IP Library Granted Patent US 9,155,638
Granted Patent B2
US 9,155,638 · App. 13/891,574 · Granted Oct 13, 2015

Drug eluting medical implant

Inventors: Maria Palasis (Wellesley, MA); Changcheng You (Burlington, MA); Danny Concagh (Medfield, MA); Lee Core (Needham, MA); Kicherl Ho (Groton, MA); Upma Sharma (Somerville, MA); Gregory T. Zugates (Chelmsford, MA)
Assignee: 480 BIOMEDICAL, INC.
A61F2/86A61F2/90A61L31/06A61L31/10A61L31/14A61L31/16D04C1/06A61F2230/0054D10B2403/0112D10B2509/06
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Quick Facts
Patent No.
US 9,155,638
App. No.
13/891,574
Granted
Oct 13, 2015
Kind
B2
Abstract

Disclosed are self-expanding medical implants for placement within a lumen of a patient. The implants comprise a woven or non-woven structure having a substantially tubular configuration, and are designed to be low-profile such that they are deliverable with a small diameter catheter. The implants have a high recoverability and desired mechanical properties.

Claims (32)

1. A medical implant comprising:

a tubular structure comprising a first polymeric material;

a first conformal coating comprising poly (lactic acid-co-caprolactone), said first conformal coating at least partially coating said tubular structure and increasing the mass of said tubular structure by at least about 20 percent;

a second conformal coating at least partially coating said first conformal coating and comprising a second polymeric material and paclitaxel, said second conformal coating comprising between 0.3 weight percent and 5 weight percent of paclitaxel; and

a third conformal coating at least partially coating said second conformal coating and comprising a third polymeric material.

2. The medical implant of claim 1 , wherein said poly (lactic acid-co-caprolactone) comprises about 50 weight percent of lactic acid and about 50 weight percent of caprolactone.

3. The medical implant of claim 1 , wherein said poly (lactic acid-co-caprolactone) is prepared by a process that comprises the step of crosslinking said poly (lactic acid-co-caprolactone) with diisocyanate.

4. The medical implant of claim 3 , wherein said diisocyanate is hexamethylene diisocyanate.

5. The medical implant of claim 1 , wherein said first polymeric material comprises poly(lactic acid co-glycolic acid).

6. The medical implant of claim 1 , wherein said second conformal coating has a thickness up to 8 microns.

7. The medical implant of claim 1 , wherein the medical implant comprises between 2.5 micrograms and 20 micrograms of paclitaxel per 10 millimeters of length of the tubular structure.

8. The medical implant of claim 7 , wherein the medical implant comprises between 5 micrograms and 13 micrograms of paclitaxel per 10 millimeters of length of the tubular structure.

9. The medical implant of claim 1 , wherein the third conformal coating is biodegradable.

10. The medical implant of claim 1 , wherein at least a portion of said third conformal coating does not include paclitaxel.

11. The medical implant of claim 1 , wherein said second and third polymeric materials are the same.

12. The medical implant of claim 1 , wherein said second and third polymeric materials are different.

13. A medical implant comprising:

a tubular structure comprising a first polymeric material;

a first conformal coating comprising poly (lactic acid-co-caprolactone), said first conformal coating at least partially coating said tubular structure and increasing the mass of said tubular structure by at least about 20 percent;

a second conformal coating at least partially coating said first conformal coating and comprising a second polymeric material and paclitaxel, said second conformal coating comprising between 2.5 micrograms and 20 micrograms of paclitaxel per 10 millimeters of length of the tubular structure; and

a third conformal coating at least partially coating said second conformal coating and comprising a third polymeric material.

14. The medical implant of claim 13 , wherein said second conformal coating comprises between 5 micrograms and 13 micrograms of paclitaxel per 10 millimeters of length of the tubular structure.

15. The medical implant of claim 13 , wherein said poly (lactic acid-co-caprolactone) comprises about 50 weight percent of lactic acid and about 50 weight percent of caprolactone.

16. The medical implant of claim 13 , wherein said poly (lactic acid-co-caprolactone) is prepared by a process that comprises the step of crosslinking said poly (lactic acid-co-caprolactone) with diisocyanate.

17. The medical implant of claim 16 , wherein said diisocyanate is hexamethylene diisocyanate.

18. The medical implant of claim 13 , wherein said first polymeric material comprises poly(lactic acid co-glycolic acid).

19. The medical implant of claim 13 , wherein said second conformal coating has a thickness up to 8 microns.

20. The medical implant of claim 13 , wherein the second conformal coating comprises between 0.3 weight percent and 5 weight percent of paclitaxel.

21. The medical implant of claim 13 , wherein the third conformal coating is biodegradable.

22. The medical implant of claim 13 , wherein at least a portion of said third conformal coating does not include paclitaxel.

23. The medical implant of claim 13 , wherein said second and third polymeric materials are the same.

24. The medical implant of claim 13 , wherein said second and third polymeric materials are different.

Assignments (2)
CHANGE OF NAME Recorded Jan 17, 2020
From: 480 BIOMEDICAL, INC.
To: LYRA THERAPEUTICS, INC.
Reel/Frame 051637/0116 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2013
From: PALASIS, MARIA; YOU, CHANGCHENG; CONCAGH, DANNY; CORE, LEE; HO, KICHERL; SHARMA, UPMA; ZUGATES, GREG
To: 480 BIOMEDICAL, INC.
Reel/Frame 030509/0514 →
Continuity (12)
Continuation 13863632 · Apr 16, 2013
Continuation In Part 13766294 · Feb 13, 2013
Continuation In Part 13370025 · Feb 9, 2012
Continuation In Part 13253720 · Oct 2, 2011
Continuation In Part 13183104 · Jul 14, 2011
Continuation In Part 13032281 · Feb 22, 2011
Continuation In Part 12783261 · May 19, 2010
Provisional Application 61179834 · May 20, 2009
Provisional Application 61227308 · Jul 21, 2009
Provisional Application 61251984 · Oct 15, 2009
Provisional Application 61624607 · Apr 16, 2012
Related Publication 20130304177A1 · Nov 14, 2013