Nitrogen-doped carbon quantum dot with high fluorescence quantum yield and preparation method and application of nitrogen-doped carbon quantum dot
A fluorescence quantum yield, carbon quantum dot technology, applied in fluorescence/phosphorescence, chemical instruments and methods, preparations for in vivo experiments, etc. Meet the needs of industrial applications, high fluorescence quantum efficiency, good biocompatibility
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Embodiment 1
[0033] Add 3 g of urea and 1 mL of HOOC-PEG-COOH (Mw 600) into a three-necked flask filled with 25 mL of glycerol or diethylene glycol, and put it in a water bath at 80°C until the urea is completely dissolved. Under the protection of inert gas, heat to 120 °C and keep it for 1 h to remove water, then raise the temperature to 220 °C and keep it for 4 h, then stop heating. The resulting mixture was dialyzed for two days using a dialysis bag with a molecular weight cut-off of 1K, and then the product was concentrated by a rotary evaporator, and the obtained viscous brown liquid, namely fluorescent carbon dots, was freeze-dried. According to transmission electron microscopy analysis, the size of carbon dots is 2-4 nm, and the nitrogen content is 9wt% as measured by elemental analysis. It shows bright blue fluorescence under excitation at 365 nm wavelength.
[0034] Seed 1*10 in each well of 96-well plate 4 HeLa cells were cultured for 24 h. Add different concentrations (6, 12, ...
Embodiment 2
[0037] Add 0.1 g of urea and 0.1 mL of HOOC-PEG-COOH (Mw 600) into a three-necked flask filled with 5 mL of glycerol or diethylene glycol, and bathe in 80°C water until the urea is completely dissolved. Under the protection of inert gas, heat to 120 °C and keep it for 1 h to remove water, then raise the temperature to 200 °C and keep it for 8 h, then stop heating. The resulting mixture was dialyzed for two days using a dialysis bag with a molecular weight cut-off of 1K, and then the product was concentrated by a rotary evaporator, and the obtained viscous brown liquid, namely fluorescent carbon dots, was freeze-dried. According to transmission electron microscopy analysis, the size of carbon dots is 2-4 nm, and the nitrogen content is 6wt% as measured by elemental analysis. It shows bright blue fluorescence under excitation at 365 nm wavelength.
[0038] Seed 1*10 in each well of 96-well plate 4 HeLa cells were cultured for 24 h. Add different concentrations (6, 12, 25, 50, ...
Embodiment 3
[0041] Add 5 g of urea and 1 mL of HOOC-PEG-COOH (Mw 600) into a three-necked flask filled with 25 mL of glycerol or diethylene glycol, and put it in a water bath at 80°C until the urea is completely dissolved. Under the protection of inert gas, heat to 120°C and keep it for 1 hour to remove water, then raise the temperature to 240°C and keep it for 1 hour, then stop heating. The resulting mixture was dialyzed for two days using a dialysis bag with a molecular weight cut-off of 1K, and then the product was concentrated by a rotary evaporator, and the obtained viscous brown liquid, namely fluorescent carbon dots, was freeze-dried. According to transmission electron microscopy analysis, the size of carbon dots is 2-4 nm, and the nitrogen content is 10wt% as measured by elemental analysis. It shows bright blue fluorescence under excitation at 365 nm wavelength.
[0042] Seed 1*10 in each well of 96-well plate 4 HeLa cells were cultured for 24 h. Add different concentrations (6,...
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