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Colorimetric detection method for antibiotics based on regulation and control of nano-enzyme catalytic activity by nucleic acid aptamer

A technology of nucleic acid aptamer and catalytic activity, which is applied in the field of biosensing, can solve the problems of restricting wide application, and achieve the effect of high catalytic ability, simple preparation process and high stability

Pending Publication Date: 2022-04-12
HUNAN UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, it is still a challenge to obtain nanozymes with high catalytic activity and high substrate selectivity, which greatly limits their wide application.

Method used

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  • Colorimetric detection method for antibiotics based on regulation and control of nano-enzyme catalytic activity by nucleic acid aptamer
  • Colorimetric detection method for antibiotics based on regulation and control of nano-enzyme catalytic activity by nucleic acid aptamer
  • Colorimetric detection method for antibiotics based on regulation and control of nano-enzyme catalytic activity by nucleic acid aptamer

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Embodiment 1

[0043] A method for colorimetric detection of antibiotics based on nucleic acid aptamer-regulated nanozyme catalytic activity of the present invention, comprising the following steps:

[0044] (1) BNQDs / CeO 2 Preparation of nanozymes:

[0045] (1.1) Dissolve and mix cerium nitrate and sodium hydroxide in water respectively, stir for 1 h, the mass ratio of cerium nitrate and sodium hydroxide is 1:10, carry out hydrothermal reaction at 100°C to obtain CeO 2 Nanorod precursors;

[0046] (1.2) CeO to be prepared 2 The nanorod precursor was redispersed in water, and then an aqueous solution of boron nitride quantum dots (BNQDs) with a concentration of 0.1 mg / mL was added, and the boron nitride quantum dots and CeO 2 The mass ratio of the nanorod precursor is 1:20, and the stirring is continued for 2 hours to obtain a mixed solution;

[0047] (1.3) Put the mixed solution obtained in step (1.2) in a reaction kettle, and perform a hydrothermal reaction at 180 ° C to obtain porous ...

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Abstract

The invention discloses a colorimetric detection method for antibiotics based on regulation and control of nano-enzyme catalytic activity by nucleic acid aptamers, and the method comprises the following steps: preparing BNQDs / CeO2 nano-enzyme, functionalizing the BNQDs / CeO2 nano-enzyme by using the nucleic acid aptamers, respectively adding the functionalized BNQDs / CeO2 nano-enzyme into a plurality of sodium acetate-acetic acid buffer solution samples containing antibiotics with different concentrations, incubating, and detecting the antibiotic activity by using the nucleic acid aptamers. Adding H2O2 and a chromogenic substrate 3, 3 ', 5, 5'-tetramethyl benzidine to react, recording the absorbance value A of each sample at the wavelength of 652nm after the reaction to obtain a detection linear relation between the antibiotic concentration and the absorbance value A, and obtaining the antibiotic concentration in the to-be-detected sample according to the detection linear relation and the absorbance value of the to-be-detected sample containing the antibiotic. The colorimetric detection method has the advantages of simplicity and rapidness in operation, low cost, high sensitivity, strong specificity, strong anti-interference capability, wide detection range, low detection limit and the like.

Description

technical field [0001] The invention belongs to the technical field of biosensing and relates to a colorimetric detection method for antibiotics, in particular to a colorimetric detection method for antibiotics based on nucleic acid aptamer-regulated nanozyme catalytic activity. Background technique [0002] Antibiotics are a class of drugs with antibacterial activity, and the increase of antibiotic resistance due to abuse has attracted people's attention. Kanamycin (KAN), as a broad-spectrum antibiotic, is widely used in animal husbandry and aquaculture because of its low cost and strong antibacterial properties, but it has toxicity and serious side effects to humans. The current methods for determining KAN include: high performance liquid chromatography, liquid chromatography-mass spectrometry, or enzyme-linked immunoassay, etc. These methods have problems such as complex equipment, cumbersome operations, high detection costs, and long detection cycles. Therefore, there i...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N21/31G01N21/78
Inventor 汤琳朱旭彭博欧阳细莲冯浩鹏余江芳
Owner HUNAN UNIV
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