Preparation of carbon quantum dots having catalysis performance, and applications of kit based on carbon quantum dots
A catalytic performance and kit technology, applied in the field of chemical applications, can solve problems such as personal and social hazards, and achieve the effects of obvious phenomena, high sensitivity and good stability
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Embodiment 1
[0031]Take 0.5g of polyethyleneimine, 0.1g of cysteine, 10mL of ethylene glycol, and 2mL of distilled water in a 50mL beaker, add 4g of solid phosphoric acid, and heat in an oil bath (180°C) until the solution is light yellow gel , add 2 mL of secondary water; repeat this step 5 times until a brown gel is formed, and cool to room temperature naturally. Then dissolve the gel with 20 mL of secondary water, and adjust the pH of the solution to ≈7 with 10 mol / L NaOH solution. Add another 50mL of absolute ethanol, let it stand for 12h, and the solution is separated. Aspirate the supernatant, remove the insoluble matter in the lower layer, and obtain the ethanol solution of carbon dots. The ethanol solution of carbon dots is subjected to rotary evaporation treatment, and rotated to almost no liquid state to obtain solid carbon dots. Dissolve solid carbon dots with secondary water, and dialyze with a dialysis bag with a molecular weight cut-off of 1000 to obtain a pure carbon dot s...
Embodiment 2
[0033] Chromogenic reaction to breast cancer antigen. Breast cancer antigen standard solution, that is, the sample diluent, is to dilute the pure breast cancer antigen standard product with pH=7.2-7.4 and PBS buffer solution with a concentration of 0.01mol / L into solutions of different concentrations; the carbon dot-labeled breast cancer antibody is After activating the carbon dots with activators EDC and NHS, breast cancer antibodies were added to the activated carbon dot solution, reacted for 1 hour, and dialyzed for 24 hours. First, breast cancer antibody was added to a 96-well polystyrene microwell plate, reacted overnight at 4°C, washed three times with PBS buffer solution, added BSA solution and reacted for 1 hour, washed three times with PBS buffer solution, and then added different concentrations of breast cancer Antigen standard solution (1×10 -12 to 1×10 -14 U / mL) reaction for 1 hour, after washing with PBS buffer solution three times again, add the breast cancer a...
Embodiment 3
[0035] Take 5 serum samples from breast cancer patients, firstly add breast cancer antibody to 5 wells of 96-well polystyrene microwell plate, react overnight at 4°C, wash with PBS buffer solution three times, add BSA solution and react for 1 hour, Wash three times with PBS buffer solution and add dilution 10 10 times human serum samples. Reaction for 1 hour, after washing with PBS buffer solution three times again, add breast cancer antibody that has been connected to carbon dots for reaction for 1 hour, also wash with PBS buffer solution three times, add 100 μL of 4 mM trisodium citrate solution and 100 μL of 320 μmol / L hydrogen peroxide solution was reacted for 40 minutes, and then 100 μL of chloroauric acid solution with a concentration of 2 mmol / L was added. After 30 minutes, its color changes as Figure 4 As shown, when the concentration of breast cancer antigen is 0, the color of gold nanoparticles in the microwell plate is red, and in the microwell plate after addin...
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