Resorbable complex shape memory poly(propylene fumarate) star scaffolds for 4D printing applications

US11987668B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11987668-B2
Application numberUS-202118005643-A
CountryUS
Kind codeB2
Filing dateJul 15, 2021
Priority dateJul 15, 2020
Publication dateMay 21, 2024
Grant dateMay 21, 2024

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

In one or more embodiments, the present invention provides am method of making a poly(propylene fumarate-co-succinate) (PPFS) copolymer containing a random incorporation of succinate groups and targetable reduction profiles without the need for three or more monomer units. To achieve this, a time-dependent sonication-promoted zinc/acetic acid reduction of the PPM unsaturated double bonds has been used to create a random PPMS copolymer which may be isomerized into the PPFS equivalent. By changing the sonication time as well as the ratios of acetic acid, zinc, and PPM unsaturated alkenes, partial reduction of the PPM alkenes has been shown to give PPMS products containing varying compositions of succinic and maleate units, which may then be isomerized to the PPFS product.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for making poly(propylene fumarate-co-succinate) polymer comprising the time-dependent partial reduction of poly(propylene maleate) double bonds by sonication mediated by zinc and acetic acid to form a poly(propylene maleate-co-succinate) intermediate, followed by isomerization of the poly(propylene maleate-co-succinate) intermediate using an organic base to produce the poly(propylene fumarate-co-succinate) polymer. 2. The method for producing a poly(propylene fumarate-co-succinate) polymer of claim 1 comprising: A) obtaining or synthesizing poly(propylene maleate) and. dissolving it in acetic acid or a solvent combination comprising acetic acid; B) adding zinc to the poly(propylene maleate) solution; C) sonicating the combination of step B to reduce at least some of the maleate groups in the poly(propylene maleate) to succinate groups to form a poly(propylene maleate-co-succinate) intermediate; and D) dissolving the poly(propylene maleate-co-succinate) intermediate in a solvent and isomerizing it with the organic base wherein said organic base is selected from the group consisting of diethylamine, trimethylamine, pyridine, and combinations thereof, to produce a poly(propylene fumarate-co-succinate) polymer. 3. The method of claim 2 wherein the acetic acid is glacial acetic acid. 4. The method of claim 2 wherein the solvent combination comprising acetic acid in step A comprises glacial acetic acid and a solvent selected from the group consisting of dichloromethane, chloroform, toluene, and combinations thereof. 5. The method of claim 2 wherein. the solvent combination comprising acetic acid in step A is a co--solvent solution of glacial acetic acid and toluene. 6. The method of claim 2 wherein the solvent combination comprising acetic acid in step A is a co-solvent solution of glacial acetic acid and one of dichloromethane, chloroform, or both dichloromethane and chloroform. 7. The method of claim 2 wherein the step of combining (step B) comprises adding an amount of zinc that is from about 0.5 to about 5.0 equivalents relative to the alkene bonds in the poly(propylene maleate) polymer. 8. The method of claim 2 wherein the step of adding zinc (step B) comprises adding an amount of zinc that is from about 0.5 to about 3.0 equivalents relative to the alkene bonds in the poly(propylene maleate) polymer. 9. The method of claim 2 wherein the step of sonication comprises sonicating the combination of step C for from about 1 to about 60 minutes. 10. The method of claim 2 wherein the step of sonication comprises sonicating the combination of step C until a desired mole percent of succinate groups is present in the poly(propylene maleate-co-succinate) polymer produced. 11. The method of claim 2 wherein the solvent in the step of dissolving (step D) is an organic solvent. 12. The method of claim 2 wherein the solvent in the step of dissolving (step D) is selected from the group consisting of chloroform, dichloromethane and combinations thereof.

Assignees

Inventors

Classifications

  • C08G63/83Primary

    Alkali metals, alkaline earth metals, beryllium, magnesium, copper, silver, gold, zinc, cadmium, mercury, manganese, or compounds thereof {(C08G63/823 takes precedence)} · CPC title

  • C08G63/52Primary

    Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation · CPC title

  • Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation · CPC title

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What does patent US11987668B2 cover?
In one or more embodiments, the present invention provides am method of making a poly(propylene fumarate-co-succinate) (PPFS) copolymer containing a random incorporation of succinate groups and targetable reduction profiles without the need for three or more monomer units. To achieve this, a time-dependent sonication-promoted zinc/acetic acid reduction of the PPM unsaturated double bonds has be…
Who is the assignee on this patent?
Becker Matthew, Bass Garrett Fredric, Univ Akron
What technology area does this patent fall under?
Primary CPC classification C08G63/83. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).