Black phosphorus wrapped with cell protein and preparation method of black phosphorus
A cell protein and black phosphorus technology, applied in the field of biomedical engineering, can solve the problems of affecting the performance of black phosphorus, reducing the bioactive degradability of black phosphorus nanosheets, etc., and achieve the effects of low cost, prevention of black phosphorus oxidation, and simple preparation process
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Embodiment 1
[0022] Take 30 mg blocky black phosphorus crystals (made in the laboratory) and grind them into black phosphorus powder in an agate mortar dropwise added with N,N-dimethylformamide (DMF), then put the above powder in 20ml DMF, Ultrasonic cell disruptor probe was used to sonicate in an ice bath for 10 h to obtain black phosphorus nanosheet dispersion.
[0023] Centrifuge the dispersion at a speed of 4000 rpm for 15 min to remove oversized products, then centrifuge the supernatant at a speed of 13000 rpm for 20 min, and wash the obtained precipitate with isopropanol and deoxygenated water for 2-3 times. Freeze-dried samples were obtained to obtain black phosphorus nanosheets; the supernatant was centrifuged at a speed of 50,000 rpm for 4 hours to obtain precipitates as black phosphorus quantum dots. Exosomes were extracted by gradient centrifugation.
[0024] Culture human osteosarcoma cells MG63 to 80% with DMEM complete medium, remove the cell supernatant, add 10ml Tris-HCl b...
Embodiment 2
[0027]Take 40 mg blocky black phosphorus crystals (made in the laboratory) and grind them into black phosphorus powder in an agate mortar dropwise added with N,N-dimethylformamide (DMF), then put the above powder in 20ml DMF, Ultrasonic cell disruptor probe was used to sonicate in an ice bath for 10 h to obtain black phosphorus nanosheet dispersion. Centrifuge the dispersion at a speed of 4000 rpm for 15 min to remove oversized products, then centrifuge the supernatant at a speed of 13000 rpm for 20 min, and wash the obtained precipitate with isopropanol and deoxygenated water for 2-3 times , freeze-dry the sample to obtain black phosphorus nanosheets; then centrifuge the supernatant at a speed of 50,000 rpm for 4 hours to obtain precipitates as black phosphorus quantum dots. Exosomes were extracted by gradient centrifugation. Culture mouse embryonic osteoblast precursor cells MC3T3-E1 with DMEM complete medium to 80%, remove the cell supernatant, add 10ml Tris-HCl buffer sol...
Embodiment 3
[0029] Take 40 mg blocky black phosphorus crystals (made in the laboratory) and grind them into black phosphorus powder in an agate mortar dropwise added with N,N-dimethylformamide (DMF), then put the above powder in 20ml DMF, Ultrasonic cell disruptor probe was used to sonicate in an ice bath for 10 h to obtain black phosphorus nanosheet dispersion. Centrifuge the dispersion at a speed of 4000 rpm for 15 min to remove oversized products, then centrifuge the supernatant at a speed of 13000 rpm for 20 min, and wash the obtained precipitate with isopropanol and deoxygenated water for 2-3 times , freeze-dry the sample to obtain black phosphorus nanosheets; then centrifuge the supernatant at a speed of 50,000 rpm for 4 hours to obtain precipitates as black phosphorus quantum dots. Exosomes were extracted by gradient centrifugation. Cultivate human cervical cancer cells HeLa to 80% with DMEM complete medium, remove the cell supernatant, add 10ml of Tris-HCl buffer solution with a ...
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