Parathion-methyl electrochemical biosensor based on sulfonic functionalized grapheme-chitosan
A methyl parathion electric and biosensor technology, applied in the field of ultra-sensitivity and easy operability, can solve the problems of expensive, high cost, bulky and bulky instruments, and achieve the advantages of improving accuracy and sensitivity, preventing interference, and improving response current. Effect
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Embodiment 1
[0016] The prepared electrochemical enzyme sensor was placed in the methyl parathion standard solution for reaction, and the concentration of the standard solution was as follows: 0ng / mL, 0.01ng / mL, 0.05ng / mL, 0.1ng / mL, 0.5ng / mL mL, 1ng / mL, 5ng / mL, 10ng / mL, 50ng / mL, 100ng / mL, the working voltage is 0.2V~1.0V, the scan rate is 100mV / s, and the working buffer system is NaH 2 PO 4 -Na 2 HPO 4 (pH=7.0), each concentration was inhibited for 16 min respectively; after the electrode was taken out, the surface of the electrode was cleaned with ultrapure water to remove residual pesticides, and then the electrode was placed in a reaction pool with a concentration of 5 mM acetylcholine chloride to react for 2 min. Formula A%=(I 0 -I p ) / I 0 ×100% (A% represents enzyme inhibition rate, 1 0 and I p Represent not being inhibited by pesticides and the peak current value of the reaction after being inhibited by pesticides) Calculate the inhibition rate of immobilized enzyme, and estab...
Embodiment 2
[0018] Tear off the cabbage leaves and spread out, spray the pesticide evenly on the leaves, then chop and mix well. Weigh 10.00g of the mixed sample, place it in a 250mL Erlenmeyer flask with stopper, add 30g of anhydrous sodium sulfate for dehydration, and shake vigorously; then add 0.25g of activated carbon for decolorization; then add 70mL of dichloromethane, and shake Shake for 30 min, and filter the mixture with filter paper. Measure 35mL of the filtrate, volatilize naturally in a fume hood at room temperature until nearly dry, grind and wash the residue 3 times with a small amount of dichloromethane, transfer to a 5mL graduated centrifuge tube, and dilute to 2.0mL for later use. The selected working voltage is 0.2V~1.0V, the scanning speed is 100mV / s, and the working buffer system is NaH 2 PO 4 -Na 2 HPO 4 (pH=7.0), the prepared enzyme electrode was placed in the extract solution for 16min, after taking out the electrode, the surface of the electrode was cleaned wit...
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