Low-density lipoprotein adsorption microspheres, preparation method and adsorption material
A low-density lipoprotein and adsorption microsphere technology, which is applied in the field of low-density lipoprotein adsorption microspheres, preparation methods and adsorption materials, can solve the problems of severe reinfusion in fat-removed patients, expensive antibodies, and limited promotion. Suitable for large-scale promotion and application, high adsorption selectivity, fast filtration effect
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Embodiment 1
[0026] Embodiment 1, LDL adsorption microspheres H1
[0027] Made by the following steps:
[0028] A) 10ml porous polyvinyl alcohol microspheres are placed in the conical flask, and the concentration of 10mlDMSO, 10ml is added successively to be 1.0mol / L sodium hydroxide solution, 5ml of 1,4-butanediol diglycidyl ether, At 30°C for 6 hours, after the reaction is complete, filter with suction, wash with 50% acetone until 1,4-butanediol diglycidyl ether remains, and then wash with distilled water until no acetone remains;
[0029] B) Add 5ml DMSO, 5ml of 1.5mol / L sodium hydroxide solution, 0.12g of δ-tocopherol and 1.88g of α-tocopherol to the porous polyvinyl alcohol microspheres after the above treatment, at 35°C Stir and react for 12 hours, rinse with ethanol solution after the reaction is completed, and then wash with distilled water;
[0030] C) Add 10 ml of distilled water, 5 ml of 0.1 mol / L sodium hydroxide solution and 2 g of sulfonated dextran to the porous polyvinyl ...
Embodiment 2
[0031] Embodiment 2, LDL adsorption microspheres H2
[0032] The difference between Example 2 and Example 1 is that 0.1 g of δ-tocopherol and 1.9 g of α-tocopherol are added in step B), and the remaining parameters and operations are as shown in Example 1.
Embodiment 3
[0033] Embodiment 3, LDL adsorption microspheres H3
[0034] The difference between Example 3 and Example 1 is that 0.16 g of δ-tocopherol and 1.84 g of α-tocopherol are added in step B), and the remaining parameters and operations are as shown in Example 1.
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