Blood fat adsorbent and preparation method thereof
A technology of adsorbent and blood lipid, which is applied in the field of blood lipid adsorbent and its preparation, can solve the problems of low reaction efficiency, inability to obtain blood lipid adsorbent, and low utilization rate of ligand, so as to improve adsorption efficiency, improve catalytic ring-opening and coupling The effect of improving the efficiency of the coupling reaction and the efficiency of the coupling reaction
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[0026] The invention provides a preparation method of a blood lipid adsorbent, comprising the following steps:
[0027] S1. Activating the adsorption carrier to obtain an epoxy-containing activation carrier;
[0028] The epoxy-containing activation carrier includes, but is not limited to, one or more of epoxy-containing sepharose, cellulose gel and resin, preferably sepharose microspheres. For example, epichlorohydrin is used to activate the agarose gel microspheres to obtain epoxy group-containing agarose gel microspheres.
[0029] S2. adding the lipid adsorption ligand into the buffer to obtain a ligand solution;
[0030] The blood lipid adsorption ligand is a dextran sulfate solution or a heparin solution; the buffer is a glycine-sodium hydroxide buffer.
[0031] S3. The epoxy-containing activation carrier obtained in step S1 is mixed with a tertiary amine reagent, and then added to the ligand solution obtained in step S2, and the coupling reaction is carried out with mix...
Embodiment 1
[0040] A preparation method of a blood lipid adsorbent, comprising the following steps:
[0041] S1. Take a certain amount of agarose gel microspheres, add 1.0mol / L sodium hydroxide solution and epichlorohydrin in a ratio of 1g:1.5ml:450μl to the microspheres, mix well, and react at 40°C for 2 hours , washed and drained to obtain activated agarose gel microspheres;
[0042] S2. Dissolve dextran sulfate sodium salt in a glycine-sodium hydroxide buffer with a pH value of 10.6 at a ratio of 200mg: 1ml to prepare a dextran sulfate ligand solution;
[0043] S3. Mix the activated sepharose microspheres with dodecyl tertiary amine by 1g:0.6ml, and then press the ratio of activated sepharose microspheres to dextran sulfate ligand solution to be 1g:2.5ml , adding it into the dextran sulfate ligand solution, carrying out a coupling reaction at 50° C. for 8 hours, and then washing the adsorption carrier with purified water, brine, ethanol and purified water in turn to obtain the blood l...
Embodiment 2
[0045] A preparation method of a blood lipid adsorbent, compared with Example 1, is different in that the dodecyl tertiary amine in step S3 is replaced with hexadecyl tertiary amine. Others are basically the same as those in Embodiment 1, and are not repeated here.
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