Methods for making encapsulated stent-grafts

• US 7,306,756 B2
• Filed: 06/21/2004
• Issued: 12/11/2007
• Est. Priority Date: 03/10/1995
• Status: Expired due to Fees

• Current Assignee: Bard Peripheral Vascular Incorporated (Becton, Dickinson & Co)
• Original Assignee: Bard Peripheral Vascular Incorporated (Becton, Dickinson & Co)
• Inventors: Banas, Christopher E., Edwin, Tarun J., McCrea, Brendan
• Primary Examiner(s): Johnson; Christina
• Assistant Examiner(s): Daniels; Matthew J.
• Application Number:
  US10/873,514
• Publication Number:
  US 20040232588A1
• Time in Patent Office: 1,268 Days
• Field of Search: 264/249, 264/266, 264/273, 264/294, 264/229, 264/230, 623/901
• US Class Current: 264/229
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/82 Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents stent-grafts for tubular structures of the body other than blood vessels A61F2/04; stent-grafts for blood vessels A61F2/07; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95; for closing wounds, or holding wounds closed A61B17/04 - A61B17/115; dilators A61M29/00
• 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: A61L 2400/16 Materials with shape-memory or superelastic properties
• CPC Class Codes: A61L 27/507 for artificial blood vessels apparatus for applying cells on a blood vessel prosthesis A61F2/062
• CPC Class Codes: A61L 31/048 obtained by reactions only involving carbon-to-carbon unsaturated bonds A61L31/041 takes precedence
• CPC Class Codes: A61L 31/10 Macromolecular materials
• CPC Class Codes: B29C 55/005 characterised by the choice of materials
• CPC Class Codes: B29C 55/22 of tubes B29C61/08 takes precedence
• CPC Class Codes: B29K 2027/18 PTFE, i.e. polytetrafluorethene , e.g. ePTFE, i.e. expanded polytetrafluorethene
• CPC Class Codes: C08L 27/18 Homopolymers or copolymers or tetrafluoroethene
• CPC Class Codes: Y10S 623/901 Method of manufacturing prosthetic device

Abstract

A method for making an encapsulated stent-graft having an essentially tubular configuration with a central longitudinal lumen and having a first diameter and a second diameter, wherein the first diameter is larger than the second diameter. The stent-graft may include a self-expanding stent and a first and second tube of biocompatible material between which the stent is positioned. The stent-graft may also include an interlayer member between the first and second tube. The method generally includes applying pressure and heat to a stent-graft assembly to form a monolithic layer of biocompatible material around the stent.

Claims

1. A method for making an encapsulated stent-graft, the stent-graft comprising a self-expanding stent having an essentially tubular configuration with a central longitudinal lumen and having a first diameter and a second diameter, wherein the first diameter is larger than the second diameter, comprising the steps of:

placing a first tube of biocompatible material over a mandrel;

manipulating said stent from said first diameter to said second diameter;

concentrically engaging said stent about said first tube at said second diameter;

positioning an interlayer member about said stent;

concentrically engaging a second tube of biocompatible material about said interlayer member, said stent and said first tube, forming a stent-graft assembly;

applying pressure to said assembly by winding a layer of tape over said second tube to compress said assembly against said mandrel; and

heating said assembly, wherein said first tube is joined to said second tube through openings in the wall of said stent, forming a monolithic layer of biocompatible material that applies a constraining force on said stent, preventing said stent from expanding to said first diameter, the monolithic layer of biocompatible material being radially deformable to release said constraining force on said stent.

2. The method according to claim 1, wherein the biocompatible material in said first and second tubes comprises seamless expanded polytetrafluoroethylene having a node-fibril microstructure.

3. The method according to claim 2, wherein at least one of said first and second tubes is initially unsintered.

4. The method according to claim 2, wherein said node-fibril microstructure of said first and second tubes contains fibrils having a parallel orientation with respect to the longitudinal axis of the stent.

5. The method according to claim 2, wherein said node-fibril microstructure of said first and second tubes contains fibrils having a perpendicular orientation with respect to the longitudinal axis of the stent.

6. The method according to claim 1, wherein said stent is comprised of shape memory alloy having an Austenite phase and a Martensite phase, the manipulating step further comprising cooling said stent to a temperature below the martensitic transformation temperature thereof.

7. The method according to claim 1, wherein said stent is comprised of shape memory alloy having an Austenite phase and a Martensite phase, and wherein the manipulating step is performed at a temperature above the martensitic transformation temperature of the stent.

8. The method according to claim 2, wherein said interlayer member comprises a pair of unsintered rings of expanded polytetrafluoroethylene.

9. The method according to claim 8, wherein said positioning step comprises wrapping unsintered films of expanded polytetrafluoroethylene concentrically about opposing ends of said stent to create said rings, such that the node-fibril microstructure of said films contains fibrils having a perpendicular orientation with respect to the longitudinal axis of said stent.

10. The method according to claim 2, wherein at least one of said first and second tubes is initially fully sintered.

11. The method according to claim 10, wherein said positioning step comprises wrapping unsintered films of expanded polytetrafluoroethylene concentrically about opposing ends of said stent to create a pair of rings, such that the node-fibril microstructure of said films contains fibrils having a perpendicular orientation with respect to the longitudinal axis of said stent.

12. The method according to claim 4, wherein said positioning step comprises concentrically engaging at least one pre-formed tubular ring of unsintered expanded polytetrafluoroethylene about said stent, such that the node-fibril microstructure of said ring contains fibrils having a parallel orientation with respect to the longitudinal axis of said stent.

13. The method according to claim 4, wherein at least one of said first and second tubes is initially fully sintered.

14. The method according to claim 13, wherein said positioning step comprises concentrically engaging at least one pre-formed tubular ring of unsintered expanded polytetrafluoroethylene about said stent, such that the node-fibril microstructure of said ring contains fibrils having a parallel orientation with respect to the longitudinal axis of said stent.

15. A method for making an encapsulated stent-graft, the stent-graft comprising a self-expanding stent having an essentially tubular configuration with a central longitudinal lumen and having a first diameter and a second diameter, wherein the first diameter is larger than the second diameter, comprising the steps of:

placing a first tube of biocompatible material over a mandrel;

concentrically engaging said stent about said first tube at said first diameter;

positioning an interlayer member about said stent;

concentrically engaging a second tube of biocompatible material about said interlayer member, said stent and said first tube, forming a stent-graft assembly;

applying pressure to said assembly by winding a layer of tape over said second tube to compress said assembly against said mandrel;

heating said assembly, wherein said first tube is joined to said second tube through openings in the wall of said stent, forming a monolithic layer of biocompatible material; and

manipulating said assembly to said second diameter, wherein a constraining force in the form of a delivery sheath is applied to said assembly, preventing said assembly from expanding to said first diameter.

16. The method according to claim 15, wherein the biocompatible material in said first and second tubes comprises seamless expanded polytetrafluoroethylene having a node-fibril microstructure.

17. The method according to claim 16, wherein at least one of said first and second tubes is initially unsintered.

18. The method according to claim 16, wherein said node-fibril microstructure of said first and second tubes contains fibrils having a parallel orientation with respect to the longitudinal axis of the stent.

19. The method according to claim 16, wherein said node-fibril microstructure of said first and second tubes contains fibrils having a perpendicular orientation with respect to the longitudinal axis of the stent.

20. The method according to claim 15, wherein said stent is comprised of shape memory alloy having an Austenite phase and a Martensite phase, the manipulating step further comprising cooling said stent to a temperature below the martensitic transformation temperature thereof.

21. The method according to claim 15, wherein said stent is comprised of shape memory alloy having an Austenite phase and a Martensite phase, and wherein the manipulating step is performed at a temperature above the martensitic transformation temperature of the stent.

22. The method according to claim 16, wherein said interlayer member comprises a pair of unsintered rings of expanded polytetrafluoroethylene.

23. The method according to claim 22, wherein said positioning step comprises wrapping unsintered films of expanded polytetrafluoroethylene concentrically about opposing ends of said stent to create said rings, such that the node-fibril microstructure of said films contains fibrils having a perpendicular orientation with respect to the longitudinal axis of said stent.

24. The method according to claim 16, wherein at least one of said first and second tubes is initially fully sintered.

25. The method according to claim 24, wherein said positioning step comprises wrapping unsintered films of expanded polytetrafluoroethylene concentrically about opposing ends of said stent to create a pair of rings, such that the node-fibril microstructure of said films contains fibrils having a perpendicular orientation with respect to the longitudinal axis of said stent.

26. The method according to claim 18, wherein said positioning step comprises concentrically engaging at least one pre-formed tubular ring of unsintered expanded polytetrafluoroethylene about said stent, such that the node-fibril microstructure of said ring contains fibrils having a parallel orientation with respect to the longitudinal axis of said stent.

27. The method according to claim 18, wherein at least one of said first and second tubes is initially fully sintered.

28. The method according to claim 27, wherein said positioning step comprises concentrically engaging at least one pre-formed tubular ring of unsintered expanded polytetrafluoroethylene about said stent, such that the node-fibril microstructure of said ring contains fibrils having a parallel orientation with respect to the longitudinal axis of said stent.

29. A method for making an encapsulated stent-graft, the stent-graft comprising a self-expanding stent having an essentially tubular configuration with a central longitudinal lumen and having a first diameter and a second diameter, wherein the first diameter is larger than the second diameter, comprising the steps of:

placing a first tube of biocompatible material over a mandrel;

positioning an interlayer member about said first tube;

manipulating said stent from said first diameter to said second diameter;

concentrically engaging said stent about said first tube and said interlayer member at said second diameter;

concentrically engaging a second tube of biocompatible material about said stent, said interlayer member and said first tube, forming a stent-graft assembly;

applying pressure to said assembly by winding a layer of tape over said second tube to compress said assembly against said mandrel; and

heating said assembly, wherein said first tube is joined to said second tube through openings in the wall of said stent, forming a monolithic layer of biocompatible material that applies a constraining force on said stent, preventing said stent from expanding to said first diameter, the monolithic layer of biocompatible material being radially deformable to release said constraining force on said stent.

30. A method for making an encapsulated stent-graft, the stent-graft comprising a self-expanding stent having an essentially tubular configuration with a central longitudinal lumen and having a first diameter and a second diameter, wherein the first diameter is larger than the second diameter, comprising the steps of:

placing a first tube of biocompatible material over a mandrel;

positioning an interlayer member about said first tube;

concentrically engaging said stent about said first tube at said first diameter;

concentrically engaging a second tube of biocompatible material about said stent, said interlayer member and said first tube, forming a stent-graft assembly;

applying pressure to said assembly by winding a layer of tape over said second tube to compress said assembly against said mandrel;

heating said assembly, wherein said first tube is joined to said second tube through openings in the wall of said stent, forming a monolithic layer of biocompatible material; and

manipulating said assembly to said second diameter, wherein a constraining force in the form of a delivery sheath is applied to said assembly, preventing said assembly from expanding to said first diameter.