Preparation method of Cu nanometer material and cancer cell detection method
A technology of nano-materials and detection methods, applied in the direction of analysis materials, metal material coating technology, measurement devices, etc., can solve the problems of cardiac pacemaker patients who cannot be used, malignant tumors, leukemia, and expensive CT equipment, etc., to achieve decentralized Good performance, simple preparation and low cost
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Embodiment 1
[0024] The preparation method of embodiment 1Cu nanometer material
[0025] The preparation method of the Cu nanomaterial modified by hyaluronic acid of the present invention comprises the following steps:
[0026] Preparation of rod-like ZnO by direct deposition method;
[0027] Ni is plated on ZnO, and it comprises the following steps: ZnO is sensitized in the solution of tin dichloride and hydrochloric acid, puts into the solution of palladium dichloride and hydrochloric acid to activate again, and the activated ZnO is cleaned with deionized water , and then put ZnO into the electroless plating pool containing nickel sulfate, sodium hypophosphite, ammonium chloride, sodium citrate, succinic acid and lactic acid for electroless plating, and finally filter the nickel-plated ZnO with deionized water After washing and drying, nickel-plated ZnO is obtained.
[0028] Coating nickel-plated ZnO with Cu comprises the following steps: moving the prepared nickel-plated ZnO into deio...
Embodiment 2
[0030] Embodiment 2 cancer cell detection method
[0031] Cancer cell detection method of the present invention comprises the following steps:
[0032] a) Fluorescein labeling, dissolving the Cu nanomaterial in deionized water, adding fluorescein isothiocyanate for labeling, the particle size range of the Cu nanomaterial is 40-60nm, hyaluronic acid in the Cu nanomaterial The loading capacity on the surface is 0.4~0.5mmol / g;
[0033] b) Cultivation of cancer cells, wherein the cancer cells are one of lung cancer cells, liver cancer cells, breast cancer cells or gastric cancer cells. 10 5 Each well was inoculated in a well plate, incubated at 30-37°C, 5% CO2 for 24 hours, washed with alkaline phosphate solution, added copper nanomaterial solution labeled with fluorescein isothiocyanate, incubated for 24 hours, washed with alkali Fully wash with alkaline phosphate solution, add 1ml 4% paraformaldehyde solution to each well and fix for 20min, then wash with alkaline phosphate s...
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