Degradable hydrogels for pulp dentin regeneration
A hydrogel and dentin technology, applied in the field of medicine, can solve the problems of poor proliferation and limited application of dental pulp stem cells
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Embodiment 1
[0022] Embodiment 1: Preparation of degradable hydrogel
[0023] (1) Dissolve chitosan in aqueous acetic acid solution to obtain a 3w / w% chitosan solution, and dissolve di-4-formylbenzoic acid polyethylene glycol (DF-PEG) in deionized water to obtain a 20w / w % aqueous solution, add 25ml DF-PEG aqueous solution to 70ml chitosan solution, then add 0.1mg epidermal growth factor (EGF) and 0.2mg interleukin-2, stir and react at room temperature for 40 seconds to obtain a hydrogel;
[0024] (2) Adult dental pulp cells were cultured by tissue block method, trypsinized and passaged, and the dental pulp cells passed to the fifth passage were trypsinized to collect the cells, and the cell suspension was 5.0×10 6 cells / g gel inoculation, 37°C, CO 2 Box overnight, use the next day, test the number of viable dental pulp cells in the gel before use, and detect by cell counting method, which contains 5.8×10 6 unit / g gel.
Embodiment 2
[0026] Using the same preparation as in Example 1, the difference is that the epidermal growth factor (EGF) is 0.2 mg, and the interleukin-2 is 0.1 mg. The number of viable dental pulp cells in the test gel before use is detected by cell counting. Which contains 4.2×10 6 unit / g gel.
Embodiment 3
[0028] Using the same preparation as in Example 1, the difference is that the epidermal growth factor (EGF) is 0.2 mg, and the interleukin-2 is 0.2 mg. The number of viable dental pulp cells in the test gel before use is detected by cell counting. Which contains 4.6×10 6 unit / g gel.
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