MEDICAL DEVICE HAVING COUPLED SEGMENTS
20180318116 ยท 2018-11-08
Inventors
- Erik David Eli (Redwood City, CA)
- Syed Hossainy (Hayward, CA)
- Mikael Trollsas (San Jose, CA)
- Michael H. Ngo (San Jose, CA)
- Stephen Pacetti (San Jose, CA)
- Michael Green (Pleasanton, CA, US)
- John Papp (Temecula, CA)
Cpc classification
A61F2/958
HUMAN NECESSITIES
A61F2/915
HUMAN NECESSITIES
A61F2220/0075
HUMAN NECESSITIES
A61F2220/0091
HUMAN NECESSITIES
A61F2002/91591
HUMAN NECESSITIES
A61F2/91
HUMAN NECESSITIES
International classification
Abstract
A scaffold is formed by several segments joined or connected to each other by only at least one coupling. The coupling decouples the segments in the axial direction over a finite distance of axial displacement. The scaffold when implanted in a peripheral vessel reduces loading on rings of a segment due to the decoupling of the segments in the axial direction over the finite distance.
Claims
1-20. (canceled)
21. A medical device, comprising: a first stent or scaffold segment and a second stent or scaffold segment, the first segment and the second segment having a pattern of adjoined rings, comprising: a first ring, a second ring, a third ring and a fourth ring, each ring forming peak and valley undulations, wherein a peak of the first ring is adjoined with a valley of the second ring, a peak of the third ring is adjoined with a valley of the fourth ring, the adjoined rings form a plurality diamond shape cells, and the first ring and fourth ring are end rings; and a mechanical connection comprising at least one coupling having a lost motion distance (LMD) and a maximum axial distance (Z1); wherein the first segment and the second segment are joined to each other by only the coupling.
22. The medical device of claim 21, wherein each of the first and second segments are made from a polymer comprising poly(L-lactide).
23. The medical device of claim 21, wherein each of the first and second segments are self-expanding segments made from a metal.
24. The medical device of claim 21, wherein the coupling extends from a valley of the first segment's fourth ring to a peak of the second segment's first ring.
25. The scaffold of claim 21, wherein the diamond shape cells have circumferentially aligned vertices.
26. The scaffold of claim 21, wherein the coupling is a male-female coupling, a pin and socket coupling, a flexible band coupling, or a stiff band coupling.
27. The scaffold of claim 21, wherein the LMD accounts for displacement of the first segment relative to the second segment, such that when implanted in a vessel the LMD is equal to about D (TAN()), where D is an outer, expanded diameter of the first segment and is between 10 and 30 degrees.
28. The scaffold of claim 21, wherein the LMD or Z1 is equal to about 7% to about 10% of a length of the first segment to account for an expected 7% to about 10% axial compression of the first segment when the first segment is implanted in a vessel.
29. The medical device of claim 21, wherein Z1 is equal to at least a width of a diamond shape.
30. The medical device of claim 21, wherein the coupling is a beam, string or thread; and wherein when the coupling is a thread or string, the string or thread joins together one pair of adjacent peaks of the first and second segments, or a plurality of pairs of adjacent peaks of the first and second segments.
31. The medical device of claim 21, wherein the coupling comprises a first portion integrally formed with the first segment, a second portion integrally formed with the second segment, and a connection formed between the first and second portion and defining the LMD.
32. The medical device of claim 21, further comprising a balloon catheter having a balloon, the first segment and second segments are crimped to the balloon, and the coupling is configured such that the first segment and the second segment are separated by a distance Z2 to account for a shortening of a length of the segments when the segments are expanded by the balloon.
33. A medical device, comprising: a stent segment, comprising: a first ring, a second ring, a third ring, and a fourth ring, a peak of the first ring is adjoined with a valley of the second ring, a peak of the third ring is adjoined with a valley of the fourth ring, the first ring is an end ring forming peak and valley undulations, the fourth ring is an end ring forming peak and valley undulations, and a male portion of a male-female connector, the male portion being formed integrally with the fourth ring and extending from a peak of the fourth ring.
34. The medical device of claim 33, wherein the stent segment has one, and only one male portion.
35. The medical device of claim 33, wherein the stent segment is a self-expanding stent segment made from a metal.
36. The medical device of claim 33, wherein the male portion forms a bulbous head configured for being received within a complementary shaped female portion of the male-female connector.
37. The medical device of claim 33, wherein the first ring, the second ring, the third ring, and the fourth ring form a plurality of diamond shape cells.
38. The medical device of claim 33, wherein the peak and valley undulations of the fourth ring are offset circumferentially from the peak and valley undulations of the first ring, such that a peak of the fourth ring is longitudinally aligned with a valley of the first ring.
39. The medical device of claim 33, wherein the stent segment is a first stent segment, further comprising: the first stent segment, a second stent segment and a third stent segment mounted to a catheter and contained within a sheath, wherein the second and third stent segments each comprise: a first ring, a second ring, a third ring, and a fourth ring, a peak of the first ring is adjoined with a valley of the second ring, a peak of the third ring is adjoined with a valley of the fourth ring, the first ring is an end ring forming peak and valley undulations, the fourth ring is an end ring forming peak and valley undulations, and a male portion of a male-female connector integral with the fourth ring and extending from a peak of the fourth ring; wherein each of the first, second and third segments are self-expanding; and wherein each of the first, second and third segments are axially decoupled from each other when the sheath is withdrawn and the segments thereby self-expand, such that the first segment, second segment and third segment can be located at different axial locations relative to each other at an implant site
40. The medical device of claim 39, wherein the first segment and the second segment are coupled to each other by the first segment's male portion and the second segment's male portion engaging with respective first and second female portions of the male-female connectors.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0067] For purposes of this disclosure, the following terms and definitions apply:
[0068] The term about means 20%, 10%, 5%, 2% or 1% less or more than a stated value, a range or each endpoint of a stated range, or a one-sigma variation from a stated mean value.
[0069] Inflated diameter or expanded diameter refers to the diameter the scaffold attains when its supporting balloon is inflated to expand the scaffold from its crimped configuration to implant the scaffold within a vessel. The inflated diameter may refer to a post-dilation balloon diameter which is beyond the nominal balloon diameter, e.g., a 6.5 mm balloon has about a 7.4 mm post-dilation diameter, or a 6.0 mm balloon has about a 6.5 mm post-dilation diameter. The nominal to post dilation ratios for a balloon may range from 1.05 to 1.15 (i.e., a post-dilation diameter may be 5% to 15% greater than a nominal inflated balloon diameter). The scaffold diameter, after attaining an inflated diameter by balloon pressure, will to some degree decrease in diameter due to recoil effects related primarily to, any or all of, the manner in which the scaffold was fabricated and processed, the scaffold material and the scaffold design.
[0070] Post-dilation diameter (PDD) of a scaffold refers to the diameter of the scaffold after being increased to its expanded diameter and the balloon removed from the patient's vasculature. The PDD accounts for the effects of recoil. For example, an acute PDD refers to the scaffold diameter that accounts for an acute recoil in the scaffold.
[0071] A pre-crimp diameter means an OD of a tube, or the scaffold before it is crimped to a balloon. Similarly, a crimped diameter means the OD of the scaffold when crimped to a balloon. The pre-crimp diameter can be 2, 2.5, 3.0 times greater than the crimped diameter and about 0.9, 1.0, 1.1, 1.3 and about 1-1.5 times higher than an expanded diameter or post-dilation diameter. A partial crimp diameter is a diameter attained after a scaffold or segment is crimped to a diameter less than a pre-crimp diameter and greater than a final crimp diameter. A partial crimp diameter can be an intermediate diameter after crimping from a pre-crimp diameter to about the nominal or over inflated diameter of the balloon to which the scaffold will be crimped. An example of a partial crimping diameter is described by the scaffold diameter following Stage II in
[0072] Recoil means the response of a material following the plastic/inelastic deformation of the material and in the absence of externally applied forces, e.g., vessel contraction. When the scaffold is radially deformed well beyond its elastic range and the external pressure (e.g., a balloon pressure on the luminal surface) is removed the scaffold diameter will tend to revert back to its earlier state before the external pressure was applied. Thus, when a scaffold is radially expanded by applied balloon pressure and the balloon removed, the scaffold will tend to return towards the smaller diameter it had, i.e., crimped diameter, before balloon pressure was applied. A scaffold that has recoil of 10% within hour following implantation and an expanded diameter of 6 mm has an acute post-dilation diameter of 5.4 mm. The recoil effect for balloon-expanded scaffolds can occur over a long period of time. Post-implant inspection of scaffolds shows that recoil can increase over a period of about one week following implantation. Unless stated otherwise, when reference is made to recoil it is meant to mean recoil along a radial direction (as opposed to axial or along longitudinal direction) of the scaffold.
[0073] Acute Recoil is defined as the percentage decrease in scaffold diameter within the first about hour following implantation within a vessel.
[0074] Axial and longitudinal are used interchangeably and refer to a direction, orientation, or line that is parallel or substantially parallel to the central axis of a stent or the central axis of a tubular construct. The term circumferential refers to the direction along a circumference of the stent or tubular construct. Thus, a link spaced 180 degrees from another link means 180 degrees as measured about the circumference of the tubular construct.
[0075] Radial refers to a direction, orientation, or line that is perpendicular or substantially perpendicular to the central axis of the stent or the central axis of a tubular construct and is sometimes used to describe a circumferential property, i.e. radial strength.
[0076] A coupling is a structure that connects or joins a scaffold segment A with a scaffold segment B so as to form a linkage having at least one joint. For example, shown in
[0093] A maximum axial distance means Z1, or the maximum amount of separation between the segment A and segment B when joined by one or more couplings. In some embodiments LMD=Z1. Every coupling has an inherent maximum axial distance when the coupling is joining the two segments.
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[0095] Following are examples of structure forming a coupling that connects a segment A and B. With regard to the segment A and B connected by the coupling, the structure of the segments can be the same or different between A and B. Preferred embodiments of segments according to the disclosure are found in
[0096] In the examples of
[0097] It will be understood that various combinations of structural or functional features of the embodiments of couplings, including those embodiments illustrated in the examples of
[0098] According to any of the embodiments, the segment A may be connected via one coupling or via two couplings 50 spaced 180 degrees apart from each other, three couplings spaced 120 degrees apart or four couplings spaced 90 degrees apart.
[0099] According to some embodiments, the segment A and segment B are connected only by a coupling. Thus, for any of the disclosed methods of assembly, or assembled scaffolds, only couplings connect adjacent segments, or couplings are the only in-plane connecting structure between adjacent segments. In other embodiments, additional structure may connect the adjacent segments.
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[0101] The DOF of the joint defined by coupling 50 is Z translation only.
[0102] The Z1 distance for coupling 50 is created when the head 56 of the male portion 52 is proximal the opening 72 into the female space 68 and distal an abutting surface 70 offset in the Z-axis direction from the opening 70; or when the head 56 is spaced by about the LMD from the surface 70.
[0103] The Z2 distance for coupling 50 occurs when the surface 56a of head 56 of male portion 52 abuts surface 70 of female portion 62 or in this example crown surface 70 of segment B, and/or edges 66a, b of arms 64 of female portion 62 come into contact or abut a surface 58 of segment A, as illustrated. The LMD for coupling 50 may be defined in two alternate ways. The LMD may be LMD1, in which case the LMD is defined by the length of the male portion 52. And/or the LMD may be LMD2, in which case the LMD is defined by about the length of the female portion upper and/or lower arms 64. The illustration of
[0104] In a method of assembly, the segment A and B are connected by forcible pressing the male head 56 into the female space 68. To facilitate this assembly, a chamfered surface may be formed at the edges 66, which are sized to flex outwardly when the rounded male head 56 is forcibly pressed against surfaces of the edges 66. Once pressed into the space 68 the shapes of the edges 66 of arms 64 prevent or discourage dislodgement of the male portion 52 from the female portion 62.
[0105] Referring to
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[0107] The DOF of the joint defined by coupling 100 is Z translation only and rotation about the one of the X or Y axes in two places, i.e., where the flexible band 106 is engaged about the left and right pieces 114 as shown in
[0108] When the segments A and B are spaced by Z1,
[0109] The Z1 distance for coupling 100 is created when the flexible band 106 comes into tension, or when a restoring force in the flexible band becomes non-zero if the segments A and B are pulled farther apart.
[0110] The Z2 distance for coupling 100 occurs when the ends 114a and 114b abut one another, as shown in
[0111] The LMD for coupling 100 is the maximum space formed between the ends 114a, 114b before the flexible band 106 begins to impart a restoring force tending to resist the segments A and B being pulled away from each other.
[0112] The arms 102 and 112 of coupling 100 may be formed from the tube from which the scaffold segments are formed.
[0113] Additionally, coupling 100, like coupling 50 has Z1 not equal to about the LMD. In the case of couplings 50 and 100 the LMD is less than Z1, as can be appreciated by the fact that Z2 is non-zero. In the case of coupling 50 the Z2 is equal to about the shorter-in-length (in Z axis direction) of the male portion 52 and female portion 62. In the case of the coupling 100 the Z2 length is about equal to 2 the length of an arm 102/112.
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[0115] The DOF of the joint defined by coupling 150 is Z translation only and rotation about only the Z axis in two places, i.e., where the ends of the beam 165 are received in the holes 152a, 152b. Z axis rotation is available when the beam 150 has a round cross-section and is received in a round hole.
[0116] When the segments A and B are spaced by Z1,
[0117] The Z1 distance for coupling 150 is created when the segments A and B are pulled apart until the ends 156 of the beam 165 both reach the respective holes 152a, 152b, or about when the beam 150 is brought into tension. The Z2 distance is zero, as can be appreciated from
[0118] Alternatively, a connection may be made between the segments A and B by a thread or string 190 made from a bioresorbable material. The string or thread by its nature cannot sustain a bending load or transverse. As such, in the configuration of
[0119] In a method of making the scaffold segments configured for receiving either the beam 165 or the string 190 a hole may be bored out of the tube by a laser, or a wire embedded then later removed to form the passageway for the string 190 or beam 165. Then the segments may be cut from the tube using a laser and the segments connected to each other by the thread 190 and/or beam 165.
[0120] Another embodiment of a string connecting segments A and B is shown in
[0121] The LMD is equal to Z1 in the case of a string or thread 170 or 190.
[0122] Referring again to
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[0126] The DOF of the joint defined by coupling 200 is translational motion in both Z and Y and rotation about Y, or Z and X and rotation about X. There is such a joint between Segment A and pin 202 and segment B and pin 202. When the segments A and B are spaced by Z1,
[0127] Referring to
[0128] Referring to
[0129] The LMD is illustrated in
[0130] Segments
[0131] A segment according to the invention may include a portion of one, two, or three couplings at one or both ends. For example, a segment connected by a coupling formed, at least in part, with the segment, i.e., integral with the segment, such as the example in
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[0133] Ls is the length of the segment 320. Ls may be 3 to 6 mm, 6 to 8 mm, 8 to 10 mm, 10 to 12 mm, or greater than 12 mm in an as cut or as fabricated configuration. For this type of segment, Ls increases when the segment is crimped to a decreased diameter and then decreases when expanded from a crimped configuration. Length change is affected by the number of peaks in a ring and the width of the diamonds. The length change (increases or decreases) with the number of peaks and (increases or decreases) with the width of the diamonds.
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[0135] may be 90 degrees, 90 to 95 degrees, 95 to 100 degrees, 100 to 110 degrees, or greater than 110 degrees. may be 90 degrees, 85 to 90 degrees, 80 to 85 degrees, 70 to 80 degrees, or less than 70 degrees. may be 90 degrees, 85 to 90 degrees, 80 to 85 degrees, 70 to 80 degrees, or less than 70 degrees. may be 90 degrees, 90 to 95 degrees, 95 to 100 degrees, 100 to 110 degrees, or greater than 110 degrees.
[0136] Exemplary values for and are about 70 and 110 degrees, respectively. Values in this range tend to reduce segment shortening from crimping to deployment. Other exemplary values for and are about 110 and 70 degrees, respectively. Values in this range tend to increase segment's radial strength and crush resistance. Another variable that affects the angles above is the lased tube diameter and the final deployed diameter. Generally, for polymers, the lased tube diameter is slightly larger than the final deployed diameter.
[0137] The segments can include radiopaque marker embedded within holes in the scaffold segment to aid in visualization of the implanted scaffold. In some embodiments, the markers are embedded in holes in the short link struts 330 of
[0138] Referring to
[0139] The segment properties of radial strength and stiffness can be modified through adjustment of the as-cut geometrical parameters of the diamond-shaped elements. For example, radial strength and stiffness is increased by increasing He which results in a decrease in We and also corresponds to a decrease in and an increase in .
[0140] In some segment design embodiments, the diamond-shaped elements are square-shape or approximately square-shaped in the as-cut condition. In such embodiments, is the same or approximately the same as . For example, ABS() may be 2 or about 2 degrees or less than 2 degrees.
[0141] In other segment design embodiments, the diamond-shaped elements can be taller or greater in the circumferential direction or, Hc>Wc and >. In such embodiments, the may be greater than 2 degrees, 2 to 4 degrees, 4 to 8 degrees, greater than 8, about 3 degrees, about 4 degrees, or about 5 degrees.
[0142] L.sub.l may be less than 10% or 10% to 20%, 20% to 30%, 30 to 40%, or greater than 40% of a ring strut length between a crest and a trough. Exemplary link struts may have a length of less than 0.01 in, 0.01 to 0.02 in, 0.02 to 0.04 in, 0.04 to 0.06 in, or greater than 0.06 in. In some embodiments, adjacent rings are connected at an intersection of the opposing crests and troughs such that a length of the link strut is effectively the width of the intersection and L.sub.l is zero.
[0143] As discussed in US20140046431a scaffold including a plurality of unconnected segments presents challenges with regard to crimping on a delivery balloon including maintaining the desired spacing between segments, placing segments and ensuring no overlapping of segments.
[0144] Generally, scaffold crimping is the act of affixing a radially expandable scaffold or stent to a delivery catheter or delivery balloon so that it remains affixed to the catheter or delivery balloon until the physician desires to deliver the stent at the treatment site. Examples of crimping methods are described. According to one aspect of the invention crimping of a scaffold according to the disclosure includes one or more of the crimping steps set forth in
[0145] Examples of crimping technology include a roll crimper; a collet crimper; and an iris or sliding-wedge crimper. In the sliding wedge or iris crimper, for example, adjacent pie-piece-shaped sections move inward and twist toward a scaffold in a cavity formed by the sections, much like the leaves in a camera aperture.
[0146] The Z1 distance or Z2 distance between segments may be pre-set for a scaffold in relation to crimping. One or the other distance may be set prior to crimping, or after a partial crimping (e.g. after Stage II in
[0147] A scaffold segment having rings forming zig-zag patterns interconnected by links tend to not shorten or lengthen during crimping and deployment. Scaffold segments having diamond-shaped elements, on the other hand, by nature lengthen as they are crimped and shorten as they are deployed. It may be desirable for the scaffold having the expanded or post-dilation diameter in the vessel to have the distance Z1 between segments. As stated above, during crimping initial or interim adjustments in segment spacing can be made to counteract a lengthening of segments during diameter decrease. It should be noted that, in some embodiments, during crimping Z1 does not need to be controlled or pre-set, because when deployment occurs, the coupling will lengthen to Z1 and the final deployed spacing will be Z1. This may be ideal as implants are made with a patient's leg mostly straight or in the non-compressed artery state. Any subsequent movement of the artery will then be essentially compression.
[0148] The scaffold segments may be crimped tightly on a delivery balloon using a crimping apparatus such as an iris crimper. The crimping process may include two stages, a pre-crimping process and a final crimp process. In the pre-crimp process, the diameter of the scaffold segments are reduced to a diameter between the initial diameter and the balloon diameter prior to loading the scaffold segments on the balloon. This process is illustrated in the examples of
[0149] Crimping of the scaffold, as detailed in US20130025110, includes heating the polymer material to a temperature less then, but near to the glass transition temperature of the polymer. In one embodiment the temperature of the scaffold during crimping is raised to about 5 to 15 degrees below the lower end of the glass transition temperature of the bioresorbable polymer; e.g., about 54 to 40 degrees for PLLA. When crimped to the final, crimped diameter, the crimping jaws are held at the final crimp diameter for final dwell period. This method for crimping a polymer scaffold having crush recovery is advantageous to reduce recoil when the crimp jaws are released. After the final dwell period, the scaffold is removed from the crimper and a constraining sheath is immediately placed over the scaffold to minimize recoil. Examples of such a sheath are described in US20120302955.
[0150] The diamond pattern disclosed herein tends to maximize the relative friction between the vessel wall and the segments. With this and the high radial and axial rigidity of the diamond pattern, endothelialization of the segments may be sped up and vessel irritation may be reduced. With rapid endothelialization, the scaffold/vessel wall becomes a composite structure which in itself enhances the radial strength and hence crush resistance of the vessel/scaffold composite. With most, if not all of the movement transferred to the gaps between the segments, the design utilizes the natural flexibility of the vessel walls to handle any compression, bending and torsional movements.
[0151] In some embodiments, a single high radial strength and stiff scaffold segment, such as described above, may be implanted at an implant site. Implanting a single segment without additional segments may be useful in treatments involving vessels that do not undergo axial compression, torsion, or bending. Examples include the Iliac and Renal artery.
[0152] During deployment at a lesion site of a conventional balloon expandable stent or scaffold, the balloons generally start to expand at the proximal and distal ends first, producing a dog bone shape. As pressure is increased, the balloon expands in the center, expanding the scaffold in the center also.
[0153] With the segmented scaffold, which can include several short scaffolds on a single balloon, the balloon can expand in a similar manner, i.e., expanding at the proximal and distal ends first, followed by expansion of a center section. Expansion at the ends first has the tendency to push the segments axially towards the center of the balloon which decreases the segment to segment gap. The gap may be decreased to the point that the segments collide with each other. This movement of the individual segments axially along the balloon during deployment, therefore, can change the segment to segment gap to an undesirably small size which can result in interference of the segments. Additionally, the segment to segment spacing will not necessarily be the same between all segments. A reduced gap or zero gap may be acceptable where non-pulsatile forces are virtually zero.
[0154] In pre-clinical animal studies, bioresorbable polymer fully disconnected segmented scaffolds have been shown to have high radial strength and fracture resistance. The sections of the artery along the segments are held open at a desired diameter. However, in some cases, the sections of the artery at the gaps between the segments are not held open to the same degree as along the segments. There appears to be prolapse or focal restenosis of the vessel wall inward into the artery lumen at the gaps between segments. For example, in a case where the gaps between the segments were on the order of 5 mm, prolapse or focal restenosis was observed.
[0155] Embodiments of the present invention include segmented scaffolds and delivery thereof that reduce or prevent the vessel prolapse between the segments while maintaining high radial strength and fracture resistance.
[0156] Embodiments of the present invention include deploying a segmented scaffold in such a manner that the ends of the adjacent scaffolds segments overlap or are interlinked. The segments that are overlapped or interlinked are disconnected and are not in contact. The segment ends overlap. Therefore, there is no gap between segments that is a circumferential strip or band with no support that completely encircles the vessel wall. Equivalently, there is no longitudinal position without support from a segment between the ends of adjacent segments that extends completely around the circumference of the vessel wall or scaffold.
[0157] Embodiments also include segmented scaffold segments in a crimped reduced state with ends of the adjacent scaffolds segments that overlap or are interlinked. The crimped scaffold segments can be crimped over a delivery balloon to allow balloon assisted delivery of the segments to a deployed state in a vessel. The scaffold segments are interlinked in a manner that upon expansion of the segments to a deployed state, the deployed segments are interlinked as described.
[0158] Although specific embodiments are described herein, the embodiments generally apply to segmented scaffolds made up of segments composed of struts forming a plurality of circumferential undulating rings, the undulations include peaks and valleys, as exemplified above. Undulating can refer to, but is not limited to, to a wave-like appearance or form. The wave-like appearance can be smooth, such as sinusoidal from, or jagged, such as a zigzag form. The ends of the segments, therefore, include an undulating ring also with peaks and valleys. A peak or valley undulation refers generally to the portion of an undulation or wave on either side of a peak or valley. The peak undulations project longitudinally outward or away from the end of the segment and the valley undulations extend longitudinally inward or toward the segment.
[0159] The interlinking of two adjacent scaffold segments with the above general structure is described with respect to the peak undulation and valley undulation of neighboring end rings of adjacent segments. The peak undulations of a first ring overlap or extend into the valley undulation of an adjacent ring. Likewise, the peak undulations of the adjacent ring overlap or extend into the valleys of the first ring. The degree of overlap or interlinking can be described in terms of the degree of extension of the peak undulations into the valley undulations.
[0160] The peak and valley undulations in the crimped state are compressed close to one another relative to the expanded or deployed state. The segments described are provided in the crimped state with the interlinking of the neighboring rings of adjacent segments. The degree of overlap may be greater in the crimped state than the deployed state since the degree of overlap may decrease as the segments are expanded.
[0161] A scaffold having overlapping segments can be formed using the scaffolds segments described, for example, in
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[0163] As shown in
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[0165] As shown in
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[0167] As shown in
[0168] In order for deployed segments to have overlap, the couplings are connected with an LMD that preserves a degree of overlap even when the scaffold segments are located at the Z1 distance from each other. According to this aspect of the disclosure, a scaffold includes a first scaffold segment connected to a second scaffold segment only by one or more couplings where there is overlapping of the segments when the segments are a maximum axial distance from each other, i.e., the axial or Z-axis distance from each other is Z1, and each of the couplings' LMD is equal to or less than Z1.
[0169] The scaffold segments of the present invention can be made from variety of biodegradable polymers including, but not limited to, poly(L-lactide) (PLLA), polymandelide (PM), poly(DL-lactide) (PDLLA), polyglycolide (PGA), polycaprolactone (PCL), poly(trimethylene carbonate) (PTMC), polydioxanone (PDO), poly(4-hydroxy butyrate) (PHB), and poly(butylene succinate) (PBS). The scaffold segments can also be made from random and block copolymers of the above polymers, in particular, poly(L-lactide-co-glycolide) (PLGA) and poly(L-Lactide-co-caprolactone) PLLA-PCL. The scaffold can also be made of a physical blending of the above polymers. The scaffold segments can be made from PLGA including any molar ratio of L-lactide (LLA) to glycolide (GA). In particular, the stent can be made from PLGA with a molar ratio of (LA:GA) including 85:15 (or a range of 82:18 to 88:12), 95:5 (or a range of 93:7 to 97:3), or commercially available PLGA products identified as having these molar ratios. High strength, semicrystalline polymers with a Tg above body temperature include PLLA, PGA, and PLGA.
[0170] Embodiments of the invention further may include couplings joining scaffold segments, methods of making or methods of crimping such segments as described in US20140046431. It will be understood that use of the word linkage herein refers specifically and exclusively to the coupling's feature (as stated earlier) of having or providing, among other things, a joint defining a DOF including at least in the Z-axis translation direction. This is different from use of the word link or connecting links as those terms simply describe a connection without having or defining a DOF or joint in the structure.
[0171] The width and/or radial thickness of struts of a scaffold may be 80 to 400 microns, or more narrowly, 100 to 250 microns, 140 to 180 microns, 200 to 400 microns, 140 to 160 microns, or 300 to 350 microns. The thickness and width can be different. For example, the width can be at or about 350 microns (e.g., 10 microns) and the thickness can be at or about 300 microns (e.g., 10 microns).
[0172] Semi-crystalline polymers such as poly(L-lactide) (PLLA) with glass transition temperature (Tg) above human body temperature may be suitable as materials for a totally bioresorbable scaffold since they are relatively stiff and strong at the conditions of the human body. However, they tend to be brittle at these conditions. These polymer systems exhibit a brittle fracture mechanism in which there is little plastic deformation prior to failure. As a result, a stent fabricated from such polymers can be vulnerable to fracture during fabrication and use of a scaffold, i.e., crimping, delivery, deployment, and during a desired treatment period post-implantation.
[0173] Embodiments of the present invention are applicable to endovascular treatment of coronary and peripheral disease in coronary arteries and various peripheral vessels including the superficial femoral artery, the iliac artery, and carotid artery. The embodiments are further applicable to various stent types, such as self-expandable and balloon expandable stents. The embodiments are further applicable to various stent designs including scaffolding structures formed from tubes, wire structures, and woven mesh structures. Embodiments also applicable to different materials that are permanent implants such as polymers and metals like Nitinol, Egeloy, stainless steel and cobalt chrome.
[0174] In general, the initial clinical need for a bioresorbable scaffold is to provide mechanical/structural support to maintain patency or keep a vessel open at or near the deployment diameter. The scaffold is designed to have sufficient radial strength or vessel wall support for a period of time. The vessel wall support provided by the scaffold allows the segment of the vessel to undergo healing and remodeling at the increased diameter. Remodeling refers generally to structural changes in the vessel wall that enhance its load-bearing ability.
[0175] A period of vessel wall support is required in order to obtain permanent positive remodeling and vessel healing and hence maintenance of vessel patency. As the polymer of the scaffold degrades, the radial strength of the scaffold decreases and the load of the vessel is gradually transferred from the scaffold to the remodeled vessel wall. In addition to the decline in radial strength, the degradation of the scaffold also causes a gradual decline in the mechanical integrity, i.e., connectivity of struts and the size and shape of the overall scaffold structure. The struts gradually resorb and disappear from the vessel.
[0176] As discussed earlier, the amount of movement experienced by a peripheral scaffold in the peripheral artery is greater than what a coronary scaffold experiences in the coronary artery. A peripheral scaffold can be subjected to a high degree of flexing, axial elongation/compression, pinching, bending, and torsion after implantation. Axial stresses on the scaffold can arise from the axial compression and extension, flexural stresses are imposed by lateral flexing, and crushing forces are imparted by pinching, while helical stress can arise from torsional forces. Resulting stresses are propagated along the length of the scaffold and can impart significant forces throughout the scaffold structure. When the load-path for the equilibrating axial forces are present in the scaffold structure, the axial forces can cause failure in ring struts, resulting in a decrease or loss in vessel wall support provided by the scaffold. According to the disclosure, for a limited range of axial movement the axial load transmission to a ring, as might induce significant bending loads at a crown, the LMD provided by the coupling can reduce the loading over time. It is of chief interest to reduce the amount of loading that contribute to fatigue failure.
[0177] While particular embodiments of the present invention have been shown and described, it will be obvious to those skilled in the art that changes and modifications can be made without departing from this invention in its broader aspects. Therefore, the appended claims are to encompass within their scope all such changes and modifications as fall within the true spirit and scope of this invention.