Plasticizers for a biodegradable scaffolding and methods of forming same
US-2015359947-A1 · Dec 17, 2015 · US
US9675478B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9675478-B2 |
| Application number | US-201414302295-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2014 |
| Priority date | Jun 11, 2014 |
| Publication date | Jun 13, 2017 |
| Grant date | Jun 13, 2017 |
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Methods of making polymeric devices, such as stents, using solvent based processes. More particularly, methods of making bioabsorbable stents.
Opening claim text (preview).
What is claimed is: 1. A method of making a stent body for supporting a vascular lumen, comprising providing or forming a polymer solution comprising a solvent and a polymer with an inherent viscosity of at least 3.3 dl/g, a number average molecular weight greater than 250,000 g/mole as measured by gel permeation chromatography using polystyrene standards, or both; either (a) immersing a cylindrical member into the polymer solution and removing the cylindrical member from the polymer solution; wherein a portion of the polymer solution remains on the surface of the cylindrical member upon removal from the polymer solution; and removing at least a portion of the solvent from the polymer solution remaining on the cylindrical member to form a tubular layer of the polymer on the cylindrical member; or (b) spraying the polymer solution onto the cylindrical member; and substantially removing the solvent during, after, or both during and after the spraying to form a tubular layer of the polymer on the cylindrical member; optionally, repeating (a) on one or more occasions, repeating (b) on one or more occasions, or both, with repeating of the providing or forming prior to repeating (a), (b), or both, being optional, to form a final tubular layer of polymer on the cylindrical member of a desired thickness, removing residual solvent from the final tubular layer; and forming a stent body from the final tubular layer; wherein if the optional providing or forming is repeated, for each repetition, the solvent, the polymer, or both, of the polymer solution may be different from the polymer, the solvent, or both used in the prior execution of (a), (b), or both; and wherein removal of the residual solvent from the final tubular layer comprises removal in an environment of solvent vapor, the solvent of the solvent vapor being a removal solvent, where the removal solvent is different from the solvent of the polymer solution; and wherein the removal solvent is selected from the group consisting of acetonitrile, methanol, ethanol, n-propanol, isopropanol, butanol, fluoroform, freons, methylene chloride (CH 2 Cl 2 ), and combinations thereof. 2. The method of claim 1 , wherein the environment of removal solvent vapor is at a temperature not less than 30° C. but not more than the glass transition temperature of the polymer. 3. The method of claim 1 , wherein the environment of removal solvent vapor is at a temperature not less than the glass transition temperature of the polymer, or not less than 28° C., if the glass transition temperature is lower than 25° C., and not more than the melting temperature of the polymer, if the polymer has a melting temperature of at least 45° C., or not more than the higher of 50° C. above the glass transition temperature of the polymer, and 45° C. 4. The method of claim 1 , wherein the removal solvent plasticizes the polymer. 5. The method of claim 1 , wherein the removal solvent partial pressure is at least 100 Torr. 6. The method of claim 1 , wherein the removal solvent partial pressure is at least 50% of the vapor pressure of the pure removal solvent at the temperature of the environment. 7. The method of claim 1 , wherein the removal of residual solvent from the final tubular layer in an environment of removal solvent vapor comprises placing the tubular layer in an environment of solvent vapor for at least 0.2 hour and not more than 1,000 hours. 8. The method of claim 1 , wherein the environment of removal solvent vapor is at a pressure of 760 Torr±100 Torr. 9. The method of claim 1 , wherein the environment of removal solvent vapor is at a pressure of not more than 380 Torr, but at least 0.001 Torr. 10. The method of claim 1 , wherein the removal solvent is selected from the group consisting of acetonitrile, methanol, ethanol, n-propanol, isopropanol, butanol, fluoroform, methylene chloride (CH 2 Cl 2 ), and combinations thereof. 11. A method of making a stent body for supporting a vascular lumen, comprising: coating a web with a polymer solution comprising a solvent and a polymer, wherein the polymer has an inherent viscosity greater than 3.3 dl/g, has a weight average molecular weight greater than 500,000 g/mole, or both; removing at least a portion of the solvent from the polymer solution remaining on the web to form a polymer film on the web; separating the polymer film from the web; and wrapping the polymer film around a cylindrical member, subject to the constraint that the edges of the film at least touch each other, and optionally overlap; heating at least part of the polymer film to fuse the polymer film into a polymer tube; removing the polymer tube from the cylindrical member; and forming a stent body from the polymer tube. 12. The method of claim 11 , wherein the wrapping occurs when the polymer film is at a temperature not less than the glass transition temperature of the polymer, and not more than the melting temperature of the polymer, if there is a melting temperature of at least 40° C., or not more than the higher of 50° C. above the glass transition temperature of the polymer and 40° C. 13. The method of claim 11 , wherein the wrapping occurs when the polymer film is at a temperature not less than the glass transition temperature of the polymer, and not more than 15° C. above the glass transition temperature of the polymer, or the melting temperature of the polymer, if the polymer exhibits a melting temperature, whichever is lower. 14. The method of claim 11 , wherein the polymer film is wrapped around the cylindrical member such that the edges touch each other but do not overlap, or do not overlap by more than 4 times the film thickness. 15. The method of claim 11 , wherein heating at least a region of the polymer film comprises heating the edges of the polymer film and the optional overlapping regions of the polymer film to fuse the polymer film to form the polymer tube. 16. The method of claim 11 , wherein the polymer film is wrapped around the cylindrical member at least 2 times but not more than 100 times. 17. The method of claim 16 , wherein heating at least a region of the polymer film comprises heating all or substantially all of the polymer film to fuse the polymer film to form the polymer tube. 18. The method of claim 17 , wherein prior to wrapping the polymer film around the cylindrical member, the polymer film is heated to a temperature, the temperature being at least the glass transition temperature of the polymer, and not more than 15° C. above the glass transition temperature of the polymer, or the melting temperature of the polymer, if the polymer exhibits a melting temperature, whichever is lower; wherein after wrapping the polymer film, the polymer film is maintained at the temperature for a duration of time, heated to a higher temperature and maintained at the higher temperature for a second duration of time, or both; wherein the higher temperature is not greater than the melting temperature, if there is a melting temperature, or not more than 50° C. above the glass transition temperature of the polymer, if the polymer does not have melting temperature, or 40° C., if 40° C. is greater than 50° C. above the glass transition temperature of the polymer; and wherein the first and second durations of time are at least 2 minutes and not more than 120 minutes. 19. The method of claim 17 , wherein prior to wrapping the polymer film around the cylindrical member, the polymer film is heated to a temperature being at least the glass transition temperature of the polymer, and n
characterised by a net-like or mesh-like structure · CPC title
obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds {(A61L31/041 takes precedence)} · CPC title
Materials characterised by their function or physical properties {, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials} · CPC title
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