Copper-cobalt-sulfur nano-enzyme material as well as preparation method and antibacterial application thereof

A technology of nanozyme and copper cobalt sulfur, which is applied in the field of nanozyme, can solve the problems of limited application and low catalytic activity, and achieve the effects of good biocompatibility, good dispersion and stable properties

Pending Publication Date: 2020-06-02
YANGZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, most nanozymes exhibit optimal activity at a pH of 3-5, and their catalytic activity is low at neutral physiological pH, which limits their application in the biomedical field.

Method used

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  • Copper-cobalt-sulfur nano-enzyme material as well as preparation method and antibacterial application thereof
  • Copper-cobalt-sulfur nano-enzyme material as well as preparation method and antibacterial application thereof
  • Copper-cobalt-sulfur nano-enzyme material as well as preparation method and antibacterial application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] The preparation of embodiment 1 copper-cobalt-sulfur nanozyme:

[0033] Dissolve 0.5 g of dextran (molecular weight: 500,000) in 30 mL of ultrapure water, and stir magnetically for 30 minutes to fully dissolve the dextran. Then add 0.25mmol of CuCl 2 .2H 2 O, 0.5 mmol CoCl 2 .6H 2 O, and 1.5mmol thiourea, magnetically stirred for 30 minutes to obtain a mixed solution. Then slowly add 100 μL of ethylenediamine dropwise, stir and mix thoroughly to obtain a reaction solution. The reaction solution was poured into a 50 ml polytetrafluoroethylene reactor, transferred to an oven, and reacted at 160° C. for 20 hours. After the reaction product was naturally cooled to room temperature, it was centrifuged, washed three times with water and ethanol, and freeze-dried in vacuum to finally obtain 150 mg of black copper-cobalt-sulfur nano-powder with a yield of 54.4%. XRD analysis showed that the obtained product was copper cobalt sulfur (CuCo 2 S 4 )(See image 3 ), with a ...

Embodiment 2

[0034] Preparation of embodiment 2 copper-cobalt-sulfur nanozyme:

[0035] Dissolve 0.5 g of dextran (molecular weight: 70,000) in 30 mL of ultrapure water, and stir magnetically for 30 minutes to fully dissolve the dextran. Then add 0.25mmol of CuCl 2 .2H 2 O, 0.5 mmol CoCl 2 .6H 2 O, and 1.5mmol thiourea, magnetically stirred for 30 minutes to obtain a mixed solution. Then slowly add 100 μL of ethylenediamine dropwise, stir and mix thoroughly to obtain a reaction solution. The reaction solution was poured into a 50 ml polytetrafluoroethylene reactor, transferred to an oven, and reacted at 160° C. for 20 hours. After the reaction product is naturally cooled to room temperature, it is centrifuged, washed three times with water and ethanol, and freeze-dried in a vacuum to finally obtain copper-cobalt-sulfur nanoparticles.

Embodiment 3

[0036] Preparation of embodiment 3 copper-cobalt-sulfur nanozyme:

[0037] Dissolve 0.5 g of dextran (molecular weight: 10,000) in 30 mL of ultrapure water, and stir magnetically for 30 minutes to fully dissolve the dextran. Then add 0.25mmol of CuCl 2 .2H 2 O, 0.5 mmol CoCl 2 .6H 2 O, and 1.5mmol thiourea, magnetically stirred for 30 minutes to obtain a mixed solution. Then slowly add 100 μL of ethylenediamine dropwise, stir and mix thoroughly to obtain a reaction solution. The reaction solution was poured into a 50 ml polytetrafluoroethylene reactor, transferred to an oven, and reacted at 160° C. for 20 hours. After the reaction product is naturally cooled to room temperature, it is centrifuged, washed three times with water and ethanol, and freeze-dried in a vacuum to finally obtain copper-cobalt-sulfur nanoparticles.

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Abstract

The invention discloses a copper-cobalt-sulfur nano-enzyme material as well as a preparation method and antibacterial application thereof, and the preparation method of the nano-enzyme material comprises the following steps: (1) fully dissolving biocompatible macromolecules in a solvent to obtain a uniform solution; (2) under a stirring condition, adding CuCl2.2H2O, CoCl2.6H2O and thiourea into the solution obtained in the step (1), then adding ethylenediamine, and carrying out stirring to fully mix the mixture to form clear liquid; and (3) taking the clear solution obtained in the step (2), carrying out reacting at 160-180 DEG C, and then carrying out cooling, centrifuging, washing and drying to obtain the copper-cobalt-sulfur nano-enzyme material. The obtained copper-cobalt-sulfur nano-enzyme has the activity of simulated peroxidase and can catalyze hydrogen peroxide to generate hydroxyl radicals under the physiological pH condition. The preparation method of the copper-cobalt-sulfurnano-enzyme is simple and easy to implement, good in dispersity and good in antibacterial property, and can be applied to treatment of bacterial infection.

Description

technical field [0001] The technical field of nanozyme of the present invention particularly relates to a copper-cobalt-sulfur nanozyme material and its preparation method and antibacterial application. Background technique [0002] Bacterial infection is a serious threat to human health, causing illness and death of millions of people every year, and bacterial resistance associated with biofilms often leads to more serious persistent infectious diseases. The increasingly serious problem of antibiotic resistance forces people to look for new antibacterial strategies. With the development of nanotechnology, it has been found that inorganic nanomaterials have the advantages of no drug resistance, broad-spectrum antibacterial properties, and good stability in antibacterial aspects. The widely studied antibacterial mechanism of inorganic nanomaterials is to affect the function of bacteria by generating reactive oxygen species (ROS) or inducing oxidative stress, thereby destroyi...

Claims

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Application Information

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IPC IPC(8): C01G51/00B82Y40/00B01J27/043A61K33/34A61P31/04A61P17/02A61K33/24
CPCC01G51/006B82Y40/00B01J27/043A61K33/34A61K33/24A61P31/04A61P17/02C01P2004/03C01P2004/04C01P2002/72C01P2002/86C01P2004/64A61K2300/00
Inventor郭倩倩李丹丹高利增
OwnerYANGZHOU UNIV