Biodegradable absorbents and methods of preparation
View Patent ↗A biodegradable microfiber absorbent comprises a substantially homogeneous mixture of at least one hydrophilic polymer and at least one biodegradable polymer. The absorbent can be prepared by an electro hydrodynamic spinning of a substantially homogeneous polymer mixture. Medical dressings for burns and wounds, cavity dressings, drug delivery patches, face masks, implants, drug carriers that comprises at least one microfiber electrospun from a polymer mixture are provided. The dressings can have variable water vapor penetration characteristics and variable biodegradation times.
1. A biodegradable structure comprising an electrohydrodynamic processed mixture containing:
(a) a solvent;
(b) poly-(N-vinyl)pyrrolidone; and
(c) a biodegradable polyester which includes a caprolactone or a dioxanon of a molecular mass at least 150000 Dalton, with a component ratio of the poly-(N-vinyl)pyrrolidone to the caprolactone or diaxanon by weight being about 10:90 to about 50:50.
2. The biodegradable structure of claim 1 , wherein said mixture further comprises one or more low molecular weight biodegradable polyesters with hydroxyl, carboxyl or amino-terminal groups, or one or more polyoxyethylene glycols, or one or more low molecular weight alcohols selected from the group containing alcohols, including alcohols of natural origin.
3. The biodegradable structure of claim 1 , further comprising one or more of living cells, proteins, peptides, antibiotic compounds, bacteriocidal compounds, fungicidal compounds, bacteriostatic compounds, analgesic compounds, and trombogenic compounds.
4. The biodegradable structure of claim 1 , wherein the mixture further comprises one or more biodegradable polyesters with hydroxyl, carboxyl or amino-terminal groups, and/or one or more polyoxyethylene glycols, or one or more alcohols.
5. The biodegradable structure of claim 1 , wherein the mixture further comprises a compound selected from the group consisting of polyoxyethylene glycol, salicylates, methylsalicylate, salicylic acid, and nicotenates.
6. The biodegradable structure of claim 1 , wherein the mixture further comprises an antimicrobial substance.
7. The biodegradable structure of claim 1 , wherein the mixture further comprises a compound selected from the group consisting of tetracycline, neomycin, oxytetracycline, triclosan, sodium cefazolin, doxorubicin, toxol, insulin, and interferon.
8. The biodegradable structure of claim 1 , further comprising one or more alpha hydroxy acids.
9. The biodegradable structure of claim 1 , wherein the electrohydrodynamic process mixture is processed by an electrospinning technique.
10. The biodegradable structure of claim 1 , wherein the mixture further comprises at least one copolymer that includes a polyether or a polyoxyethylene glycol and a polymer of a lactides, a dioxanon, a caprolactone or a glycolide.
11. A method for preparing a biodegradable microfiber absorbent, the method comprising electrohydrodynamic processing of a mixture containing:
(a) a solvent;
(b) poly-(N-vinyl)pyrrolidone; and
(c) a biodegradable polyester which includes a caprolactone or a dioxanon of a molecular mass at least 150000 Dalton, with a component ratio of the poly-(N-vinyl)pyrrolidone to the caprolactone or diaxanon by weight being about 10:90 to about 50:50.
12. The method of claim 11 , wherein said mixture further comprises one or more low molecular weight biodegradable polyesters with hydroxyl, carboxyl or amino-terminal groups, or one or more polyoxyethylene glycols, or one or more low molecular weight alcohols selected from the group containing alcohols, including alcohols of natural origin.
13. The method of claim 11 , further comprising incorporating into the absorbent at least one therapeutic performance enhancing additive comprising one or more of living cells, proteins, peptides, antibiotic compounds, bacteriocidal compounds, fungicidal compounds, bacteriostatic compounds, analgesic compounds, and trombogenic compounds.
14. The method of claim 11 , wherein the electrohydrodynamic processing comprises emitting a flow of said mixture into an area in which said mixture flies in an electrical field towards a substrate; and the method further comprises emitting a flow of dry particles into said area and the dry particles being deposited over said substrate.
15. The method of claim 14 , wherein the flow of dry particles and the flow of said mixture are emitted into said area in overlapping periods of time.
16. The method of claim 11 , wherein the mixture further comprises at least one therapeutic performance-enhancing additive.
17. The method of claim 11 , wherein the mixture has an intrinsic viscosity from about 0.1 to about 10 poise.
18. The method of claim 11 , wherein the mixture further comprises one or more biodegradable polyesters with hydroxyl, carboxyl or amino-terminal groups, and/or one or more polyoxyethylene glycols, or one or more alcohols.
19. The method of claim 11 , wherein the mixture further comprises a compound selected from the group consisting of polyoxyethylene glycol, salicylates, methylsalicylate, salicylic acid, and nicotenates.
20. The method of claim 11 , wherein the mixture further comprises an antimicrobial substance.
21. The method of claim 11 , wherein the mixture further comprises a compound selected from the group consisting of tetracycline, neomycin, oxytetracycline, triclosan, sodium cefazolin, doxorubicin, toxol, insulin, and interferon.
22. The method of claim 11 , further comprising including into the mixture one or more alpha hydroxy acids.
23. The method of claim 11 , wherein the mixture further comprises at least one copolymer that includes a polyether or a polyoxyethylene glycol and a polymer of a lactides, a dioxanon, a caprolactone or a glycolide.