Fabrication method of enzyme-free glucose sensor and use of enzyme-free glucose sensor fabricated by the same

Patent metadata

Field	Value
Publication number	US-11733199-B2
Application number	US-202117610443-A
Country	US
Kind code	B2
Filing date	Apr 30, 2021
Priority date	Sep 24, 2020
Publication date	Aug 22, 2023
Grant date	Aug 22, 2023

Abstract

The present invention relates to the technical field of glucose detection, and in particular to an enzyme-free glucose sensor and a fabrication method and use thereof. In the present invention, Magnolia grandiflora L. leaves are used as a carbon-based catalyst, which serve as a base material to well disperse nickel atoms and improve the catalytic activity of a material. A prepared Ni@NSiC nano-molecular layer is used to modify a pretreated white glassy carbon electrode (GCE) to obtain a highly-active material-modified working electrode Ni@NSiC/GCE, and then glucose is detected through cyclic voltammetry (CV) and chronoamperometry (CA).

First claim

What is claimed is:

1. A fabrication method of an enzyme-free glucose sensor, comprising the following specific steps:
step (1): subjecting washed and dried Magnolia grandiflora L. leaves to calcination in a high-temperature tube furnace to obtain a biochar;
step (2): soaking the biochar in hydrochloric acid, adding the hydrochloric acid-treated biochar, pyromellitic acid, nickel acetylacetonate, and N,N-dimethylformamide to a mixed solution of ethanol and ultrapure water to obtain a resulting mixture, and stirring the resulting mixture for dispersion to obtain a mixed solution A;
step (3): subjecting the mixed solution A to a reaction in a microwave synthesizer to obtain a mixed solution precursor B, wherein in the step (3), the reaction in the microwave synthesizer is conducted under the following process parameters: a microwave power: 180 W to 200 W, a reaction temperature: 160° C. to 180° C., and a reaction time: 2 h;
step (4): pouring the mixed solution precursor B into a centrifuge tube, then centrifuging and drying the mixed solution precursor B to obtain a product C;
step (5): flowing NH 3 in the high-temperature tube furnace and subjecting the product C to high-temperature calcination at 900° C. for 2 h in the high-temperature tube furnace to obtain a Ni@NSiC nano-electrode composite material; and
step (6): mixing the Ni@NSiC nano-electrode composite material, water, ethanol, and a 5 wt % Nafion solution to prepare a Ni@NSiC solution, pipetting the Ni@NSiC solution with a pipette and adding dropwise onto a pretreated electrode, and air-drying the electrode to obtain a Ni@NSiC/GCE electrode,
wherein in the step (6), in the Ni@NSiC solution, the Ni@NsiC nano-electrode composite material has a concentration of 5 mg/mL, and the water, the ethanol, and the 5 wt % Nafion solution have a volume ratio of 665 μL:335 μL:25 μL; 5 μL of the Ni@NsiC solution is pipetted with the pipette; and the pretreated electrode is prepared by polishing a glassy carbon electrode (GCE) successively with 1.0 μm, 0.3 μm, and 0.05 μm Al 2 O 3 polishing powders; rinsing the GCE with deionized water, and subjecting the GCE to ultrasonic treatment three times with deionized water and then to ultrasonic treatment once with absolute ethanol, wherein each ultrasonic treatment is conducted for no more than 30 s; and finally blow-drying the GCE with nitrogen.

2. The fabrication method of the enzyme-free glucose sensor according to claim 1 , wherein in the step (1), the calcination in the high-temperature tube furnace is conducted under the following process parameters: a N 2 atmosphere; a heating rate: 5° C./min; a calcination temperature: 600° C.; a calcination time: 2 h; and a N 2 flow rate: 0.5 L/min.

3. An use of the enzyme-free glucose sensor fabricated by the fabrication method according to claim 2 in high-sensitivity detection of glucose, wherein the glucose detection uses cyclic voltammetry, chronoamperometry, and a three-electrode system; the three-electrode system is composed of a working electrode, a reference electrode, and a counter electrode; the working electrode is the Ni@NSiC/GCE electrode, the reference electrode is an Ag/AgCl electrode, and a platinum wire is used as the counter electrode; and a 0.1 M NaOH solution is used as an electrolyte,
wherein the enzyme-free glucose sensor is the Ni@NSiC/GCE electrode.

4. The fabrication method of the enzyme-free glucose sensor according to claim 1 , wherein in the step (2), the biochar is soaked in 0.5 M/L hydrochloric acid for 12 h, then filtered out, and dried; in the mixed solution A, the hydrochloric acid-treated biochar, the pyromellitic acid, the nickel acetylacetonate, the N,N-dimethylformamide, the ethanol, and the ultrapure water have a ratio of 0.04 g:0.2542 g:0.2569 g:5 ml:10 ml; and in the mixed solution of ethanol and ultrapure water, a volume ratio of the ethanol to the ultrapure water is 1:1.

5. An use of the enzyme-free glucose sensor fabricated by the fabrication method according to claim 4 in high-sensitivity detection of glucose, wherein the glucose detection uses cyclic voltammetry, chronoamperometry, and a three-electrode system; the three-electrode system is composed of a working electrode, a reference electrode, and a counter electrode; the working electrode is the Ni@NSiC/GCE electrode, the reference electrode is an Ag/AgCl electrode, and a platinum wire is used as the counter electrode; and a 0.1 M NaOH solution is used as an electrolyte,
wherein the enzyme-free glucose sensor is the Ni@NSiC/GCE electrode.

6. The fabrication method of the enzyme-free glucose sensor according to claim 1 , wherein in the step (5), a flow rate of the NH 3 is 0.1 L/min.

7. An use of the enzyme-free glucose sensor fabricated by the fabrication method according to claim 6 in high-sensitivity detection of glucose, wherein the glucose detection uses cyclic voltammetry, chronoamperometry, and a three-electrode system; the three-electrode system is composed of a working electrode, a reference electrode, and a counter electrode; the working electrode is the Ni@NSiC/GCE electrode, the reference electrode is an Ag/AgCl electrode, and a platinum wire is used as the counter electrode; and a 0.1 M NaOH solution is used as an electrolyte,
wherein the enzyme-free glucose sensor is the Ni@NSiC/GCE electrode.

8. An use of the enzyme-free glucose sensor fabricated by the fabrication method according to claim 1 in high-sensitivity detection of glucose, wherein the glucose detection uses cyclic voltammetry, chronoamperometry, and a three-electrode system; the three-electrode system is composed of a working electrode, a reference electrode, and a counter electrode; the working electrode is the Ni@NSiC/GCE electrode, the reference electrode is an Ag/AgCl electrode, and a platinum wire is used as the counter electrode; and a 0.1 M NaOH solution is used as an electrolyte,
wherein the enzyme-free glucose sensor is the Ni@NSiC/GCE electrode.

Assignees

• Univ Jiangsu

Inventors

• Bu Quan
• Cai Jin
• Long Hairong
• Wang Mei
• Mao Hanping

Classifications

• G01N27/3277 Primary

  being a redox reaction, e.g. detection by cyclic voltammetry (voltammetry per se G01N27/42, G01N27/48) · CPC title

• G01N27/308 Primary

  at least partially made of carbon · CPC title

• G01N27/3278 Primary

  involving nanosized elements, e.g. nanogaps or nanoparticles (nanopores G01N33/48721; magnetic beads G01N27/745) · CPC title

• G01N27/4163

  checking the operation of, or calibrating, the measuring apparatus (G01N27/3274, G01N27/4175 and G01N33/0006 take precedence) · CPC title

• B82Y5/00

  Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title