Implantable expandable medical devices having regions of differential mechanical properties and methods of making same
View Patent ↗An implantable expandable medical device in which selected regions of the device are in a martensite phase and selected regions are in an austenite phase. The martensitic regions exhibit pseudoplastic behavior in vivo and may be deformed without recovery under in vivo body conditions. In contrast the austenitic regions exhibit superelastic behavior in vivo and will recover their pre-programmed configuration upon deformation or release of an applied strain.
1. An implantable medical device, comprising: a generally tubular member having a plurality of interconnected structural members in spaced apart relationship and a plurality of interstitial openings passing through a wall surface of the generally tubular member, at least some of the plurality of interconnected structural members being interconnected in an articulated fashion defining hinge regions such that the generally tubular member is circumferentially expansible and longitudinally flexible, wherein at least some of the hinge regions comprise first hinge regions that operate to permit at least one of elastic or pseudoelastic circumferential expansion in vivo and at least some of the hinge regions comprise second hinge regions that operate to permit at least one of plastic or pseudoplastic deformation along the longitudinal axis of the device in vivo, wherein the generally tubular member further comprises a nickel-titanium alloy, and wherein the second hinge regions further have a higher transition temperature than the remainder of the generally tubular member.
2. The implantable medical device according to claim 1 , wherein the first hinge regions further comprise regions that are sufficiently austenitic under in vivo conditions to allow at least about 90% recovery of an unstrained configuration of the device.
3. An implantable, geometrically expandable, generally tubular, nickel-titanium medical device, comprising:
a) a plurality of circumferentially self-expansible members;
b) a plurality of interconnecting members interconnecting adjacent pairs of circumferentially self-expansible members; and
c) a plurality of first hinge regions within each of the plurality of circumferentially self-expansible members, each of the plurality of first hinge regions permitting circumferential expansion of the device by at least one of elastic or pseudoelastic deformation in vivo; and
d) a plurality of second hinge regions formed in the interconnecting members, each of the plurality of second hinge regions being capable of deforming by at least one of plastic or pseudoplastic deformation along a longitudinal axis of the device in vivo under the influence of a flexing load and the plurality of second hinge regions isolating stress transmission between adjacent pairs of circumferentially self-expansible members by a U-shape; and wherein the plurality of second hinge regions further have a higher transition temperature than the remainder of the generally tubular medical device.
4. The device according to claim 3 , wherein each of the plurality of circumferentially self-expansible members further comprises a ring member having of a plurality of generally linear structural members interconnected at opposing ends thereof by one of the plurality of first hinge regions.
5. The device according to claim 4 , wherein each of the plurality of generally linear structural members and each of the plurality of first hinge regions further comprise a nickel-titanium alloy in a sufficiently austenite phase to behave pseudoelastically in vivo.
6. The device according to claim 5 , wherein each of the plurality of interconnecting members have regions thereof that are in a sufficiently austenitic phase to operate in at least one of an elastic or pseudoelastic manner in vivo.
7. The device according to claim 3 , wherein each of the plurality of circumferentially self-expansible members further comprises a material selected from the group consisting of biocompatible metals, metal alloys and pseudometals that are capable of behaving elastically or pseudoelastically in vivo.
8. The device according to claim 7 , wherein each of the plurality of interconnecting members further comprises a material selected from the group consisting of biocompatible metals, metal alloys and pseudometals that are capable of behaving plastically or pseudoplastically in vivo.