TECHNICAL FIELD
This invention generally relates to stents and methods of making a stent from a tubular member for placement within a body lumen or interior space of a body during a medical procedure.
BACKGROUND
Stents are expandable endoprosthetic devices adapted to be placed in a body lumen in order to maintain the patency of a body lumen by providing a flow pathway and/or structural support, for example. Stents are typically used in the treatment of atherosclerotic stenosis in blood vessels and the like to reinforce body vessels and to prevent restenosis following angioplasty in the vascular system. Additionally, stents may be used in the treatment of aortic aneurysms, by providing strength to a weakened vascular wall. They have also been implanted in other body lumens, such as urinary tracts and bile ducts. Stents are generally tubular structures that may be radially expandable between an unexpanded size and an expanded size greater than the unexpanded size. Therefore, a stent may be inserted through a body lumen in an unexpanded state and then expanded at a specific location within the lumen to an expanded state.
As the use of stents in a variety of medical procedures is gaining widespread acceptance, it is desirable to provide improved methods of manufacturing stents in order to increase efficiency, reduce costs, and/or minimize material waste. The disclosed stents and accompanying methods of manufacturing a stent may be deemed advantageous in view of the increased usage of stents during medical procedures.
SUMMARY
The invention is directed to a stent manufactured from a tubular member. The stent may be cut from a tubular member such that a pattern and an opening extending from the first end to the second end of the tubular member are cut therein. The opening may define a first edge and a second edge through the wall of the tubular member. One or more connectors may be cut along either the first or second edge and may extend into the opening.
Accordingly, a process of making a stent from a tubular member is disclosed. A tubular structure having a pattern configured to provide expansion and an opening defining a first edge and a second edge may be cut from a tubular member. The opening may be cut such that one or more connectors may be cut along either the first or second edge and extend into the opening.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention may be more completely understood in consideration of the following detailed description of various embodiments in connection with the accompanying drawings, in which:
FIG. 1A is a perspective view of an exemplary stent within the scope of the invention;
FIG. 1B is a perspective view of an exemplary embodiment of a pattern cut in a tubular member to form a stent within the scope of the invention;
FIG. 1C is a cut away view of the tubular member of FIG. 1B, more easily showing an opening cut along the tubular member including exemplary connectors within the scope of the invention;
FIG. 1D is a perspective view of the tubular structure formed after expansion of the tubular member of FIG. 1B;
FIGS. 1E-1F are enlarged views of exemplary embodiments of connectors within the scope of the invention;
FIG. 2A is a perspective view of another exemplary stent within the scope of the invention including a plurality of connectors extending across an opening;
FIG. 2B is a perspective view of an exemplary embodiment of a pattern cut in a tubular member to form a stent within the scope of the invention;
FIG. 2C is a cut away view of the tubular member of FIG. 2B, more easily showing an opening cut along the tubular member including exemplary connectors within the scope of the invention;
FIG. 2D is an enlarged view of an exemplary connector extending across an opening cut in a tubular member within the scope of the invention;
FIG. 3A is a perspective view of another exemplary stent within the scope of the invention;
FIG. 3B is a perspective view of an exemplary embodiment of a pattern cut in a tubular member to form a stent within the scope of the invention;
FIG. 3C is a cut away view of the tubular member of FIG. 3B, more easily showing an opening cut along the tubular member including exemplary connectors within the scope of the invention;
FIGS. 3D-3G are enlarged views of exemplary embodiments of connectors comprising tooling nodes within the scope of the invention;
FIG. 4A is a perspective view of an exemplary embodiment of another tubular member to form a stent within the scope of the invention;
FIG. 4B is a cut away view of the tubular member of FIG. 4A, more easily showing an opening cut along the tubular member including a spine extending along the opening within the scope of the invention;
FIG. 5 is a plan view illustrating an exemplary device for elongating and/or forming the tubular member of FIG. 3B;
FIG. 6 is a plan view illustrating forming an exemplary stent having overlapping edges within the scope of the invention; and
FIG. 7 is a plan view illustrating forming an exemplary stent having a C-shape within the scope of the invention.
DETAILED DESCRIPTION
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
The following detailed description should be read with reference to the drawings in which similar elements in different drawings are numbered the same. The detailed description and the drawings, which are not necessarily to scale, depict illustrative embodiments and are not intended to limit the scope of the invention. The illustrative embodiments depicted are intended only as exemplary. Selected features of any illustrative embodiment may be incorporated into an additional embodiment unless clearly stated to the contrary.
Referring now to the drawings, and particularly FIG. 1A, illustrates an exemplary stent 10 within the scope of the invention. As discussed herein, stent 10 may be formed from a tubular member. Stent 10 may be manufactured from a variety of materials. For example, stent 10 may include a nickel-titanium alloy, such as a shape memory material commonly referred to as nitinol, which may provide the stent 10 with superelastic properties, psuedoeleastic properties, or linear elastic properties. Other suitable materials for the stent include, but are not limited to, stainless steels and their alloys, composites, platinum enhanced stainless steel, layered materials, niobium (Nb), zirconium (Zr), Nb—Zr alloys, tantalum (Ta), platinum (Pt), titanium (Ti), gold (Au), silver (Ag), magnesium (Mg), and alloys and compositions comprising the same. Polymers, polymer composites, and combinations and mixtures thereof, may also be used. Stent 10 may be treated or coated with an anti-thrombogenic agent, an anti-proliferative agent, an anti-inflammatory agent, or an anti-coagulant. Additionally or alternatively, stent 10 may be treated or coated with a medication, such as a time-release drug. Stent 10 may also desirably have radiopaque characteristics for visualization on a fluoroscopy device, which may aid in proper placement of the stent 10 during a medical procedure. For example, stent 10 may be doped with, plated with, or otherwise include a radiopaque material. Radiopaque materials are understood to be materials capable of producing a relatively bright image on a fluoroscopy screen or another imaging technique during a medical procedure. Some examples of radiopaque materials include, but are not limited to, gold (Au), platinum (Pt), palladium (Pd), tantalum (Ta), tungsten (W), plastic material loaded with radiopaque filler, and the like. Stent 10 may, alternatively or additionally, include MRI compatible materials and/or be coated with one or more MRI compatible coatings.
Now referring to FIG. 1B, stent 10 may be formed from a tubular member 50. Tubular member 50 may be a thin-walled tube having appropriate dimensions. A pattern 60 may be cut into tubular member 50. Although a relatively simple pattern of interconnected segments is shown in FIG. 1B, numerous patterns of varying design and complexity are possible. A selected pattern 60 may dictate the degree of expansion and/or flexibility of stent 10. Pattern 60 may be cut into tubular member 50 by a laser cutting device controlled by a computer automated system, for example a computer numerically controlled (CNC) machine. Such a laser cutting device may be able to replicate a very intricate and precise pattern 60. A laser beam, for example, or a laser beam traveling through a fluid jet may be directed at the tubular member 50. The tubular member 50 may be translated and/or rotated relative to the position of the laser, or vise versa, in order to cut the desired pattern 60. The lumen 20 of the tubular member 50 may be subjected to a fluid column to flush dross from the tubular member, provide cooling to the cutting zone, and/or deflect the laser beam from the opposing wall of the tubular member 50 during the cutting process. The fluid column may be a gas and/or a liquid, and a single or multiple fluid columns may be provided through the lumen 20. For example, two fluid columns may be separated by a tubular mandrel disposed within the lumen 20 of the tubular member 50, such that a first column of fluid is positioned in the annular space between the tubular member 50 and the mandrel and a second fluid column is positioned in the lumen of the tubular mandrel. Such a laser cutting process is disclosed in U.S. Pat. No. 6,696,666 entitled Tubular Cutting Process and System, which is herein incorporated by reference in its entirety. Other cutting techniques may include optical etching, chemical etching, electron beam ablation, material deposition, as well as other laser ablation techniques.
FIG. 1C shows a cut away view of tubular member 50. An opening 30 may be cut through tubular member 50 during the cutting process or during an additional cutting process. Opening 30 may extend from the first end 22 of the tubular member 50 to the second end 24 of the tubular member 50. Opening 30 defines a first edge 32 and an opposing second edge 34 of the wall of the tubular member 50 and may extend from the first end 22 to the second end 24. Edges 32, 34 may extend from the outer surface to the inner surface of the wall of the tubular member 50. Opening 30 may extend substantially longitudinally along tubular member 50. However, opening 30 may extend helically around the tubular member 50, providing a helical configuration of opening 30 along the length of tubular member 50, undulate along at least a portion of the length of tubular member 50, or otherwise extend along tubular member 50 in a regular or irregular manner.
One or more connectors 40 may be cut along the first edge 32 and extend into the opening 30. Additionally or alternatively, one or more connectors 40 may be cut along the second edge 34 and extend into the opening 30. Connectors 40 may be positioned adjacent one another and extend from opposing edges 32, 34 of the tubular member 50, or connectors 40 may be alternated along at least a portion of the length of the opening 30. A connector 40 may extend from the first edge 32 toward the second edge 34 and be attached to a connector 40 extending from the second edge 34 toward the first edge 32, thus creating one continuous connector 40 spanning the opening 30 between the first edge 32 to the second edge 34. Alternatively, opposing connectors 40 may not be attached to one another, thus a space may remain between opposing connectors 40.
FIGS. 1E and 1F show two possible embodiments of connector 40. As shown in FIG. 1E, connector 40 may be a serpentine or zig-zag shaped strut extending from the first edge 32 to the second edge 34. The shape and size of connector 40 may be dimensioned such that the connector 40 may be elongated a predetermined amount during a subsequent expansion process. FIG. 1F shows another embodiment of a connector 40 similar to that shown in FIG. 1E. Connector 40 may have a serpentine or zig-zag shape having a grasping portion, such as an eyelet 42. The eyelet 42 may be substantially located in the central portion of the connector 40, or eyelet 42 may be located at any position along connector 40. An aperture, such as hole 44 may extend through eyelet 42. Hole 44 may allow a tooling device to be coupled or otherwise be engaged with the connector 40. Eyelet 42 may be used to retain and/or manipulate the stent 10 during a subsequent manufacturing process. The aperture may extend through eyelet 42 or the aperture may be a recess or pocket with a terminus within the thickness of connector 40. Other configurations of connectors, such as connectors with a grasping portion such as tabs, slots, slits, projections, grooves, loops, or hooks are contemplated to be within the scope of the invention.
Referring now to FIG. 1D, the tubular member 50 may be expanded subsequent to cutting the pattern 60 in the tubular member 50. The resulting tubular structure 70 may have an outer diameter greater than the initial diameter of the tubular member 50. Tubular member 50 may be expanded by placing a mandrel through the lumen 20 of tubular member 50 or by other means for expanding the tubular member 50. The expanded tubular structure 70 may be a mesh 65 including a plurality of interconnected segments 66 formed from the material of the tubular member 50 remaining after cutting the pattern 60 in the tubular member 50. The interconnected segments 66 are spaced farther apart after expansion to create the mesh 65 having a plurality of interstices 67 disposed therein. The specific pattern 60 cut into the tubular member 50 and/or the material used may dictate the degree of expansion of the tubular structure 70.
As a result of the expansion of the tubular structure 70, connectors 40 may become elongated. Connectors 40 may provide support and/or continuous structure in order to ensure uniform, non-uniform or an otherwise predetermined expansion of the tubular structure 70. Therefore, the tubular shape of the structure 70 may be maintained throughout the expansion process. For example, connectors 40 may be configured to have a degree of expansion similar to that of the pattern 60. Therefore, the circumferential expansion of the tubular structure 70 may be uniform at all locations around the circumference of the tubular structure 70. Connectors 40 may be configured to provide visual confirmation of proper expansion, such as when the connectors 40 are sufficiently straightened. Therefore, the tubular structure 70 may reach its proper expanded dimensions when the connectors 40 have reached a sufficient elongated configuration. Alternatively, connectors may be configured to provide visual confirmation of proper expansion of the tubular member 50 at the point where elongation of connectors 40 commences or at the point of fracture of connectors 40 from tubular member 50.
Connectors 40 may be sufficiently frangible such that connectors 40, or a portion thereof, may be separated from the tubular structure 70 subsequent expansion of the tubular structure 70, or connectors 40 may be retained with the tubular structure 70. Connectors 40 may be removed during a subsequent process using mechanical, electrical or chemical techniques. A cutting process may be used to provide separation from the edge 32, 34 of the structure 70. For example, a laser ablation technique may be used to separate the connectors 40 from the tubular structure 70 or weaken the interface between connector 40 and tubular structure 70. Connectors 40 may be removed by mechanically cutting, snipping, breaking or otherwise severing the connectors, or by grinding, sandblasting or otherwise eroding away material. Additionally or alternatively, a chemical etching or electro-polishing process may be used to remove connectors 40 or a portion thereof. Connectors 40 may be dissolved or weakened during a subsequent manufacturing process in which a portion of the material is eroded away.
FIG. 2A shows a tubular structure 170 forming another stent 110, similar to stent 10. Stent 110 may be similarly formed from a tubular member 150. Tubular structure 170, shown in FIG. 2A, includes connectors 140 coupled to stent 110 subsequent to expansion of the stent 110. However, connectors 140 may be removed from stent 110 during or subsequent the expansion process, as discussed herein. With connectors 140 removed, stent 110 may substantially replicate stent 10 illustrated in FIG. 1A. As shown in FIG. 2B, a pattern 160 may be cut through tubular member 150. Additionally, an opening 130 may extend from the first end 122 to the second end 124 of the tubular member 150. As shown in the cut away view in FIG. 2C, the opening 130 defines a first edge 132 and a second edge 134 of the wall of the tubular member 150. One or more connectors 140 may be cut in the tubular member 150 such that connector 140 extends across the opening 130 from the first edge 132 to the second edge 134. Connector 140, which may more clearly be understood from FIG. 2D, may be connected to opposing edges 132, 134 of the tubular member 150. Connector 140 may have one or more apertures, such as holes 144 used to retain and/or manipulate the tubular structure 170 during a manufacturing process. The aperture may extend through the wall of tubular structure 170 or the aperture may be a recess or pocket with a terminus within the wall of tubular structure 170. Other configurations of connectors, such as connectors having a grasping portion including tabs, slots, slits, projections, grooves, loops, or hooks are contemplated to be within the scope of the invention. Hole 144 may be located in the central portion of connector 140, or hole 144 may be located at another location of connector 140. Connector 140 may provide support and/or continuous structure in order to ensure uniform, non-uniform or otherwise proper expansion of the tubular structure 170 during expansion of the stent 110. Therefore, the tubular shape of the structure 170 may be maintained throughout the expansion process. Connector 140 may allow the tubular structure 170 to retain a uniform diameter during expansion of the stent 110. The connection between the connector 140 and the edge 132, 134 of the tubular structure 170 may be a weakened zone or an otherwise frangible region, such that prior to providing the finished product stent 110, connector 140 may be removed. The connector 140, or a portion thereof, may be removed by mechanically cutting, snipping, breaking, grinding, sandblasting, laser ablation, chemical etching, electro-polishing, or other processes wherein the connector 140 is separated, eroded or dissolved from the tubular structure 170.
FIG. 3A illustrates a stent 210 similar to stent 10 in an expanded configuration. Stent 210 may include one or more connectors 240, as discussed herein. As shown in FIG. 3B, stent 210 may be cut from a tubular member 250 such as discussed above. An opening 230, which may more easily be shown in the cut away view of FIG. 3C, may be cut along tubular member during a cutting process and may extend from the first end 222 to the second end 224 of the tubular member 250. One or more connectors 240 may be cut in tubular member 250, such that connectors 240 extend from edge 232, 234 of tubular member 250 into opening 230. As more clearly shown in FIGS. 3D-3G, connectors 240 may be tooling nodes. Connectors 240 may be configured to be coupled to or otherwise engaged with a tooling apparatus. Connectors 240 may be used to retain and/or manipulate the tubular structure 270 during a subsequent manufacturing process. As shown in FIG. 3D, connectors 240 may extend from edge 232, 234 toward an opposing edge. However, connectors 240 may not be connected to one another. Instead, a gap may be maintained between adjacent connectors 240. Although connectors 240 are shown adjacent one another, opposing connectors 240 may alternate along the length of the tubular structure 270, such as shown in FIG. 3G. Alternatively, connectors 240 may extend toward an adjacent connector 240 and be connected to an adjacent connector 240, as shown in FIG. 3E. The connection between adjacent connectors 240 may be a weakened zone or an otherwise frangible region. For example, the connection may be a region of reduced cross sectional area or an area scored during a cutting process. Such a configuration of connectors 240 may be separated during a subsequent manufacturing process. For example, connectors 240 may be separated by mechanically cutting, snipping, breaking, grinding, sandblasting, laser ablation, chemical etching, or electro-polishing. FIG. 3F illustrates yet another embodiment of connectors 240. A strut 242 may bridge a pair of connectors 240 extending from opposing edges 232, 234 of the tubular structure 270. Strut 242 may have a serpentine or zig-zag shape or otherwise have an extendable shape. During an expansion process, strut 242 may be elongated similar to connectors 40 discussed above regarding FIGS. 1A-1F. Therefore, strut 242 may provide support and/or continuous structure around the circumference of the tubular structure 270 in order to ensure uniform, non-uniform or otherwise proper expansion of the tubular structure 270. Therefore, the tubular shape of the structure 270 may be maintained throughout the expansion process. Elongation of the strut 242 may be a visual indicator of proper expansion of the tubular structure 270. Sufficient elongation of the strut 242 may indicate the tubular structure 270 has reached its predetermined expanded configuration. Subsequent to expansion of the tubular structure 270, strut 242 may be removed by mechanical, electrical or chemical means. For example, strut 242 may be removed by laser ablation, cutting, snipping, breaking, grinding, sandblasting, or prior to or during a chemical etching or electro-polishing process.
Alternatively or additionally, a wire or filament may be extend between connectors 240 to join opposing or alternating connectors. For example, the wire may be laced or threaded through holes 244 of connectors 240. The wire may be a temporary connector which extends across opening 230. The wire may substantially restrain separation of opposing edges 232, 234 or tubular structure 270. The wire may provide support and/or continuous structure to the tubular member 250 to ensure uniform, non-uniform or an otherwise predetermined expansion of the tubular structure 270. Therefore, the tubular shape of the structure 270 may be maintained throughout the expansion process. Subsequent expansion and/or forming of the tubular structure 270, the wire may be removed from the structure 270. The wire may be removed by mechanical, electrical or chemical means. The wire may be dissolvable whereby it is dissolved with a solvent, by a thermal process, a chemical process or an electrical process. The wire may have characteristics similar to a dissolvable suture. Alternatively, wire may be mechanically removed by a laser, grinding, sandblasting, cutting, snipping, etching, breaking, or by another process.
Additionally or alternatively, connectors, such as connectors 240, having an aperture such as a recess, may include an adhesive. The adhesive, which may be disposed in the recess of the connector 240, may be used to secure one portion of the tubular structure 270 with another portion of the tubular structure 270. For example, one connector 240 may be adhesively secured to an opposing connector 240. The adhesive may also be used to secure the tubular structure 270 to another apparatus for forming and/or processing of the tubular structure 270. The adhesive may be dissolvable, or otherwise provide temporary securement, or the adhesive may be intended to provide permanent securement.
Alternatively or additionally, an apparatus such as a mandrel having hooks, tines, clips, or other engagement means, may be used to engage connectors 240. The mandrel may substantially couple opposing edges 232, 234 such that edges 232, 234 are restrained from separation during expansion of the tubular structure 270. For example, the hooks of the mandrel may be inserted in holes 244 of connectors 240. The mandrel may provide support and/or continuous structure to the tubular member 250 to ensure uniform, non-uniform or an otherwise predetermined expansion of the tubular structure 270. Therefore, the tubular shape of the structure 270 may be maintained throughout the expansion process. Subsequent expansion and/or forming of the tubular structure 270, the mandrel may be removed from the structure 270. Although the mandrel may engage connectors 240, mandrel may also engage another portion of the stent to restrain separation of opposing edges 232, 234.
FIG. 4A shows another embodiment of a tubular member 350 for forming a stent within the scope of the invention. As more easily shown in FIG. 4B, tubular member 350 may be cut with an opening 330 extending from a first end 322 to a second end 324. A connecting spine 345 may be disposed along opening 330. One or more connectors 340 may extend from edge 332, 334 to connecting spine 345. An electrical current of a sufficient magnitude may be applied to the connecting spine 345 to remove the connectors 340. The connectors 340 may be sufficiently thin relative to the other portions of the tubular member 350, such that the magnitude of the electrical current and/or the geometry of the connectors 340 is sufficient to remove the connectors 340 from the stent. Alternatively, an electrical current may be directly applied to the connectors 340, thus alleviating the need for the connecting spine 345.
Connectors 240, characterized as tooling nodes as shown in FIGS. 3D-3G, may be used to retain and manipulate tubular structure 250 during a subsequent process. For example, FIG. 5 illustrates an exemplary process wherein a tooling device 400 is coupled to or otherwise engaged with one or more connectors 240. Tooling device 400 may be manipulated such that tubular member 250 is unrolled and/or elongated into a substantially planar sheet 280. Thus, interconnected segments 266 may be sufficiently directed away from one another to form a mesh 265 with a plurality of interstices 267 disposed thereon. While elongated in a substantially planar sheet 280, the sheet may be subjected to one or more additional processes, such as a heat treatment process, a cleaning process, a chemical etching process, an electro-polishing process, a quenching process, a coating process, or another chosen process. Sheet 280 may undergo a forming process, wherein the sheet 280 is rolled into a tubular stent. Additional processes, such as a heat treatment process, a cleaning process, an electro-polishing process and/or a coating process may follow rolling the sheet 280 into a tubular stent. Tooling device 400, or an additional tooling device, may be used to re-roll or otherwise form the sheet 280 into a tubular stent or an intermediate form. For example, a mandrel having clips, tines, hooks or other means of engaging the structure may be used to expand, roll, form, wrap or otherwise manipulate the structure to form a stent.
Any one of the previously disclosed tubular structures may further be rolled into a coil stent. As shown in FIG. 6, a stent, such as stent 10 may be wrapped such that the first edge 32 of the tubular structure 70 overlaps the second edge 34. The degree of overlap may be determined by the profile necessary to provide sufficient clearance through a body lumen, such as a blood vessel, and/or the degree of expansion necessary to provide sufficient patency of a body lumen. A tooling device, such as a mandrel, may be coupled to one or more connectors 40 along one edge of stent 10 and rotated such that the first edge 32 is urged toward the second edge 34. Thus the stent 10 may be wrapped into a chosen tubular shape such as a coiled overlapping configuration. However, stent 10 may be rolled into a coil using other mechanical means. Alternatively, stent 10 may be rolled such that edge 32 substantially abuts edge 34 to form a generally continuous tubular structure. Edge 32 may be secured to edge 34 by welding, brazing, soldering, bonding, adhesive, mechanically coupling, crimping, or the like, or edges 32, 34 may remain unconnected.
Alternatively, one of the previously disclosed tubular structures may be formed in a C-shape such as shown in FIG. 7. A stent 10 having a C-shape may be readily expanded within a lumen to provide necessary patency of the lumen. The opening 30 extending along the length of the stent 10 allows opposing edges 32, 34 to deflect away from one another when stent 10 is allowed to expand within a lumen. Stent 10 may be formed into a C-shape during a subsequent forming/rolling process, or C-shape may be the result of cutting a tubular member 50 and expanding into a tubular structure 70 having a longitudinal, helical, undulating or otherwise elongate opening 30 as discussed above.
Any one of the previously described stent forming processes may include one or more further processing steps. For example, the tubular member may be subjected to a cleaning process to remove dross or residue subsequent a cutting process. For instance, an alcohol and/or water solution may be used to clean foreign material from the tubular structure. A chemical etching process may be used to remove connectors and/or other material from the tubular structure to provide a surface with no sharp edges or burrs. An electro-polishing process may be used to reduce the surface roughness of the machined tubular member and provide a stent having a substantially smooth outer surface. An electro-polishing process, or similar electrical process, may also be used to dissolve or otherwise separate a connector from the stent. For example, an electro-polishing process may dissolve a percentage of the mass of the material forming the stent. By dimensioning the connectors relatively small compared to the material of the interconnected segments of the stent, the connectors will completely dissolve, erode or otherwise be separated from the stent without fully dissolving the interconnected segments during an electro-polishing process. An electrical current of a sufficient magnitude may be applied to the connectors to separate the connectors from the stent. Additionally, a stent may be subjected to one or more heat treating processes in order to remove residual stresses and/or provide favorable characteristics to the stent, such as shape memory properties.
One illustrative stent forming process may include a plurality of processes. Initially a stent may be laser cut from a tubular member as discussed above. The stent may then be subjected to a chemical etching and/or electro-polishing process to remove residue, connectors and/or rough edges remaining after being cut from the tubular member. Alternatively or additionally, the stent may be placed in an ultrasonic cleaning process. Next, the stent may be expanded or otherwise formed by rolling and/or tucking the ends of the stent. Once formed, the stent may be heat treated to remove any residual stresses and/or provide shape memory properties and then quenched. The stent may then undergo a final cleaning process to remove any remaining residue. Additional processes, such as chemical etching, electro-polishing, cleaning or heat treating, may be included throughout. For example, the stent may be subjected to a chemical etching or electro-polishing process subsequent to being expanded in order to remove temporary connectors from the stent.
It is contemplated that the disclosed process of forming a stent may be substantially used to form other similar products from a tubular member. For example, a filter mesh or frame for an intravenous filter or distal protection device may be formed utilizing the disclosed process.
Those skilled in the art will recognize that the present invention may be manifested in a variety of forms other than the specific embodiments described and contemplated herein. Accordingly, departure in form and detail may be made without departing from the scope and spirit of the present invention as described in the appended claims.
Patent Application
20060248698
