Method for determining microcystic toxins concentration
A technology of microcystin and concentration, which is applied in the direction of measuring devices, instruments, fluorescence/phosphorescence, etc., can solve the problems of low selectivity, high cost, and complicated operation of detection methods, and achieve simple operation, low detection limit, and avoid background The effect of fluorescence interference
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Embodiment 1
[0037] 1) Preparation of molybdenum disulfide quantum dot stock solution with upconversion fluorescence:
[0038] Ammonium molybdate tetrahydrate, N-acetyl-L-cysteine and thiourea were weighed according to the mass ratio of 3.16:1:0.39, and they were added to water and fully mixed under an ice bath to obtain a mixed solution, wherein, For each gram of sodium molybdate tetrahydrate, 64.7 mL of water needs to be added, and then the mixed solution is transferred to a hydrothermal reaction kettle for 4 hours at 200°C, cooled naturally, and then subjected to a centrifuge with a speed of 20,000 r / min. After centrifugation for 10 min, the supernatant was taken to obtain the original solution of molybdenum disulfide quantum dots.
[0039] 2) Draw a standard curve:
[0040] Take the microcystin nucleic acid aptamer solution with a concentration of 2 μM, the gold nanometer solution reduced with sodium borohydride with a concentration of 14.4 nM, the NaCl solution with a concentration...
Embodiment 2
[0048] 1) Preparation of molybdenum disulfide quantum dot stock solution with upconversion fluorescence:
[0049] Ammonium molybdate tetrahydrate, N-acetyl-L-cysteine and thiourea were weighed according to the mass ratio of 3.16:1:0.39, and they were added to water and fully mixed under an ice bath to obtain a mixed solution, wherein, For each gram of sodium molybdate tetrahydrate, 64.7 mL of water needs to be added, and then the mixed solution is transferred to a hydrothermal reaction kettle for 4 hours at 220°C, cooled naturally, and then subjected to a centrifuge with a speed of 20,000 r / min. After centrifugation for 10 min, the supernatant was taken to obtain the original solution of molybdenum disulfide quantum dots.
[0050] 2) Draw a standard curve:
[0051] Take 5 μL of 2 μM microcystin nucleic acid aptamer solution, 100 μL of 14.4 nM sodium borohydride-reduced gold nano-solution and 30 μL of 100 mM KCl solution to obtain a mixed solution, and then add to the above ...
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