Glucosyl core-shell structure carrier material, preparation and application thereof
A carrier material, dextran-based shell technology, which can be used in applications, preparations for skin care, medical preparations with inactive ingredients, etc., and can solve the problems of complex production process, high loss of raw materials, and low yield of carrier complexes. , to achieve the effects of controllable reaction conditions, simple steps and excellent biocompatibility
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Embodiment 1
[0042] 1 g of water-soluble starch particles was weighed and dissolved in Tris-HCl buffer solution (50 mmol / L, pH 7.0) to prepare a homogeneous solution with a mass concentration of 0.5%. Continue to add 1.5 g of glucose-1-phosphate and 40 U of glycosyltransferase, stir evenly, and react at a constant temperature of 40° C. and pH 7.0 for 12 hours. Heat to inactivate the enzyme and centrifuge, and vacuum-dry the obtained precipitate to obtain the glucosyl-core-shell structure carrier material.
[0043] like figure 1As shown, a represents spherical hyperbranched water-soluble starch particles; b represents the initial stage of graft chain extension of starch particles modified by biotechnology, that is, glycosyltransferase connects the glucose group to the Non-reducing ends of spherical starch granules. c indicates that starch particles have been modified by biotechnology, and the late stage of graft chain extension, that is, the linear structure formed by grafting is wound an...
Embodiment 2
[0048] 1 g of water-soluble starch particles was weighed and dissolved in Tris-HCl buffer solution (50 mmol / L, pH 7.0) to prepare a homogeneous solution with a mass concentration of 1.0%. Continue to add 2.5 g of glucose-1-phosphate and 60 U of glycosyltransferase, stir evenly, and react at a constant temperature of 40° C. and pH 7.0 for 18 hours. Heat to inactivate the enzyme and centrifuge, and vacuum-dry the obtained precipitate to obtain the glucosyl-core-shell structure carrier material.
Embodiment 3
[0050] 1 g of water-soluble starch particles was weighed and dissolved in Tris-HCl buffer solution (50 mmol / L, pH 7.0) to prepare a homogeneous solution with a mass concentration of 1.5%. Continue to add 5.0 g of glucose-1-phosphate and 100 U of glycosyltransferase, stir evenly, and react at a constant temperature of 40° C. and pH 7.0 for 24 hours. Heat to inactivate the enzyme and centrifuge, and vacuum-dry the obtained precipitate to obtain the glucosyl-core-shell structure carrier material.
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