisting of tantalum, molybdenum, tungsten, niobium, rhenium, carbon, germanium, silicon and alloys thereof.

3. The method of claim 2 , wherein the outer member is tantalum.

4. The method of claim 2 , wherein the shaping step comprises forming the composite wire into a two-dimensional waveform and then wrapping the waveform around a mandrel.

5. The method of claim 1 , wherein the step of processing the composite wire such that the outer member is removed comprises exposing the composite wire to xenon difluoride gas.

6. The method of claim 1 , wherein a diameter of the inner member is up to 90% of an outer diameter of the outer member.

7. The method of claim 1 , wherein a diameter of the inner member is in the range of 0.0025 inch to 0.0100 inch.

8. The method of claim 7 , wherein an outer diameter of the outer member is in the range of 0.0030 inch to 0.0140 inch.

9. The method of claim 1 , wherein the outer member is more plastically deformable than the inner member, and wherein the outer member is sufficiently stiff to hold the inner member in the stent pattern after the shaping step and prior to the heating step.

10. The method of claim 1 , wherein the outer member is a metal or metal alloy.

11. A method of forming a stent comprising the steps of:
shaping a composite wire into a stent pattern, wherein the composite wire comprises an inner member disposed within a lumen of an outer member, wherein the inner member is a solid Nitinol material, wherein shaping step begins with the outer member in a solid state surrounding the inner member;
heat treating the composite wire in the stent pattern, wherein the outer member holds the inner member in the stent pattern during the heat treating step;
after the heat treating step, processing the composite wire such that the outer member is completely removed from around the inner member while preserving the solid inner member and the stent pattern.

12. The method of claim 11 , wherein the outer member is selected from the group consisting of tantalum, molybdenum, tungsten, niobium, rhenium, carbon, germanium, silicon and alloys thereof.

13. The method of claim 12 , wherein the outer member is tantalum.

14. The method of claim 11 , wherein the step of processing the composite wire such that the outer member is removed comprises exposing the composite wire to xenon difluoride gas.

15. The method of claim 11 , wherein a diameter of the inner member is up to 90% of an outer diameter of the outer member.

16. The method of claim 11 , wherein a diameter of the inner member is in the range of 0.0025 inch to 0.0100 inch.

17. The method of claim 16 , wherein an outer diameter of the outer member is in the range of 0.0030 inch to 0.0140 inch.

18. The method of claim 11 , wherein the outer member is more plastically deformable than the inner member, and wherein the outer member is sufficiently stiff to hold the inner member in the stent pattern after the shaping step and prior to the heating step.

19. The method of claim 11 , wherein the shaping step comprises forming the composite wire into a two-dimensional waveform and then wrapping the waveform around a mandrel.

20. The method of claim 11 , wherein the outer member is a metal or metal alloy.

Assignees

• Medtronic Vascular Inc

Inventors

• Thompson Dustin M

Classifications

• A61F2250/0068

  the pharmaceutical product being in a reservoir · CPC title

• A61F2240/001

  Designing or manufacturing processes · CPC title

• C22F1/10

  of nickel or cobalt or alloys based thereon · CPC title

• A61L31/022

  Metals or alloys · CPC title

• A61F2/88 Primary

  the wire-like elements formed as helical or spiral coils · CPC title