Factors controlling drug release in cross-linked poly(valerolactone) based matrices
US-2024368351-A1 · Nov 7, 2024 · US
US9598534B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9598534-B2 |
| Application number | US-201514926624-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 29, 2015 |
| Priority date | Oct 29, 2014 |
| Publication date | Mar 21, 2017 |
| Grant date | Mar 21, 2017 |
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Described are shape memory polymers and methods of making shape memory polymers and actuators from the shape memory polymers.
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What is claimed is: 1. A method of making a shape memory polymer, comprising: partially crosslinking a prepolymer to form a partially crosslinked polymer, wherein the prepolymer comprises a semi-crystalline polymer; stretching the partially crosslinked polymer to form a stretched, partially crosslinked polymer; and crosslinking the stretched, partially crosslinked polymer, thereby making the shape memory polymer. 2. The method of claim 1 , wherein the semi-crystalline polymer comprises a polyethylene, polyethylene terephthalate, polytetrafluoroethylene, isotactic polypropylene, polyphenylene sulfide, polyetherketone, polyetheretherketone, polyphthalamide, polyetherketoneketone, thermoplastic polyimide, polybutylene terephthalate, polyoxymethylene, nylon, polyester, polyether, poly(caprolactone), or a copolymer thereof. 3. The method of claim 1 , wherein the prepolymer comprises acrylate end groups and partially crosslinking the prepolymer comprises base-catalyzed Michael addition of at least a portion of the acrylate end groups of the polymer and a multifunctional thiol. 4. The method of claim 1 , wherein the partially crosslinked polymer has a pre-stretched length; the stretched, partially crosslinked polymer has a post-stretched length; and the post-stretched length is from greater than 0% to 1000% longer than the pre-stretched length. 5. The method of claim 4 , wherein the post-stretched length is 100% or more longer than the pre-stretched length. 6. The method of claim 1 , wherein crosslinking the stretched, partially crosslinked polymer comprises a photocrosslinking reaction. 7. The method of claim 6 , wherein the photocrosslinking reaction comprises photocuring with UV irradiation in the presence of a photoinitiator. 8. The method of claim 1 , wherein the method occurs at a temperature above the melting temperature of the shape memory polymer. 9. The method of claim 1 , wherein stretching the partially crosslinked polymer comprises applying a load to the partially crosslinked polymer, and the method further comprises removing the load from the shape memory polymer, thereby making an actuator with a loadless length. 10. The method of claim 9 , wherein the partially crosslinked polymer has a pre-stretched length; the stretched, partially crosslinked polymer has a post-stretched length; and the loadless length is between the pre-stretched length and the post-stretched length. 11. The method of claim 9 , further comprising cooling the actuator to a temperature below the melting temperature of the shape memory polymer, thereby elongating the actuator along the direction to an elongated length. 12. The method of claim 10 , wherein the elongated length is from greater than 0% to 50% longer than the loadless length. 13. The method of claim 10 , further comprising heating the actuator to a temperature above the melting temperature of the shape memory polymer, thereby contracting the actuator along the direction to the loadless length. 14. The method of claim 11 , further comprising cooling the actuator to a temperature below the melting temperature of the shape memory polymer, thereby elongating the actuator along the direction to the elongated length. 15. A method of making a shape memory polymer, comprising: providing a semi-crystalline polymer with photosensitive crosslinks and permanent crosslinks; stretching and heating the semi-crystalline polymer; and irradiating the stretched and heated semi-crystalline polymer, to thereby reshuffle the photosensitive crosslinks.
having terminal carbon-to-carbon unsaturated bonds · CPC title
Polyesters derived from hydroxy carboxylic acids, e.g. lactones (C08J2367/06 takes precedence) · CPC title
derived from hydroxycarboxylic acids · CPC title
Two or more independent types of crosslinking for one or more polymers · CPC title
Treatment by wave energy or particle radiation · CPC title
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