Nondegradable Hydrogels For Medical Device Application

• US 20090238815A1
• Filed: 03/18/2008
• Published: 09/24/2009
• Est. Priority Date: 03/18/2008
• Status: Abandoned Application

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Guo, Ya, Udipi, Kishore, Trudel, Julie
• Application Number:
  US12/050,309
• Publication Number:
  US 20090238815A1
• Time in Patent Office: Days
• US Class Current: 424/130.100
• CPC Class Codes: A61L 2300/416 Anti-neoplastic or anti-proliferative or anti-restenosis or anti-angiogenic agents, e.g. paclitaxel, sirolimus
• CPC Class Codes: A61L 27/18 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• 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 29/06 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• 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 31/06 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds A61L31/041 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
• CPC Class Codes: A61P 41/00 Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution
• CPC Class Codes: C08L 71/02 Polyalkylene oxides

Abstract

Disclosed are nondegradable hydrogels used to coat or form at least a portion of a medical device. The hydrogels may be formed from functionalized PEG based macromers. These hydrogels are easy to sterilize, transport and store. Methods of forming these hydrogels as described herein are included.

Claims

1. A polymeric material formed from macromers of a general formula 1:

wherein W, W′

are each independently O or CH₂, n is between about 1 and about 500, macromers of a general formula 2;

wherein W, W′ and

W″

are each independently O or CH₂, x, y, and z are each independently between about 1 and about 500, or combinations thereof, and wherein at least two macromers are cross-linked thereby forming a hydrogel.

2. A polymeric material according to claim 1, wherein said hydrogel is non-degradable.

3. A polymeric material according to claim 1, wherein at least one of n, x, y, or z is the following:

n is between 1 and 250;

x is between 1 and 250;

y is between 1 and 250; and

z is between 1 and 250.

4. A polymeric material according to claim 1, wherein said hydrogel further comprises at least one bioactive agent selected from the group consisting of anti-proliferatives, estrogens, chaperone inhibitors, protease inhibitors, protein-tyrosine kinase inhibitors, leptomycin B, peroxisome proliferator-activated receptor gamma ligands (PPARγ

), hypothemycin, nitric oxide, bisphosphonates, epidermal growth factor inhibitors, antibodies, proteasome inhibitors, antibiotics, anti-inflammatories, anti-sense nucleotides and transforming nucleic acids.

5. A polymeric material according to claim 1, wherein said hydrogel further comprises at least one bioactive agent selected from the group consisting of sirolimus (rapamycin), tacrolimus (FK506), everolimus (certican), temsirolimus (CCI-779) and zotarolimus (ABT-578).

6. A polymeric material according to claim 1, wherein said hydrogel comprises any ratio of formula 1:

formula 2.

7. An implantable medical device comprising a polymeric material, said polymeric material formed from macromers of a general formula 1:

wherein n is between about 1 and about 500, macromers of a general formula 2;

wherein x, y, and z are each independently between about 1 and about 500, or combinations thereof, and wherein at least two macromers are cross-linked thereby forming a hydrogel.

8. An implantable medical device according to claim 7, wherein said hydrogel is non-degradable.

9. An implantable medical device according to claim 7, wherein said hydrogel comprises at least one of n, x, y, or z with the following:

n is between 1 and 250;

x is between 1 and 250;

y is between 1 and 250; and

z is between 1 and 250.

10. An implantable medical device according to claim 7, wherein said polymeric material further comprises at least one bioactive agent selected from the group consisting of anti-proliferatives, estrogens, chaperone inhibitors, protease inhibitors, protein-tyrosine kinase inhibitors, leptomycin B, peroxisome proliferator-activated receptor gamma ligands (PPARγ

), hypothemycin, nitric oxide, bisphosphonates, epidermal growth factor inhibitors, antibodies, proteasome inhibitors, antibiotics, anti-inflammatories, anti-sense nucleotides and transforming nucleic acids.

11. An implantable medical device according to claim 7, wherein said hydrogel further comprises at least one bioactive agent selected from the group consisting of sirolimus (rapamycin), tacrolimus (FK506), everolimus (certican), temsirolimus (CCI-779) and zotarolimus (ABT-578).

12. An implantable medical device according to claim 7, wherein said hydrogel comprises any ratio of formula 1:

formula 2.

13. An implantable medical device according to claim 7, wherein said hydrogel is coated onto said implantable medical device.

14. An implantable medical device according to claim 7, wherein said implantable medical device is selected from the group consisting of vascular stents, shunts, vascular grafts, stent grafts, heart valves, catheters, pacemakers, pacemaker leads, bile duct stents and defibrillators.

15. A method of forming a hydrogel comprising the steps of:

a) choosing at least one macromer selected from the group consisting of Formula 1

wherein n is between about 1 and about 500, Formula 2

wherein x, y, and z are each independently between about 1 and about 500, or a combination thereof;

b) choosing appropriate concentrations of said macromer(s);

c) selecting an appropriate initiator; and

d) reacting said macromers and said initiator, thereby forming a hydrogel.

16. A method according to claim 15, wherein the method further comprises the step of:

e) coating at least a portion of a medical device, forming at least a portion of a medical device, or a combination of thereof with said hydrogel.

17. A method according to claim 15, wherein said initiator is selected from the group consisting of light, Eosin Y, triethanolamine, a free radical, or combinations thereof.

18. A method according to claim 15, wherein said medical device is selected from the group consisting of vascular stents, shunts, vascular grafts, stent grafts, heart valves, catheters, pacemakers, pacemaker leads, bile duct stents and defibrillators.