Fluorescent carbon quantum dot having peroxidase catalytic activity and preparation method of same
A technology of peroxidase and carbon quantum dots, applied in the field of nanomaterials, can solve problems such as lack of catalytic activity, and achieve the effects of high reproducibility, easy procurement, and simple preparation methods
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Embodiment 1
[0026] 1) At room temperature, take 1g of pig blood and put it into a mortar to grind it into a paste, add it to a 50mL small beaker, add 10mL of deionized water, mix well, put it into an ultrasonic instrument and continue to sonicate for 20 minutes to make it well mixed.
[0027] 2) Take out the above suspension and add it into a 20mL autoclave, and heat it in a constant temperature drying oven. The reaction temperature was set at 180° C. for 8 hours. After the reaction was completed, it was naturally cooled to room temperature.
[0028] 3) Pour the above reaction solution into a syringe equipped with a 0.22 μm filter membrane and filter to remove the residue. Then the obtained filtrate was put into a centrifuge tube, and centrifuged at a speed of 8000 rpm for 10 minutes to remove insoluble matter.
[0029] 4) The supernatant was then rotary-evaporated to increase the concentration of the carbon quantum dot solution, and then freeze-dried for 24 hours to obtain a fluorescen...
Embodiment 2
[0037] 1) At room temperature, take 1g of sheep blood and put it into a mortar to grind it into a paste, add it to a 50mL small beaker, add 10mL of deionized water, mix well, put it into an ultrasonic instrument and continue to sonicate for 20 minutes to make it well mixed.
[0038] 2) Take out the above suspension and add it into a 20mL autoclave, and heat it in a constant temperature drying oven. The reaction temperature was set at 200° C. for 6 hours. After the reaction was completed, it was naturally cooled to room temperature.
[0039] 3) Pour the above reaction solution into a syringe equipped with a 0.22 μm filter membrane and filter to remove the residue. Then the obtained filtrate was put into a centrifuge tube, and centrifuged at a speed of 8000 rpm for 10 minutes to remove insoluble matter.
[0040] 4) The supernatant was then rotary-evaporated to increase the concentration of the carbon quantum dot solution, and then freeze-dried for 24 hours to obtain a fluoresc...
Embodiment 3
[0043] 1) At room temperature, take 1g of chicken blood and put it into a mortar to grind it into a paste, add it to a 50mL small beaker, add 10mL of distilled water, mix well, put it into an ultrasonic instrument and continue to sonicate for 20 minutes to make it evenly mixed .
[0044] 2) Take out the above suspension and add it into a 20mL autoclave, and heat it in a constant temperature drying oven. The reaction temperature was set at 160° C. for 10 hours. After the reaction was completed, it was naturally cooled to room temperature.
[0045] 3) Pour the above reaction solution into a syringe equipped with a 0.22 μm filter membrane and filter to remove the residue. Then the obtained filtrate was put into a centrifuge tube, and centrifuged at a speed of 8000 rpm for 10 minutes to remove insoluble matter.
[0046] 4) The supernatant was then rotary-evaporated to increase the concentration of the carbon quantum dot solution, and then freeze-dried for 24 hours to obtain a fl...
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