Sodium alginate-dopamine/polyvinyl alcohol hydrogel, and preparation method and application thereof
A sodium alginate and polyvinyl alcohol technology, applied in medical science, bandages, etc., can solve the problems of poor wound healing, complicated preparation process, and high reaction conditions, and achieve broad biomedical application prospects, improve mechanical properties, and absorb water. The effect of sexual comfort
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Embodiment 1
[0040] (1) Sterilization of experimental raw materials and instruments
[0041] The experimental raw materials were sterilized by irradiating the raw materials with ultra-clean bench for 1 hour, and the glass instruments were sterilized at 121°C for 20 minutes under high-pressure conditions.
[0042] (2) Preparation of sodium alginate-dopamine
[0043] Take 2g of sodium alginate (SA) and add it into 100ml of distilled water, stir and dissolve at 800rpm for 12h, and prepare an SA solution for later use. Add 0.5755g N-hydroxysuccinimide (NHS) and 0.9585g 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride to the SA solution according to the molar ratio of 1:1 and add Stir at 800 rpm for 20 min, then add 1.5473 g of dopamine (DA) at room temperature and stir at 800 rpm for 24 hours. After the reaction is completed, the prepared sodium alginate-dopamine (SA-DA) solution is sealed and stored at 2-8°C.
[0044] (3) Preparation of sodium alginate-dopamine / polyvinyl alcohol...
Embodiment 2
[0060] In Vitro Cell Experiment of Sodium Alginate-Dopamine / Polyvinyl Alcohol Hydrogel
[0061] Before the in vitro cytotoxicity test, the freeze-dried hydrogel sample prepared in Example 1 was sterilized by Co60 γ-ray radiation.
[0062] (1) Take out NIH 3T3 cells (purchased from Wuhan Punuosai Life Technology Co., Ltd.) in liquid nitrogen and resuscitate them with DMEM culture medium.
[0063] (2) Subculture several times with DMEM culture medium, take the cells in the logarithmic growth phase and count the NIH3T3 cells with a cell counting plate, adjust the cell density to 5×10 4 individual / mL.
[0064] (3) Take a 96-well plate and add 100 μL to 30 wells of it. Step (2) The cell density is 5×10 4 cells / mL of DMEM culture solution was used as the experimental group; at the same time, another 3 wells were taken and set as a blank control group, that is, only 100 μL of DMEM culture solution (without cells) was added, and placed at 37°C, 5% CO 2 Incubate for 24 hours in a ce...
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