Fluorescent antibacterial carbon dot as well as preparation method and application thereof
A carbon dot and fluorescence technology, applied in antibacterial drugs, nano-carbon, pharmaceutical formulations, etc., can solve the problems of cumbersome preparation method of fluorescent antibacterial carbon dots, low antibacterial activity of carbon dots, and easy formation of drug resistance, etc. Bactericidal efficacy, avoidance of drug resistance, high antibacterial activity
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[0042]In the prior art, carbon dots are usually coupled and modified with substances with antibacterial function to achieve bacterial imaging and inhibition, or fluorescent antibacterial carbon dots are prepared through cumbersome preparation methods, but most of the prepared carbon dots have low antibacterial activity. Poor biocompatibility, poor stability, etc. In view of these problems, the present invention creatively proposes a preparation method of fluorescent antibacterial carbon dots, by specially selecting chitosan quaternary ammonium salt or chitosan as a carbon source to heat and prepare carbon dots, which can be synthesized in one step to obtain At the same time, blue luminescent carbon dots for imaging and killing bacteria can be realized, and the preparation method is simple and green. The prepared antibacterial functional carbon dots not only have high antibacterial activity, but also have good water dispersibility, low cost, low cytotoxicity and hemolysis. The ...
Embodiment 1
[0066] (1) Weigh 200 mg of chitosan quaternary ammonium salt and disperse it in 20 mL of ultrapure water, then stir under a magnetic stirrer to obtain a uniformly dispersed transparent solution.
[0067] (2) Transfer the transparent solution obtained in step (1) to a polytetrafluoroethylene reactor, and react in an oven at 200° C. for 4 hours to obtain a carbon dot solution, whose fluorescence spectrum is as follows: figure 2 As shown, the particle size characterization results are shown in image 3 .
[0068] (3) Put the carbon dot solution obtained in step (2) directly into a 500D dialysis bag for 24 hours of dialysis and then dry to obtain solid carbon dots.
Embodiment 2
[0070] (1) Weigh 200 mg of chitosan quaternary ammonium salt and disperse it in 20 mL of ultrapure water, then stir under a magnetic stirrer to obtain a uniformly dispersed transparent solution.
[0071] (2) Transfer the transparent solution obtained in step (1) to a polytetrafluoroethylene reactor, and react in an oven at 200° C. for 6 hours to obtain a carbon dot solution, whose fluorescence spectrum is as follows: figure 2 As shown, the fluorescence intensity is relatively weak compared with Example 1, and its MIC to Staphylococcus aureus is 40 μg / mL.
[0072] (3) Put the carbon dot solution obtained in step (2) directly into a 500D dialysis bag for 24 hours of dialysis and then dry to obtain solid carbon dots.
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