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Material with antibacterial and biocompatible surface and preparing method and application thereof

A biocompatible and antibacterial technology, applied in the field of material surface modification, can solve the problems of toxic effects on cells, decrease in the content of antibacterial active components, implantation failure, etc., and achieve the effect of good cell compatibility.

Active Publication Date: 2016-01-20
广州佰斯伦生物技术有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The representative technology of the former is surface coupling or coating antibacterial materials, such as organic small molecule antibacterial agents and synthetic polymer antibacterial agents containing quaternary ammonium, haloamine, guanidine and quaternary phosphine, chitosan and its derivatives, silver-containing compounds Inorganic antibacterial agents, etc., can effectively kill surrounding bacteria and microorganisms, but on the one hand, the bacteria and microorganisms killed on the surface of implanted materials or devices may still cause immune reactions and inflammation; on the other hand, the content of antibacterial active components continues to decline over time , affect the antibacterial effective period, and may have toxic effects on normal cells
The representative technology of the latter is the introduction of polyethylene glycol or polyzwitterions (such as phosphorylcholine, sulfobetaine, etc.) compounds with anti-protein and bacterial adhesion functions on the surface, which can effectively reduce bacterial adhesion and inhibit biofilm formation. Formation, and has good hemocompatibility and cell compatibility, but there is still the risk of bacterial introduction and implantation failure in clinical use

Method used

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  • Material with antibacterial and biocompatible surface and preparing method and application thereof
  • Material with antibacterial and biocompatible surface and preparing method and application thereof
  • Material with antibacterial and biocompatible surface and preparing method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Embodiment 1 Preparation of phosphoric acid dicholine chitosan hydrochloride.

[0039] Take 200mg of 6-O-triphenyl methyl etherified chitosan (CsTr) modified by chitosan (x / n=0) and dissolve it in 20mL of anhydrous dimethylacetamide, and add 0.42mL of Tris Ethylamine and 0.19mL of carbon tetrachloride; slowly add 0.46g of disubstituted choline phosphonate, wherein the molar ratio of the amino group in CsTr to phosphonate is 1:3, stir and react at 0°C for 6 hours; spin to dry the solvent , add formic acid, stir at room temperature for 1 hour; spin dry formic acid, dialyze with physiological saline and deionized water for 3 days, and freeze-dry to obtain phosphoric acid dicholine chitosan hydrochloride. Wherein the degree of substitution of the phosphoric acid dicholine group is 30%.

Embodiment 2

[0040] Example 2 Preparation of phosphoric acid dicholine chitosan hydrochloride.

[0041] Get 500mg of 6-O-triphenyl methyl etherified chitosan (CsTr) modified by chitosan (x / n=0.2) and dissolve it in 40mL of anhydrous dimethylacetamide, add 1.05mL of Tris Ethylamine and 0.49mL of carbon tetrachloride; slowly add 2.3g of disubstituted choline phosphonate, wherein the molar ratio of the amino group in CsTr to phosphonate is 1:6, stir and react at 40°C for 12 hours; spin to dry the solvent , add formic acid, stir at room temperature for 3 hours; spin dry formic acid, dialyze with normal saline and deionized water for 3 days, and freeze-dry to obtain phosphoric acid dicholine chitosan hydrochloride. Wherein the degree of substitution of the phosphoric acid dicholine group is 50%.

Embodiment 3

[0042] Example 3 Preparation of phosphoric acid dicholine chitosan hydrochloride.

[0043] Get 300mg of 6-O-triphenylmethyl etherified chitosan (CsTr) modified by chitosan (x / n=0.1) and dissolve it in 30mL of anhydrous dimethylacetamide, add 0.63mL of Tris Ethylamine and 0.29mL of carbon tetrachloride; slowly add 1.84g of disubstituted choline phosphonate, wherein the molar ratio of the amino group in CsTr to phosphonate is 1:8, stir and react at 25°C for 24 hours; spin to dry the solvent , add formic acid, stir at room temperature for 6 hours; spin dry formic acid, dialyze with normal saline and deionized water for 3 days, and freeze-dry to obtain phosphoric acid dicholine chitosan hydrochloride. Wherein the degree of substitution of the phosphoric acid dicholine group is 75%.

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PUM

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Abstract

The invention discloses a material with an antibacterial and biocompatible surface and a preparing method and application thereof. The preparing method comprises the steps that amination of the surface of a material is achieved with an amino silane coupling agent, so that a surface-aminated material is obtained; the obtained surface-aminated material is made to react with dialdehyde to achieve formylation of the surface of the material, so that a surface-formylated material is obtained; the obtained surface-formylated material is made to react with citicoline chitosan salt to achieve citicoline chitosan salt immobilization of the surface of the material, and washing is conducted to obtain the material with the antibacterial and biocompatible surface. The adopted citicoline chitosan salt has high cytocompatibility, blood compatibility and broad-spectrum antibacterial property in the physiological environment and is biodegradable; furthermore, the citicoline chitosan salt can be fixed to the surface of the material under a mild condition to generate the material with the antibacterial and biocompatible surface, and the material is suitable for implantable and interventional medical devices.

Description

technical field [0001] The invention belongs to the technical field of material surface modification, and in particular relates to a material with antibacterial properties and biocompatibility on the surface, a preparation method and an application. Background technique [0002] The adhesion of microorganisms such as bacteria on the surface of implanted biomaterials or medical devices and the subsequent formation of biofilms are one of the main reasons for implant infection and medical device failure, which seriously threaten human health and life safety. At present, the application of antimicrobial agent coating (active antibacterial) and the formation of anti-bioadhesive surface (inert antibacterial) are two strategies to solve the complications or failure of implanted devices caused by microbial infection. The representative technology of the former is surface coupling or coating antibacterial materials, such as organic small molecule antibacterial agents and synthetic po...

Claims

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Application Information

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IPC IPC(8): A61L27/34A61L27/50A61L31/10A61L31/14
Inventor 曾戎尤德强屠美赵剑豪李卫
Owner 广州佰斯伦生物技术有限公司
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