Progenitor Endothelial Cell Capturing with a Drug Eluting Implantable Medical Device

• US 20070141107A1
• Filed: 11/15/2006
• Published: 06/21/2007
• Est. Priority Date: 03/15/2000
• Status: Abandoned Application

• Current Assignee: OrbusNeich Medical Pte Ltd
• Original Assignee: Orbusneich Medical Incorporated (Orbusneich Medical)
• Inventors: Rowland, Stephen, Cottone, Robert, Kutryk, Michael, Yoklavich, Margaret
• Application Number:
  US11/560,356
• Publication Number:
  US 20070141107A1
• Time in Patent Office: Days
• US Class Current: 424/423
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61L 2300/256 Antibodies, e.g. immunoglobulins, vaccines
• CPC Class Codes: A61L 2300/438 Antigens
• CPC Class Codes: A61L 2300/64 Animal cells
• CPC Class Codes: A61L 2400/12 Nanosized materials, e.g. nanofibres, nanoparticles, nanowires, nanotubes; Nanostructured surfaces
• CPC Class Codes: A61L 27/34 Macromolecular materials
• CPC Class Codes: A61L 27/54 Biologically active materials, e.g. therapeutic substances A61L27/227 takes precedence
• CPC Class Codes: A61L 29/085 Macromolecular materials
• CPC Class Codes: A61L 29/16 Biologically active materials, e.g. therapeutic substances A61L29/048 takes precedence
• CPC Class Codes: A61L 31/10 Macromolecular materials
• CPC Class Codes: A61L 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence

Abstract

A medical device for implantation into vessels or luminal structures within the body is provided, which stimulates positive blood vessel remodeling. The medical device, such as a stent and a synthetic graft, is provided with a coating with a pharmaceutical composition containing a controlled-release matrix and one or more pharmaceutical substances for direct delivery of drugs to surrounding tissues. The coating on the medical device further comprises one or more barrier layers, and a ligand such as a peptide, an antibody or a small molecule for capturing progenitor endothelial cells in the blood contacting surface of the device for restoring an endothelium at the site of injury. In particular, the drug-coated stents are for use, for example, in balloon angioplasty procedures for preventing or inhibiting restenosis.

Claims

1. A method for in vivo positive blood vessel remodeling in a patient with vascular disease, comprising implanting into a blood vessel of a patient a medical device having a coating comprising one or more layers of a matrix, one or more pharmaceutical substances, and one or more ligands designed to bind to a specific molecule on the cell membrane of a target cell.

2. The method of claim 1, wherein the medical device is a stent, a vascular graft, a synthetic graft, a heart valve, a catheter, a vascular prosthetic filter, a pacemaker, a pacemaker lead, a defibrillator, a patent foramen ovale (PFO) septal closure device, a vascular clip, a vascular aneurysm occluder, a hemodialysis graft, a hemodialysis catheter, an atrioventricular shunt, an aortic aneurysm graft device or components, a venous valve, a sensor, a suture, a vascular anastomosis clip, an indwelling venous or arterial catheter, a vascular sheath and a drug delivery port.

3. The method of claim 1, further comprising the step of providing to said patient genetically modified target cells after implantation of said medical device, and wherein said target cells have at least one cell membrane receptor which binds to said one or more ligands on said medical device, and secrete one or more vasodilator substances.

4. The method of claim 1, wherein said one or more ligands comprise a peptide, a protein, a small molecule, or combinations thereof, which are designed to bind to a cell membrane molecule on a target cell.

5. The method of claim 2, wherein said medical device comprises one or more structural material selected from group consisting of stainless steel, Nitinol, MP35N, gold, tantalum, platinum or platinum iridium, biocompatible metals and/or alloys, carbon fiber, cellulose acetate, cellulose nitrate, silicone, cross-linked polyvinyl acetate (PVA) hydrogel, cross-linked PVA hydrogel foam, polyurethane, polyamide, styrene isobutylene-styrene block copolymer (Kraton), polyethylene teraphthalate, polyurethane, polyamide, polyester, polyorthoester, polyanhidride, polyether sulfone, polycarbonate, polypropylene, high molecular weight polyethylene, polytetrafluoroethylene, polyesters of polylactic acid, polyglycolic acid, copolymers of polylactic acid and polyglygolic acid, a polyanhydride, polycaprolactone, polyhydroxybutyrate valerate, extracellular matrix components, proteins, elastin, tropoelastin, cross-linked tropoelastin, collagen, tropocollagen, fibrin, and mixtures thereof.

6. The method of claim 1, wherein said biocompatible matrix comprises a non-polymer porous structure, dextran, tropoelastin, elastin, cross-linked tropoelastin, fibrin, or combinations thereof.

7. The method of claim 6, wherein the non-polymer porous structure are metallic nanoparticles or nanospheres of from about 5 nm to about 5 μ

m in pore size.

8. The method of claim 1, wherein said one or more pharmaceutical substance(s) is selected from the group consisting of vasodilators, antibiotics/antimicrobials, antiproliferative agents, antineoplastic agents, antioxidants, endothelial cell growth factors, smooth muscle cell growth and/or migration inhibitors, thrombin inhibitors, immunosuppressive agents, anti-platelet aggregation agents, collagen synthesis inhibitors, therapeutic antibodies, nitric oxide donors, antisense oligonucleotides, wound healing agents, therapeutic gene transfer constructs, peptides, proteins, extracellular matrix components, thrombolytics, anti-metabolites, growth factor agonists, antimitotics, steroids, steroidal antiinflammatory agents, chemokines, proliferator-activated receptor-alpha agonists, proliferator-activated receptor-delta agonists;

proliferator-activated receptor-gamma agonists, nonsterodial antiinflammatory agents, angiotensin converting enzyme (ACE) inhibitors, free radical scavengers, inhibitors of the CX3CR1 receptor and anti-cancer chemotherapeutic agents.

9. The method of claim 1, wherein said pharmaceutical substance is selected from the group consisting of peroxisome proliferator-activated receptor-alpha agonists, peroxisome proliferator-activated receptor-delta agonists, peroxisome proliferator-activated receptor-gamma agonists, calcitonin gene related peptide (α

-CGRP), monocyte chemoattractant protein-1, adenosine, prostacyclins, tachykinins, sialokinins, neurokinins, plasminogen activator, erythropoietin, darbepotin, serine proteinase-1 (SERP-1), and metalloproteinases.

10. The method of claim 1, wherein said vasodilator substance comprises from about 1 to about 99% (w/w) of the composition.

11. The method of claim 1, wherein said coating on said medical device comprises multiple layers comprising one or more vasodilator substances.

12. The medical device of claim 1, wherein said ligand is covalently attached to the blood contacting surface of said medical device and binds to a prostate specific antigen on the surface of said target cells.

13. The method of claim 1, wherein said ligand is an antibody, a peptide, or a small molecule which binds to a cell surface molecule on said target cell.

14. The method of claim 1, wherein said cell surface molecule on said target cell is a membrane receptor and/or a cell surface antigen.

15. The method of claim 1, wherein said specific molecule on the surface of said target cell is a prostate specific antigen.

16. The method of claim 1, wherein said target cell is a genetically altered target cell comprising a vector with DNA or RNA sequences encoding a vasodilator substance and a prostate specific antigen.

17. The method of claim 16, wherein said vector is a plasmid vector.

18. A method for coating the medical device of claim 1, comprising:

applying to a surface of said medical device at least one or more layers of a matrix, one or more pharmaceutical substance(s), and a basement membrane component;

applying to said at least one layer of said composition on said medical device a solution comprising at least one type of ligand for binding and immobilizing genetically-modified target cells; and

drying said coating on the stent under vacuum at low temperatures.

19. A method of treating mammals with restenosis or artherosclerosis, comprising implanting into a patient a medical device comprising a coating for controlled release of one or more pharmaceutical substances to adjacent tissues, wherein the coating comprises a biocompatible matrix, one or more pharmaceutical substances, and at least one ligand for capturing and immobilizing genetically modified target cells on the blood contacting surface of the medical device.

20. The method of claim 19, wherein said genetically modified target cells comprise a vector comprising a nucleic acid sequence encoding a vasodilator substance and a prostate specific antigen.

21. The method of claim 19, wherein said ligand is an antibody, a peptide, or a small molecule which binds to a cell surface molecule on said target cell.

22. The method of claim 21, wherein the ligand binds to a prostate specific antigen on the surface of said genetically-modified target cell.

23. The method of claim 19, wherein said genetically-modified target cells secrete a vasodilator.

24. The method of claim 23, wherein the vasodilator is selected from the group consisting of peroxisome proliferator-activated receptor-gamma agonists, calcitonin gene related peptide (α

-CGRP), monocyte chemoattractant protein-1, adenosine, prostacyclins, tachykinins, sialokinins, nerokinins, plasminogen activator, erythropoietin, darbepotin, serine proteinase-1 (SERP-1) and metalloproteinases.

25. The method of claim 19, wherein the biocompatible matrix is selected from the group consisting of a non-polymer based porous structure, dextran, elastin, tropoelastin and cross-linked tropoelastin.

26. The method of claim 25, wherein the non-polymer based porous structure comprises metallic nanospheres or nanoparticles of from about 5 nm to about 5 μ

m in pore size.

27. A method for in vivo positive blood vessel remodeling comprising:

implanting into a blood vessel of a patient a medical device having a coating comprising at least one layer of a matrix selected from the group consisting of a non-polymer porous structure, tropoelastin, elastin, and crossed-linked tropoelastin matrix, or combinations thereof;

one or more pharmaceutical substances, and one or more ligands which bind to specific molecules on the cell membrane of a target cell;

wherein said target cell secretes a vasodilator substance.

28. The method of claim 27, wherein said one or more pharmaceutical substance(s) is selected from the group consisting of vasodilators, antibiotics/antimicrobials, antiproliferative agents, antineoplastic agents, antioxidants, endothelial cell growth factors, smooth muscle cell growth and/or migration inhibitors, thrombin inhibitors, immunosuppressive agents, anti-platelet aggregation agents, collagen synthesis inhibitors, therapeutic antibodies, nitric oxide donors, antisense oligonucleotides, wound healing agents, therapeutic gene transfer constructs, peptides, proteins, extracellular matrix components, thrombolytics, anti-metabolites, growth factor agonists, antimitotics, steroids, steroidal antiinflammatory agents, chemokines, proliferator-activated receptor-gamma agonists, proliferator-activated receptor-alpha agonists, proliferator-activated receptor-delta agonists, nonsterodial antiinflammatory agents, angiotensin converting enzyme (ACE) inhibitors, free radical scavengers, inhibitors of the CX3CR1 receptor and anti-cancer chemotherapeutic agents.

29. The method of claim 27, wherein said pharmaceutical substance is selected from the group consisting of peroxisome proliferator-activated receptor-gamma agonists, calcitonin gene related peptide (α

-CGRP), monocyte chemoattractant protein-1, adenosine, prostacyclins, tachykinins, sialokinins, nerokinins, plasminogen activator, erythropoietin, darbepotin, serine proteinase-1 (SERP-1), aromatase inhibitors and metalloproteinases.

30. An implantable medical device having a luminal surface and a coating;

wherein the coating comprises a non-polymer matrix;

one or more pharmaceutical substances and a ligand attached to said matrix and configured to attach to circulating progenitor cells on the luminal surface of the device when implanted into a blood vessel of a patient.

31. The medical device of claim 30, wherein the non-polymer matrix is formed of nanoparticles and the ligand is an antibody, antibody fragments or combinations thereof.

32. The medical device of claim 31, wherein the non-polymer matrix is formed of nanoparticles made from a metallic alloy.

33. The medical device of claim 31, wherein the ligand is an antibody, antibody fragment or combinations thereof.

34. The medical device of claim 33, wherein the antibody has specificity to an antigen selected from the group consisting of CD133, CD34, CD14, CDw90, CD117, VEGFR-1, VEGFR-2, Muc-18 (CD146), CD130, stem cell antigen (Sca-1), stem cell factor 1 (SCF/c-Kit ligand), Tie-2, MHC such as H-2Kk and HLA-DR.