IP Library Granted Patent US 9,320,628
Granted Patent B2
US 9,320,628 · App. 14/479,912 · Granted Apr 26, 2016

Endoprosthesis devices including biostable and bioabsorable regions

Inventors: Jan Weber (Maastricht, NL); James M. Anderson (Fridley, MN); Derek C. Sutermeister (Ham Lake, MN); Cass Alexander Hanson (St. Paul, MN); Timothy A. Ostroot (Cokato, MN)
Assignee: BOSTON SCIENTIFIC SCIMED, INC.
A61F2/915A61F2/856A61F2002/061A61F2002/825A61F2002/91541A61F2002/91575A61F2250/0018A61F2250/0029A61F2250/0031A61F2250/0036A61F2250/0039
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,320,628
App. No.
14/479,912
Granted
Apr 26, 2016
Kind
B2
Abstract

Some embodiments are directed to medical devices, and methods for making and using the medical devices. An exemplary endoprosthesis includes an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough. The tubular framework includes a number of interconnected biostable struts. The tubular framework has a proximal region extending distally from the proximal end to an intermediate location, and a distal region extending proximally from the distal end to the intermediate location. The distal region of the tubular framework is more flexible than the proximal region.

Claims (50)

1. An endoprosthesis comprising:

an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected biostable struts;

the expandable tubular framework having a proximal region extending distally from the proximal end to an intermediate location and a distal region extending proximally from the distal end to the intermediate location;

wherein the distal region of the expandable tubular framework is more flexible than the proximal region;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of a bioabsorbable material;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable tubular structure disposed around the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of the bioabsorbable tubular structure; and

wherein the expandable tubular framework has a first outer diameter in the proximal region and a second diameter in the distal region, the first diameter being less than the second diameter.

2. The endoprosthesis of claim 1 , wherein the bioabsorbable tubular structure has an outer diameter approximately equal to the second diameter.

3. An endoprosthesis comprising:

an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected biostable struts;

the expandable tubular framework having a proximal region extending distally from the proximal end to an intermediate location and a distal region extending proximally from the distal end to the intermediate location;

wherein the distal region of the expandable tubular framework is more flexible than the proximal region;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of a bioabsorbable material; and

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed in a groove formed in the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of the bioabsorbable material.

4. An endoprosthesis comprising:

an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected biostable struts;

the expandable tubular framework having a proximal region extending distally from the proximal end to an intermediate location and a distal region extending proximally from the distal end to the intermediate location;

wherein the distal region of the expandable tubular framework is more flexible than the proximal region;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of a bioabsorbable material; and

wherein the interconnected biostable struts have a first thickness in the proximal region and the interconnected biostable struts have a second thickness in the distal region, wherein the first thickness is greater than the second thickness.

5. The endoprosthesis of claim 4 , wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts.

6. An endoprosthesis comprising:

an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected biostable struts;

the expandable tubular framework having a proximal region extending distally from the proximal end to an intermediate location and a distal region extending proximally from the distal end to the intermediate location;

wherein the distal region of the expandable tubular framework is more flexible than the proximal region;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of a bioabsorbable material; and

wherein the interconnected biostable struts have a first width in the proximal region and the interconnected biostable struts have a second width in the distal region, wherein the first width is greater than the second width.

7. The endoprosthesis of claim 6 , wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts.

8. An endoprosthesis comprising:

an expandable tubular framework having a proximal end, a distal end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected biostable struts;

the expandable tubular framework having a proximal region extending distally from the proximal end to an intermediate location and a distal region extending proximally from the distal end to the intermediate location;

wherein the distal region of the expandable tubular framework is more flexible than the proximal region;

wherein the proximal region of the expandable tubular framework includes a bioabsorbable material disposed on the interconnected biostable struts and the distal region of the expandable tubular framework is devoid of a bioabsorbable material; and

wherein the interconnected biostable struts have a continuously changing thickness from the proximal region to the distal region, wherein a thickness of the interconnected biostable struts at the proximal end of the expandable tubular framework is greater than a thickness of the interconnected biostable struts at a distal end of the expandable tubular framework.

9. An endoprosthesis comprising:

an expandable tubular framework having a first end, a second end, and a lumen extending therethrough, the expandable tubular framework including a plurality of interconnected bioabsorbable struts;

at least one biostable wire extending generally longitudinally along the expandable tubular framework;

wherein at least one biostable wire is configured to provide longitudinal support to a vessel wall after the expandable tubular framework is absorbed.

10. The endoprosthesis of claim 9 , wherein the at least one biostable wire includes a plurality of biostable wires circumferentially arranged around a circumference of the expandable tubular framework.

11. The endoprosthesis of claim 10 , further comprising a biostable ring attached to the plurality of biostable wires.

12. The endoprosthesis of claim 10 , wherein a first end of the plurality of biostable wires is attached to a first biostable ring and a second end of the plurality of biostable wires is attached to a second biostable ring.

13. A method of implanting an endoprosthesis in a coronary artery proximate an aortic ostium, the method comprising:

positioning the endoprosthesis in the coronary artery with a proximal end of the endoprosthesis proximate the aortic ostium, the endoprosthesis including an expandable tubular framework and having a lumen extending therethrough from the proximal end to a distal end, the expandable tubular framework including a plurality of interconnected biostable struts and a bioabsorbable material disposed on at least a portion of the interconnected biostable struts; and

expanding the expandable tubular framework to exert a radially outward force against the coronary artery;

wherein a proximal region of the endoprosthesis proximate the proximal end has an initial stiffness when expanded greater than an initial stiffness of a distal region of the endoprosthesis; and

wherein the proximal region is configured to have a reduced stiffness less than the initial stiffness over a period of time as the bioabsorbable material is absorbed.

14. The method of claim 13 , wherein the stiffness of the proximal region is reduced at a greater rate than the stiffness of the distal region over the period of time.

15. The method of claim 13 , wherein the proximal region of the expandable tubular framework includes the bioabsorbable material and the distal region of the expandable tubular framework is devoid of a bioabsorbable material, wherein the bioabsorbable material is absorbed over a period of time to reduce the difference in stiffness of the proximal portion relative to the stiffness of the distal portion.

16. The method of claim 13 , wherein the bioabsorbable material is disposed in a groove formed in the interconnected biostable struts in the proximal region.

17. The method of claim 13 , wherein the interconnected biostable struts have a continuously changing thickness from the proximal region to the distal region, wherein a thickness of the interconnected biostable struts at the proximal end of the expandable tubular framework is greater than a thickness of the interconnected biostable struts at a distal end of the expandable tubular framework.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2014
From: WEBER, JAN; ANDERSON, JAMES M.; SUTERMEISTER, DEREK C.; HANSON, CASS A.; OSTROOT, TIMOTHY A.
To: BOSTON SCIENTIFIC SCIMED, INC.
Reel/Frame 033690/0892 →
Continuity (2)
Provisional Application 61875370 · Sep 9, 2013
Related Publication 20150073522A1 · Mar 12, 2015