Blood fat adsorbent and preparation method thereof
An adsorbent and blood lipid technology, which is applied in the field of blood lipid adsorbent and its preparation, can solve the problems that the spraying process of tertiary amine reagent is not easy to operate, affect the environment and reaction results, and cannot obtain blood lipid adsorbent, etc., so as to improve the reaction rate and ligand. Utilization rate, lowering reaction temperature, increasing the effect of fixed amount
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[0028] The invention provides a preparation method of a blood lipid adsorbent, comprising the following steps:
[0029] S1, using polyepoxy glyceryl ether to activate the adsorption carrier to obtain an activated carrier containing polyepoxy groups;
[0030] S2, adding the lipid adsorption ligand into the acidic solution to obtain a ligand solution;
[0031] S3, adding the epoxy group-containing activated carrier obtained in step S1 to the ligand solution obtained in step S2, mixing and stirring to carry out coupling reaction, after the reaction is completed, solid-liquid separation, cleaning and drying are performed to obtain a blood lipid adsorbent.
[0032] Preferably, in step S1, the polyglycidyl ethers include but not limited to trimethylolpropane triglycidyl ether, glycerol triglycidyl ether, castor oil triglycidyl ether and triisocyanurate One or more mixtures of glycidyl ethers.
[0033] Preferably, in step S1, the activation carrier containing polyepoxy groups inclu...
Embodiment 1
[0045] Embodiment 1 of the present invention provides a preparation method of a blood lipid adsorbent, comprising the following steps:
[0046] S1, take a certain amount of agarose microspheres, add trimethylolpropane triglycidyl ether with a ratio of 1g:1.0mL to the agarose microspheres, mix well, react at 50°C for 2h, wash and drain, Obtain activated agarose microspheres containing multiple epoxy groups;
[0047] S2, dissolving heparin in a hydrochloric acid solution with a pH value of 4 at a ratio of 200mg: 1mL to prepare a heparin ligand solution;
[0048] S3, the ratio of the activated agarose microspheres to the heparin ligand solution is 1g: 3.0mL, which is added to the heparin ligand solution, and the coupling reaction is carried out at 50°C for 10 hours, followed by purified water and saline 1. Washing the adsorption carrier with purified water to obtain a blood lipid adsorbent.
Embodiment 2
[0050] Compared with Example 1, the difference is that the ratio in step S1 is replaced by 1 g: 2.0 mL.
[0051] Others are basically the same as in Embodiment 1, and will not be repeated here.
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