초록 ▼

Thermal spray processing and cold spray processing are utilized to manufacture porous starting materials (such as tube stock, wire and substrate sheets) from biocompatible metals, metal alloys, ceramics and polymers that may be further processed into porous medical devices, such as stents. The spray

Thermal spray processing and cold spray processing are utilized to manufacture porous starting materials (such as tube stock, wire and substrate sheets) from biocompatible metals, metal alloys, ceramics and polymers that may be further processed into porous medical devices, such as stents. The spray processes are also used to form porous coatings on consolidated biocompatible medical devices. The porous substrates and coatings may be used as a reservoir to hold a drug or therapeutic agent for elution in the body. The spray-formed porous substrates and coatings may be functionally graded to allow direct control of drug elution without an additional polymer topcoat. The spray processes are also used to apply the drug or agent to the porous substrate or coating when drug or agent is robust enough to withstand the temperatures and velocities of the spray process with minimal degradation.

대표청구항 ▼

What is claimed: 1. A method of manufacturing a medical device, comprising: providing a biocompatible material; using a spray process to form a porous substrate from the biocompatible material; and processing the porous substrate into a medical device. 2. The method of claim 1, further comprisin

What is claimed: 1. A method of manufacturing a medical device, comprising: providing a biocompatible material; using a spray process to form a porous substrate from the biocompatible material; and processing the porous substrate into a medical device. 2. The method of claim 1, further comprising applying a therapeutic agent to the porous substrate. 3. The method of claim 2, wherein applying the therapeutic agent to the porous substrate includes selecting the therapeutic agent from the group consisting of antiplatelets, anticoagulants, antifibrins, antiinflammatories, antithrombins, and antiproliferatives. 4. The method of claim 2, wherein applying the therapeutic agent to the porous substrate includes impregnating the porous substrate with paclitaxel. 5. The method of claim 1, wherein providing the biocompatible material includes providing a metal alloy selected from the group consisting of iron-based, cobalt-based and titanium-based alloys. 6. The method of claim 1, wherein processing the porous substrate includes forming a stent. 7. The method of claim 6, further comprising applying a polymer layer on an outer surface of the stent. 8. The method of claim 6, further comprising using a spray process to form a porous layer of the biocompatible materials on an outer surface of the stent. 9. A method of manufacturing a drug eluting stent, comprising: providing a biocompatible material; forming a porous substrate from the biocompatible material, wherein a spray process is used; processing the porous substrate into a porous tube stock; and forming a pattern in the porous tube stock to form a porous stent. 10. The method of claim 9, further comprising applying a therapeutic agent to the porous substrate. 11. The method of claim 10, wherein applying the therapeutic agent to the porous substrate includes selecting the therapeutic agent from the group consisting of antiplatelets, anticoagulants, antifibrins, antiinflammatories, antithrombins, and antiproliferatives. 12. The method of claim 10, wherein applying the therapeutic agent to the porous substrate includes impregnating the porous substrate with paclitaxel. 13. The method of claim 9, wherein providing the biocompatible material includes providing a metal alloy selected from the group consisting of iron-based, cobalt-based and titanium-based alloys. 14. The method of claim 9, further comprising applying a polymer layer on an outer surface of the stent. 15. The method of claim 9, further comprising using a spray process to form a porous layer of the biocompatible material on an outer surface of the stent. 16. A method of coating a medical device, comprising: providing a medical device; providing a coating material; applying the coating material to the medical device by cold spray thermal processing wherein powder particles are introduced into a high pressure gas where both the gas and particles enter a supersonic jet which is directed against the medical device forming a porous coating, and wherein the medical device is selected from the group consisting of a stent, guide wires, lead tips, catheters, and markers; wherein the porous coating is functionally graded, wherein the thickness of the coating on the medical device is varied, and applying a drug to the porous coating on the medical device. 17. The method of claim 16, wherein applying the drug to the porous coating includes selecting the drug from the group consisting of antiplatelets, anticoagulants, antifibrins, antiinflammatories, antithrombins, and antiproliferatives. 18. The method of claim 16, wherein providing the coating material includes providing a metal alloy selected from the group consisting of iron-based, cobalt-based and titanium-based alloys. 19. The method of claim 16, wherein providing the medical device includes forming a stent. 20. A method of manufacturing a medical device, comprising: providing a biocompatible material; and using a spray process to form a porous substrate from the biocompatible material on a medical device, such that the formed porous substrate exhibits a functionally graded coating over at least a portion of the medical device; wherein the using a spray process to form a porous substrate step is such that the formed porous substrate includes a first porous layer having a first density and a second porous layer having a second density greater than the first density. 21. A method of manufacturing a medical device, comprising: providing a biocompatible material; and using a spray process to form a porous substrate from the biocompatible material on a medical device, such that the formed porous substrate exhibits a functionally graded coating over at least a portion of the medical device; wherein the using a spray process to form a porous substrate step is such that different degrees of density and porosity are formed over at least a portion of the medical device. 22. A method of manufacturing a medical device, comprising: providing a biocompatible material; and using a spray process to form a porous substrate from the biocompatible material on a medical device, such that the formed porous substrate exhibits a functionally graded coating over at least a portion of the medical device; further including the step of impregnating the porous substrate with a drug or therapeutic agent. 23. A method of manufacturing a medical device, comprising: providing a biocompatible material; and using a spray process to form a porous substrate from the biocompatible material on a medical device, such that the formed porous substrate exhibits a functionally graded coating over at least a portion of the medical device; further including the step of varying the thickness of the porous substrate. 24. A method of manufacturing a medical device, comprising: providing a biocompatible material; using a spray process to form a porous substrate from the biocompatible material on a base material, such that the formed porous substrate exhibits a functionally graded coating over at least a portion of the medical device; and processing the porous substrate into a medical device.