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Biological 3D printing ink and preparation method thereof

A 3D printing and biological technology, applied in medical science, prosthesis, etc., can solve the problems of low hardness of printing glue block, difficult to apply wound model, soft texture, etc., to achieve rich pores, good cell loading potential, and excellent clinical application potential Effect

Active Publication Date: 2020-01-24
GENERAL HOSPITAL OF PLA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Unlike the previous tissue engineering seed cells that migrate to the scaffold material and assist in promoting the microenvironment of regeneration, the cell-loaded bioink can integrate biomaterials, seed cells, and the regenerative microenvironment, which greatly improves the tissue engineered skin in the skin. The possibility of clinical application, and in the development of cell-loaded hydrogel, the selection and application of biomaterials and the appropriate addition of regenerative microenvironment are the focus of current research. Gelatin is due to its excellent biodegradability, biocompatibility, high Cell attachment and proliferation and low immunogenicity have been widely used in the research of wound dressings. In previous studies, gelatin-sodium alginate cell-loaded bioink not only has good biocompatibility, but also improves cell migration. , proliferation and differentiation, however, in the process of practical application, the gelatin-sodium alginate bioink printed with cell-loaded bioink has low hardness, resulting in a soft texture, which is difficult to apply to animal wound models

Method used

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  • Biological 3D printing ink and preparation method thereof
  • Biological 3D printing ink and preparation method thereof
  • Biological 3D printing ink and preparation method thereof

Examples

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Embodiment 1

[0029] This embodiment provides a modified nano-biological glass particle. The modified nano-biological glass particle is prepared by the following method: weigh 1.65g of calcium hydroxide solid powder and place it in a beaker, add 1000ml of deionized water and use a constant temperature Stir with a magnetic stirrer, the stirring speed is 1500r / min, and the stirring time is 12h. During the stirring process, seal the beaker, centrifuge after the stirring, discard the precipitate, and take the supernatant to obtain a saturated solution of calcium hydroxide. Take 400ml calcium hydroxide saturated solution. Put the solution in a beaker, add 67ml of 40wt% silica nanoparticle suspension, place the beaker on a constant temperature magnetic stirrer, stir for 72 hours, and stir at a speed of 200r / min, keep the beaker in a sealed state during the stirring process , after stirring, centrifuge at 5500rpm for 10min, take the precipitate, add deionized water to wash, centrifuge again, take t...

Embodiment 2

[0031] The present embodiment provides a kind of preparation method of biological 3D printing ink, and this preparation method comprises the following steps:

[0032]S1: Weigh 1.65g of calcium hydroxide solid powder and place it in a beaker, add 1000ml of deionized water and stir with a constant temperature magnetic stirrer at a stirring speed of 1500r / min for 12 hours. During the stirring process, seal the beaker and finish the stirring Centrifuge afterward, discard the precipitate, take the supernatant to obtain a saturated calcium hydroxide solution, put 400ml of the saturated calcium hydroxide solution in a beaker, add 67ml of 40wt% silica nanoparticle suspension, place the beaker under constant temperature magnetic stirring Stir on the mixer, the stirring time is 72h, the stirring speed is 200r / min, keep the beaker in a sealed state during the stirring process, centrifuge at 5500rpm for 10min after stirring, take the precipitate, add deionized water to wash, centrifuge aga...

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PUM

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Abstract

The invention provides a biological 3D printing ink and a preparation method thereof. The preparation method comprises the following steps: S1: preparing a calcium hydroxide saturated solution, addinga silica nanoparticle suspension to the calcium hydroxide saturated solution, centrifuging and taking a precipitate to obtain modified nano-bioglass particles; S2: dissolving gelatin and sodium alginate in deionized water, then adding the modified nano-bioglass particles prepared in the Step S1, stirring evenly to prepare liquid hydrogel, sterilizing and equilibrating to obtain a gelatin-sodium alginate composite hydrogel; S3: dissolving solid calcium chloride powder in deionized water to prepare a calcium chloride solution, and sterilizing to obtain a cross-linking agent; and S4: adding thecross-linking agent to the gelatin-sodium alginate composite hydrogel for cross-linking to obtain the biological 3D printing ink. The biological 3D printing ink prepared by the invention has not onlysignificantly improved mechanical properties but also good gelling performance, rich pores and good cell-carrying potential.

Description

technical field [0001] The invention relates to the field of medical model manufacturing and application, in particular to a biological 3D printing ink and a preparation method thereof. Background technique [0002] The skin is the largest organ of the human body, which plays a very important role in maintaining the stability of the internal environment of the human body and the normal physiological functions of the body. Due to exposure to the external environment, skin damage and loss often occur. For small skin defects, the body Complete regeneration can be achieved to a certain extent through self-compensation, but for larger wounds, the skin generally undergoes scar repair, and for larger wounds, skin defects often delay healing or fail to heal. The body is directly exposed to the external environment, which not only fails to maintain the body’s fluid balance, but also exposes the patient to a high risk of infection. Therefore, it is very necessary to seal the wound in ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L27/44A61L27/52A61L27/56A61L27/60
CPCA61L27/446A61L27/52A61L27/56A61L27/60C08L89/00C08L5/04
Inventor 宋薇姚斌黄沙付小兵
Owner GENERAL HOSPITAL OF PLA
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