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Antibacterial self-repairing hydrogel as well as preparation method and application thereof

A self-healing and antibacterial technology, which can be used in pharmaceutical formulations, medical preparations with non-active ingredients, and medical science. Longevity, good biocompatibility and long-term activity

Inactive Publication Date: 2019-11-22
HEBEI UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, to date, the antibacterial properties of self-healing hydrogels have not been well studied, although heavy metal ions and natural extracts have been used in antibacterial applications.

Method used

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  • Antibacterial self-repairing hydrogel as well as preparation method and application thereof
  • Antibacterial self-repairing hydrogel as well as preparation method and application thereof
  • Antibacterial self-repairing hydrogel as well as preparation method and application thereof

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preparation example Construction

[0040] The embodiment of the present invention also discloses the preparation method of antibacterial hydrogel, comprising the following steps:

[0041]a, copolymerization, 200 parts by weight of N-(3-dimethylaminopropyl) methacrylamide and 10~300 parts (preferably 20~100 parts) of diacetone acrylamide are dissolved in a solvent, and the Free radical copolymerization (preferably controlled free radical polymerization), the reaction temperature is 30~120°C (preferably 60~100°C), the reaction time is 2~24h (preferably 12~24h), after the polymerization is completed, add to the reaction solution Add a precipitating agent to remove the residual monomer by precipitation to obtain N-(3-dimethylaminopropyl) methacrylamide and diacetone acrylamide copolymer. Wherein, the solvent used is N,N-dimethylformamide, dioxane or dimethyl sulfoxide, and the amount of solvent used is 120-1000 parts.

[0042] b, quaternization, the obtained N-(3-dimethylaminopropyl) methacrylamide and diacetone a...

Embodiment 1

[0045] Copolymerization: 20 g N-(3-dimethylaminopropyl) methacrylamide, 20 g diacetone acrylamide, 30 mg azobisisobutyronitrile (AIBN) and 300 mg DDMAT chain transfer agent (i.e. dodecyltri Thiocarbonate) was dissolved in 40 mL of dioxane, and it was added to a 100 mL reaction flask. After removing the oxygen in the system, the temperature was raised to 60°C under magnetic stirring to perform reversible addition-fragmentation chain transfer radical polymerization. The reaction time is 24 hours. After the reaction is over, cool the reaction system, precipitate twice with petroleum ether, remove the unreacted monomer, and dry it in vacuum to obtain a white powder, which is N-(3-dimethylaminopropyl) methacrylic acid Amide-diacetone acrylamide copolymer, weighted calculation of monomer conversion rate and average molecular weight, the mass ratio of repeating unit N-(3-dimethylaminopropyl) methacrylamide to repeating unit diacetone acrylamide in the copolymer About 50:50.

[0046]...

Embodiment 2

[0054] Copolymerization: 20 g N-(3-dimethylaminopropyl) methacrylamide, 15 g diacetone acrylamide, 27 mg azobisisobutyronitrile (AIBN) and 270 mg DDMAT chain transfer agent (i.e. dodecyltri Thiocarbonate) was dissolved in 35 mL of dioxane, and added to a 100 mL reaction flask. After removing the oxygen in the system, the temperature was raised to 60°C under magnetic stirring to perform reversible addition-fragmentation chain transfer radical polymerization. The reaction time is 24 hours. After the reaction is over, cool the reaction system, precipitate twice with petroleum ether, remove the unreacted monomer, and dry it in vacuum to obtain a white powder, which is N-(3-dimethylaminopropyl) methacrylic acid Amide-diacetone acrylamide copolymer, weighted calculation of monomer conversion rate and average molecular weight, the mass ratio of repeating unit N-(3-dimethylaminopropyl) methacrylamide to repeating unit diacetone acrylamide in the copolymer About 20:10.

[0055] Quater...

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Abstract

The invention provides antibacterial self-repairing hydrogel as well as a preparation method and application thereof. The self-repairing hydrogel is prepared by carrying out a reaction on a copolymerof quaternized N-(3-dimethylaminopropyl) methacrylamide (DMAPMA) and diacetone acrylamide (DAA) and a hydrazide compound in an aqueous solution, wherein the copolymer comprises a repeating unit A anda repeating unit B, and the repeating unit A as a functional group containing quaternary ammonium salt accounts for 50-95% by mass of the copolymer. The hydrogel provided by the invention is good in stability under a neutral condition; the hydrogel has self-repairability, does not need any external catalyst or other stimulation in the self-repairing process, has a self-repairing behavior similar to that of a living body, has a certain antibacterial function, and has very wide application prospects in wound dressing, drug loading, controllable release and other biological medicine related fields.

Description

technical field [0001] The invention relates to a self-repairing hydrogel and its preparation method and application, in particular to a self-repairing hydrogel with antibacterial function and its preparation method and application. Background technique [0002] Hydrogel is a polymer material with a three-dimensional network structure that absorbs a large amount of water, is soft in nature and can maintain a certain shape. Hydrogels with self-healing properties, whose repair process is close to the self-healing of living organisms, have very realistic application prospects in the fields of bioscience and engineering, such as wound dressings, tissue engineering and controlled release of drugs, and are expected to help Human beings uncover the mysteries of self-healing of living organisms. Therefore, self-healing materials, especially hydrogels, have attracted extensive attention from the scientific community. [0003] Wound healing is a dynamic and complex process involving...

Claims

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Application Information

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IPC IPC(8): C08J3/075C08L33/24C08L71/02C08F220/60C08F220/58C08F8/44A61K9/06A61K47/32A61L15/26A61L15/46A61L26/00
CPCA61K9/06A61K47/32A61L15/26A61L15/46A61L26/0014A61L26/0066A61L26/008C08F8/44C08F220/58C08F220/60C08J3/075C08J2333/24C08J2371/02C08J2433/24C08J2471/02
Inventor 秦江雷安恒莘佳富
Owner HEBEI UNIVERSITY