Heavy metal adsorbent for extracorporeal perfusion method and preparation method of heavy metal absorbent
An in vitro perfusion and heavy metal technology is applied in the field of biomedical materials to achieve the effects of large adsorption capacity, low preparation cost and treatment of heavy metal poisoning
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Embodiment 1
[0016] Measure 20ml (sedimentation volume) of Sepharose FF medium microspheres stored in 20% ethanol aqueous solution, wash repeatedly with excess deionized water to remove ethanol; place the washed gel in a G3 sintered glass funnel Vacuum-dry 5min; Back successively with each 40ml of dimethyl sulfoxide aqueous solution of 20%, 50%, 70% clean the medium after the suction filtration; Then, add a certain amount of dimethyl sulfoxide (30ml) successively in the treated medium %), dichloroethane, epichlorohydrin (10%), sodium hydroxide (0.8M), water; the medium suspension was reacted at 40° C. for 2 hours under shaking conditions. After the reaction, it was repeatedly washed with excess deionized water until there was no residual epoxy group in the cleaning solution, and epichlorohydrin-activated agarose gel microspheres were obtained, and the agarose epoxy modification density was 60 μmol / ml gel.
Embodiment 2
[0018] Mix 8.5 volumes of 0.2M K2HPO4 solution with 1.5 volumes of 0.2M KH2PO4 solution to make the coupling buffer. Take 5 g of the epichlorohydrin-activated sepharose microspheres in Example 1 and suspend them in 10 ml of coupling buffer. Take a certain amount of metallothionein and dissolve it in the coupling buffer solution to completely dissolve it. Mix the gel suspension and the coupling buffer solution at a ratio of 1:0.5 to 1:1 for suspension reaction, seal in a water bath at 20°C-45°C, and keep stirring (or vibrating, shaking) for 20 hours. Wash with coupling buffer to remove excess ligand. Suspend the reacted and washed gel in a solution of 1 mol / L ethanolamine (pH 8.0), and react at 40°C-50°C for a minimum of 4 hours or overnight at room temperature to eliminate residual active groups on the surface of the medium. After the reaction, wash alternately with 0.1M acetate buffer (pH 4.0) containing 0.5M NaCl and coupling buffer (pH 8.3) containing 0.5M NaCl, and repea...
Embodiment 3
[0020] Measure 20ml (sedimentation volume) of Sepharose FF medium microspheres stored in 20% ethanol aqueous solution, wash repeatedly with excess deionized water to remove ethanol; place the washed gel in a G3 sintered glass funnel Vacuum dry for 5 minutes; then wash the medium after suction and filtration with 5 times the volume of 30% and 70% acetone aqueous solution; finally wash 5 times with 5 times the volume of 100% dioxane, drain and transfer to a 200ml flask ; Add a certain amount of allyl glycidyl ether and boron trifluoride-ether to the treated medium in turn; react the medium suspension at 35°C for 1-2 hours under shaking conditions. After the reaction, the medium was washed with 5 times the volume of 30% and 70% acetone aqueous solutions in sequence, and then repeatedly washed with excess deionized water until there was no residual epoxy group in the cleaning solution, and allyl glycidyl ether activated agarose gel was obtained. Microspheres, allyl modification de...
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