Copper nanocluster with various mimic enzyme activities and preparation method and application thereof
A technology of copper nano and clusters, applied in chemical instruments and methods, analyzing materials through chemical reactions, and analyzing materials through observing the influence of chemical indicators, can solve the problems of non-selectivity and achieve The preparation method is simple, the stability is good, and the effect of broad development prospects
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Embodiment 1
[0071] Add cysteine hydrochloride (10mM, 20mL) dropwise to a copper sulfate solution containing copper ions (100mM, 2mL) at room temperature. After stirring for 15 minutes, add hydrazine hydrate (50μL), and continue stirring for 1.5 hours. have to.
Embodiment 2
[0073] Validation of Mimic Peroxidase Activity of Copper Nanoclusters:
[0074] Experimental system a: The catalytic reaction system is composed of acetate buffer solution (pH 4, 100mM), organic chromogen TMB (1mM) and hydrogen peroxide (1mM) after the copper nanoclusters (0.182mM) obtained in the above example. Then react in a water bath at 37° C. for 20 minutes, and measure its visible absorption spectrum in the range of 400-800 nm with a microplate reader.
[0075] In addition, do control experiment b: Include acetate buffer (pH 4, 100mM) and copper nanoclusters (0.182mM) in the catalytic system, and the rest of the reaction conditions are the same as the above-mentioned experimental system, and the absorbance value is measured after 20 minutes . Another control experiment c: no copper nanoclusters were added to the catalytic reaction system, and the absorbance value was detected after reacting for 20 minutes under the same conditions as the above-mentioned experimental sy...
Embodiment 3
[0078] Validation of Mimic Catalase Activity of Copper Nanoclusters:
[0079] Experimental system b: The catalytic reaction system contains phosphate buffer (pH 7.8, 100mM) and H 2 o 2 (5mM), the above copper nanoclusters (1.82mM), reacted at 37°C for 30 minutes, took the supernatant, then added horseradish peroxidase (25μg / mL) and ABTS (0.02mM), at room temperature After reacting for 10 minutes, record its visible absorption spectrum in the range of 380-500 nm with a UV spectrophotometer.
[0080] Another control experiment system a: the catalytic reaction system is composed of phosphate buffer (pH 7.8, 100mM), H 2 o 2 (5mM), take its supernatant, react at 37°C for 30 minutes, then add horseradish peroxidase (25μg / mL) and ABTS (0.02mM), react at room temperature for 10 minutes and record with a UV spectrophotometer Its visible absorption spectrum in the range of 380-500nm.
[0081] Such as image 3 As shown, the absorbance value of the control system b at 417nm is lower...
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