Hydrogel capable of releasing nitric oxide and preparation method thereof
A technology of nitric oxide and hydrogel, applied in medical science, bandages, etc., can solve the problems of short action time, high power density damage to surrounding healthy tissues, and high frequency of administration, so as to promote healing, promote collagen deposition, and be good The effect of biocompatibility
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Embodiment 1
[0041] A preparation method for releasing nitric oxide hydrogel as an embodiment of the present invention, the method comprises the following steps:
[0042] (1) The 2-methylimidazole of 35.48g and the zinc acetate of 2g are dissolved in 200ml deionized water to obtain the mixed aqueous solution of 2-methylimidazole and zinc acetate, the mixed aqueous solution of 2-methylimidazole and zinc acetate at 20 Stirring and reacting at 700 rpm at ~30°C for 5 hours, collecting the reaction solution, centrifuging at 8000 rpm for 20 minutes, collecting the precipitate, washing the precipitate with deionized water, and freeze-drying to obtain the first nanoparticle (ZIF-8);
[0043] (2) Dissolve 200 mg of the first nanoparticles and 100 mg of N, N'-di-sec-butyl-N, N'-dinitroso-1,4-phenylenediamine (BNN6) in 30 mL with a volume fraction of 40% After stirring at 700rpm / min in aqueous ethanol solution for 24h to obtain solution A, add 60mg of dopamine hydrochloride and 0.26mL of 1M sodium hy...
Embodiment 2
[0049] As a preparation method of nitric oxide releasing hydrogel in the embodiment of the present invention, the only difference between this embodiment and embodiment 1 is that in step (3), 1.0 mg of the second nanoparticle (BZP), 50 mg Methacrylated gelatin (GelMA) and 12.5 mg oxidized dextran (oDex) were uniformly dispersed in 1 mL of PBS solution to obtain the mixed system B.
Embodiment 3
[0051] As a preparation method of nitric oxide releasing hydrogel in the embodiment of the present invention, the only difference between this embodiment and embodiment 1 is that in step (3), 1.0 mg of the second nanoparticle (BZP), 50 mg Methacrylated gelatin (GelMA) and 25 mg oxidized dextran (oDex) were uniformly dispersed in 1 mL of PBS solution to obtain the mixed system B.
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