Preparation method of graphene quantum dots for Hg<2+> detection and tumor diagnosis
A graphene quantum dot and tumor diagnosis technology, applied in the chemical industry, can solve the problems of inconvenient detection of trace Hg2+, unsatisfactory requirements, large number of samples, etc., and achieve the effects of small background interference, good fat solubility, and simple preparation method
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Embodiment 1
[0023] Weigh 2g of citric acid and 0.005g of folic acid into a beaker, add 10mL of twice distilled water and stir until dissolved, heat, stir, and evaporate the water to dryness, and react at 200°C for 3 hours, and prepare the pH of the graphene quantum dots with sodium hydroxide solution For 6, the cultured normal cells and tumor cells were incubated in a solution containing 25ug / mL functionalized graphene quantum dots for 24 hours at a constant temperature of 37°C, and observed under a laser confocal microscope to achieve specific recognition of tumor cells.
Embodiment 2
[0025] Weigh 2g of citric acid and 0.01g of dihydrofolic acid into a beaker, add 10mL of twice distilled water and stir until dissolved, heat, stir, and evaporate the water to dryness, and react at 120°C for 2h, and use sodium hydroxide solution to dissolve the graphene quantum dots Prepare a pH of 6, and incubate the cultured normal cells and tumor cells in a functionalized graphene quantum dot solution containing 25ug / mL at a constant temperature of 37°C for 24 hours, and observe under a laser confocal microscope to achieve specific tumor recognition cell.
Embodiment 3
[0027] Weigh 2g of maleic acid and 0.03g of folic acid in a beaker, add 10mL of twice distilled water and stir until dissolved, heat, stir, and evaporate the water to dryness, and react at 150°C for 4h, and use sodium hydroxide solution to dissolve the graphene quantum The dot preparation pH is 6, and the cultured normal cells and tumor cells are incubated in the functionalized graphene quantum dot solution containing 25ug / mL at a constant temperature of 37°C for 24h, and observed under a laser confocal microscope to achieve specific recognition tumor cells.
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