Stent having an expandable web structure

• US 7,887,578 B2
• Filed: 11/16/2006
• Issued: 02/15/2011
• Est. Priority Date: 09/05/1998
• Status: Expired due to Fees

• Current Assignee: Abbott International Enterprises Ltd. (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Laboratories Limited (Abbott Laboratories Incorporated)
• Inventors: Schneider, Ralph
• Primary Examiner(s): Bui; Vy Q
• Application Number:
  US11/601,475
• Publication Number:
  US 20070135891A1
• Time in Patent Office: 1,552 Days
• Field of Search: 623/1.15, 606/198, 606/108, 606/195
• US Class Current: 623/1.15
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91508 the meander having a difference in amplitude along the band
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2210/0076 multilayered, e.g. laminated structures
• CPC Class Codes: A61F 2230/0054 V-shaped

Abstract

A stent comprises a tubular flexible body composed of a web structure that is expandable from a contracted delivery configuration to a deployed configuration and that comprises neighboring web patterns of alternating concavities extending circumferentially and adjoined by X-shaped transition sections. The web pattern may comprise either arcuate struts interconnected by bends, or a plurality of substantially straight sections with the transition sections formed by the junctions between pairs of adjacent bends of opposite curvatures.

Claims

1. A stent comprising:

a tubular body having a longitudinal axis, and having a proximal, a distal end, and a lumen extending longitudinally therebetween, and a wall having areas thereof removed to define a web structure configured for circumferential expansion from a contracted delivery configuration to an expanded deployed configuration;

the web structure comprising a plurality of web patterns interconnected with one another at a plurality of X-shaped transition sections, and that are arranged so that the web patterns are situated side-by-side along the longitudinal length of the tubular body, with each web pattern also extending circumferentially around the wall;

at least one of said interconnected web patterns comprising,

at least three webs joined end-to-end so as to extend between a pair of X-shaped transition sections with no other X-shaped transition sections between the pair of X-shaped transition sections;

said three webs that are joined end-to-end being joined by two bends so that the bends permit the three webs to be generally foldable between the pair of X-shaped transition sections when said tubular body is in the contracted delivery configuration, and then unfolded when said tubular body is expanded to the deployed configuration; and

said at least three webs each comprising a plurality of web sections, with one of the web sections being angled relative to one other web section when the stent is in the expanded deployed configuration.

2. The stent of claim 1, wherein the X-shaped transition sections are disposed at an angle relative to a longitudinal axis of the stent.

3. The stent of claim 2, wherein each X-shaped transition section is formed by a junction between the upward end of a bend interconnecting two struts with a downward end of a bend interconnecting two other struts.

4. The stent of claim 1, wherein the X-shaped transition sections connect one out of every three pairs of adjacent bends around the circumference of the web patterns.

5. The stent of claim 4, wherein the X-shaped transition sections extending from one end of each web pattern are staggered relative to the X-shaped transition sections extending from an opposite end of the web pattern.

6. The stent of claim 1, wherein the stent is formed using a material so that the stent is balloon expandable when deployed.

7. The stent of claim 6, wherein the stent is manufactured from a deformable material.

8. The stent of claim 7, wherein the deformable material is chosen from the group consisting of stainless steel and titanium.

9. The stent of claim 1, wherein the stent is formed using a shape memory alloy so that the stent is self-expanding when deployed.

10. The stent of claim 1, wherein the stent is manufactured from a polymeric material, a metallic material, or a metal alloy.

11. The stent of claim 10, wherein the polymeric material is a poly-L-lactid material.

12. The stent of claim 10, wherein the metallic material is stainless steel, titanium, platinum, tantalum, or a combination thereof.

13. The stent of claim 10, wherein the metal alloy is a titanium alloy, a platinum alloy, a nickel-titanium alloy, a platinum-nickel-titanium alloy, a tantalum alloy, a cobalt-chromium alloy, or a combination thereof.

14. The stent of claim 1, wherein at least a portion of the stent comprises a radiopaque material.

15. The stent of claim 14, wherein the stent is formed using a shape memory alloy so that the stent is self-expanding when deployed.

16. The stent of claim 1, wherein the web structure comprises a therapeutic coating.

17. The stent of claim 16, wherein the therapeutic coating is selected from the group consisting of therapeutic agents that retard thrombus formation, therapeutic agents that retard restenosis, and therapeutic agents for systemic or local delivery via the blood system.

18. The stent of claim 1, wherein the stent is manufactured as a single layer structure.

19. The stent of claim 1, wherein the stent is manufactured as a multi-layer structure.

20. A stent comprising:

a tubular body having a longitudinal axis, and having a proximal end, a distal end, and a lumen extending longitudinally therebetween, and a wall having areas thereof removed to define a web structure configured for circumferential expansion from a contracted delivery configuration to an expanded deployed configuration;

the web structure comprising a plurality of web patterns interconnected with one another at a plurality of X-shaped transition sections, and that are arranged so that the web patterns are situated side-by-side along the longitudinal length of the tubular body, with each web pattern also extending circumferentially around the wall;

at least one of said interconnected web patterns comprising,

at least three webs joined end-to-end so as to extend between a pair of X-shaped transition sections with no intervening X-shaped transition sections between the pair of X-shaped transition sections;

said three webs that are joined end-to-end being joined by two bends so that the bends permit the three webs to be generally foldable between the pair of X-shaped transition sections when said tubular body is in the contracted delivery configuration, and then unfolded when said tubular body is expanded to the deployed configuration;

each web comprising three web sections, with one of the web sections being a central section joined at opposite ends thereof to two lateral sections, each of the lateral sections being angled relative to the central section when the stent is in the expanded deployed configuration.

21. The stent of claim 20, wherein each of the struts comprises three substantially straight sections.

22. The stent of claim 20, wherein each X-shaped transition section is disposed at an angle relative to a longitudinal axis of the stent.

23. The stent of claim 22, wherein each X-shaped transition section is formed by a junction between an upward end of a bend interconnecting two struts with a downward end of a bend interconnecting two other struts.

24. The stent of claim 20, wherein the X-shaped transition sections connect one out of every three pairs of adjacent bends around the circumference of the web pattern.

25. The stent of claim 24, wherein the X-shaped transition sections extending from one end of each web pattern are staggered relative to the X-shaped transition sections extending from an opposite end of the web pattern.

26. The stent of claim 20, wherein the stent is formed using a material so that the stent is balloon expandable when deployed.

27. The stent of claim 26, wherein the stent is manufactured from a deformable material.

28. The stent of claim 27, wherein the deformable material is chosen from the group consisting of stainless steel and titanium.

29. The stent of claim 20, wherein the stent is manufactured from a polymeric material, a metallic material, or a metal alloy.

30. The stent of claim 29, wherein the polymeric material is a poly-L-lactid material.

31. The stent of claim 29, wherein the metallic material is stainless steel, titanium, platinum, tantalum, or a combination thereof.

32. The stent of claim 29, wherein the metal alloy is a titanium alloy, a platinum alloy, a nickel-titanium alloy, a platinum-nickel-titanium alloy, a tantalum alloy, a cobalt-chromium alloy, or a combination thereof.

33. The stent of claim 20, wherein at least a portion of the stent comprises a radiopaque material.

34. The stent of claim 20, wherein the web structure comprises a therapeutic coating.

35. The stent of claim 34, wherein the therapeutic coating is selected from the group consisting of therapeutic agents that retard thrombus formation, therapeutic agents that retard restenosis, and therapeutic agents for systemic or local delivery via the blood system.

36. The stent of claim 20, wherein the stent is manufactured as a single layer structure.

37. The stent of claim 20, wherein the stent is manufactured as a multi-layer structure.