Medical devices and methods of making the same
An endoprosthesis, such as a stent, having a layer that can enhance the biocompatibility of the endoprosthesis, and methods of making the endoprosthesis are disclosed.
1. A stent, comprising:
a tubular member defined by struts and openings, the tubular member including at least a first portion comprising an alloy of two or more elements, the alloy having a concentration gradient of at least one radiopaque element within the alloy, the first portion defining an outer surface of the tubular member, wherein the concentration of the at least one radiopaque element increases as a function of distance from the outer surface.
2. The stent of claim 1 , wherein the concentration gradient varies substantially linearly along a thickness of the first portion.
3. The stent of claim 1 , wherein the first portion is capable of attenuating an incident X-ray beam by more than about 70%.
4. The stent of claim 1 , wherein the at least one radiopaque element is selected from a group consisting of gold, platinum, palladium, and tantalum.
5. The stent of claim 1 , wherein the first portion is formed of an alloy comprising the at least one radiopaque element and a second element.
6. The stent of claim 1 , wherein the member further includes a second portion disposed inwardly of the first portion, the second portion being more radiolucent than the first portion.
7. A stent, comprising:
a tubular member defined by struts and openings having
a first portion; and
a second portion disposed outwardly of the first portion, the second portion being more radiopaque than the first layer and including an alloy of two or more elements, the alloy having a concentration gradient of at least one radiopaque element within the alloy, wherein the concentration of the at least one radiopaque element increases as a function of distance from the outer surface
an outer layer of the second portion having a lower oxidation potential than an oxidation potential of an inner layer of the second portion.
8. The stent of claim 7 , wherein the second portion is capable of attenuating an incident X-ray beam by more than about 70%.
9. The stent of claim 7 , wherein the at least one radiopaque element is selected from the group consisting of gold, platinum, palladium, and tantalum.
10. The stent of claim 7 , wherein the alloy includes a second element is selected from the group consisting of titanium, niobium, palladium, chromium, and silicon.
11. The stent of claim 7 , wherein the first portion comprises a material selected from the group consisting of stainless steel and a nickel-titanium alloy.
12. The stent of claim 7 , wherein the first portion is the innermost portion of the member.
13. The stent of claim 7 , wherein the first portion contacts the second portion.
14. The stent of claim 7 , wherein the first and second portions have different compositions.
15. The stent of claim 7 , further comprising a polymeric layer on the member.
16. The stent of claim 7 , further comprising a drug-releasing layer on the member.
17. A stent, comprising:
a tubular member defined by struts and openings, the tubular member having at least a first portion including
a first layer comprising a radiopaque material, and
a second layer comprising an alloy of the radiopaque material and at least one additional element, the second layer defining an outer surface of the member, the second layer having a lower oxidation potential than an oxidation potential of the first layer, wherein the alloy of the second layer has concentration gradient of the radiopaque material that varies substantially linearly along a thickness of the second layer.
18. The stent of claim 17 , wherein the radiopaque material comprises gold and the at least one additional element is titanium.
19. The stent of claim 1 , wherein the radiopaque material is selected from a group consisting of gold, platinum, palladium, and tantalum.
20. The stent of claim 1 , wherein the radiopaque material is gold and the at least one additional element is titanium.