Black phosphorus wrapped with polymer as well as preparation method and application thereof
A technology of polymer and black phosphorus, which can be used in medical preparations without active ingredients, medical preparations containing active ingredients, and drug combinations, etc., can solve the problems of inability to protect anti-oxidation and stability of black phosphorus.
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Embodiment 1
[0078]The present embodiment provides a kind of PLGA-wrapped black phosphorus quantum dots and a preparation method thereof, the method comprising the following steps:
[0079] (1) Preparation of black phosphorus quantum dots: Weigh 25 mg of black phosphorus block in a nitrogen-filled glove box, grind it and disperse it into 25 mL of N-methylpyrrolidone and seal it to obtain a 1 mg / mL dispersion ; Sonicate for 3 hours under 1200W probe ultrasonic power, and then immediately ultrasonicate for 10 hours in a water bath with 300W power. The whole ultrasonic process is completed under the condition that the stability is controlled below 277K by ice bath; Centrifuge at a speed of 1 / min for 20 minutes, take the supernatant, and obtain small-sized black phosphorus quantum dots (concentration 1-100 μg / mL) dispersed in N-methylpyrrolidone.
[0080] The black phosphorus quantum dot solution prepared above was dropped on the carbon-coated copper grid with filter paper as the bottom, and a...
Embodiment 2
[0087] The photothermal therapy effect of the PLGA-wrapped black phosphorus quantum dots prepared in Example 1 on tumor cells was tested, and the cell apoptosis was detected by the Calcein-AM / PI live cell / dead cell double staining method. The specific steps are as follows: Digest logarithmically growing breast cancer cells (MCF7) from the culture flask with trypsin (1:250) to make a cell suspension and adjust the cell density to 5×10 4 cells / mL. Add 1 mL of cell suspension to each well of a 12-well plate, and add 5% volume fraction of CO 2 Culture in an incubator at 37°C. When the cell monolayer covered the bottom of the 24-well plate, the PBS solutions of PLGA-wrapped black phosphorus quantum dots with black phosphorus concentrations of 0 ppm, 2 ppm, 5 ppm, 10 ppm and 20 ppm were added respectively, and PBS was used as a blank control. After standing in the incubator for 4 hours, remove the medium containing the drug, carefully add 1mL PBS to each well to wash it two to thr...
Embodiment 3
[0089] Detect the photothermal therapy effect of the black phosphorus quantum dots wrapped in PLGA prepared in Example 1 on tumor cells, and use the CCK-8 method to detect the cell survival rate. The specific steps are as follows: use trypsin (1:250) to grow logarithmically Breast cancer cells (MCF7) were digested from the culture flask to make a cell suspension, and the cell density was adjusted to 5×10 4 cells / mL. Add 1 mL of cell suspension to each well of a 12-well plate, and add 5% volume fraction of CO 2 Culture in an incubator at 37°C. When the cell monolayer covered the bottom of the 24-well plate, the PBS solutions of PLGA-wrapped black phosphorus quantum dots with black phosphorus concentrations of 0 ppm, 2 ppm, 5 ppm, 10 ppm and 20 ppm were added respectively, and PBS was used as a blank control. After standing in the incubator for 4 hours, remove the medium containing the drug, carefully add 1mL PBS to each well to wash it two to three times, absorb the PBS, add ...
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