Electrode loaded with multi-layer glucose oxidase magnetic nanospheres and preparation method of electrode

A technology of glucose oxidase and magnetic nanometers, which is applied in the direction of material analysis, measuring devices, and instruments through electromagnetic means, can solve the problems of uncompensable reaction enzymes, no continuity of reactions, difficult detection and judgment, etc. Long-lasting, enhanced reaction efficiency, and high-strength effects

Inactive Publication Date: 2012-10-24
SUZHOU WENXI MEDICAL ELECTRONICS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Glucose-reactive enzymes are difficult to form a stacked structure on the electrode surface, that is, only a small amount of reaction enzymes exist at a certain reaction point, and they are easily consumed in the glucose decomposition reaction. In the concentration zone, glucose molecules will permeate into this reaction zone, but because the reaction enzyme is not compensable, the point no longer has the reaction enzyme, so the reaction has no continuity
The resulting current is small and lasts for a short time, making it difficult to detect and judge

Method used

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  • Electrode loaded with multi-layer glucose oxidase magnetic nanospheres and preparation method of electrode
  • Electrode loaded with multi-layer glucose oxidase magnetic nanospheres and preparation method of electrode
  • Electrode loaded with multi-layer glucose oxidase magnetic nanospheres and preparation method of electrode

Examples

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example 1

[0036] Fe will be prepared by bubble liquid film method and co-deposition reaction 3 o 4 The ferrite precursor is placed in a container and sintered at 210 degrees centigrade for 10 hours to obtain a consolidated ferrite nanopowder. 1g glucose oxidase, 10ml ethanol, 100ml deionized water, 1.5g SiO 2 Put nanoparticles and 1.5g ferrite nanopowder into a three-neck bottle, reflux and stir for 30 minutes at a temperature of 20 degrees Celsius, so that glucose oxidase is hydrolyzed to form a transparent sol, and the sol is transferred into a PVC mold, and heated at 25 degrees Celsius temperature, in a constant temperature water bath for 2 hours, drying and grinding at a constant temperature of 42.5° C. to prepare nano-microspheres loaded with glucose oxidase. The obtained nano-microspheres and 25% ethanol solution are configured into a mixed solution at a molar ratio of 1:20, and electromagnetically stirred at room temperature until completely dissolved; the dissolved system is t...

Embodiment 2

[0038] Fe will be prepared by bubble liquid film method and co-deposition reaction 3 o 4 The ferrite precursor is placed in a container and sintered at 210 degrees centigrade for 10 hours to obtain a consolidated ferrite nanopowder. 1g glucose oxidase, 10ml ethanol, 100ml deionized water, 2.5g SiO 2 Put nanoparticles and 2.5g of ferrite nanopowder into a three-neck bottle, and stir at 25 degrees Celsius for 20 minutes under reflux to hydrolyze glucose oxidase to form a transparent sol. temperature, in a constant temperature water bath for 2 hours, drying and grinding at a constant temperature of 40° C. to prepare nano-microspheres loaded with glucose oxidase. The obtained nano-microspheres and 25% ethanol solution are configured into a mixed solution at a molar ratio of 1:20, and electromagnetically stirred at room temperature until completely dissolved; the dissolved system is transferred to an ice-water bath, and 5% analytically pure ammonia water is added, Continue to st...

example 3

[0040] Fe will be prepared by bubble liquid film method and co-deposition reaction 3 o 4 The precursor of the ferrite is placed in a container and sintered at 220 degrees centigrade for 12 hours to obtain a consolidated ferrite nanopowder. 1g glucose oxidase, 10ml ethanol, 100ml deionized water, 1.5g SiO 2 Put nanoparticles and 1.5g ferrite nanopowder into a three-neck bottle, reflux and stir for 30 minutes at a temperature of 20 degrees Celsius, so that glucose oxidase is hydrolyzed to form a transparent sol, and the sol is transferred into a PVC mold, and heated at 25 degrees Celsius temperature, in a constant temperature water bath for 2 hours, drying and grinding at a constant temperature of 40° C. to prepare nano-microspheres loaded with glucose oxidase. The obtained nano-microspheres and 25% ethanol solution are configured into a mixed solution at a molar ratio of 1:20, and electromagnetically stirred at room temperature until completely dissolved; the dissolved system...

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Abstract

The invention discloses a preparation method of an electrode loaded with glucose oxidase magnetic nanospheres. The preparation method comprises the following steps of: preparing the nanospheres and 25 percent ethanol solution into mixed solution with molar ratio of 1:20-1:30 and electromagnetically stirring at room temperature until complete dissolution; transferring a dissolution system into an ice water bath; adding a proper amount of 5-10 percent analytically pure ammonia water, continuously stirring for 0.5-1 hour and aging the colloid at normal temperature for 1-2 hours to prepare nanoparticle sol; taking an electrode substrate, coating the prepared nanoparticle sol on the electrode substrate by using a pulling method at the pulling speed of 6-8 cm / min and standing to prepare a coated substrate; preparing the nanoparticles, toluene solution and water into mixed solution according to a certain molar ratio; vertically soaking the prepared coated substrate in a reactor with mixed solution; applying a horizontal magnetic field to the reactor; and reacting under the magnetic field condition of 5,000-10,000 gausses for 0.5-1 hour to prepare the electrode loaded with the multi-layer nanospheres with enzyme.

Description

technical field [0001] The invention relates to a method for preparing an electrode, in particular to a method for preparing an electrode loaded with multilayer glucose oxidase magnetic nano microspheres. Background technique [0002] Such as Figure 4 Shown: It reflects the basic process of converting the blood sugar detection process from a chemical reaction to an electrical signal. Under the catalysis of chemical decomposition reaction, charged particles (such as hydroxide ions, hydrogen ions and electrons) are released. The charged particles are transmitted to the electrical signal detection system through the electrodes and the wires connected to the electrodes. According to the generated current The size judges the intensity of the reaction, and the greater the intensity of the reaction, the more severe the reaction and the higher the glucose content; and vice versa. [0003] In the prior art, the enzyme layer mainly uses the method of directly coating the reaction so...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N27/327
Inventor 张勐鲍文生肖红梅
Owner SUZHOU WENXI MEDICAL ELECTRONICS
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