Lipid droplet targeting carbon dot and preparation method and application thereof
A technology of carbon dots and lipid droplets, applied in the field of fluorescent nanomaterials manufacturing, can solve problems such as limiting the in-depth research of carbon dots
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Embodiment 1
[0048] A method for preparing carbon dots, comprising the following steps:
[0049] First weigh 50 mg of 4-(1-piperidinyl)aniline and dissolve it in 5 mL of absolute ethanol, then transfer the solution to a polytetrafluoroethylene-lined autoclave, and place the autoclave in an oven In a dry box, heated to 160 °C for 12 h. After the reaction was completed, the reactor was cooled to room temperature to obtain a brownish-red solution, and then the crude product was purified by silica gel column chromatography, using different proportions of petroleum ether and ethyl acetate as eluents, rotary evaporation and further drying, Purified fluorescent carbon dots were obtained.
Embodiment 2
[0055] Fluorescence intensity changes of carbon dots in different solvents
[0056] Add 2 mL of different solvents to the cuvette, add 4 μL of carbon dot stock solution, and measure the fluorescence spectrum. The experimental results show that: if figure 1 As shown, the fluorescence of carbon dots in aqueous solution is very weak and negligible, which has the potential for wash-free cell imaging.
Embodiment 3
[0058] Fluorescence intensity changes in 1,4-dioxane solutions with different water contents (0-100%)
[0059] Add 2 mL of 1,4-dioxane solution with different water content (0-100%) to the cuvette, add 4 μL of carbon dot stock solution, and measure the fluorescence spectrum. The experimental results show that: if figure 2 As shown, the fluorescence of carbon dots in pure 1,4-dioxane solution is very strong, which is conducive to the targeting of carbon dots to lipid droplets. Moreover, the fluorescence of carbon dots in aqueous solution is very weak and can be ignored, which has the potential of no-wash lipid droplet imaging.
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