Preparation method of layered double hydroxide nanosheet-copper sulfide quantum dot heterogeneous nano composite
A nanocomposite, hydroxide technology, applied in the field of medical materials, can solve the problem of no anti-cancer effect, and achieve the effect of improving production efficiency and utilization rate
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Embodiment 1
[0036] (1) 16.0mmol sodium hydroxide was dissolved in 37.5mL deionized water to obtain sodium hydroxide solution;
[0037] (2) 1.7mmol aluminum nitrate and 5.1mmol magnesium nitrate were dissolved in 12.5mL deionized water to obtain a metal salt solution;
[0038] (3) Under a nitrogen atmosphere, slowly drop sodium hydroxide solution into the metal salt solution, stir vigorously at room temperature for 1 hour, then centrifuge at 12,000 rpm for 15 minutes, wash with water three times, and collect the layered double hydroxide Nanosheet crude product;
[0039] (4) The crude product of layered double hydroxide nanosheets was dispersed in 40 mL of deionized water, placed in a hydrothermal reaction kettle, and placed in an oven at 120° C. for 8 hours to obtain layered double hydroxide nanosheets.
[0040] (5) 7.25 mg of the prepared layered double hydroxide nanosheets, 6.8 mg of copper chloride, and 27 mg of polyvinylpyrrolidone were dissolved in 9 mL of deionized water to obtain a...
Embodiment 2
[0044] Take 2 mg of the layered double hydroxide-copper sulfide quantum dot nanocomposite prepared in Example 1, disperse it in 2 mL of water and place it in a cuvette. cm 2 The 808nm near-infrared laser irradiates the solution, and the temperature of the solution changes with time. figure 2 It can be seen that the obtained nanocomposite undergoes obvious photothermal conversion under illumination, and the temperature of the solution continues to rise as the illumination time prolongs.
Embodiment 3
[0046] The layered double hydroxide-copper sulfide quantum dot nanocomposite prepared in Example 1 was used for intracellular lysosome localization experiments.
[0047] (1) The layered double hydroxide-copper sulfide quantum dot nanocomposite prepared in Example 1 was stirred in an aqueous solution of an equal amount of green fluorescent marker (FITC) for 4 hours. Human breast cancer cells 4T1 were inoculated in a 12-well cell culture plate, 1×10 per well 5 For each cell, add 1 mL of DMEM medium to the culture medium in each well. After the cells were adhered to the wall for 24 hours, the original medium was taken out, and 500 μL of nanocomplexes labeled with FITC containing 10 μg / mL were added to the experimental group, and the culture was continued for 4 hours;
[0048](2) Aspirate the supernatant in the well plate, wash the cells with phosphate buffer solution, and mark the cell lysosomes with the lysosome probe LysoTracker Rad, observe and take pictures under the laser co...
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