Blood purification adsorption agent for clearing immune body and preparation method thereof
A blood purification and adsorbent technology, applied in chemical instruments and methods, blood circulation treatment, other chemical processes, etc., can solve the problems of insignificant treatment effect, high price of protein A adsorbent, and limited scope of application.
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Embodiment 1
[0024] Take the gel with a volume of 10mL after fully settling (overnight), wash it with 200mL of anhydrous acetone several times to remove the water contained in the gel, then disperse the agarose gel evenly in an equal volume of acetone, and ensure that the whole system is free of water. water. Weigh 0.8 g of CDI and mix it with the gel suspension, and stir the resulting mixture at 15° C. for 1 hour. After the reaction, the gel was washed several times with 200 mL of anhydrous acetone. A cross-linked agarose gel with imidazole carbamate active groups was obtained, and the degree of substitution was 1.6 mmol / g dry gel according to elemental analysis, and 1 g of dry gel was equivalent to a wet volume of 35 mL.
[0025] 10 mL of CDI-activated gel was evenly dispersed in an equal volume of acetone, and hexamethylenediamine was added to the gel system in a 5-fold excess, and the resulting mixture was suspended and stirred at 20°C for 2 hours. After the reaction, wash with 100 m...
Embodiment 2
[0028] The specific steps are the same as in Example 1, except that the amount of CDI is increased to 1.2 g / 10 mL of wet glue, and the activation reaction is carried out at 30° C. for 2 hours. After the activation, the elemental analysis showed that the degree of substitution was 3.6 mmol / g dry glue. The amount of hexamethylenediamine used in the arm grafting reaction was 10 times excess, and the arm grafting reaction was carried out at 35° C. for 3 hours. When coupling benzoic acid, the reaction was carried out in a pH 6.5 buffer solution at 35° C. for 4 hours. NaOH solution at pH 13 was used for hydrolysis of remaining imidazole activating groups. The coupling density of its product is 2.6mmol / g dry glue through elemental analysis.
Embodiment 3
[0030] The specific steps are the same as in Example 1, except that the amount of CDI is 1.0 g / 10 mL of wet glue, and the activation reaction is carried out at 30° C. for 1 hour. After the activation, the elemental analysis showed that the degree of substitution was 3.1 mmol / g dry glue. The amount of hexamethylenediamine used in the arm grafting reaction was 10-fold excess, and the arm grafting reaction was carried out at 30°C for 2.5 hours. When coupling benzoic acid, the reaction was carried out in a pH 6.5 buffer solution at 30°C for 3 hours. The coupling density of its product is 2.1mmol / g dry glue through elemental analysis.
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