Self-expanding valve for the venous system

• US 20090062907A1
• Filed: 08/31/2007
• Published: 03/05/2009
• Est. Priority Date: 08/31/2007
• Status: Abandoned Application

• Current Assignee: Hosheng Tu, Rodolfo C. Quijano
• Original Assignee: Hosheng Tu, Rodolfo C. Quijano
• Inventors: Tu, Hosheng, Quijano, Rodolfo C.
• Application Number:
  US11/897,794
• Publication Number:
  US 20090062907A1
• Time in Patent Office: Days
• US Class Current: 623/1.240
• CPC Class Codes: A61F 2/01 Filters implantable into blood vessels
• CPC Class Codes: A61F 2/2415 Manufacturing methods
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2230/0026 trapezoidal
• CPC Class Codes: A61F 2230/0095 Saddle-shaped

Abstract

A venous valve device and method of formation are described to provide antegrade blood flow in the deep venous vessels of the leg or in other venous vessels of the body having incompetent or irreversibly dysfunctional valves. The venous valve device is made of a sheet of biocompatible material, comprising a longitudinal wire-frame structure that is a continuous seamless wire loop and plural anchoring mesh-lattice wing members spaced apart and connected to the base of the wire-frame structure.

Claims

1. An implantable venous device made of a sheet of biocompatible material, comprising:

a longitudinal wire-frame structure having a base, wherein the wire-frame structure is a continuous seamless wire loop, the base of the wire-frame structure being radially inwardly compressible; and

plural anchoring mesh lattice wing members spaced apart and connected to the base of the wire-frame structure, wherein each mesh lattice wing member and the wire-frame are integral parts from said sheet of biocompatible material.

2. The venous device of claim 1, wherein the wire-frame structure is mounted with at least one leaflet to provide a unidirectional fluid flow.

3. The venous device of claim 2, wherein the leaflet is made of a polymer membrane.

4. The venous device of claim 2, wherein the leaflet is a tissue leaflet.

5. The venous device of claim 2, wherein the leaflet is a decellularized tissue leaflet.

6. The venous device of claim 2, wherein the leaflet is a crosslinked tissue leaflet.

7. The venous device of claim 2, wherein the leaflet is a crosslinked tissue leaflet with a crosslinking agent of epoxy compounds.

8. The venous device of claim 2, wherein the leaflet is a crosslinked pericardium tissue leaflet.

9. The venous device of claim 2, wherein the leaflet is made of a crosslinked pericardium, wherein the pericardium is selected from a group consisting of bovine pericardium, equine pericardium, porcine pericardium, ovine pericardium, caprine pericardium, and kangaroo pericardium.

10. The venous device of claim 1, wherein the wire-frame structure comprises a filter mechanism.

11. The venous device of claim 2, wherein the leaflet is a tissue leaflet made of a process comprising steps of:

providing a tissue sheet having cells and extracellular matrix;

subjecting said sheet to a solution containing bile acid or bile salts that effect the solubilization of cell membranes of the cells present in said tissue sheet;

removing said solubilized cell membranes by flushing the tissue sheet with filtered water or saline; and

treating said tissue sheet with a crosslinking agent.

12. The venous device of claim 11, wherein the bile acid is cholic acid or deoxycholic acid.

13. The venous device of claim 11, wherein the bile salts are glycocholate or deoxycholate.

14. The venous device of claim 11, wherein the process further comprises dehydrating said decellularized tissue.

15. The venous device of claim 11, wherein the process further comprises soaking said decellularized tissue in glycerol or glycerol-alcohol mixture.

16. The venous device of claim 11, wherein the process further comprises lyophilizing said decellularized tissue.

17. The venous device of claim 1, wherein the wire-frame is made of a shape memory Nitinol alloy.

18. The venous device of claim 1, wherein said anchoring mesh lattice wing members are neither radially inwardly compressible nor outwardly expansible.

19. The venous device of claim 1, wherein a ratio of the wing-member axial length to the wire-frame axial length is between about 1.01 and 10.

20. The venous device of claim 1, wherein a process of manufacturing said device comprises:

(a) providing the sheet of biocompatible material;

(b) laser-cutting the sheet to form the plurality of mesh lattice wing members and a central wire member that connects the plural mesh lattice wing members on a plane, wherein the central wire member has at least two wire sections being detached from said plural mesh lattice wing member;

(c) forming an individual wire-frame configuration on each of the at least two wire sections by pushing upward a central part of each wire section while holding the mesh lattice wing members on the plane; and

(d) bending the mesh lattice wing members to be substantially parallel to a direction of said wire-frame configuration.