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Establishment method of ratio electrochemical sensor of prostate-specific antigen detection and application thereof

A prostate-specific and construction method technology, applied in the direction of material electrochemical variables, scientific instruments, instruments, etc., to achieve high sensitivity, good reproducibility, and easy operation

Active Publication Date: 2019-12-20
JIANGNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] This application aims at the deficiency of a single signal sensor, and the present invention provides a method for constructing a ratiometric electrochemical sensor for prostate-specific antigen detection

Method used

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  • Establishment method of ratio electrochemical sensor of prostate-specific antigen detection and application thereof
  • Establishment method of ratio electrochemical sensor of prostate-specific antigen detection and application thereof
  • Establishment method of ratio electrochemical sensor of prostate-specific antigen detection and application thereof

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] 1. The synthesis of materials, the specific method is as follows:

[0033] (1) Synthesis of Ag@RF NPs: 20 mL of 0.5 mg / mL resorcinol aqueous solution, 0.014 mL of 37% formaldehyde solution and 0.5 mL of 0.005 mol / L AgNO 3 Mix in a three-necked flask, heat to boiling at 90°C under magnetic stirring, then add 0.05mL of 2wt% ammonium hydroxide solution, continue to reflux for 20min, naturally cool to room temperature, centrifugally wash, and dry under vacuum to obtain Ag @RF NPs;

[0034] (2) Synthesis of Ag@RF-Ag NPs: Place the Ag@RF NPs prepared in step (1) in an ammonia environment, put 80 mg of dry Ag@RF NPs on clean filter paper, and place the filter paper on The etching reaction was carried out on a 20mL beaker containing 5mL ammonia water with a volume concentration of 20%. After standing for a certain period of time, the etched nanoparticles were dissolved in 5mL water to obtain Ag@RF-Ag NPs with a concentration of 16mg / mL. solution;

[0035] (3) Preparation of ...

Embodiment 2

[0041] 1. The synthesis of materials, the specific method is as follows:

[0042] (1) Synthesis of Ag@RF NPs: 30 mL of 0.5 mg / mL resorcinol aqueous solution, 0.014 mL of 38% formaldehyde solution and 1 mL of 0.01 mol / L AgNO 3 Mixed in a three-necked flask, heated to boiling at 100°C under magnetic stirring, then added 0.1mL, 2.5wt% ammonium hydroxide solution, continued to reflux for 30min, naturally cooled to room temperature, centrifugally washed, and dried under vacuum to obtain Ag@RF NPs, the particle size analysis of the synthesized nanomaterial Ag@RF NPs, the results are as follows figure 1 as shown ( figure 1 A is the particle size statistics of the Ag core in the synthesized nanomaterial Ag@RF NPs, figure 1 B is the particle size statistics of the synthesized whole nanomaterial Ag@RF NPs). from figure 1 In A, it can be seen that the average particle size of the Ag core is 18.02±4.50nm, and the thickness of the outer polymer RF shell is 44.7±4.0nm (Note: Ag@RF NPs c...

Embodiment 3

[0050] 1. The synthesis of materials, the specific method is as follows:

[0051] (1) Synthesis of Ag@RF NPs: 40 mL of 0.5 mg / mL resorcinol aqueous solution, 0.014 mL of 40% formaldehyde solution and 1.5 mL of 0.015 mol / L AgNO 3 The solution was mixed in a three-necked flask, heated to boiling at 110°C under magnetic stirring, then added 0.15mL, 3wt% ammonium hydroxide solution, continued to reflux for 40min, cooled naturally to room temperature, washed by centrifugation, and dried under vacuum to obtain Ag@RF NPs.

[0052] (2) Synthesis of Ag@RF-Ag NPs: Put the Ag@RF NPs prepared in step (1) in an ammonia atmosphere, put 120 mg of dry Ag@RF NPs on a clean filter paper, and put the filter paper in a container On a 20mL beaker with 15mL ammonia water with a volume concentration of 30%, the etching reaction was carried out, and after standing for a certain period of time, the etched nanoparticles were dissolved in 15mL water to obtain Ag@RF-Ag NPs with a concentration of 8mg / mL...

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Abstract

The invention provides an establishment method of a ratio electrochemical sensor of prostate-specific antigen detection, and belongs to the technical field of electrochemical analysis. The main content of the establishment method comprises providing a synthesis method of nanometer materials Ag@RF-Ag NP and rGO / Fe3O4 / Cu2O. Based on a strong electrochemical oxidation peak of Ag NPs in Ag@RF-Ag NPs,a stable electrochemical oxidation peak of Cu2O NPs in rGO / Fe3O4 / Cu2O Ns and avoidance of mutual interference of peak potentials thereof, a magnetic ratio electrochemical sensor is designed by regarding the electrochemical oxidation peak of Ag NPs in Ag@RF-Ag NPs as a detection signal and regarding the electrochemical oxidation peak of Cu2O NPs in rGO / Fe3O4 / Cu2O Ns as reference signal. According to the method, the operation is simple, the sensitivity is high, and the specificity is high. The ratio electrochemical sensor is applied to detection of PSA.

Description

technical field [0001] The application of the present invention belongs to the technical field of electrochemical analysis, and in particular relates to a construction method of a ratiometric electrochemical sensor for prostate specific antigen detection. Background technique [0002] The specific antigen (PSA) secreted by prostate epithelial cells is a biomarker, which generally exists in human serum. When the content in serum reaches 4ng / mL, there is a risk of cancer. Therefore, early and accurate diagnosis of PSA can increase the chance of successful treatment. So far, several techniques have been used for PSA detection, including surface-enhanced Raman scattering, fluorescence measurement, chromatographic methods, etc., but these experimental methods have the disadvantages of cumbersome operation, instability, and expensive instruments. However, the early diagnosis of cancer plays an important role in the later treatment, so it is urgent to develop a method for detectin...

Claims

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Application Information

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IPC IPC(8): G01N33/53G01N27/48G01N27/327B22F9/24B22F1/00
CPCG01N33/5302G01N27/327G01N27/48B22F9/24B22F1/07B22F1/054
Inventor 赵媛刘瀚施丽霞
Owner JIANGNAN UNIV