Methods and devices for delivering therapeutic agents to target vessels
View Patent ↗The present disclosure pertains to stents having a coating applied thereto, wherein the coating comprises a biocompatible polymer/drug mixture, as well as devices comprising a metallic stent, a biocompatible polymeric carrier and a drug.
1. A stent having a coating applied thereto, wherein said coating comprises a biocompatible polymer/drug mixture, said polymer is a nonabsorbable polymer, and said drug is rapamycin and is contained in the coating in weight percentage of about 30%.
2. The stent according to claim 1 comprising a generally thin walled cylinder containing a plurality of generally solid struts to which said coating is applied.
3. The stent according to claim 2 further comprising a channel formed in at least one of said struts.
4. The stent according to claim 3 , wherein said channel has a closed perimeter on all sides, an open top and a generally rectangular perimeter, and said channel is smaller in all dimensions than said strut.
5. The stent according to claim 1 wherein the coating is dip-coated onto the stent.
6. The stent according to claim 1 wherein the coating is spray-coated onto the stent.
7. The stent according to claim 1 wherein the coating comprises a polydimethylsiloxane; a poly(ethylene)vinylacetate; a poly(hydroxy)ethylmethylmethacrylate; an acrylate based polymer; an acrylate based copolymer; a polyvinyl pyrrolidone; a cellulose ester; a fluorinated polymer; or a blend thereof.
8. The stent according to claim 7 wherein the coating comprises a fluorinated polymer.
9. The stent according to claim 1 that provides a controlled release of said rapamycin over a period of several weeks.
10. The stent according to claim 1 wherein said rapamycin is present in a therapeutically beneficial amount to inhibit neointimal proliferation.
11. A device comprising a metallic stent, a biocompatible polymeric carrier and a drug that are present in a weight ratio of about 7:3, wherein said polymer is a nonabsorbable polymer, said drug is rapamycin and is present in an amount effective to inhibit neointimal proliferation.
12. The device according to claim 11 wherein said polymeric carrier and drug are mixed together.
13. The device according to claim 11 wherein said polymeric carrier is bound to the drug.
14. The device according to claim 11 wherein the drug is entrapped on the surface of the stent by said polymeric carrier.
15. The device according to claim 11 wherein said stent comprises a generally thin walled cylinder containing a plurality of generally solid struts to which said polymeric carrier and drug are applied.
16. The device according to claim 15 further comprising a channel formed in at least one of said struts.
17. The device according to claim 16 , wherein said channel has a closed perimeter on all sides, an open top and a generally rectangular perimeter, and said channel is smaller in all dimensions than said strut.
18. The device according to claim 11 wherein the polymeric carrier and drug are dip-coated onto the stent.
19. The device according to claim 11 wherein the polymeric carrier and drug are spray-coated onto the stent.
20. The device according to claim 11 wherein the polymeric carrier comprises a polydimethylsiloxane; a poly(ethylene)vinylacetate; a poly(hydroxy)ethylmethylmethacrylate; an acrylate based polymer; an acrylate based copolymer; a polyvinyl pyrrolidone; a cellulose ester; a fluorinated polymer; or a blend thereof.
21. The device according to claim 11 wherein the polymeric carrier comprises a fluorinated polymer.
22. The device according to claim 11 that provides a controlled release of said rapamycin over a period of several weeks.