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Preparation method of bionic tissue engineering scaffold with photo-thermal responsiveness and controllable drug release

A tissue engineering scaffold and responsive technology, which is applied in the field of preparation of bionic tissue engineering scaffolds, can solve problems such as accelerating nerve regeneration, achieve the effects of improving success rate, benefiting long-term treatment and rehabilitation, and improving biological functionality

Active Publication Date: 2020-08-25
NANTONG UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Purpose of the invention: In view of the existing problems and the deficiencies of the prior art, the technical problem to be solved by the present invention is to construct an artificial nerve graft that contains intelligent responsive controlled release bioactive molecules and has a bionic micro-nano topology on the surface. In order to better realize the function of accelerating nerve regeneration, it provides a beneficial choice for patients with peripheral nerve injury in clinical practice

Method used

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  • Preparation method of bionic tissue engineering scaffold with photo-thermal responsiveness and controllable drug release
  • Preparation method of bionic tissue engineering scaffold with photo-thermal responsiveness and controllable drug release
  • Preparation method of bionic tissue engineering scaffold with photo-thermal responsiveness and controllable drug release

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specific Embodiment 1

[0061] The first step is to prepare a nanoparticle with photothermal effect loaded with bioactive molecules:

[0062] Take tris-tris to prepare a Tris solution with a pH of 8.5, then add Dopa powder to the Tris solution to prepare a polydopamine solution, and finally add 50 mg of nanoparticles to 10 ml of the polydopamine solution. Wrap the container containing the mixed solution with tin foil to avoid light, ventilate it, and shake it in a mechanical shaker. After shaking, remove the solution from the shaker container, discard the supernatant, take out the precipitate and dry it. Then dry the obtained powder and wash it again with Milli-Q. After centrifuging again, the supernatant was discarded, and the precipitate was dried to obtain Dopa@MWCNT powder. Add Dopa@MWCNT powder into 20ml of DFO / YR mixed solution, and shake it in a mechanical shaker. After shaking, the solution was taken out from the shaker and placed in a centrifuge for centrifugation. Finally, discard the s...

specific Embodiment 2

[0070] The first step is to prepare a nanoparticle with photothermal effect loaded with bioactive molecules:

[0071] Take tris-tris to prepare a Tris solution with a pH of 8.5, then add Dopa powder to the Tris solution to prepare a polydopamine solution, and finally add 100 mg of nanoparticles to 10 ml of the polydopamine solution. Wrap the container containing the mixed solution with tin foil to avoid light, ventilate it, and shake it in a mechanical shaker. After shaking, remove the solution from the shaker container, discard the supernatant, take out the precipitate and dry it. Then dry the obtained powder and wash it again with Milli-Q. After centrifuging again, the supernatant was discarded, and the precipitate was dried to obtain Dopa@MWCNT powder. Add Dopa@MWCNT powder into 20ml of DFO / YR mixed solution, and shake it in a mechanical shaker. After shaking, the solution was taken out from the shaker and placed in a centrifuge for centrifugation. Finally, discard the ...

specific Embodiment 3

[0079] The first step is to prepare a nanoparticle with photothermal effect loaded with bioactive molecules:

[0080] Take tris-tris to prepare a Tris solution with a pH of 8.5, then add Dopa powder to the Tris solution to prepare a polydopamine solution, and finally add 150 mg of nanoparticles to 10 ml of the polydopamine solution. Wrap the container containing the mixed solution with tin foil to avoid light, ventilate it, and shake it in a mechanical shaker. After shaking, remove the solution from the shaker container, discard the supernatant, take out the precipitate and dry it. Then dry the obtained powder and wash it again with Milli-Q. After centrifuging again, the supernatant was discarded, and the precipitate was dried to obtain Dopa@MWCNT powder. Add Dopa@MWCNT powder into 20ml of DFO / YR mixed solution, and shake it in a mechanical shaker. After shaking, the solution was taken out from the shaker and placed in a centrifuge for centrifugation. Finally, discard the ...

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Abstract

The invention discloses a preparation method of a bionic tissue engineering scaffold with photo-thermal responsiveness and controllable drug release. The scaffold comprises bioactive molecules which have a nerve regeneration promoting function and can be released in a photo-controlled mode, the surface of the scaffold is provided with an anisotropic topological structure for regulating and controlling cell orientation growth, and the microenvironment of nerve regeneration can be well simulated. The preparation method comprises the following specific steps that bioactive nano-particles are prepared; an electrostatic spinning receiving substrate is prepared; a high-molecular biological material solution is prepared, and the bioactive nano-particles and the high-molecular biological materialsolution are blended and subjected to electrospinning; the scaffold is stripped, and the scaffold is obtained. The scaffold has excellent biocompatibility, mechanical property, intelligent responsiveness and drug controlled release performance, nerve regeneration can be accelerated, and the problems that the long-distance nerve defect repairing effect is not ideal, and function recovery is deficient are solved. An ideal material and a preparation method are provided for nerve recovery badness of nerve injury patients.

Description

technical field [0001] The invention belongs to the technical field of biomedical materials, and in particular relates to a preparation method of a bionic tissue engineering scaffold with photothermal responsiveness and controllable drug release. Background technique [0002] Peripheral nerve injury is a common clinical disease. For those with short defect gaps, precision suture or small gap cannula can be used to directly repair the defect, but for long-distance nerve injuries, direct suture is not feasible. At present, with the development of microsurgical equipment and technology, the clinical treatment effect of peripheral nerve injury has been continuously improved. More methods are used to bridge tissue engineering grafts, which has been proved to be an effective method for repairing peripheral nerve injury. However, Compared with autologous nerve grafts, there is still a gap in its repair effect. Therefore, it is urgent to develop new tissue engineered nerve grafts. ...

Claims

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Application Information

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IPC IPC(8): A61L27/54A61L27/50A61L27/58A61L27/22A61L27/26A61L27/08D01D5/00D04H1/4382D04H1/728
CPCA61L27/54A61L27/50A61L27/58A61L27/227A61L27/08A61L27/26D04H1/4382D04H1/728D01D5/003D01D5/0092D01D5/0069D01D5/0061A61L2300/624A61L2430/32C08L5/08C08L67/04
Inventor 李贵才刘逸凡慕函朔刘毅恒韩琦梁佳琦张林辉刘恒全张鲁中杨宇民
Owner NANTONG UNIVERSITY