Microelectrode sensor for detecting Staphylococcus aureus and preparation and application methods thereof

Patent metadata

Field	Value
Publication number	US-11835482-B2
Application number	US-202318314552-A
Country	US
Kind code	B2
Filing date	May 9, 2023
Priority date	Nov 11, 2021
Publication date	Dec 5, 2023
Grant date	Dec 5, 2023

Abstract

A microelectrode sensor for detecting Staphylococcus aureus and a preparation method and an application method thereof are provided. The microelectrode sensor is a three-electrode system sensor with a platinum wire electrode as a counter electrode and an Ag/AgCl electrode as a reference electrode, and a working electrode is a silver microelectrode modified by chitosan, catechol and Staphylococcus aureus aptamers. The microelectrode sensor is constructed based on the microelectrode with micro/nano structure on the surface, dual media (Fc-Ru3+), chitosan, and catechol. The working electrode can specifically capture Staphylococcus aureus. During the CV test of the microelectrode sensor, the Cl− in bacteria will be leaked to a surface of the working electrode under the action of local high-field strength, and when Cl− ions exists, the cathodic reduction peak of the working electrode can be specifically enhanced between 0 to −0.1 V, the goal of specific detection of bacteria can be achieved.

First claim

What is claimed is:

1. A microelectrode sensor for detecting Staphylococcus aureus , wherein the microelectrode sensor is a three-electrode system sensor with a platinum wire electrode as a counter electrode and a silver/silver chloride (Ag/AgCl) electrode as a reference electrode;
wherein a working electrode is a silver microelectrode modified by chitosan, catechol and Staphylococcus aureus aptamers; the working electrode takes the silver microelectrode as a matrix, is coated with the chitosan on a surface of the silver microelectrode and grafted with the catechol and the Staphylococcus aureus aptamers onto the chitosan individually; and the surface of the silver microelectrode is distributed with micro and nano scale protrusions and gaps;
wherein the modified silver microelectrode of the microelectrode sensor is modified by:
step (1), constructing a two-electrode system with the silver microelectrode as a working electrode and a platinum wire as an auxiliary electrode to electrochemically deposit the chitosan on a surface of the working electrode to thereby obtain a chitosan-silver (Chi-Ag) electrode;
step (2), taking the Chi-Ag electrode obtained in the step (1) as a working electrode, Ag/AgCl as the reference electrode, and the platinum wire as the counter electrode, and electrochemically grafting the catechol onto a surface of the Chi-Ag electrode to thereby obtain a catechol-chitosan-silver (Cat-Chi-Ag) electrode; and
step (3), soaking the Cat-Chi-Ag electrode in an aptamer solution, modifying the aptamers onto a surface of the Cat-Chi-Ag electrode through a reaction between an aldehyde group on the aptamers and an amino group on the chitosan, thereby forming an aptamer-modified electrode;
wherein the silver microelectrode in the step (1) is a silver microelectrode prepared in one step by using a local electrodeposition method;
wherein the electrochemical deposition in the step (1) is to place the silver microelectrode in a chitosan solution for electrochemical deposition for 200-500 seconds, and then take out the deposited electrode, rinse the deposited electrode with ultrapure water, and dry the rinsed electrode at room temperature;
wherein a pH value of the catechol solution used for grafting the catechol in the step (2) is in a range of 7.0-7.6, with a concentration in a range of 4-5 millimoles per liter (mM); nitrogen gas is injected to the catechol solution before preparation to remove air, and the nitrogen gas is continuously injected during the preparation process;
wherein a linear range of the microelectrode sensor is 1-10 5 colony-forming units per milliliter (CFU/mL), and a detection limit of the microelectrode sensor is 1 CFU/mL.

2. The microelectrode sensor according to claim 1 , wherein the aptamer solution in the step (3) is a solution with the aptamers dissolved in a phosphate-buffered saline (PBS) buffer, with a modification time in a range of 8-24 hours and a temperature in a range of 0-25° C.

3. An application method of the microelectrode sensor for detecting Staphylococcus aureus according to claim 1 , comprising:
(a) acquiring peak currents of specific response signals of the aptamer modified electrode corresponding to standard solutions of Staphylococcus aureus of respective concentrations by cyclic voltammetry test at room temperature, and establishing a standard curve equation according to a relationship between the concentrations of Staphylococcus aureus and the peak currents;
(b) taking or preparing a sample solution to be detected;
(c) detecting a peak current of a characteristic peak of the sample solution to be detected in the step (b) by cyclic voltammetry; and
(d) substituting the peak current obtained in the step (c) into the standard curve equation in the step (a) to calculate a concentration of Staphylococcus aureus in the sample solution to be detected.

4. The application method according to claim 3 , wherein the standard curve equation in the step (a) is obtained by adding the standard solutions of Staphylococcus aureus of respective concentrations to a ferrocene-ruthenium 3+ (Fc-Ru 3+ ) double-electron medium solution of the microelectrode sensor, and the standard curve equation is a two-section equation;
when the concentration C of Staphylococcus aureus is taken as 1≤C≤10 CFU/mL, the standard curve equation is P=0.3115C+0.3024, where R 2 =0.9939, P represents the peak current, in units of microampere (μA), and C represents the concentration of Staphylococcus aureus , in CFU/mL;
when the concentration C of Staphylococcus aureus is taken as 10 1 <C≤10 5 CFU/mL, the standard curve equation is P=0.7318 log[C]+3.4108, where R 2 =0.9927, P represents the peak current, in units of μA, and C represents the concentration of Staphylococcus aureus , in CFU/mL.

5. The application method according to claim 4 , wherein the Fc-Ru 3+ double-electron medium solution comprises 50 micromoles per liter (μM) Fc, 50 μM ruthenium 3+ (Ru 3+ ), and a PBS buffer; before the cyclic voltammetry test, the Fc-Ru 3+ double-electron medium solution after adding the Staphylococcus aureus solution is degassed with nitrogen, and continuously injected nitrogen during the cyclic voltammetry test.

6. An application method of a microelectrode sensor for detecting Staphylococcus aureus , wherein the microelectrode sensor is a three-electrode system sensor with a platinum wire electrode as a counter electrode and a silver/silver chloride (Ag/AgCl) electrode as a reference electrode; a working electrode is a silver microelectrode modified by chitosan, catechol and Staphylococcus aureus aptamers; the working electrode takes the silver microelectrode as a matrix, is coated with the chitosan on a surface of the silver microelectrode and grafted with the catechol and the Staphylococcus aureus aptamers onto the chitosan individually; and the surface of the silver microelectrode is distributed with micro and nano scale protrusions and gaps; and the application method comprises:
(a) acquiring peak currents of specific response signals of an aptamer modified electrode corresponding to standard solutions of Staphylococcus aureus of respective concentrations by cyclic voltammetry test at room temperature, and establishing a standard curve equation according to a relationship between the concentrations of Staphylococcus aureus and the peak currents;
(b) taking or preparing a sample solution to be detected;
(c) detecting a peak current of a characteristic peak of the sample solution to be detected in the step (b) by cyclic voltammetry; and
(d) substituting the peak current obtained in the step (c) into the standard curve equation in the step (a) to calculate a concentration of Staphylococcus aureus in the sample solution to be detected;
wherein the standard curve equation in the step (a) is obtained by adding the standard solutions of Staphylococcus aureus of respective concentrations to a Fc-R u 3+ double-electron medium solution of the microelectrode sensor, and the standard curve equation is a two-section equation;
when the concentration C of Staphylococcus aureus is taken as 1<C<10 CFU/mL, the standard curve equation is P=0.3115C+0.3024, where R 2 =0.9939, P represents the peak current, in units of microampere (μA), and C represents the concentration of Staphylococcus aureus , in CFU/mL;
when the concentration C of Staphylococcus aureus is taken as 10 1 <C<10 5 CFU/mL, the standard curve equation is P=0.7318 log[C]+3.4108, where R 2 =0.9927, P represents the peak current, in units of μA, and C represents the concentration of Staphylococcus aureus , in CFU/mL.

7. A microelectrode sensor for detecting Staphylococcus aureus , wherein the microelectrode sensor is a three-electrode system sensor with a platinum wire electrode a

Assignees

• Univ Central South

Inventors

• Liu Zhengchun
• Lai Qingteng
• Niu Qibin
• Chen Wei
• Zhang Yanke
• Wang Fuliang
• Long Mengqiu
• Liang Bo

Classifications

• G01N27/3278 Primary

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

• G01N27/48

  using polarography, i.e. measuring changes in current under a slowly-varying voltage · CPC title

• G01N27/3275 Primary

  Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction · CPC title

• G01N27/3277

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