Electrochemical sensor for simultaneously detecting PAT and OTA, preparation method and detection method
A sensor and electrochemical technology, applied in the field of rapid detection of food safety, to achieve the effect of low detection concentration, low cost and simple operation
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[0044] The preparation method of the working electrode of the electrochemical sensor that simultaneously detects PAT and ochratoxin A of the present invention comprises the following steps:
[0045] Step 1, use alumina slurry to polish the working electrode, then ultrasonically clean it several times with a mixture of ethanol and ultrapure water, and finally ultrasonically clean it several times with ultrapure water;
[0046] Step 2, drop-coating the AuNPs-BP nanocomposite prepared by the present invention on the treated working electrode, and drying at room temperature to obtain the AuNPs-BP / GCE electrode;
[0047] Step 3, apply the first mixed solution onto the surface of the AuNPs-BP / GCE electrode, incubate at room temperature for 2-14 hours, then rinse with Tris-HCl, and then coat the surface with 6-mercapto-1-hexanol at room temperature The reaction time is 0.2~2h, which is used to seal the uncovered active sites on the surface of AuNPs-BP / GCE and prevent other electroact...
Embodiment 1
[0056] Preparation of working electrodes for electrochemical sensors that simultaneously detect PAT and OTA:
[0057] Step 1, use alumina slurry to polish the glassy carbon electrode, then use the mixture of ethanol and ultrapure water to ultrasonically clean it several times, and finally use ultrapure water to ultrasonically clean it several times;
[0058] Step 2, centrifugally concentrate the commercially available BP dispersion (0.2 mg / mL) to 2.0 mg / mL, and put it in the refrigerator (temperature 4°C) for later use;
[0059] 350 μL of 10 mM chloroauric acid (HAuCl 4 ) was added to 24.65mL ultrapure water to obtain a uniform mixed solution; the mixed solution was heated on a heating plate to nearly 150°C; then 2.5mL of sodium citrate with a concentration of 10mM was added and reacted for about 25 minutes to obtain a nano-gold solution;
[0060] 2.0 mg / mL BP dispersion and 0.13 mM nano-gold solution were mixed at a volume ratio of 3:1, and reacted for 1 h to obtain AuNPs-BP...
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