U.S. patent application number 11/708448 was filed with the patent office on 2007-06-28 for stent.
This patent application is currently assigned to BOSTON SCIENTIFIC SCIMED, INC.. Invention is credited to Jason T. Lenz.
Application Number | 20070150050 11/708448 |
Document ID | / |
Family ID | 32868413 |
Filed Date | 2007-06-28 |
United States Patent
Application |
20070150050 |
Kind Code |
A1 |
Lenz; Jason T. |
June 28, 2007 |
Stent
Abstract
A stent comprises a plurality of serpentine circumferential
bands and a plurality of connector columns. Each connector column
is located between two adjacent serpentine circumferential bands
and comprises a plurality connector struts. Each connector strut is
connected at one end to one serpentine circumferential band and at
another end to another serpentine circumferential band. Each
connector strut has step sections and at least one riser. Each step
section extends substantially in a circumferential direction and
each riser extends in a substantially longitudinal direction. The
steps in a connector are connected to one another via a riser.
Inventors: |
Lenz; Jason T.; (Maplewood,
MN) |
Correspondence
Address: |
VIDAS, ARRETT & STEINKRAUS, P.A.
6109 BLUE CIRCLE DRIVE
SUITE 2000
MINNETONKA
MN
55343-9185
US
|
Assignee: |
BOSTON SCIENTIFIC SCIMED,
INC.
Maple Grove
MN
|
Family ID: |
32868413 |
Appl. No.: |
11/708448 |
Filed: |
February 20, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10371804 |
Feb 21, 2003 |
7179286 |
|
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11708448 |
Feb 20, 2007 |
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Current U.S.
Class: |
623/1.16 ;
623/1.42 |
Current CPC
Class: |
A61F 2230/0054 20130101;
A61F 2002/91533 20130101; A61F 2002/91558 20130101; A61F 2/91
20130101; A61F 2/915 20130101 |
Class at
Publication: |
623/001.16 ;
623/001.42 |
International
Class: |
A61F 2/06 20060101
A61F002/06 |
Claims
1-24. (canceled)
25. A stent comprising: a plurality of serpentine bands; and a
plurality of connector columns, each connector column located
between two adjacent serpentine bands, each connector column
comprising a plurality of connector struts, each connector strut
attached at one end to one serpentine band and attached at another
end to another serpentine band, each connector strut attached only
to said serpentine bands; at least one connector column comprising
a first connector strut and a second connector strut, the first
connector strut contacting the second connector strut at a first
location, the first connector strut spaced apart from the second
connector strut in a stent axial direction at a second
location.
26. The stent of claim 25, the first connector strut contacting the
second connector strut at a third location.
27. The stent of claim 26, wherein the first location and the third
location define corners of a substantially rectangular or
parallelogram shaped space bounded by the first connector strut and
the second connector strut.
28. The stent of claim 27, further comprising a third connector
strut contacting the second connector strut at a fourth location,
the third connector strut spaced apart from the second connector
strut in a stent axial direction at a fifth location.
29. The stent of claim 28, the third connector strut contacting the
second connector strut at a sixth location.
30. The stent of claim 29, wherein the fourth location and the
sixth location define corners of a substantially rectangular or
parallelogram shaped space bounded by the third connector strut and
the second connector strut.
31. The stent of claim 25, further comprising a third connector
strut contacting the second connector strut at a third location,
the third connector strut spaced apart from the second connector
strut in a stent axial direction at a fourth location.
32. The stent of claim 25, wherein the spacing between the first
connector strut and the second connector strut at the second
location is approximately four times a width of the first connector
strut.
33. The stent of claim 25, wherein connector struts of a first
connector column reverse orientation from connector struts of a
second connector column.
34. The stent of claim 25, wherein each connector strut contacts
two adjacent connector struts.
35. The stent of claim 34, wherein each connector strut further
comprises a portion that is spaced apart from a circumferentially
adjacent connector strut in a stent axial direction.
36. The stent of claim 25, wherein the first connector strut and
the second connector strut each comprise a plurality of step
sections and at least one riser.
37. The stent of claim 36, wherein the step sections are parallel
to one another when the stent is viewed as a flat pattern.
38. The stent of claim 36, wherein the risers are parallel to one
another when the stent is viewed as a flat pattern.
39. The stent of claim 25, wherein a connector strut attaches at
one end to an upper half of a peak of one serpentine band and
attaches at the other end to a lower half of a trough of another
serpentine band.
40. A stent comprising: a plurality of serpentine bands; and a
first connector strut, a second connector strut and a third
connector strut connected between two adjacent serpentine bands,
said connector struts not attached to one another, the first
connector strut contacting the second connector strut at a first
location, the first connector strut spaced apart from the second
connector strut in a stent axial direction at a second location,
the third connector strut contacting the second connector strut at
a third location, the third connector strut spaced apart from the
second connector strut in a stent axial direction at a fourth
location.
41. The stent of claim 40, a first serpentine band comprising a
peak, a second serpentine band comprising a trough, a portion of
each of the first, second and third connector struts located
between the peak and the trough.
42. The stent of claim 41, wherein the peak and trough are aligned
in a stent axial direction.
43. The stent of claim 42, wherein the first location and the third
location are located between the peak and trough.
44. The stent of claim 42, wherein the first connector strut
extends from an upper half of the peak in a downward direction, and
the third connector strut extends from a lower half of the trough
in an upward direction.
Description
BACKGROUND OF THE INVENTION
[0001] The use of stents in bodily lumen is well known. A stent is
typically delivered in an unexpanded state to a desired location in
a bodily lumen via a stent delivery device such as a catheter. Once
the stent is at the desired bodily location, it is either expanded
with a balloon or other suitable device or allowed to expand by,
for example, withdrawing a restraining sheath. Typically, the stent
is delivered bare to the body. During the past several years,
however, there has been a great deal of interest in drug-coated
stents. Specifically, a number of drug-coated stents have been
developed which allow for time-release of a drug. These stents are
believed to offer the possibility of reduced restenosis. The
presence of drug-coatings on stents, however, presents new
challenges in the area of stent design. Conventional bare stent
designs may prove difficult to coat uniformly because of the
proximity of different structural features.
[0002] There is a need for flexible stents that are designed to be
coated with drugs.
[0003] All US patents and applications and all other published
documents mentioned anywhere in this application are incorporated
herein by reference in their entirety.
[0004] Without limiting the scope of the invention a brief summary
of some of the claimed embodiments of the invention is set forth
below. Additional details of the summarized embodiments of the
invention and/or additional embodiments of the invention may be
found in the Detailed Description of the Invention below.
[0005] A brief abstract of the technical disclosure in the
specification is provided as well for the purposes of complying
with 37 C.F.R. 1.72.
BRIEF SUMMARY OF THE INVENTION
[0006] In one embodiment, the invention is directed to a stent
comprising a plurality of serpentine circumferential bands, and a
plurality of connector columns. Each connector column is located
between two adjacent circumferential bands and comprises one or
more connector struts. Each connector strut is connected at one end
to one serpentine circumferential band and at another end to
another serpentine circumferential band. Each connector strut
further comprises step and riser elements. Desirably each connector
strut comprises only two step sections and no more than three riser
elements.
[0007] In another embodiment, the invention is directed to a stent
comprising a plurality of serpentine circumferential bands
comprising alternating peaks and troughs, and a plurality of
connector columns. Each connector column is located between two
adjacent circumferential bands and includes a plurality connector
struts. Typical connector struts within a connector column are
distributed such that between each peak on one serpentine
circumferential band and a facing trough on an adjacent serpentine
circumferential band, there are at least three different connector
struts.
[0008] Additional details and/or embodiments of the invention are
discussed below.
BRIEF DESCRIPTION OF DRAWINGS
[0009] FIG. 1a shows a flat pattern of an inventive stent.
[0010] FIG. 1b shows an expanded view of a connector strut of FIG.
1a.
[0011] FIG. 2 shows the stent of FIG. 1 in a crimped state, such as
crimped onto a balloon.
[0012] FIG. 3 shows the stent of FIG. 1 in a crimped state.
DETAILED DESCRIPTION OF THE INVENTION
[0013] While this invention may be embodied in many different
forms, there are described in detail herein specific embodiments of
the invention. This description is an exemplification of the
principles of the invention and is not intended to limit the
invention to the particular embodiments illustrated.
[0014] For the purposes of this disclosure, like reference numerals
in the figures shall refer to like features unless otherwise
indicated.
[0015] In one embodiment, the invention is directed to a stent such
as that shown generally at 100 in FIG. 1a, having a first free end
104 and a second free end 108, comprising a plurality of serpentine
circumferential bands 112, and a plurality of connector columns
120. Each serpentine circumferential band 112 may form a plurality
of alternating peaks and troughs. Each connector column 120 is
located between two adjacent serpentine circumferential bands 112
and comprises one or more connector struts 124. Each connector
strut 124 is connected at one end 128 to one serpentine
circumferential band and at another end 132 to another serpentine
circumferential band.
[0016] Each connector strut 124 may further be comprised of one or
more. step sections 136 and one or more risers 140. The step
sections 136 may be perpendicular to the longitudinal axis of the
stent 100, and the risers 140 may be parallel to the longitudinal
axis of the stent 100. Thus, the connector struts 124 may be
characterized as forming stair-steps. The connector struts 124 may
further be characterized as being substantially straight with a jog
therein.
[0017] Optionally, the step sections 136 may be slanted or arranged
at a slight to moderate angle to an axis perpendicular to the
longitudinal axis of the stent 100. Likewise, the risers 140 may be
arranged at a slight to moderate angle to the longitudinal axis of
the stent 100. Slanted step sections 136 and risers 140 are
depicted in FIGS. 1a-3.
[0018] As best shown in FIGS. 2 and 3, which depict an embodiment
of the stent 100 in a crimped, unexpanded state, such as about an
expansion balloon or catheter, the risers 140 may act to space the
step sections 136 laterally with respect to each other. In the
embodiment shown, there are three different connector struts 124
located between each peak on one serpentine circumferential band
112 and a facing trough on an adjacent serpentine circumferential
band 112. Thus, each connector strut 124 contacts two
circumferentially adjacent connector struts 124. Further, adjacent
connector struts 124 define a substantially parallelogram shaped
space 142 bounded by two risers 140 and two step sections 136. This
provides the stent 100 with added flexibility in bending about the
length of the stent 100 while still retaining structural rigidity
against compressive axial forces.
[0019] Lateral spacing S of the step sections 136 is directly
affected by the length of the risers 140 and the angle formed
between the risers 140 and the step sections 136. While lateral
spacing of the step sections 136 may be set to any practical
configuration, the embodiment depicted in FIGS. 2 and 3 utilizes a
lateral spacing S in the unexpanded state of approximately four
times the width W of the step sections 136.
[0020] A further benefit of the risers 140, and the subsequent
lateral spacing of the step sections 136, may be realized when the
present stent 100 is used with a coating, such as a drug coating.
Because adjacent step sections 136 are not in lateral contact with
each other for a substantial portion of their length, coatings may
be applied more uniformly to the entire surface area of the stent
100. The lateral spacing helps to assure that the sides of the step
sections 136 are properly coated.
[0021] The lateral spacing also helps to prevent a coating from
forming a thick film extending across multiple adjacent step
sections 136 over substantial lengths of the step sections 136.
This is beneficial because a thick film extending across multiple
adjacent step sections 136 can cause the step sections 136 to stick
together upon expansion, interfering with proper deployment and
functionality after placement.
[0022] Although FIGS. 1a-3 depict an embodiment of the stent 100
having a plurality of similar serpentine circumferential bands 112,
various embodiments may include different serpentine forms, such as
bands of different length, bands of different widths, bands having
varying numbers of peaks and troughs, and the like.
[0023] Similarly, the stent 100 embodiment shown in FIGS. 1a-3
includes connector columns 120 wherein the connector struts 124
reverse orientation from column to column. Additional embodiments
may include configurations wherein all connector struts 124 are
similarly aligned. Further, various other shapes of connecting
struts 124 may be utilized in accordance with the present inventive
stent 100.
[0024] Suitable methods for manufacturing the inventive stents
include laser cutting, chemical etching or stamping of a tube. The
inventive stents may also be manufactured by laser cutting,
chemically etching, stamping a flat sheet, rolling the sheet and
welding the sheet, by electrode discharge machining, or by molding
the stent with the desired design. The stent may also be
manufactured by assembling a plurality of serpentine
circumferential bands and welding or adhesively joining them to one
another via connectors.
[0025] Any suitable stent material may be used in the manufacture
of the inventive stents disclosed herein. Examples of such
materials include polymeric materials, metals, ceramics and
composites. Suitable polymeric materials include thermotropic
liquid crystal polymers (LCP's). Where the stent is made of metal,
the metal may be stainless steel, cobalt chrome alloys such as
elgiloy, tantalum or other plastically deformable metals. Other
suitable metals include shape-memory metals such as nickel titanium
alloys generically known as "nitinol," platinum/tungsten alloys and
titanium alloys. The invention also contemplates the use of more
than one material in the inventive stents. For example, the first
serpentine bands and the second serpentine bands may be made of
different materials. Optionally, the connectors may be made of a
different material than the first and/or second serpentine
bands.
[0026] The inventive stents disclosed herein may be
balloon-expandable, self-expanding or a hybrid of the two.
[0027] In the case of balloon-expandable stents, a balloon catheter
may be used to deliver the stent to a desired bodily location. The
balloon is then expanded, causing the stent to expand. The balloon
may then be deflated and the catheter withdrawn. In the case of a
self-expanding stent, the stent may be delivered on a catheter
suited for delivery of self-expanding stents. Typically, such
catheters include will include a retention sheath to maintain the
stent in position until it is to be deployed. At the time of
deployment, the sheath is withdrawn and the stent allowed to
expand.
[0028] The invention is also directed to a stent-delivery catheter
and any of the inventive stents disclosed herein. Details of
stent-delivery catheters may be found in U.S. Pat. No. 6,120,522
and U.S. Pat. No. 6,506,201.
[0029] The inventive stents disclosed herein may include suitable
radiopaque coatings. For example, the stents may be coated with
gold or other noble metals or sputtered with tantalum or other
metals. The stents may also be made directly from a radiopaque
material to obviate the need for a radiopaque coating or may be
made of a material having a radiopaque inner core. Other radiopaque
metals which may be used include platinum, platinum-tungsten,
palladium, platinum-iridium, rhodium, tantalum, or alloys or
composites of these metals.
[0030] The inventive stents may also be provided with various
bio-compatible coatings to enhance various properties of the stent.
For example, the inventive stents may be provided with lubricious
coatings. The inventive stents may also be provided with
drug-containing coatings which release drugs over time.
[0031] The inventive stents may also be provided with a sugar or
more generally a carbohydrate and/or a gelatin to maintain the
stent on a balloon during delivery of the stent to a desired bodily
location. Other suitable compounds for treating the stent include
biodegradable polymers and polymers which are dissolvable in bodily
fluids. Portions of the interior and/or exterior of the stent may
be coated or impregnated with the compound. Mechanical retention
devices may also be used to maintain the stent on the balloon
during delivery.
[0032] The inventive medical devices may also be provided with
various bio-compatible coatings to enhance various properties of
the inventive medical devices. For example, the inventive medical
devices may be provided with lubricious coatings or other polymeric
coatings. An example of a suitable polymeric coating is PTFE.
[0033] The inventive stents may include one or more coatings which
comprise one or more therapeutic agents, cellular materials,
polymeric agents, and the like. Coatings may be applied to the
stent in numerous ways, including spray coatings, dip coatings, or
any other method that is known in the art.
[0034] The therapeutic agent may be non-genetic or genetic.
Suitable non-genetic therapeutic agents include anti-thrombogenic
agents such as heparin, heparin derivatives, urokinase, and PPack
(dextrophenylalanine proline arginine chloromethylketone),
anti-proliferative agents such as enoxaprin, angiopeptin, or
monoclonal antibodies capable of blocking smooth muscle cell
proliferation, hirudin, and acetylsalicylic acid, anti-inflammatory
agents such as dexamethasone, prednisolone, corticosterone,
budesonide, estrogen, sulfasalazine, and mesalamine,
antineoplastic/antiproliferative/anti-miotic agents such as
paclitaxel, 5-fluorouracil, cisplatin, vinblastine, vincristine,
epothilones, endostatin, angiostatin and thymidine kinase
inhibitors, anesthetic agents such as lidocaine, bupivacaine, and
ropivacaine, anti-coagulants such as D-Phe-Pro-Arg chloromethyl
keton, an RGD peptide-containing compound, heparin, antithrombin
compounds, platelet receptor antagonists, anti-thrombin antibodies,
anti-platelet receptor antibodies, aspirin, prostaglandin
inhibitors, platelet inhibitors and tick antiplatelet peptides,
vascular cell growth promoters such as growth factor inhibitors,
growth factor receptor antagonists, transcriptional activators, and
translational promoters, vascular cell growth inhibitors such as
growth factor inhibitors, growth factor receptor antagonists,
transcriptional repressors, translational repressors, replication
inhibitors, inhibitory antibodies, antibodies directed against
growth factors, bifunctional molecules consisting of a growth
factor and a cytotoxin, bifunctional molecules consisting of an
antibody and a cytotoxin, cholesterol-lowering agents; vasodilating
agents; and agents which interfere with endogenous vascoactive
mechanisms.
[0035] Suitable genetic materials include anti-sense DNA and RNA,
DNA coding for anti-sense RNA, tRNA or rRNA to replace defective or
deficient endogenous molecules, angiogenic factors including growth
factors such as acidic and basic fibroblast growth factors,
vascular endothelial growth factor, epidermal growth factor,
transforming growth factor .alpha. and .beta., platelet-derived
endothelial growth factor, platelet-derived growth factor, tumor
necrosis factor .alpha., hepatocyte growth factor and insulin like
growth factor, cell cycle inhibitors including CD inhibitors,
thymidine kinase ("TK") and other agents useful for interfering
with cell proliferation, the family of bone morphogenic proteins
("BMP's"), BMP-2, BMP-3, BMP-4, BMP-5, BMP-6 (Vgr-1), BMP-7 (OP-1),
BMP-8, BMP-9, BMP-10, BMP-11, BMP-12, BMP-13, BMP-14, BMP-15, and
BMP-16. Any of BMP-2, BMP-3, BMP-4, BMP-5, BMP-6 and BMP-7 are
particularly desirable. These dimeric proteins can be provided as
homodimers, heterodimers, or combinations thereof, alone or
together with other molecules. Alternatively or, in addition,
molecules capable of inducing an upstream or downstream effect of a
BMP can be provided. Such molecules include any of the "hedgehog"
proteins, or the DNA's encoding them.
[0036] Suitable cellular materials include cells of human origin
(autologous or allogeneic) or from an animal source (xenogeneic),
genetically engineered if desired to deliver proteins of interest
at the transplant site. The delivery media can be formulated as
needed to maintain cell function and viability.
[0037] Suitable polymer coating materials include polycarboxylic
acids, cellulosic polymers, including cellulose acetate and
cellulose nitrate, gelatin, polyvinylpyrrolidone, cross-linked
polyvinylpyrrolidone, polyanhydrides including maleic anhydride
polymers, polyamides, polyvinyl alcohols, copolymers of vinyl
monomers such as EVA, polyvinyl ethers, polyvinyl aromatics,
polyethylene oxides, glycosaminoglycans, polysaccharides,
polyesters including polyethylene terephthalate, polyacrylamides,
polyethers, polyether sulfone, polycarbonate, polyalkylenes
including polypropylene, polyethylene and high molecular weight
polyethylene, halogenated polyalkylenes including
polytetrafluoroethylene, polyurethanes, polyorthoesters, proteins,
polypeptides, silicones, siloxane polymers, polylactic acid,
polyglycolic acid, polycaprolactone, polyhydroxybutyrate valerate
and blends and copolymers thereof, coatings from polymer
dispersions such as polyurethane dispersions (BAYHDROL.RTM., etc.),
fibrin, collagen and derivatives thereof, polysaccharides such as
celluloses, starches, dextrans, alginates and derivatives,
hyaluronic acid, squalene emulsions. Desirably, polyacrylic acid,
available as HYDROPLUS.RTM. (Boston Scientific Corporation, Natick,
Mass.), and described in U.S. Pat. No. 5,091,205, the disclosure of
which is hereby incorporated herein by reference, may be used. Also
desirably, the polymer may be a copolymer of polylactic acid and
polycaprolactone. Other materials include selected medical-grade
biodegradable materials such as PGA-TMC, Tyrosine-Derived
Polycarbonates and arylates, polycaprolactone co butyl acrylate and
other co polymers, Poly-L-lactic acid blends with DL-Lactic Acid,
Poly(lactic acid-co-glycolic acid), polycaprolactone co PLA,
polycaprolactone co butyl acrylate and other copolymers,
Tyrosine-Derived Polycarbonates and arylate, poly amino acid,
polyphosphazenes, polyiminocarbonates,
polydimethyltrimethylcarbonates, biodegradable CA/PO.sub.4'S,
cyanoacrylate, 50/50 DLPLG, polydioxanone, polypropylene fumarate,
or polydepsipeptides.
[0038] Other suitable coatings include macromolecules such as
chitosan and Hydroxylpropylmethylcellulose. Surface erodible
materials may also be used. Coatings may also comprise maleic
anhydride copolymers, zinc-calcium phosphate and amorphous
polyanhydrides.
[0039] The inventive stents may also be used as the framework for a
graft. Suitable coverings include nylon, collagen, PTFE and
expanded PTFE, polyethylene terephthalate and KEVLAR, or any of the
materials disclosed in U.S. Pat. No. 5,824,046 and U.S. Pat. No.
5,755,770. More generally, any known graft material may be used
including synthetic polymers such as polyethylene, polypropylene,
polyurethane, polyglycolic acid, polyesters, polyamides, their
mixtures, blends, copolymers, mixtures, blends and copolymers.
[0040] The above disclosure is intended to be illustrative and not
exhaustive. This description will suggest many variations and
alternatives to one of ordinary skill in this art. All these
alternatives and variations are intended to be included within the
scope of the claims where the term "comprising" means "including,
but not limited to". Those familiar with the art may recognize
other equivalents to the specific embodiments described herein
which equivalents are also intended to be encompassed by the
claims.
[0041] In addition to the specific embodiments claimed below, the
invention is also directed to other embodiments having any other
possible combination of the dependent features claimed below. As
such, the particular features presented in the dependent claims can
be combined with each other in other manners within the scope of
the invention such that the invention should be recognized as also
specifically directed to other embodiments having any other
possible combination of the features of the dependent claims. For
instance, for purposes of claim publication, any dependent claim
which follows should be taken as alternatively written in a
multiple dependent form from all prior claims which possess all
antecedents referenced in such dependent claim if such multiple
dependent format is an accepted format within the jurisdiction
(e.g. each claim depending directly from claim 1 should be
alternatively taken as depending from all previous claims). In
jurisdictions where multiple dependent claim formats are
restricted, the following dependent claims should each be also
taken as alternatively written in each singly dependent claim
format which creates a dependency from a prior
antecedent-possessing claim other than the specific claim listed in
such dependent claim below (e.g. claim 3 may be taken as
alternatively dependent from claim 1 or claim 2; claim 11 may be
taken as alternatively dependent on any of claims 9-10; claim 12
may be taken as alternatively dependent on any of claims 9-11
etc.).
[0042] Those familiar with the art may recognize other equivalents
to the specific embodiments described herein which equivalents are
also intended to be encompassed by the claims attached hereto.
* * * * *