IP Library Granted Patent US 8,992,601
Granted Patent B2
US 8,992,601 · App. 13/766,294 · Granted Mar 31, 2015

Medical implants

Inventors: Maria Palasis (Wellesley, MA); Changcheng You (Northbridge, MA); Daniel Concagh (Medfield, MA); Lee Core (Needham, MA); Kicherl Ho (Groton, MA); Upma Sharma (Somerville, MA); Gregory T. Zugates (Chelmsford, MA)
Assignee: 480 Biomedical, Inc.
A61F2/82A61L29/06A61L29/085A61L29/16A61L31/10A61F2/90A61L31/14A61F2230/0054
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Quick Facts
Patent No.
US 8,992,601
App. No.
13/766,294
Granted
Mar 31, 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 (27)

1. A medical implant comprising:

a tubular structure being characterized, as manufactured and when unconstrained, by a first diameter and comprising a first polymeric material;

a conformal coating comprising a second polymeric material, said coating at least partially coating said tubular structure;

wherein said coating increases the mass of said tubular structure by at least 15%;

wherein said tubular structure is characterized by a radial resistive force that does not decrease by more than 50% after being placed into a configuration that is 55% to 90% of said first diameter in an aqueous environment at 37° C. for eight weeks.

2. The medical implant of claim 1 , wherein said second polymeric material is a thermoset elastomer.

3. The medical implant of claim 2 , wherein said thermoset elastomer is a polyester urethane.

4. The medical implant of claim 3 , wherein the thermoset elastomer is poly (lactic acid-co-caprolactone).

5. The medical implant of claim 4 , wherein said poly (lactic acid-co-caprolactone) comprises about 50weight percent of lactic acid and about 50 weight percent of caprolactone.

6. The medical implant of claim 2 , wherein said thermoset elastomer is prepared by a process that comprises the steps of:

at least partially dissolving a polyester polymer in a solvent to form a solution;

adding a diisocyanate crosslinker to said solution;

adding a chain terminator to said solution; and

curing said solution.

7. The medical implant of claim 6 , wherein said diisocyanate crosslinker is hexamethylene diisocyanate.

8. The medical implant of claim 6 , wherein said chain terminator comprises a monoisocyanate.

9. The medical implant of claim 8 , wherein said monoisocyanate is 1-dodecylisocyanate.

10. The medical implant of claim 6 , wherein said chain terminator comprises a monoalcohol.

11. The medical implant of claim 10 , wherein said monoalcohol is 1-dodecanol.

12. The medical implant of claim 2 , wherein said first polymeric material comprises poly(lactic acid co-glycolic acid).

13. The medical implant of claim 6 , wherein said thermoset elastomer comprises at least 1.5 wt % of said chain terminator.

14. The medical implant of claim 13 , wherein said thermoset elastomer comprises at least 2.0 wt % of said chain terminator.

15. The medical implant of claim 13 , wherein said thermoset elastomer comprises at least 4.0 wt % of said chain terminator.

16. The medical implant of claim 1 , wherein said tubular structure is characterized by a chronic outward force that does not decrease by more than 50% after being placed into a configuration that is 55% to 90% of said first diameter in an aqueous environment at 37° C. for twelve weeks.

17. The medical implant of claim 1 , wherein said tubular structure is characterized by a radial resistive force that does not decrease by more than 50% after being placed into a configuration that is not greater than 75 % of said first diameter in an aqueous environment at 37° C. for twelve weeks.

18. The medical implant of claim 17 , wherein said tubular structure is characterized by a chronic outward force that does not decrease by more than 50% after being placed into a configuration that is not greater than 75% of said first diameter in an aqueous environment at 37° C. for twelve weeks.

19. The medical implant of claim 1 , wherein said tubular structure is characterized by a chronic outward force that does not decrease by more than 25% after being placed into a configuration that is 55% to 90% of said first diameter in an aqueous environment at 37° C. for eight weeks.

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 Apr 17, 2013
From: PALASIS, MARIA; YOU, CHANGCHENG; CONCAGH, DANIEL; CORE, LEE; HO, KICHERL; SHARMA, UPMA; ZUGATES, GREG
To: 480 BIOMEDICAL, INC.
Reel/Frame 030231/0682 →
Continuity (9)
Continuation In Part 13370025 · Feb 9, 2012
Continuation In Part 13253720 · Oct 5, 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
Related Publication 20130158652A1 · Jun 20, 2013