SPR sensor for detecting microcystic toxin based on nucleic acid aptamer signal amplification strategy and preparation method and application thereof
A technology of microcystin and nucleic acid aptamer, which is applied in the direction of instruments, measuring devices, scientific instruments, etc., can solve the problems of restricting the dynamics of microcystin pollution in a timely manner, restricting large-scale promotion and use, and expensive probes, etc. , to achieve the effects of easy construction of portable detection instruments for field monitoring, real-time analysis, and simple preparation methods
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Embodiment 1
[0031] A preparation method of an SPR sensor for detecting microcystins based on a nucleic acid aptamer signal amplification strategy. The specific steps of the preparation method are as follows:
[0032] (1) Preparation of glass chips: Clean the glass slides with a mixed solution of ammonia water: hydrogen peroxide: ultrapure water with a volume ratio of 1:1:1 for 1 hour, and then place them in ammonia with a volume fraction of 10% under anhydrous conditions. Propyltrimethoxysilane in ethanol solution for 10min, then wash with ultrapure water to make the surface positively charged amino groups, and finally immerse in citric acid stabilized gold nano solution for 2h to deposit gold nanoparticles on the treated surface through electrostatic force On the glass slide, a glass chip was obtained;
[0033] (2) DNA probe 1 modification of the glass chip: immerse the glass chip obtained in step (1) in a solution containing 0.03 μM DNA probe 1 for 1 h, so that the DNA probe 1 can be bo...
Embodiment 2
[0040] The method for detecting the content of microcystin in water by an SPR sensor for detecting microcystin based on a nucleic acid aptamer signal amplification strategy comprises the following steps:
[0041] (1) Carry out the preparation of sensor according to the method step of preparing SPR sensor in embodiment 1;
[0042] (2) The sensor in step (1) was immersed in the PBS buffer solution containing 0 μ M, 10 μ M, and 100 μ M microcystin respectively, and then the SPR signal change was measured, and the results were as follows: image 3 It can be seen from the figure that although the sensor contains different concentrations of microcystins before being washed with water, the response values of the three groups increase at the same time because the injected DNA probe 2 modified noble metal nanoparticles stays on the surface. , but after washing with water, as the content of microcystin increases, the number of noble metal nanoparticles modified by DNA probe 2 bound to...
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