Method for preparing carbon quantum dots by using Enteromorpha
A technology for carbon quantum dots and prolifera, which is applied in chemical instruments and methods, nanocarbons, measuring devices, etc., can solve the problems of cumbersome process steps, high equipment requirements, wide particle size range, etc., and achieves simple preparation process operation, fluorescence The effect of excellent properties and low preparation cost
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Embodiment 1
[0025] (1) Weigh 2g of the collected Enteromorpha, rinse it with deionized water, put it into a 150ml polytetrafluoroethylene reactor, and then add 120ml of pH 10.0 borate buffer solution.
[0026] (2) Put the reactor into a vacuum drying oven and react at 180° C. for 6 hours, then take out the reactor and cool to room temperature to obtain a carbon quantum dot solution.
[0027] (3) The carbon quantum dot solution prepared by step (2) is centrifuged at 11900rpm for 20min to remove solid impurities and precipitates, and the supernatant is the prepared carbon quantum dot.
Embodiment 2
[0029] In this embodiment, the carbon quantum dot solution prepared in Example 1 is applied to Fe 3+ For the detection of characteristic ions, add 150μM Ag + ,Al 3+ ,Cd 2+ ,Cu 2+ ,Co 2+ , Fe 2+ , Fe 3+ ,Hg 2+ ,Mg 2+ ,Mn 2+ , Ni 2+ ,Pb 2+ ,Zn 2+ , and measured its fluorescence intensity at an excitation wavelength of 360nm, in which only Fe 3+It has an obvious quenching effect on the fluorescence intensity of carbon quantum dots, and the addition of other different metal ions will not have a significant impact on the fluorescence intensity of carbon quantum dots. In order to explore the added Fe 3+ The linear relationship between concentration and fluorescence intensity, prepare a series of concentration gradient Fe 3+ , 1 μM, 10 μM, 50 μM, 100 μM, 120 μM, 150 μM, 170 μM, 200 μM, 220 μM, 250 μM, 270 μM, 300 μM, 320 μM, 350 μM, 370 μM, 400 μM, 500 μM, 700 μM, 1000 μM, 1200 μM, 1500 μM were added to the same Concentration of carbon quantum dot solution, get a serie...
Embodiment 3
[0031] In this embodiment, the carbon quantum dot solution prepared in Example 1 is applied to cell imaging, and HeLa cells (10 6 cells / sample) placed on a square glass slide with a side length of 35mm, prepare a fresh DMEM solution containing carbon quantum dot solution concentration 1 / 10, and incubate HeLa cells with the prepared DMEM solution at 37°C for 4-24h to obtain incubated cells; At room temperature, all the incubated cells were washed three times with phosphate buffer solution to remove excess unabsorbed carbon quantum dots, the 488nm Ar ion laser was selected to excite the incubated cells, and the incubated cells were collected by a LEICA TCS SP2 laser scanning confocal microscope Obtain images, and further collect cell imaging conditions in a fixed area over time, such as Figure 7 As shown, visible cells imaged very well.
[0032] In this example, the cytotoxicity is tested, and the cells are incubated with DMEM solutions containing different concentrations of c...
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