UTILIZATION OF MURAL THROMBUS FOR LOCAL DRUG DELIVERY INTO VASCULAR TISSUE

• US 20100261662A1
• Filed: 04/09/2010
• Published: 10/14/2010
• Est. Priority Date: 04/09/2009
• Status: Abandoned Application

• Current Assignee: Endologix
• Original Assignee: Endologix
• Inventors: Schankereli, Kemal, Schreck, Stefan G., Bankert, Charles S.
• Application Number:
  US12/757,900
• Publication Number:
  US 20100261662A1
• Time in Patent Office: Days
• US Class Current: 514/25
• CPC Class Codes: A61K 31/353 3,4-Dihydrobenzopyrans, e.g. chroman, catechin
• CPC Class Codes: A61K 31/7032 attached to a polyol, i.e. compounds having two or more free or esterified hydroxy groups, including the hydroxy group involved in the glycosidic linkage, e.g. monoglucosyldiacylglycerides, lactobionic acid, gangliosides
• CPC Class Codes: A61K 9/0024 Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L
• CPC Class Codes: A61L 2300/434 of enzymes
• CPC Class Codes: A61L 29/16 Biologically active materials, e.g. therapeutic substances A61L29/048 takes precedence
• CPC Class Codes: A61L 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: A61P 7/02 Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
• CPC Class Codes: A61P 9/10 for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

The present disclosure is directed to methods and systems for stabilizing an extracellular matrix in a wall of a blood vessel. The method comprises delivering a therapeutic agent into mural thrombus, which covers the wall of the blood vessel. The agent is transported from the mural thrombus into the extracellular matrix of the vessel wall by diffusion. The agent then acts to reduce the enzymatic degradation of protein in the extracellular matrix.

Claims

1. A method for stabilizing an extracellular matrix in a wall of a blood vessel comprising:

advancing a delivery system to a treatment site positioned near a mural thrombus that covers at least a portion of the wall of the blood vessel;

advancing a delivery portion of the delivery device into the mural thrombus;

delivering a therapeutic agent through the delivery portion into the mural thrombus; and

allowing the agent to transport from the mural thrombus into the extracellular matrix of the vessel wall by diffusion to facilitate reduction of enzymatic degradation of protein in the extracellular matrix by the action of the agent.

2. The method of claim 1, wherein the agent cross-links with proteins in the extracellular matrix and protects the protein against enzymatic degradation.

3. The method of claim 1, wherein the agent is a bioflavonoid selected from the group consisting of:

proanthocyanidin, catechin, epicatechin, epigallo catechin, epicatechin gallate, epigallocatechin gallate, quercetin, tannic acid, and any combination thereof.

4. The method of claim 3, wherein the bioflavonoid is EGCG.

5. The method of claim 1, wherein the agent is in a solution.

6. The method of claim 5, wherein the solution containing the therapeutic agent has a pH less than 7.4.

7. The method of claim 5, wherein the solution has a pH close to the isoelectric point of collagen or elastin.

8. The method of claim 1, wherein the extracellular matrix layer is located in an aortic aneurysm or aortic dissection.

9. The method of claim 1, wherein delivering the therapeutic agent comprises a catheter.

10. The method of claim 9, wherein the catheter comprises at least one ejection port perpendicular to the axis of the catheter.

11. The method of claim 1, wherein a concentration of the therapeutic agent delivered into the mural thrombus is substantially higher than the concentration of the therapeutic agent in the extra-cellular matrix.

12. The method of claim 1, wherein a concentration of the therapeutic agent delivered into the mural thrombus is between approximately 2.0% and approximately 10.0%.

13. A method for stabilizing an extracellular matrix layer in the vascular system of a body comprising:

positioning a portion of a vascular catheter adjacent to or within a mural thrombus positioned adjacent to the extracellular matrix layer of a target region of the vascular system; and

delivering a therapeutic agent in solution to the mural thrombus using the vascular catheter; and

allowing the therapeutic agent to be transported to the extracellular matrix layer through the mural thrombus to promote the cross-linking protein in the extracellular matrix layer, thereby stabilizing the extracellular matrix.

14. The method of claim 13, wherein the therapeutic agent is a bioflavonoid.

15. The method of claim 14, wherein the bioflavonoid forms at least one hydrogen bond with protein in the extracellular matrix layer.

16. The method of claim 13, wherein the solution contains a keotropic agent.

17. The method of claim 16, wherein the keotropic agent is Ca(OH)₂.

18. The method of claim 13, wherein the therapeutic agent is delivered to the mural thrombus using a stent graft.

19. The method of claim 18, wherein the stent graft comprises ePTFE.

20. The method of claim 13, wherein the therapeutic agent is delivered to the mural thrombus using at least one expandable balloon configured to expand against the mural thrombus.

21. A method of claim 13, wherein the therapeutic agent is an anti-inflammatory, anti-platelet agent or a matrix-metalloproteinase inhibitor.

22. A method of claim 13, wherein the solution contains at least 2% catechin.

23. A method of claim 13, wherein the solution contains at least 10% catechin.

24. A method of claim 13, wherein the solution contains an organic solvent.

25. A method of claim 24, wherein the organic solvent is acetone, alcohol, ethyl acetate, methanol, or methyl acetate.

26. A method of claim 24, wherein the solution contains at least 10% of an organic solvent.

27. A catheter system for the delivery of a therapeutic agent into a wall of a blood vessel, comprising:

a delivery catheter, wherein the delivery catheter houses a therapeutic agent configured to promote the cross-linking of protein; and

a delivery portion of the delivery catheter, wherein the delivery portion is configured to deliver the therapeutic agent from the delivery catheter into a mural thrombus.

28. The catheter system of claim 27, wherein the delivery catheter has a first proximal end and a second distal end, wherein the first and second ends are connected by a delivery lumen and wherein the second distal end comprises an atraumatic tip.

29. The catheter system of claim 28, further comprising at least one ejection port disposed on a side of the catheter between the first and second ends, wherein the ejection port is oriented perpendicular to the axis of the catheter.

30. The catheter system of claim 28, wherein the first proximal end further comprises a reservoir.

31. The catheter system of claim 28, wherein the atraumatic tip comprises a radiopaque marker.

32. The catheter system of claim 28, wherein the lumen is configured to house a guidewire.

33. The catheter system of claim 28, wherein the atraumatic tip is articulated.