Medical devices including a metallic film and at least one filament

• US 7,901,447 B2
• Filed: 12/29/2004
• Issued: 03/08/2011
• Est. Priority Date: 12/29/2004
• Status: Active Grant

• Current Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Inventors: Molaei, Masoud, Correa, Beren W.
• Primary Examiner(s): Gherbi; Suzette J
• Application Number:
  US11/025,684
• Publication Number:
  US 20060142842A1
• Time in Patent Office: 2,260 Days
• Field of Search: 623 111- 135, 438/48, 428/461, 424/423, 423/461
• US Class Current: 623/1.15
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/072 Encapsulated stents, e.g. wire or whole stent embedded in lining
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61L 31/022 Metals or alloys
• CPC Class Codes: A61L 31/143 Stabilizers
• CPC Class Codes: Y10S 623/901 Method of manufacturing prosthetic device

Abstract

Medical devices, such as endoprostheses, and methods of making the devices are disclosed. The medical device can include a composite cover formed of a deposited metallic film. The cover may include one or more filaments, e.g., wires, which cooperate with the film to provide desirable mechanical properties. The wires may be integrated with the film by depositing the film over the wires.

Claims

1. An endoprosthesis, comprising:

a framework;

a deposited metallic film on the framework, the film defining first and second opposed surfaces and a thickness of less than about 50 μ

m therebetween; and

at least one metal filament separate from the framework, the at least one filament defining a length, at least a portion of the filament along its length being embedded within the metallic film between the first and second surfaces.

2. The endoprosthesis of claim 1, wherein the deposited metallic film comprises titanium and nickel.

3. The endoprosthesis of claim 1, wherein the framework and the deposited metallic film have a substantially tubular shape defining a longitudinal axis and the at least one filament extends generally along the longitudinal axis.

4. The endoprosthesis of claim 3, wherein the tubular shape of the film defines a length along the longitudinal axis and the length of the filament is at least about 30% of the length of the tubular shape of the film.

5. The endoprosthesis of claim 4, comprising a plurality of filaments each defining a length, at least a portion of each filament along its length being embedded within the metallic film between the first and second surfaces of the metallic film, each filament extending generally along the longitudinal axis, the length of each filament being at least 30% of the length of the tubular shape of the film.

6. The endoprosthesis of claim 4, wherein at least 75% of the filament along its length is embedded within the metallic film between the first and second surfaces of the metallic film.

7. The endoprosthesis of claim 4, wherein the filament, along its length, comprises a plurality of embedded portions and at least one non-embedded portion, each embedded portion being embedded within the metallic film between the first and second surfaces of the metallic film, adjacent embedded portions being spaced apart by a non-embedded portion of the filament.

8. The endoprosthesis of claim 1, wherein the at least one filament comprises an alloy comprising nickel and titanium.

9. The endoprosthesis of claim 8, wherein the metallic film and the at least one filament each have a respective tensile strength, the tensile strength of the filament being greater than the tensile strength of the metallic film.

21. An endoprosthesis according to claims 1 or 10, wherein the deposited metallic film is a tertiary alloy comprising nickel, titanium, and an additive in an amount between 0.2% and 20% by weight of the film.

22. An endoprosthesis according to claim 21, wherein the additive is chromium.

23. The endoprosthesis of claim 1, wherein the metal filament is formed of gold, platinum, stainless steel, or a shape memory metal.

25. The endoprosthesis of claim 1, wherein the metal filament has a circular cross section, is braided, or has a ribbon shape.

27. The endoprosthesis of claim 1, wherein the metal filament is a metal wire having a diameter of about 10 μ

m or less.

29. The endoprosthesis of claim 1, wherein the metal filament has a configuration that is circumferential, curved, or helical about the endoprosthesis.

31. An endoprosthesis according to claims 1 or 10, wherein the deposited metallic film has a thickness of about 4-35 μ

m.

10. An endoprosthesis, comprising:

a framework;

a cover on the framework, the cover comprising at least one deposited metallic film, the cover defining first and second opposed metallic film edges, the first and second opposed metallic film edges each defining a channel; and

at least one filament, the at least one filament extending through the channel of each opposed metallic film edge.

11. The endoprosthesis of claim 10, wherein the deposited metallic film comprises nickel and titanium.

12. The endoprosthesis of claim 10, wherein the framework and the cover have a substantially tubular shape defining a longitudinal axis and the at least one filament extends generally parallel to the longitudinal axis.

13. The endoprosthesis of claim 12, wherein the tubular shape defines a length along the longitudinal axis and the length of the filament is at least about 30% of the length of the shape.

14. The endoprosthesis of claim 10, wherein the first and second opposed edges each define at least one offset tab, the channel of each opposed edge being formed by the offset tab.

15. The endoprosthesis of claim 10, wherein the first and second opposed edges each define a plurality of channels, each channel being formed by a respective offset tab, the filament extending through at least some of the channels of each opposed edge.

16. The endoprosthesis of claim 12, wherein the framework is a stent body, at least a portion of the at least one filament and at least a portion of the stent body being secured together.

17. The endoprosthesis of claim 12, wherein the filament defines a longitudinal axis, an engagement between at least one of the channels and the filament restricting movement of the filament along its longitudinal axis with respect to the at least one of the channels.

18. The endoprosthesis of claim 10, wherein the first and second opposed edges are a first pair of opposed edges and the metallic film of the cover defines a plurality of pairs of first and second opposed edges, each edge of each pair defining at least one channel, a respective filament extending through the channel of each opposed edge of each pair.

19. The endoprosthesis of claim 18, wherein each pair of opposed edges extends generally along the longitudinal axis and each filament has a length at least about 30% of the length of the tubular shape.

20. The endoprosthesis of claim 19, wherein the first and second edges of each pair of opposed edges have at least some relative freedom of movement with respect to a circumference of the cover.

24. The endoprosthesis of claim 14, wherein the at least one filament is a suture, polymer, textile, metal, or a composite thereof.

26. The endoprosthesis of claim 10, wherein the at least one filament has a circular cross section, is braided, or has a ribbon shape.

28. The endoprosthesis of claim 10, wherein the filament is a metal wire having a diameter of about 10 μ

m or less.

30. The endoprosthesis of claim 10, wherein the filament has a configuration that is circumferential, curved, or helical about the endoprosthesis.

32. An endoprosthesis, comprising:

a framework;

a deposited metallic film on the framework, the film defining first and second opposed surfaces and a thickness of less than about 50 μ

m therebetween; and

at least one metal filament, the at least one filament defining a length, at least a portion of the filament along its length being embedded within the metallic film between the first and second surfaces

wherein the deposited metallic film is a tertiary alloy comprising nickel, titanium, and an additive in an amount between 0.2% and 20% by weight of the film.