Method for detecting oxytetracycline (OTC) in food by virtue of functional magnetic bead isolation-enzyme linked aptamer
An enzyme-linked aptamer and magnetic bead separation technology, which is applied in the direction of color/spectral characteristic measurement, etc., can solve the problem that the electrochemical signal of the sample matrix is easy to cause interference, cannot meet the needs of oxytetracycline detection, and the aptamer immobilization step consumes a lot of time. Time and other issues, to achieve the effect of reducing detection cost, improving specificity, and low detection cost
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Embodiment 1
[0041] Embodiment 1: Determination of milk samples
[0042] 1. Preparation of nucleic acid aptamer-magnetic nanoparticle complex probe
[0043] The nucleic acid aptamer-magnetic nanoparticle complex probes were prepared using the methods reported in the literature (Wu SJ, Duan N, Wang ZP, et al. Analyst, 2011, 136, 2306-2314).
[0044] 1. Preparation of aminated nano-magnetic beads: Add 6.5 g of 1,6-hexanediamine, 2.0 g of anhydrous sodium acetate (CH 3 COONa) and 1.0 g ferric chloride hexahydrate (FeCl 3 ·6H 2 O), stirred at 50°C to obtain a colloidal solution, and transferred the solution to a 50mL reactor lined with polytetrafluoroethylene, and reacted at 198°C for 6h. Cool to room temperature, discard the upper liquid, wash out the lower solid material with deionized water, and collect it by magnetic separation. Wash twice with deionized water and ethanol respectively, and dry at 50°C for 5-10h. Scanning electron microscope images of aminated nano-magnetic beads ref...
Embodiment 2
[0056] Embodiment 2: Determination of animal tissue samples
[0057] Method is the same as embodiment one, difference is the pretreatment method of sample:
[0058] Weigh 1.0 g of chicken sample into a 50 mL centrifuge tube, add 4 mL of extraction solution, vortex mix for 10 min, and centrifuge at 15000 r / min for 10 min. Take 200uL of the supernatant and dilute to 1 mL with 10mmol / L PBS buffer for analysis. Substitute into the standard curve to calculate the content of oxytetracycline in the sample.
Embodiment 3
[0059] Embodiment 3: honey sample determination
[0060] Method is the same as embodiment one, difference is the pretreatment method of sample:
[0061] Accurately weigh 1.0g of honey sample into a 50mL screw cap centrifuge tube, add 10mL of PBS buffer (10 mmol / L, pH 7.4), vortex for 5min, sonicate for 5min, and take 100μL of the supernatant for analysis. Calculate the content of the analyte in the sample according to the standard curve.
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