Calorimetric bionic detection method for detecting pesticide Atrazine residue
A technology of atrazine and detection method, which is applied in the field of biosensors, can solve the problems of lack of specificity, etc., and achieve the effect of simple pretreatment, good consistency and sensitive detection method
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[0021] 1. Preparation of s-MIP
[0022] (1) Dissolve 2.85g of atrazine in 100ml of N, N-dimethylformamide (DMF) acetate buffer mixed solution (DMF: acetate buffer = 9: 1, v / v; acetate buffer, 0.2 mol / L, pH3.8). Make it dissolve completely under the condition of mechanical stirring;
[0023] (2) Add 13.63g p-sodium styrene sulfonate (SSS), 1.46g methylenebisacrylamide (BIS) and 400mg controllable hollow glass beads (CPG) into the mixed solution of step (1) successively, Form an imprinted pre-polymerization system;
[0024] (3) Pre-polymerize the system for 12 hours in a water bath at 38°C with a stirrer rotating at 300 rpm;
[0025] (4) The pre-polymerization system was fed with nitrogen for 30 minutes, and ammonium persulfate (APS) was added to initiate graft imprinting polymerization, and the reaction was carried out for 10 hours;
[0026] (5) The imprinted product is separated from the system by vacuum filtration through a sand core funnel;
[0027] (6) Regenerate the p...
Embodiment 1
[0048] (1) Put the surface imprinted product (prepared according to the method in step 1) into the reactor and place it in a heat regulator, and pass through the carrier liquid (0.02mol L-1, pH3. 8 acetic acid-sodium acetate buffer solution, containing 2% DMF) equilibrium flow system, the flow rate of the system is 800 μl min-1;
[0049] (2) Use carrier liquid as solvent to prepare atrazine solution with gradient concentration of 0-120 μg mL-1.
[0050] (3) The sample solution is added, and the thermal signal changes accompanying the binding and dissociation process of the analyte to the imprinted hole are collected by the Wheatstone bridge, converted and displayed as peak signals on the calorimetric workstation (N2000 chromatography data workstation); a single sample The detection takes about 5 minutes and can be continuously detected without regeneration.
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