Preparation method and use of crosslinked hydrogel for muscle stem cell culture

US11629236B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11629236-B2
Application numberUS-202217846269-A
CountryUS
Kind codeB2
Filing dateJun 22, 2022
Priority dateDec 30, 2020
Publication dateApr 18, 2023
Grant dateApr 18, 2023

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present disclosure discloses a preparation method and use of a crosslinked hydrogel for muscle stem cell culture, and belongs to the technical field of biological food materials. Chitosan, alginate, dextran and Ca2+ are crosslinked through physical crosslinking to form a double-network hydrogel with a high mechanical strength, the hydrogel is coated with heparin and collagen through dip coating, such that the hydrogel can immobilize growth factors and adhere to cells. Meanwhile, extracted primary muscle stem cells are inoculated onto the hydrogel and cultured in a growth medium (79% of DMEM, 10% of FBS and 1% of double antibodies) for 24 h. The cells are cultured in an incubator with a differential medium (97% of DMEM, 2% of horse serum and 1% of double antibodies) for 7 d. The hydrogel can enhance the absorption to nutrient substances by the muscle stem cells and facilitate growth of the muscle stem cells. The double-network hydrogel has the potential to be a scaffold for growth of muscle stem cells for cultured meat from stem cells.

First claim

Opening claim text (preview).

What is claimed is: 1. A preparation method of a crosslinked hydrogel for muscle stem cell culture, comprising: dissolving sodium alginate to obtain a solution and adding a predetermined amount of calcium carbonate into the sodium alginate solution until the calcium carbonate is uniformly dispersed to obtain a slurry; dissolving dextran to obtain a solution and adding chitosan into the dextran solution until the chitosan is uniformly dispersed to obtain a slurry; mixing the two slurries, pouring the mixed slurry into a mold, putting the mold into a sealed container filled with hydrochloric acid, and crosslinking to obtain a double-network physically crosslinked hydrogel; and dipping into a heparin sodium solution to obtain a heparin-coated hydrogel and then dipping into a collagen solution to obtain a collagen and heparin-coated double-network crosslinked hydrogel. 2. The preparation method of a crosslinked hydrogel for muscle stem cell culture according to claim 1 , comprising the following steps: (1) preparing a first gel material: uniformly mixing and dissolving the sodium alginate (Alg) in water to obtain the sodium alginate solution, adding the predetermined amount of calcium carbonate (CaCO 3 ) into the sodium alginate solution, and stirring until the calcium carbonate is uniformly dispersed to obtain the first gel material; (2) preparing a second gel material: mixing and dissolving the dextran (Dex) in water to obtain the dextran solution, adding the chitosan (CS) to the dextran solution, and stirring until the chitosan is uniformly dispersed to obtain the second gel material; (3) preparing a chitosan/dextran/alginate/calcium ion double-network crosslinked hydrogel: uniformly mixing the first gel material and the second gel material, pouring an obtained mixture into the mold, putting the mold into the sealed container filled with hydrochloric acid, and sealing the slurry using the hydrochloric acid for 12-36 hours to obtain a double-network crosslinked CS/Dex/Alg/Ca 2+ hydrogel; (4) dip-coating heparin: dipping the hydrogel prepared in step (3) in the heparin sodium solution for 15-45 min to obtain a heparin-coated CS/Dex/Alg/Ca 2+ hydrogel; and (5) dip-coating collagen: dipping the heparin-coated CS/Dex/Alg/Ca 2+ hydrogel obtained in step (4) in the collagen solution for 15-45 min to obtain a collagen and heparin-coated CS/Dex/Alg/Ca 2+ hydrogel and freeze-drying the hydrogel. 3. The preparation method of a crosslinked hydrogel for muscle stem cell culture according to claim 2 , wherein in step (1), α-L-guluronic acid (G) and 6-D-mannuronic acid (M) in the sodium alginate has a ratio of 70/30 to 30/70. 4. The preparation method of a crosslinked hydrogel for muscle stem cell culture according to claim 2 , wherein in step (1), the content of the sodium alginate in the sodium alginate Alg solution is 1-2 wt % and the content of the CaCO 3 in the first gel material is 0.01-0.5 wt %. 5. The preparation method of a crosslinked hydrogel for muscle stem cell culture according to claim 2 , wherein the content of the dextran in the dextran solution is 0.5-2.0 wt % and the content of the chitosan in the second gel material is 0.5-3 wt %. 6. The preparation method of a crosslinked hydrogel for muscle stem cell culture according to claim 2 , wherein the first gel material and the second gel material are mixed at a mass ratio of 1:1 to 2:1.

Assignees

Inventors

Classifications

  • Heparin; Derivatives thereof · CPC title

  • Alginic acid; Derivatives thereof · CPC title

  • Alginate · CPC title

  • Dextran; Derivatives thereof · CPC title

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

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Frequently asked questions

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What does patent US11629236B2 cover?
The present disclosure discloses a preparation method and use of a crosslinked hydrogel for muscle stem cell culture, and belongs to the technical field of biological food materials. Chitosan, alginate, dextran and Ca2+ are crosslinked through physical crosslinking to form a double-network hydrogel with a high mechanical strength, the hydrogel is coated with heparin and collagen through dip coa…
Who is the assignee on this patent?
Univ Jiangnan
What technology area does this patent fall under?
Primary CPC classification C12N5/0658. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 18 2023 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).