Two-component bioink, 3D biomaterial comprising the same and method for preparing the same

US10894895B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10894895-B2
Application numberUS-201615739628-A
CountryUS
Kind codeB2
Filing dateJun 27, 2016
Priority dateJun 26, 2015
Publication dateJan 19, 2021
Grant dateJan 19, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The present invention provides a two-component bioink including a first solution and a second solution separately, wherein (i) the first solution includes a first biopolymer to which a first chemical functional group is introduced, and the second solution includes a second biopolymer to which a second chemical functional group able to chemically bond with the first chemical functional group is introduced; or (ii) the first solution includes a third biopolymer having a first electrostatic functional group, and the second solution includes a fourth biopolymer having a second electrostatic functional group able to physically bond with the first electrostatic functional group, a 3D biomaterial including the same, and a method for preparing the same.

First claim

Opening claim text (preview).

The invention claimed is: 1. A two-component bioink for 3D printing, comprising: a first solution and a second solution separately, wherein the first solution includes a first biopolymer having a first chemical functional group, and the second solution includes a second biopolymer having a second chemical functional group able to chemically bond with the first chemical functional group, wherein a combination of the first chemical functional group and the second chemical functional group is tetrazine and cyclooctene, alkyne group and azide group, alkyne group and thiol group, epoxy group and amine group, epoxy group and thiol group, acroyl group and amine group, or acroyl group and thiol group, and wherein the first chemical functional group is introduced to the first biopolymer from one or more of the material selected from the group consisting of methyltetrazine-amine, methyltetrazine-PEG4-amine, methyltetrazine-propylamine, tetrazine-PEG5-NHS ester, methyltetrazine-PEG4-NHS ester, methyltetrazine-sulfo-NHS ester, methyltetrazine-PEG4-acid, methyltetrazine-PEG12-NHS ester, methyltetrazine-NHS ester, methyltetrazine-acid, tetrazine-acid, amino-PEG4-alkyne, alkyne-PEG5-acid, alkyne-PEG-amine, oxiranylamine, 2-oxiranyl-ethylamine, acrylamide, acrylic acid and acryloyl chloride, and the second chemical functional group is introduced to the second biopolymer from one or more of the material selected from the group consisting of trans-cyclooctene-amine, trans-cyclooctene-NHS ester, trans-cyclooctene-PEG-NHS ester, trans-cyclooctene-PEG4-acid, azide-PEG4-amine, 3-amino-1-propanethiol, 11-mercaptoundecanoic acid, amino-methanethiol, thiol PEG amine, ethylene diamine, PEG diamine, (S)-3-amino-2-(hydroxymethyl)propionic acid and amino-acetic acid. 2. The bioink of claim 1 , wherein the first solution or second solution further includes one or more selected from the group consisting of cells, a material for preventing adhesion, a dye and a drug. 3. The bioink of claim 2 , wherein the cells are one or more selected from the group consisting of human-derived stem cells, muscle-derived stem cells, dental pulp stem cells, nasal concha-derived mesenchymal stromal cells, fibroblasts and smooth muscle cells. 4. A 3D biomaterial comprising the two-component bioink of claim 1 , wherein the first and second biopolymers are chemically combined by the combination of the first chemical functional group and the second chemical functional group. 5. The 3D biomaterial of claim 4 , which is a tissue-engineered scaffold, a drug carrier or an anti-adhesive agent. 6. A method for preparing a 3D biomaterial, comprising: (a) preparing a first solution by adding a material having a first chemical functional group to a first biopolymer; (b) preparing a second solution by adding a material having a second chemical functional group able to chemically bond with a first chemical functional group to a second biopolymer; and (c) chemically combining the first solution with the second solution, and wherein the material having a first chemical functional group in (a) is one or more selected from the group consisting of methyltetrazine-amine, methyltetrazine-PEG4-amine, methyltetrazine-propylamine, tetrazine-PEG5-NHS ester, methyltetrazine-PEG4-NHS ester, methyltetrazine-sulfo-NHS ester, methyltetrazine-PEG4-acid, methyltetrazine-PEG12-NHS ester, methyltetrazine-NHS ester, methyltetrazine-acid, tetrazine-acid, amino-PEG4-alkyne, alkyne-PEG5-acid, alkyne-PEG-amine, oxiranylamine, 2-oxiranyl-ethylamine, acrylamide, acrylic acid and acryloyl chloride, and wherein the material having a second chemical functional group in (b) is one or more selected from the group consisting of trans-cyclooctene-amine, trans-cyclooctene-NHS ester, trans-cyclooctene-PEG-NHS ester, trans-cyclooctene-PEG4-acid, azide-PEG4-amine, 3-amino-1-propanethiol, 11-mercaptoundecanoic acid, amino-methanethiol, thiol PEG amine, ethylene diamine, PEG diamine, (S)-3-amino-2-(hydroxymethyl)propionic acid and amino-acetic acid. 7. The method of claim 6 , wherein a molar ratio of the first biopolymer and the material having a first chemical functional group in (a) or a molar ratio of the second biopolymer and the material having a second chemical functional group in (b) is 1:400 to 1:600. 8. The method of claim 6 , wherein the content of the first biopolymer in the first solution in (a) or the content of the second biopolymer in the second solution in (b) is 1 wt % to 30 wt %.

Assignees

Inventors

Classifications

  • C09D11/08Primary

    based on natural resins · CPC title

  • Alginic acid; Derivatives thereof · CPC title

  • substituted with acid radicals (C09D101/282 takes precedence) · CPC title

  • General culture methods using substrates (for specific animal cell type C12N5/06) · CPC title

  • Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof · CPC title

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What does patent US10894895B2 cover?
The present invention provides a two-component bioink including a first solution and a second solution separately, wherein (i) the first solution includes a first biopolymer to which a first chemical functional group is introduced, and the second solution includes a second biopolymer to which a second chemical functional group able to chemically bond with the first chemical functional group is …
Who is the assignee on this patent?
Univ Ajou Ind Academic Coop Found
What technology area does this patent fall under?
Primary CPC classification C09D11/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 19 2021 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).