Nano composite fluorescent probe for visibly detecting quercetin and preparation method thereof
A nanocomposite, fluorescent probe technology for applications in nanotechnology, nanooptics, chemical instruments and methods for materials and surface science
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Embodiment 1
[0022] The present invention relates to a nanocomposite fluorescent probe for the visual detection of quercetin and its preparation method. The preparation process and principle are as follows: figure 1 As shown, the specific preparation steps are as follows:
[0023] Weigh 1g of sodium citrate and 2g of ammonium carbonate, dissolve them in 30mL of twice-distilled water under magnetic stirring, transfer the mixed solution into a 50mL autoclave with a polytetrafluoroethylene liner, stir at room temperature for 30min, and heat up to 120 ℃ after the reaction for 12h. Cool the product solution to obtain a dark brown suspension, filter through a 0.22 μm filter membrane and collect the filtrate, remove most of the solvent by rotary evaporation, centrifuge the residual filtrate, wash the precipitate with ethanol, and dry the purified carbon dots in vacuum at 60°C Prepare carbon dot powder. Disperse the carbon dot powder in phosphate saline buffer solution, add rhodamine 6G aqueous ...
Embodiment 2
[0025] Weigh 1g of sodium citrate and 4g of ammonium carbonate, dissolve them in 30mL of twice distilled water under magnetic stirring, transfer the mixed solution into a 50mL autoclave with a polytetrafluoroethylene liner, stir at room temperature for 30min, and heat up to 150 ℃ after the reaction for 10h. Cool the product solution to obtain a dark brown suspension, filter through a 0.22 μm filter membrane and collect the filtrate, remove most of the solvent by rotary evaporation, centrifuge the remaining filtrate, wash the precipitate with ethanol, and dry the purified carbon dots in vacuum at 60°C Prepare carbon dot powder. Disperse the carbon dot powder in phosphate saline buffer solution, add rhodamine 6G aqueous solution dropwise under ultrasonic and magnetic stirring, in which the mass concentration of carbon dots is 4mg mL -1, the rhodamine 6G molar concentration was 20 μM, the phosphate concentration was 20 mM, the pH of the buffer solution was 7.4, and the ultrasoni...
Embodiment 3
[0027] Weigh 1g of sodium citrate and 5g of ammonium carbonate, dissolve them in 30mL of double-distilled water under magnetic stirring, transfer the mixed solution into a 50mL autoclave with a polytetrafluoroethylene liner, stir at room temperature for 30min, and heat up to 180 After reaction at ℃ for 8h. Cool the product solution to obtain a dark brown suspension, filter through a 0.22 μm filter membrane and collect the filtrate, remove most of the solvent by rotary evaporation, centrifuge the residual filtrate, wash the precipitate with ethanol, and dry the purified carbon dots in vacuum at 60°C Prepare carbon dot powder. Disperse the carbon dots powder in phosphate saline buffer, add rhodamine 6G aqueous solution dropwise under ultrasonic and magnetic stirring, in which the mass concentration of carbon dots is 5mg mL -1 , the rhodamine 6G molar concentration was 50 μM, the phosphate concentration was 30 mM, the pH of the buffer solution was 8.0, and the mixture was kept u...
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