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

Active Publication Date: 2015-05-20
XINJIANG ACADEMY OF AGRI & RECLAMATION SCI
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Problems solved by technology

For example, Liu Bin (Jinan University master's thesis) established an aptamer-based biotin-avidin enzyme-linked detection method for oxytetracycline, but the detection limit (1.5g/L) could not meet the needs of oxytetracycline detection ( Limit value: 100mg/kg)
Kim et al. (Anal. Chim. Acta, 2009, 634: 250-254) established an analytical method for the detection of oxytetracycline with an aptamer electrochemical sensor, but the aptamer immobilization step is relatively time-consuming, and the sample matrix has a great influence on the electrolyt...

Method used

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  • Method for detecting oxytetracycline (OTC) in food by virtue of functional magnetic bead isolation-enzyme linked aptamer
  • Method for detecting oxytetracycline (OTC) in food by virtue of functional magnetic bead isolation-enzyme linked aptamer
  • Method for detecting oxytetracycline (OTC) in food by virtue of functional magnetic bead isolation-enzyme linked aptamer

Examples

Experimental program
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Effect test

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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Abstract

The invention discloses a method for detecting oxytetracycline (OTC) in food by virtue of a functional magnetic bead separation-enzyme linked aptamer. The method is characterized by comprising the following steps: with a nucleic acid aptamer-magnetic nanoparticle composite probe, binding an OTC aptamer on the surface of a magnetic bead through direct competition between HRP-OTC and OTC in a sample, and detecting the change of a light absorption value through substrate chromogenic assay so as to quantitatively analyze the content of OTC in a sample. Compared with conventional enzyme-linked immuno sorbent assay (ELISA) and enzyme linked aptamer (ELAA), the method disclosed by the invention achieves the full combination of the rapid separation and enrichment effects of magnetic nano material, the high specificity of a nucleic acid aptamer and the high-throughput screening characteristic of an ELISA plate, so as to greatly shorten detection time, improve detection sensitivity and specificity and reduce detection cost.

Description

technical field [0001] The invention relates to a detection method for oxytetracycline in food, and belongs to the technical field of food safety analysis. Background technique [0002] Oxytetracycline (OTC), also known as 5-hydroxytetracycline, oxytetracycline, oxytetracycline, oxytetracycline, etc., is a broad-spectrum antibacterial drug, often used as a preventive agent for cattle, pigs, poultry, fish and other animal diseases and treatment of infections. However, due to abuse and non-compliance with the withdrawal period regulations, its residues in animal products not only bring serious harm to human health, but also pose a serious threat to the environment. The Food and Agriculture Organization of the World, the World Health Organization, the European Union and our government have made regulations on the residue limits of oxytetracycline in food. [0003] At present, the detection methods of oxytetracycline mainly include high performance liquid chromatography (HPLC)...

Claims

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Application Information

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IPC IPC(8): G01N21/33
Inventor 卢春霞唐宗贵刘长彬孙凤霞康立超陈霞王国红
Owner XINJIANG ACADEMY OF AGRI & RECLAMATION SCI
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