Medical adsorbent, and preparation method and applications thereof
A technology of adsorbent and adsorbent carrier, which is applied in the field of medical adsorbent and its preparation, can solve the problems of difficult and effective control of pore size, failure to achieve effective screening of adsorption, poor temperature and pressure resistance, etc., to achieve good biological Compatibility, a wide range of applications, and the effect of improving the ability to withstand pressure and withstand pressure
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Examples
Embodiment 1-6
[0027] In Examples 1-6:
[0028] The carboxymethyl starch ether is prepared from carboxymethyl starch with a higher degree of substitution by etherification reaction of starch and chloroacetic acid under alkaline conditions.
[0029] The hydroxypropyl starch ether is a natural plant raw material, which is a white fine powder obtained through modification, high etherification reaction, and spray drying.
[0030] Described carboxymethyl starch ether and hydroxypropyl starch ether are all white fine powders, can dissolve in cold water, are alkaline pH value 9-11 (3.75% aqueous solution) fineness is less than 350 microns, viscosity is in 400- 1200mpas.
[0031] The molecular weight of the polyethylene glycol is 2000-40000.
Embodiment 1
[0033] 1. Carboxymethyl starch ether, Ca(HCO 3 ) 2 The total mass of powder and RO reverse osmosis water is denoted as A, will account for the carboxymethyl starch ether powder of total mass A 20wt% and account for the Ca(HCO of 65wt% of total mass A 3 ) 2 Powder, fully mixed, and gradually added RO reverse osmosis water accounting for 15wt% of the total mass A, stirred into dough, and placed in the refrigerator to cool down to 5 ° C, stored for 5 hours; Particles with a diameter of 0.5 mm were obtained. When granulating and forming, the temperature was solidified at 80° C., and the obtained particles were carbonized in a carbonization furnace at 160° C. for 4 hours to obtain adsorbent carrier particles.
[0034] 2. preparation of adsorbent solution: the total mass of polysulfone, DMAC, polyethylene glycol and PVP-K30 is recorded as B, and the polysulfone group materials accounting for 8wt% of the total mass B are mixed with the DMAC accounting for 65wt% of the total mass B,...
Embodiment 2
[0038] The difference from Example 1 is:
[0039] Starch ether described in step 1 is hydroxypropyl starch ether and accounts for 30wt%, and described Ca(HCO 3 ) 2 accounts for 70 wt%, and the RO reverse osmosis water accounts for 10 wt%.
[0040] As described in step 1, pellets with a diameter of 0.6 mm were obtained through a sieve using a round pellet granulator.
[0041] The curing temperature described in step 1 is 120°C.
[0042] The power of the ultraviolet light described in step 2 is 80W, the time of the irradiation is 40 minutes, and the time of standing for defoaming is 24h.
[0043]In step 2, the polysulfone family material is 12wt%, the DMAC is 70wt%, the heating temperature is 80°C, the PEG is 10wt%, and the PVP-K90 is 8wt%.
[0044] The spraying amount of the adsorbent solution in step 3 is 20% of the adsorbent carrier particles.
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Abstract
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