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Adsorbent for removing bacterial endotoxin, dna and peptidoglycan, preparation method and use

A technology of bacterial endotoxin and adsorbent, which is applied in the field of medicine, can solve the problem that the adsorbent can only absorb bacterial endotoxin, and achieve good adsorption effect and good adsorbent effect

Active Publication Date: 2015-10-21
CHONGQING ZHENGBO BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The purpose of the present invention is to solve the problem that the existing adsorbent can only adsorb bacterial endotoxin, and provide an adsorbent for removing bacterial endotoxin, DNA and peptidoglycan, which can simultaneously adsorb bacterial endotoxin, DNA and peptidoglycan peptidoglycan

Method used

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  • Adsorbent for removing bacterial endotoxin, dna and peptidoglycan, preparation method and use
  • Adsorbent for removing bacterial endotoxin, dna and peptidoglycan, preparation method and use

Examples

Experimental program
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Effect test

Embodiment 1

[0033] Example 1: Preparation of agarose gel-picrylamine B adsorbent

[0034] 1.1 Experimental method: Sepharose CL-4B was used for the agarose gel, purchased from GE Healthcare. Take 20ml of Sepharose CL-4B agarose gel, wash with ultrapure water, and filter to dryness. Take 4g of the dried gel, add 10ml of 0.5M NaOH solution and 10ml of epichlorohydrin, and shake at 40°C for 5 hours. After the reaction was completed, it was washed with ultrapure water and filtered to dryness. Take 100mg Kuchrysamine B, dissolve in 50ml0.1M NaHCO 3In the solution, it was mixed with agarose gel activated by epichlorohydrin, and reacted with shaking at 25°C for 24 hours. After the reaction is completed, wash with ultrapure water, and suction filter to dryness (all the filtrate is collected) to obtain Sepharose-Crysamine B adsorbent. For the collected filtrate, use high performance liquid chromatography (chromatographic column: octadecylsilane bonded silica gel as filler; mobile phase: 0.1% t...

Embodiment 2

[0038] Example 2: Preparation of polyvinyl alcohol-picrylamine B adsorbent

[0039] 2.1 Experimental method: The preparation principle of polyvinyl alcohol-picrylamine B adsorbent is similar to that of agarose gel-picrylchryl B adsorbent. Polyvinyl alcohol was purchased from Sigma-Aldrich. Dissolve 5g of polyvinyl alcohol in ultrapure water to make a 10% aqueous solution, put it in a constant temperature water bath at 90°C and stir until completely dissolved, then freeze at -20°C for 24 hours, take it out and thaw at room temperature for 4 hours, Freezing and thawing were repeated three times in this way to obtain polyvinyl alcohol hydrogel. Suction filter the gel to dryness, take 4g of the gel, add 10ml of 0.5M NaOH solution, 10ml of epichlorohydrin, shake and react at 50°C for 5 hours. After the reaction was completed, it was washed with ultrapure water and filtered to dryness. Take 100mg Kuchrysamine B, dissolve in 50ml0.1M NaHCO 3 In the solution, it was mixed with pol...

Embodiment 3

[0041] Embodiment 3: Preparation of cellulose-picrylamine B adsorbent

[0042] 3.1 Experimental method: The preparation principle of the cellulose-picrylamine B adsorbent is similar to that of the agarose gel-picrylchryl B adsorbent. Cellulose was purchased from Sigma-Aldrich. Take 5g of cellulose, add 10ml of 0.5M NaOH solution, 10ml of epichlorohydrin, and shake at 40°C for 4 hours. After the reaction was completed, it was washed with ultrapure water and suction filtered to dryness. Take 200mg Kuchrysamine B, dissolve in 100ml 0.1M NaHCO 3 In the solution, mix with the cellulose activated by epichlorohydrin, shake and react at 25°C for 24 hours. After the reaction is completed, wash with ultra-pure water and suction filter to dryness to obtain cellulose-picrylamine B adsorbent. The calculation method of the immobilization capacity of Kuchrysamine B is the same as in Example 1.

[0043] 3.2 Experimental results: After detection and calculation, the immobilization capacit...

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Abstract

The invention relates to an adsorbent for removing bacterial endotoxin, DNA and peptidoglycan. The adsorbent is connected with the surface of a carrier with good blood compatibility. The adsorbent is capable of effectively adsorbing bacterial endotoxin, DNA and peptidoglycan from blood of human body so as to achieve the aims of removing pathogene related molecular inducing the pyemia and exerting the effect of treating the pyemia, and the adsorbent has an important clinical value.

Description

technical field [0001] The invention belongs to the technical field of medicine, and particularly relates to an adsorbent for removing bacterial endotoxin, DNA and peptidoglycan, a preparation method and application thereof. Background technique [0002] Sepsis is a systemic inflammatory response syndrome triggered by infection. The occurrence of sepsis is that after pathogens invade the human body, the pathogen-related molecules contained in the pathogens are recognized by the pattern recognition receptors in the body's natural immune system, leading to the activation of inflammatory response cells and the release of a large number of inflammatory mediators, which trigger systemic inflammatory responses, resulting in tissue damage or even death. More than 90% of the pathogens that cause sepsis are bacteria, and the pathogen-related molecules contained in bacteria mainly include bacterial endotoxin (lipopolysaccharide), DNA, and peptidoglycan. Therefore, if these pathogeni...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J20/26B01J20/24B01J20/30A61M1/38C08B37/12C08B15/06C08F16/06C08F12/08C08F8/32
Inventor 郑玥
Owner CHONGQING ZHENGBO BIOTECH CO LTD
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