CA2563023A1 - Polymer-based stent assembly - Google Patents

Polymer-based stent assembly Download PDF

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Publication number
CA2563023A1
CA2563023A1 CA002563023A CA2563023A CA2563023A1 CA 2563023 A1 CA2563023 A1 CA 2563023A1 CA 002563023 A CA002563023 A CA 002563023A CA 2563023 A CA2563023 A CA 2563023A CA 2563023 A1 CA2563023 A1 CA 2563023A1
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CA
Canada
Prior art keywords
cylindrical device
polymeric
stent
diameter
polymer
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CA002563023A
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French (fr)
Other versions
CA2563023C (en
Inventor
Antoine Lafont
Serge Piranda
Patrick Sabaria
Tahmer Sharkawi
Michel Vert
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Sahajanand Medical Technologies Pvt Ltd
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Individual
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Publication of CA2563023A1 publication Critical patent/CA2563023A1/en
Application granted granted Critical
Publication of CA2563023C publication Critical patent/CA2563023C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L31/00Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
    • A61L31/04Macromolecular materials
    • A61L31/06Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/9522Means for mounting a stent or stent-graft onto or into a placement instrument
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/958Inflatable balloons for placing stents or stent-grafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2210/00Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2210/0004Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof bioabsorbable

Abstract

Methods for preparing a polymer-based stmt assembly comprising an inflatable balloon catheter and a polymer-based stmt resistant to relaxation-related negative recoil are provided. The methods comprise heating a polymeric cylindrical device which is at a final predetermined shape and diameter to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase any memory of previous processing of the polymeric cylindrical device and then quenching the polymeric cylindrical device to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape, mounting the educated cylindrical device on an inflatable balloon catheter, reducing the diameter of the educated cylindrical device by heating to a temperature at or slightly above the Tg of the polymer while evenly applying pressure on the exterior surface of the wall of the cylindrical device, and then cooling the cylindrical device below the Tg of the polymer to provide a stmt assembly comprising an inflatable balloon catheter and an expandable, educated, polymeric stmt snugly and stably disposed thereon. Assemblies comprising an inflatable balloon and a polymer based stmt that is substantially resistant to relaxation related recoil mounted snugly on the balloon are also provided.

Claims (26)

1. A method for preparing an assembly for delivering a degradable and bioresorbable polymeric stent that is resistant to relaxation-related recoil to a mammalian subject, comprising:

(a) heating a polymeric cylindrical device which is at a final predetermined radial diameter and wall thickness to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase memory of previous processing of the polymeric device, wherein the polymeric cylindrical device has a wall defining a first open end, a second open end, and a channel connecting the first and the second open end;

(b) rapidly cooling the polymeric cylindrical device at a temperature below the Tg of the polymer to quench the polymeric cylindrical device and to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape;

(c) forming slits, voids, or open spaces in the wall of the polymeric cylindrical device prior to step (a) or after step (b), wherein the slits, voids, or open spaces are configured to allow a reduction in diameter of the device without substantially altering the wall thickness of the device;

(d) mounting the educated polymeric cylindrical device on an inflatable balloon catheter;

(e) reducing the diameter of the cylindrical device by heating the cylindrical device to a temperature at or slightly above the Tg of the polymer while evenly applying pressure on the exterior surface of the wall of the cylindrical device; and (f) then rapidly cooling the cylindrical device below the Tg of the polymer to provide an assembly comprising a inflatable balloon catheter and an expandable polymeric stent which is substantially resistant to relaxation-related recoil when implanted in the lumen of a tube, duct, or vessel of the mammalian subject or when expanded and stored at 37° C for 4 to 6 weeks.
2. The method of claim 1 wherein the cylindrical device is mounted on a support for maintaining the diameter and shape of the device during step (a) and step (b).
3. The method of claim 1 wherein the stent is formed from a polymer selected from PLA
and stereocopolymers (copolymers composed of L and D units), PLAGA, Poly(lactic-co-glycolic-co-gluconic acid.
4. The method of claim 1 wherein the cylindrical device is reduced to a diameter that is less than the diameter of the lumen of the target duct, tube, or vessel during step (e).
5. The method of claim 1 wherein the wall thickness of the cylindrical device is substantially the same before and after step (e).
6. A method for preparing an assembly for delivering a degradable and bioresorbable polymeric stent into the lumen of a tube, duct, or vessel of a mammalian subject, comprising:

(a) providing a polymeric cylindrical device comprising a wall defining a first open end, a second open end, and a channel connecting said first open end and said second open end, wherein the cylindrical device has a diameter and wall thickness comparable to the final desired diameter and wall thickness of the stent;

(b) educating the device by erasing memory of previous processing of the polymeric device and establishing a memory of the desired diameter; wherein such education is achieved by heating the device to a temperature at least 8 degrees C above the Tg of the polymer;

(c) quenching the device to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape;

(d) forming slits, voids, or open spaces in the wall of the polymeric cylindrical device before or after the device is educated;

(e) mounting the educated polymeric cylindrical device on an inflatable balloon catheter;

(f) crimping the cylindrical device on the inflatable balloon catheter while heating the cylindrical device to a temperature at or slightly above the Tg of the polymer; and (g) then rapidly cooling the cylindrical device below the Tg of the polymer to provide an assembly comprising an inflatable balloon catheter and an expandable polymeric stent which is substantially resistant to relaxation-related recoil when implanted in the lumen of a tube, duct, or vessel of a mammalian subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more.
7. A method for preparing an assembly for delivering a degradable and bioresorbable polymeric stent into the lumen of a tube, duct, or vessel of a mammalian subject, comprising:

(a) providing a hollow, cylindrical device comprising a wall having slits, openings, or voids therein, wherein the hollow cylindrical device has a radial diameter that is less than the final predetermined diameter of the stent;

(b) heating the polymeric cylindrical device to a temperature close to or above the Tg of the polymer while expanding the tube to the final predetermined diameter;

(c) mounting the cylindrical device on a support for maintaining the cylindrical device at the final predetermined diameter;

(d) heating the mounted cylindrical device to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase memory of previous processing of the polymeric device;

(e) rapidly cooling the polymeric cylindrical device at a temperature below the Tg of the polymer to quench the polymeric cylindrical device and to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter;

(f) mounting the educated polymeric cylindrical device on an inflatable balloon catheter;

(g) reducing the diameter of the cylindrical device by heating the cylindrical device to a temperature at or slightly above the Tg of the polymer while evenly applying pressure on the exterior surface of the wall of the cylindrical device; and (h) then rapidly cooling the cylindrical device below the Tg of the polymer to provide an assembly comprising a inflatable balloon catheter and an expandable polymeric stent which is substantially resistant to relaxation-related recoil when implanted in the lumen of a tube, duct, or vessel of a mammalian subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more.
8. The method of claim 6 wherein the stent is formed from a polymer selected from PLA
and stereocopolymers (copolymers composed of L and D units), PLAGA, Poly(lactic-co-glycolic-co-gluconic acid.
9. The method of claim 6 wherein the wall thickness of the cylindrical device is substantially the same before and after step (g).
10. A method for preparing an assembly for delivering a degradable and bioresorbable polymeric stent into the lumen of a tube, duct, or vessel of a mammalian subject, comprising:

(a) providing a polymeric cylindrical device comprising a wall defining a first open end, a second open end, and a channel connecting said first open end and said second open end, and having slits, voids, or open spaces for permitting expansion and contraction of the device without substantially altering the thickness of the wall, wherein the cylindrical device has a radial diameter that is less than the final desired diameter of the stent, (b) expanding the polymeric device to the final desired diameter while heating to a temperature close to or above the Tg of the polymer;

(c) educating the device by erasing memory of previous processing of the polymeric device and establishing a memory of the desired diameter; wherein such education is achieved by heating the device, which is mounted on a support, to a temperature at least 8 degrees C above the Tg of the polymer;

(c) quenching the device to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape;

(d) mounting the educated polymeric cylindrical device on an inflatable balloon catheter;

(e) crimping the cylindrical device on the inflatable balloon catheter while heating the cylindrical device to a temperature at or slightly above the Tg of the polymer; and (f) then rapidly cooling the cylindrical device below the Tg of the polymer to provide an assembly comprising a inflatable balloon catheter and an expandable polymeric stent which is substantially resistant to relaxation-related recoil when implanted in the lumen of a tube, duct, or vessel of a mammalian subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more.
11. An assembly comprising an inflatable balloon and a polymeric stent prepared in accordance with the method of claim 1, 6, 7, or 10.
12. An assembly for introducing a degradable and bioresorbable stent into a vessel, tube, or duct of a mammalian subject, comprising:

an inflatable balloon catheter, and a stent formed from a degradable polymeric material having a Tg at least 45°
mounted thereon, wherein the stent comprises a wall defining a first open end, a second open end, and a channel connecting the first and second open end, and wherein the wall of stent includes voids, open spaces, or slits that allow the stent to be expanded to a larger diameter, a shorter length, and the same wall thickness when the balloon catheter is inflated or when the stent is heated to a temperature above the Tg of the polymer, and wherein the stent exhibits little to no negative recoil when deployed in the blood vessel of a subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more; and wherein the assembly has a diameter that allows it to be inserted into a tube, vessel or duct of the subject and advanced to a target site.
13. The assembly of claim 12, wherein the assembly has a diameter that allows the stent to be inserted into a blood vessel of a human subject and advanced to stenotic lesion.
14. The assembly of claim 12 wherein the stent exhibits positive recoil and adaptation to the geometry of the artery when the stent is not fully deployed up to its final diameter during deployment.
15. The assembly of claim 12 wherein the stent is formed from a polymer selected from PLA and stereocopolymers (copolymers composed of L and D units), PLAGA, Poly(lactic-co-glycolic-co-gluconic acid.
16. The assembly of claim 12 wherein the stent is stably mounted on the balloon.
17. The assembly of claim 12 further comprising a retractable sheath covering the exterior surface of the stent.
18. The assembly of claim 12 wherein bioactive agent or tracking agent is disposed within or on a surface of the stent.
19. A method for preparing a degradable and bioresorbable polymeric stent for implantation into the lumen of a tube, duct, or vessel of a mammalian subject, comprising:

(a) heating a polymeric cylindrical device which is at a final predetermined radial diameter and wall thickness to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase memory of previous processing of the polymeric device, wherein the polymeric cylindrical device has a wall defining a first open end, a second open end, and a channel connecting the first and the second open end;

(b) rapidly cooling the polymeric cylindrical device at a temperature below the Tg of the polymer to quench the polymeric cylindrical device and to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape;
and (c) forming slits, voids, or open spaces in the wall of the polymeric cylindrical device prior to step (a) or after step (b), wherein the stent is resistant to relaxation-related recoil when deployed in the blood vessel of a subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more.
20. The method of claim 19 wherein the cylindrical device is mounted on a support for maintaining the diameter and shape of the device during step (a) and step (b) .
21. The method of claim 19 wherein the stent is formed from a polymer selected from PLA and stereocopolymers (copolymers composed of L and D units), PLAGA, Poly(lactic-co-glycolic-co-gluconic acid.
22 22. A method for preparing a degradable and bioresorbable polymeric stent that is resistant to relaxation-related recoil when implanted into the lumen of a tube, duct, or vessel of a mammalian subject or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more, comprising:

(a) providing a hollow, cylindrical device comprising a wall having slits, openings, or voids therein, wherein the hollow cylindrical device has a radial diameter that is less than the final predetermined diameter of the stent;

(b) heating the polymeric cylindrical device to a temperature close to or above the Tg of the polymer while expanding the tube to the final predetermined diameter;

(c) mounting the cylindrical device on a support for maintaining the cylindrical device at the final predetermined diameter;

(d) heating the mounted cylindrical device to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase memory of previous processing of the polymeric device; and (e) rapidly cooling the polymeric cylindrical device at a temperature below the Tg of the polymer to quench the polymeric cylindrical device and to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter.
23. The method of claim 22 wherein the stent is formed from a polymer selected from PLA and stereocopolymers (copolymers composed of L and D units), PLAGA, Poly(lactic-co-glycolic-co-gluconic acid.
24. A stent made in accordance with the methods of claims 19 or 22.
25. A stent substantially resistant to relaxation-related recoil when implanted in the lumen of a duct, vessel, or tube of a mammalian subject recoil or when expanded to a final predetermined shape and diameter and stored at 37°C for 4 weeks or more, wherein said stent is formed from a polymer has a Tg of 45°C or greater, and wherein said stent lacks a memory of processing, and has a memory of a final predetermined shape and diameter.
26. A method of reducing the risk of chronic restenosis that can occur in an artery of a patient following PTC angioplasty, comprising:

delivering the assembly of claim 12 to the locus of a stenotic lesion;

inflating the balloon to expand the stent to a diameter equal to or less than the final predetermined diameter; and deflating and withdrawing the balloon.
CA2563023A 2004-04-02 2004-04-02 Polymer-based stent assembly Expired - Fee Related CA2563023C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP2004/004133 WO2005096992A1 (en) 2004-04-02 2004-04-02 Polymer-based stent assembly

Publications (2)

Publication Number Publication Date
CA2563023A1 true CA2563023A1 (en) 2005-10-20
CA2563023C CA2563023C (en) 2012-01-24

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US (2) US7731740B2 (en)
EP (1) EP1737387B1 (en)
JP (1) JP4665109B2 (en)
KR (1) KR101098267B1 (en)
CN (1) CN1960684B (en)
AT (1) ATE442822T1 (en)
AU (1) AU2004318159B8 (en)
BR (1) BRPI0418712B8 (en)
CA (1) CA2563023C (en)
DE (1) DE602004023237D1 (en)
ES (1) ES2330849T3 (en)
HK (1) HK1102420A1 (en)
WO (1) WO2005096992A1 (en)

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