Microporous articles comprising biodegradable medical polymers, method of preparation thereof and method of use thereof
View Patent ↗The present invention relates to a highly controlled method of preparation of a microporous biodegradable polymeric article. Firstly, at least one biodegradable polymer A, one polymer B, biodegradable or not, partially or totally immiscible with A, and a compatibilizer C for A and B are selected. Secondly, the selected polymers are melt-blended, thereby preparing a polymer blend, wherein said polymers A and B have an essentially continuous morphology. Thirdly, after cooling, polymer B and compatibilizer C are selectively extracted from the polymer blend by dissolution in a solvent that is a non-solvent of polymer A. The resulting polymeric article has an essentially continuous porosity with a void volume between 10 and 90% and a unimodal diameter distribution set to a predefined unimodal peak location. It can be used in tissue engineering, for controlled release applications or as an implantable medical device.
1. A microporous polymeric article having a target pore diameter d v , comprising an essentially continuous porosity with a controlled void volume from 10 to 90%, wherein pore diameters show a unimodal distribution set at a predefined unimodal peak location corresponding to said target pore diameter d v , and wherein a majority of pores have a diameter d of at least d v −50% and at most d v +50%, prepared according to a method comprising the steps of:
a) determining a target pore diameter d v ;
b) selecting at least one polymer A and at least one polymer B at least partially immiscible with A, according to the target pore diameter d v determined in step a);
c) melt blending the selected polymers from step b), thereby preparing a polymer blend, wherein said polymers A and B have an essentially continuous morphology;
d) cooling said polymer blend to room temperature, thereby retaining its morphology; and
e) extracting said polymer B, at least partially, from the polymer blend by dissolving said polymer B in a solvent that is a non-solvent of polymer A.
2. The microporous polymeric article according to claim 1 , wherein the target pore diameter d v is from 20 nm to 500 μm.
3. The microporous polymeric article according to claim 2 , wherein the target pore diameter d v is from 1 to 72 μm.
4. The microporous polymeric article according to claim 3 , wherein the majority of pores have a diameter d comprised in a range between d v −40% and d v +40%.
5. The microporous polymeric article according to claim 1 , wherein the target pore diameter d v is from 1 to 3 μm, and wherein the majority of pores have a diameter d comprised in a range between d v −25% and d v +25%.
6. The microporous biodegradable polymeric article according to claim 1 , wherein the porosity is fully continuous.
7. The microporous biodegradable polymeric article according to claim 1 , wherein the article has a symmetric morphology.
8. The microporous biodegradable polymeric article according to claim 1 , wherein the article has an asymmetric morphology.
9. The microporous biodegradable polymeric article according to claim 8 , wherein the article has a closed-cell skin.
10. The microporous biodegradable polymeric article according to claim 1 , wherein at least 95% of said article is made of a biodegradable medical polymer selected from the group consisting of poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic), polyorthoesters, polycaprolactones, polyanhydrides and their copolymers.
11. The microporous biodegradable polymeric article according to claim 1 , wherein at least 99% of said article is made of a biodegradable medical polymer selected from the group consisting of poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic), polyorthoesters, polycaprolactones, polyanhydrides and their copolymers.
12. The microporous biodegradable polymeric article according to claim 1 , wherein said article is essentially made of a biocompatible, implantable polymer.
13. A method of preparation of a microporous biodegradable polymeric article, comprising the steps:
a) selecting at least one biodegradable polymer A, one polymer B, biodegradable or not, at least partially immiscible with A, and a polymeric compatibilizer C for A and B;
b) melt blending the selected polymers from step a) and the compatibilizer C, thereby preparing a compatibilized polymer blend, wherein said polymers A and B have an essentially continuous morphology;
c) cooling said polymer blend to room temperature, thereby retaining its morphology; and
d) extracting said polymer B and said compatibilizer C, at least partially, from the polymer blend by dissolving them in a solvent that is a non-solvent of polymer A,
wherein said polymeric article has an essentially continuous porosity with a void volume from 10 to 90%, wherein pore diameters show a unimodal distribution set to a predefined unimodal peak location corresponding to a chosen pore diameter, and wherein a majority of pore has a diameter within ±50% of the chosen pore diameter.
14. The method according to claim 13 , wherein said polymer A is a biodegradable medical polymer.
15. The method according to claim 14 , wherein said polymer A is an aliphatic polyester.
16. The method according to claim 14 , wherein said polymer A is selected from the group consisting of poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic), poly(hydroxyalkanoates), polyorthoesters, polycaprolactones, polydioxanone, polyan hydrides and their copolymers.
17. The method according to claim 13 , wherein said polymer B is a non-biodegradable polymer.
18. The method according to claim 13 , wherein said polymer B is a biodegradable medical polymer.
19. The method according to claim 18 , wherein said polymer B is selected from a group consisting of poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic), poly(hydroxyalkanoates), polyorthoesters, polycaprolactones, polyanhydrides and their copolymers.
20. The method according to claim 13 , wherein said compatibilizer C is a polymeric compatibilizer.
21. The method according to claim 20 , wherein said compatibilizer C is a copolymer of A and B.
22. The method according to claim 13 , wherein said polymers A and B are fully immiscible.
23. The method according to claim 13 , wherein said polymer blend is co-continuous at more than 90%.
24. The method according to claim 13 , wherein said polymer blend may contain one or more additives.
25. The method according to claim 13 , wherein said polymer blend is submitted to a further step of controlled annealing between steps b) and c), thereby increasing the pore size of the porous article.
26. The method according to claim 13 , wherein said polymer blend is submitted to controlled cooling rates in step c).
27. The method according to claim 13 , wherein said polymer blend is further shaped into a geometrical form between steps b) and c).
28. The method according to claim 27 , wherein said polymer blend is further shaped in a mold or die, between steps b) and c).
29. The method according to claim 27 , wherein said polymer blend is shaped by injection molding, between steps b) and c).
30. The method according to claim 27 , wherein said polymer blend is formed by extrusion, between steps b) and c).
31. The method according to claim 27 , wherein said polymer blend is formed by melt spinning between steps b) and c).
32. The method according to claim 13 , wherein said polymer blend is submitted to a mechanical stress that orients the porosity in at least one specific direction, between steps b) and c).
33. The method according to claim 13 , wherein said polymer blend is submitted to a mechanical stress that orients the porosity in at least one specific direction, during step c).
34. The method according to claim 13 , wherein said polymeric article is further submitted to a controlled immersion in a solvent for its polymer A after step d), thereby creating a closed-cell skin.
35. The method according to claim 13 , wherein said polymer blend is further submitted to a controlled immersion in a common solvent for A and B between steps c) and d), thereby creating an asymmetric open-cell morphology in the porous article.
36. A method of tissue engineering utilizing a microporous article according to any one of claims 2 to 5 and 1 .
37. The microporous biodegradable article obtained by the method according to any of claims 13 - 35 , wherein said microporous biodegradable article is tissue engineering article.
38. A method of controlled release utilizing a microporous article according to any one of claims 2 to 5 and 1 as a substrate.
39. The microporous biodegradable article obtained by the method according to any of claims 13 - 35 , wherein said microporous biodegradable article is a substrate for controlled release applications.
40. A method of forming an implantable medical device utilizing a microporous article according to any one of claims 2 to 5 and 1 .
41. The microporous biodegradable article obtained by the method according to any of claims 13 - 35 , wherein said microporous biodegradable article is an implantable medical device.
42. The microporous polymeric article according to any one of claims 2 to 5 , said article being biodegradable.
43. The microporous polymeric article according to claim 1 , wherein step b) further comprises selecting a polymeric compatibilizer C for A and B; step c) comprises melt blending the selected polymers from step a) and the compatibilizer C, thereby preparing a compatibilized polymer blend; and step e) comprises extracting said polymer B and said compatibilizer C, at least partially, from the polymer blend by dissolving them in a solvent that is a non-solvent of polymer A.