A kind of preparation method of hyaluronic acid blended nanofiber immobilized enzyme
A nanofiber, hyaluronic acid technology, applied in the direction of fixation on/in organic carriers, fiber processing, fiber chemical characteristics, etc., can solve the problem of providing a mild microenvironment, easy shedding of modified materials, and poor biocompatibility and other problems, to achieve the effect of improving biocompatibility and water retention, good water retention performance and high porosity
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Embodiment 1
[0039] A preparation method for immobilizing enzymes in hyaluronic acid blended nanofibers, comprising the following steps:
[0040] (1) Configuration of hyaluronic acid solution
[0041] Measure 1.5mL of DMF solution and 1.5mL of distilled water into a test tube, weigh 4mg of sodium hyaluronate solid with an electronic balance, add it and dissolve to obtain a sodium hyaluronate solution.
[0042] (2) Configuration of PMA-AA binary interpolymer
[0043]Dissolve 2mL of acrylic acid and 14mL of methyl acrylate in 40mL of N,N-dimethylformamide (DMF), add 0.2-0.3g of azobisisopropionitrile, fill with nitrogen gas for 10-12min, and place at 60-80°C Heat in a constant temperature water bath and react for 15 to 24 hours to obtain a viscous, transparent and uniform PMA-PAA solution. (3) Configuration of spinning precursor
[0044] Measure 5mL of PMA-PAA solution and add 3mL of sodium hyaluronate solution, and shake fully to obtain the spinning precursor solution.
[0045] (4) Prep...
Embodiment 2
[0051] A preparation method for immobilizing enzymes in hyaluronic acid blended nanofibers, comprising the following steps:
[0052] (1) Configuration of hyaluronic acid solution
[0053] Measure 1.5mL of DMF solution and 1.5mL of distilled water into the test tube, weigh 4mg of sodium hyaluronate solid with an electronic balance, add it and dissolve to obtain a sodium hyaluronate solution.
[0054] (2) Configuration of PMA-AA binary interpolymer
[0055] Dissolve 2mL of acrylic acid and 14mL of methyl acrylate in 40mL of N,N-dimethylformamide (DMF), add 0.2-0.3g of azobisisopropionitrile, fill with nitrogen gas for 10-12min, and place at 60-80°C Heat in a constant temperature water bath and react for 15 to 24 hours to obtain a viscous, transparent and uniform PMA-PAA solution.
[0056] (3) Configuration of spinning precursor
[0057] Measure 5mL of PMA-PAA solution, add 0.5mL of sodium hyaluronate solution, and shake fully to obtain the spinning precursor solution.
[005...
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