Preparation method for fluorescent nano-cluster based on rare-earth metal cerium and application of fluorescent nano-cluster
A fluorescent nanocluster, rare earth metal technology, applied in the fields of nanotechnology, nanotechnology, nanotechnology for materials and surface science, can solve the problems of expensive sensitivity, not high enough, and complicated process for ordinary patients, and achieve good biological phase. Capacitance, broad application prospects, and the effect of high fluorescence properties
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Embodiment 1
[0026] The first step is to prepare a certain concentration of reduced glutathione aqueous solution, gold reagent and cerium reagent aqueous solution;
[0027] In the second step, mix 1.5 to 10 mmol / L reduced glutathione aqueous solution and 0.5 to 5 mmol / L gold reagent evenly, and shake fully until the color of the solution becomes colorless;
[0028] The third step is to put the mixed solution in a water bath and heat it for a period of time, then add 0.025 to 5 mmol / L cerium reagent to the gold reagent mixed solution, continue to react for a period of time, then take it out from the water bath, cool to obtain fluorescence Excellent gold-cerium nanocomposite material; the heating time is 0.5 to 4 hours, the heating temperature is 37 to 90°C, and the ratio of glutathione to gold reagent and cerium reagent can be adjusted to obtain nanomaterials with different fluorescence yields.
Embodiment 2
[0030] 1) Prepare a certain concentration of gold reagent and cerium reagent aqueous solution;
[0031] 2) Mix 0.0001 to 1 mmol / L cerium reagent with 0.0001 to 1 mmol / L gold reagent evenly;
[0032] 3) Liver cancer cells (HepG2) were selected as the research object, and the experimental group divided the liver cancer cells (HepG2) in the logarithmic growth phase at a ratio of 1.6×10 5 The density of cells / well was inoculated in 6-well plates, and after 8 hours of culture, sterilized and diluted with fresh sterile DMEM medium was added containing gold-cerium mixed solution with a concentration of 0.0001 to 1 mmol / L and logarithmic HepG2 cells in the growth phase were co-incubated for 4-48 hours (37 °C, 5 % CO2, RH 95%); in the control group, the liver cancer cells (HepG2) in the culture 5 Cells / well were seeded in 6-well plates and cultured under the same conditions as the experimental group. Add phosphate buffer solution (PBS, pH=7.2) to each well of the experimental group a...
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