Tissue engineering nerve graft and application thereof
A tissue engineering and graft technology, applied in the fields of medicine and biomedical engineering, can solve the problem of difficulty in obtaining materials, and achieve the effects of abundant sources, easy separation and purification, and simple preparation process.
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Embodiment 1
[0016] Example 1 Preparation of Chitosan Tissue Engineering Nerve from Autologous Bone Marrow Stem Cells
[0017] Chitosan was dissolved with 2% lactic acid to obtain a 1.5% chitosan solution. Then inject the solution into the mold, freeze and preform at -60°C, remove the material from the mold, put in 5% sodium hydroxide solution, neutralize the acid in the material, and after fixed molding, remove the excess alkali and the generated salt with distilled water After being cleaned, freeze-dried to obtain a chitosan artificial nerve graft containing neurotrophic factors, with a porosity of 87% and an average pore diameter of 220-289 μm.
[0018] Enrichment process of autologous bone marrow stem cells: extract about 40ml of subject's bone marrow, anticoagulate with heparin, pay attention to avoid clot formation as much as possible, transfer the bone marrow to two 50ml sterile centrifuge tubes in the ultra-clean bench, dilute them with PBS and Mix well, draw FICOLL10-20ml / tube×4 ...
Embodiment 2
[0021] Example 2 Chitosan Tissue Engineering Nerves Using Autologous Bone Marrow Mesenchymal Stem Cells (MSCs)
[0022] Chitosan was dissolved with 2% acetic acid to obtain a 2% solution of chitosan. Then inject the solution into the mold, freeze and preform at -70°C, remove the material from the mold, put it into a 10% sodium carbonate solution, neutralize the acid in the material and fix the molding, then remove the excess alkali and the generated salt with distilled water After cleaning, and then freeze-drying to obtain a chitosan artificial nerve graft, the porosity is 72%, and the average pore diameter is 130-180 μm.
[0023] Autologous bone marrow mesenchymal stem cell enrichment process:
[0024] (1) Cell separation
[0025] 1. Extract about 40ml of the subject's bone marrow, anticoagulate with heparin, and try to avoid clot formation
[0026] 2. Transfer the bone marrow to two 50ml sterile centrifuge tubes in the ultra-clean bench, dilute them with PBS and mix the...
Embodiment 3
[0076] Example 3 Chitosan Tissue Engineering Nerves Using Schwann Cells
[0077] Dissolve chitosan with 2% citric acid to obtain a 5% solution of chitosan, then pour the solution into the mold, freeze and preform at -80°C, and then remove the material from the mold and put it into 5% hydrogen In the sodium oxide solution, after neutralizing the acid in the material and fixing it into shape, after cleaning the excess alkali and the generated salt with distilled water, then freeze-drying to obtain the chitosan artificial nerve graft, the porosity is 51%, and the average pore size is 57-96 μm.
[0078] The chitosan artificial nerve guide prepared above was high-pressure sterilized for use. The day before the experiment, soak in DMEM+15%FBS complete medium for 24h. Dorsal root ganglia were obtained from embryonic 16d SD rats L4,5,6. Three DRGs were implanted at both ends of the prepared silk tube, cultured in DMEM+15%FBS in the bioreactor for 1 day, and then replaced with 97% n...
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