Coated implantable medical device
A coated implantable medical device 10 includes a structure 12 adapted for introduction into the vascular system, esophagus, trachea, colon, biliary tract, or urinary tract; at least one coating layer 16 posited on one surface of the structure; and at least one layer 18 of a bioactive material posited on at least a portion of the coating layer 16 , wherein the coating layer 16 provides for the controlled release of the bioactive material from the coating layer. In addition, at least one porous layer 20 can be posited over the bioactive material layer 18 , wherein the porous layer includes a polymer and provides for the controlled release of the bioactive material therethrough. Preferably, the structure 12 is a coronary stent. The porous layer 20 includes a polymer applied preferably by vapor or plasma deposition and provides for a controlled release of the bioactive material. It is particularly preferred that the polymer is a polyamide, parylene or a parylene derivative, which is deposited without solvents, heat or catalysts, and merely by condensation of a monomer vapor.
1. A coated medical device, comprising:
a vascular stent having an outer surface and a lumen surface;
a coating layer of parylene or a parylene derivative applied to at least the outer surface of the vascular stent;
a bioactive material layer posited on said coating layer, the bioactive material layer comprising a bioactive material comprising dexamethasone or a dexamethasone derivative;
a porous polymeric layer posited over said bioactive material layer, the porous polymeric layer capable of controlling the release of the dexamethasone or dexamethasone derivative from the bioactive material layer; and
an overcoat consisting of phosphatidylcholine applied to said porous polymeric layer.
2. The coated medical device of claim 1 , wherein the bioactive material layer comprises between about 0.1 and 100 μg/mm 2 of the bioactive material on the surface.
3. The coated medical device of claim 1 , wherein the bioactive material layer has a thickness of between about 0.005 μm to about 50 μm.
4. The coated medical device of claim 1 , wherein the bioactive material further comprises methotrexate.
5. The coated medical device of claim 1 , wherein the bioactive material further comprises ticlopidine.
6. The coated medical device of claim 1 , wherein the bioactive material further comprises estrogen.
7. The coated medical device of claim 1 , wherein the bioactive is selected from the group consisting of: dexamethasone sodium phosphate and dexamethasone acetate.
8. The coated medical device of claim 1 , wherein the vascular stent comprises a biocompatible metal.
9. A coated vascular stent, comprising:
a vascular stent adapted for introduction into a patient, the stent having an outer surface and a lumen surface;
a coating layer of parylene or a parylene derivative applied to at least the outer surface of the vascular stent;
a bioactive material layer posited on said coating layer, the bioactive material layer comprising an antiproliferative agent that inhibits over proliferation of smooth muscle cells;
a porous polymeric layer posited over said bioactive material layer, said porous polymeric layer capable of controlling release of the antiproliferative agent from the bioactive material layer; and
an overcoat of phosphatidylcholine applied to said porous polymeric layer.
10. The coated vascular stent of claim 9 , wherein the bioactive material layer comprises between about 0.1 and 100 μg/mm 2 of the antiproliferative agent on the outer surface of the coated vascular stent.
11. The coated medical device of claim 9 , wherein the porous polymeric layer has been prepared by applying a coating material free of any bioactive material onto said bioactive material layer.
12. The coated medical device of claim 9 , wherein the antiproliferative agent is methotrexate.