Microporous membrane osmotic emulsification method for preparing gelatin microspheres immobilized alcohol dehydrogenase
The technology of alcohol dehydrogenase and membrane emulsification method is applied in the field of microporous membrane osmotic emulsification to prepare gelatin microspheres, which can solve the problems of wide particle size distribution of microspheres, achieve simple and easy preparation process, excellent acid-base tolerance, Fixed ability strong effect
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Embodiment 1
[0026] Preparation of gelatin microspheres immobilized with alcohol dehydrogenase by membrane emulsification method:
[0027] Under the condition of magnetic stirring at 200 rpm and temperature at 55°C, add 1 gram of dry gelatin powder to 10 ml of water, and maintain magnetic stirring at this speed for 0.5 hours until the dry powder of gelatin is completely dissolved in water, and the concentration of gelatin after dissolution is 0.1 g / Milliliter, add 1 milligram of alcohol dehydrogenase to this gelatin solution, the concentration of alcohol dehydrogenase after dissolving is 0.1 mg / ml. The above gelatin / alcohol dehydrogenase aqueous solution was used as the aqueous phase.
[0028] The oil-soluble emulsifier Span-80 is added to 60 ml of liquid paraffin, and the quality of Span-80 is 1.5% of that of the liquid paraffin. Stir magnetically at a speed of 200 rpm for 30 minutes until Span-80 is completely dissolved, and heat the above solution to 60° C. as the oil phase.
[0029]...
Embodiment 2
[0037] The preparation process of this example is the same as that of Example 1, except that the microporous membrane with a membrane pore size of 3.5 microns is replaced by a microporous membrane with a membrane pore size of 5.0 microns to obtain a gelatin microporous membrane immobilized with alcohol dehydrogenase. The particle size and distribution of the balls are shown in Table 1.
Embodiment 3
[0039] The preparation process of this example is the same as that of Example 1, except that the microporous membrane with a membrane pore size of 3.5 microns is replaced by a microporous membrane with a membrane pore size of 7.2 microns to obtain a gelatin microporous membrane immobilized with alcohol dehydrogenase. The particle size and distribution of the balls are shown in Table 1.
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