Method for preparing adsorbing agent carrier for medical use

A technology of adsorbent carrier and solvent, which is applied in the field of preparation of medical adsorbent carrier, can solve the problems of poor mechanical properties, unbearable pressure, slow solution mass transfer speed, etc., and achieve the effect of improving mechanical properties

Active Publication Date: 2008-11-19
JAFRON BIOMEDICAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Cellulose can be used as the carrier of medical adsorbents, but due to the limitation of the preparation method, there are three main defects in the traditional cellulose adsorbent carriers: first, they are mostly powdery, fibrous or amorphous particles, and the The hydraulic properties are not good, which will easily cause the bed laminar flow velocity to slow down and the column pressure to increase; the second is that there is no macroporous structure, resulting in slow solution mass transfer, and it is difficult for macromolecular substances to diffuse into the pores; the third is that the mechanical properties are poor and the strength Low, unable to withstand the requirements of high flow rate and medium and h...

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] A. Preparation of Cellulose Viscose

[0028] Soak 30 grams of absorbent cotton in 270 grams of 19% sodium hydroxide aqueous solution, basify it at room temperature for 2 hours, then filter it with suction, squeeze out the lye, put it in a closed container, and age it for 3 days. Then add 18 grams of carbon disulfide to it, yellow at 30° C. for about 5 hours to obtain orange viscose, add 300 grams of 6% sodium hydroxide solution therein, and stir evenly to obtain cellulose xanthate viscose.

[0029] B. Preparation of Crosslinked Spherical Cellulose Particles

[0030] 900 grams of chlorobenzene, 320 grams of carbon tetrachloride and 2 grams of potassium oleate were mixed and stirred for 30 minutes to make it uniform. 300 grams of aqueous phase cellulose xanthate viscose, 50 grams of polyethylene glycol with a polymerization degree of 200 and 30 grams of crosslinking agent sodium trimetaphosphate are mixed uniformly, and the pH value is adjusted to 10.2, and then the Add...

Embodiment 2

[0036] A. Preparation of Cellulose Viscose

[0037] Soak 30 grams of absorbent cotton in 300 grams of 19% sodium hydroxide aqueous solution, basify it at room temperature for 2 hours, then filter it with suction, squeeze out the lye, put it in a closed container, and age it for 3 days. Then add 18 grams of carbon disulfide to it, yellow at 30° C. for about 5 hours to obtain orange viscose, add 270 grams of 6% sodium hydroxide solution therein, and stir evenly to obtain cellulose xanthate viscose.

[0038] B. Preparation of Crosslinked Spherical Cellulose Particles

[0039]1500 grams of liquid paraffin and 4.5 grams of Span80 of the oil phase dispersant were mixed and stirred for 20 minutes to make it uniform. Fully mix 300 grams of aqueous cellulose xanthate viscose, 40 grams of porogen zinc chloride, 0.6 g of surfactant (Span60: Tween60=2: 1), and 100 grams of crosslinking agent epichlorohydrin Add it evenly into the oil phase, then adjust the stirring speed to disperse the...

Embodiment 3

[0045] A. Preparation of Cellulose Viscose

[0046] Soak 10 grams of absorbent cotton in 110 grams of 19% sodium hydroxide aqueous solution, basify it at room temperature for 2 hours, then filter it with suction, squeeze out the lye, put it in a closed container, and age it for 3 days. Then add 5 grams of carbon disulfide to it, and yellow it for about 8 hours at 28° C. to obtain an orange viscose solution, add 500 grams of 6% sodium hydroxide solution therein, and stir evenly to obtain a cellulose xanthate viscose solution.

[0047] B. Preparation of Crosslinked Spherical Cellulose Particles

[0048] Mix 1050 g of vacuum pump oil and 1.0 g of Span80 as the oil phase dispersant and stir for 10 minutes to make it uniform. 300 grams of aqueous cellulose xanthate viscose, 50 grams of porogen polyvinyl alcohol, 0.5 g of surfactant (Span60: Tween60=2: 1), 80 grams of 1,4-butanediol dishrunk Glycerin ether is fully mixed and added to the oil phase, then adjust the stirring speed t...

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PUM

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Abstract

The invention relates to a method for preparing a medicinal absorbent carrier, comprising the following: a step of preparation of cellulose solution; a step of preparation of crosslinking spherical cellulose particles, which is to add pore-forming agent and crosslinking agent into the cellulose solution for uniform dispersion, to disperse the cellulose solution in dispersant which is added with surface active agent, to increase the temperature to make the crosslinking agent perform crosslinking reaction with the cellulose solution, and then to prepare the crosslinking spherical cellulose particles provided with the pore-forming agent; a step pf aftertreatment, which is to use solvent which can dissolve the pore-forming agent to process the crosslinking spherical cellulose particles, to remove the pore-forming agent, and then to prepare medicinal absorbent carrier-multiaperture crosslinking spherical cellulose particles. The method has the advantages of superior mechanical properties, capability of high pressure resistance, capability of being applied in the blood purification field and so on.

Description

technical field [0001] The invention relates to a preparation method of a medical adsorbent carrier. Background technique [0002] Cellulose can be used as the carrier of medical adsorbents, but due to the limitation of the preparation method, there are three main defects in the traditional cellulose adsorbent carriers: first, they are mostly powdery, fibrous or amorphous particles, and the The hydraulic properties are not good, which will easily cause the bed laminar flow velocity to slow down and the column pressure to increase; the second is that there is no macroporous structure, which causes the solution mass transfer rate to be slow, and it is difficult for macromolecular substances to diffuse into the pores; the third is that the mechanical properties are poor and the strength Low, unable to withstand the requirements of high flow rate and medium and high pressure. After years of research, scientists from all over the world have found a variety of improved methods, b...

Claims

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Application Information

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IPC IPC(8): C08J9/26C08J3/24C08L1/00C08K3/32C08K5/1515C08L51/02C08K5/07
Inventor 董凡
Owner JAFRON BIOMEDICAL
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