A kind of preparation method of superporous hydrogel
A technology of porous hydrogel and ultra-pure water, which is applied in the field of preparation of new ultra-porous hydrogel, can solve the problems of easy water loss closure, unstable pore structure, fast degradation rate, etc., to achieve enhanced molecular cross-linking reaction, Good biocompatibility, the effect of promoting the formation of pores
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Embodiment 1
[0034] Example 1 Preparation of porous hydrogel
[0035] (1) Dissolve the water-soluble protein HLC in 10 mL of distilled water to obtain an HLC solution with a concentration of 100 mg / mL, and add the cross-linking agent β-diimine zinc complex and 1, 2, 7, 8 with a concentration of 1%. -Diepoxyoctane each 1 mL, then add 10mg / mL KCl2mL, mix well, and adjust the pH of the solution to 4.5 with dilute hydrochloric acid;
[0036] (2) Dispense the mixed solution in (1) into a mold, keep it at 50°C for 2h, then transfer it to a high-pressure steam sterilizer and keep it at 121°C for 20min to obtain the initial gel;
[0037] (3) Soak and wash the initial gel in distilled water for 5 days, and change the washing water every 6 hours to remove salt and residual crosslinking agent; transfer the washed initial gel to a high-pressure steam sterilizer and keep at 121°C for 2 h, then soak and wash again with distilled water for 2 days, control the total amount of residual crosslinker to be less tha...
Embodiment 2
[0040] Example 2 Preparation of porous hydrogel
[0041] (1) Dissolve the water-soluble protein HSA in 10 mL of distilled water to obtain a HSA solution with a concentration of 100 mg / mL, and add the cross-linking agent β-diimine zinc complex and 1, 2, 7, 8 with a concentration of 2%. -Diepoxy octane each 1 mL, then add 10mg / mL Na 2 SO 4 2mL of the solution, mix well, and adjust the pH of the solution to 3.5 with dilute hydrochloric acid;
[0042] (2) Dispense the mixed solution in step (1) into a mold, keep it at 50°C for 2h, then transfer it to a high-pressure steam sterilizer and keep it at 110°C for 20min to obtain the initial gel;
[0043] (3) Step (2) Soak and wash with distilled water for 2 days to remove the residual cross-linking agent, and control the total amount of residual cross-linking agent to be less than 2 μg / g to obtain a porous wet gel sample;
[0044] (4) Freeze-dry the wet gel in step (3) to obtain a superporous hydrogel sample, and sterilize it by Co-60 irradiati...
Embodiment 3
[0046] Example 3 Preparation of porous hydrogel
[0047] (1) Dissolve the water-soluble protein BSA in 10 mL of distilled water to obtain a BSA solution with a concentration of 100 mg / mL, and add the cross-linking agent β-diimine zinc complex and 1, 2, 7, 8 with a concentration of 1%. -Diepoxy octane each 2 mL, then add 10mg / mL NaH 2 PO 4 Solution 2mL, mix well, and adjust the pH of the solution to 4 with dilute hydrochloric acid;
[0048] (2) Dispense the mixed solution in step (1) into a mold, keep it at 50°C for 2 hours, then transfer it to a high-pressure steam sterilizer and keep it at 121°C for 20 minutes to obtain the initial gel;
[0049] (3) The first gel in step (2) is soaked and washed with distilled water for 5 days, and the washing water is changed every 6 hours to remove salt and residual crosslinking agent; transfer the washed first gel to the autoclave Continue to keep at 121°C for 2 h, then soak and wash again with distilled water for 2 days to remove the residual c...
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