Intelligent nano-silver hydrogel
A hydrogel and nano-silver technology, applied in the directions of inorganic active ingredients, sexually transmitted diseases, aerosol delivery, etc., can solve the problems of increasing the production process, raw materials and costs, and achieve easy mass production, good stability, and low resistance. good bacteria effect
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Embodiment 1
[0029] At room temperature, dissolve 0.12g of hydroxypropyl methylcellulose in 100mL of double-distilled water to form a hydroxypropylmethylcellulose solution with a molar concentration of 0.01ml; dissolve 0.17g of silver nitrate in 10mL of double-distilled water, Form a silver nitrate solution with a molar concentration of 0.1m01 / L; take 10mL hydroxypropyl methylcellulose solution and 1.5mL silver nitrate solution and mix evenly to make the molar ratio 1:1.5. The mixed solution was irradiated under 100W self-ballasted fluorescent high-pressure mercury for 2.5 hours to prepare nano-silver hydrogel.
Embodiment 2
[0031] This embodiment is the structural characterization of the silver nano-antibacterial material in Example 1, specifically as follows: Adopt Tecnai G2F20 S-Twin 200 KV field emission transmission electron microscope to measure the morphology and elemental composition of silver nanoparticles in the nano-silver hydrogel for characterization . The sample preparation is to dissolve the nano-silver hydrogel in ultrapure water, precipitate with absolute ethanol and disperse it on the TEM copper grid. It can be seen from the TEM image that the particle size of nano-silver is between 5-10nm, and the particle size is relatively uniform. The sample mainly contains four elements: Ag, S, C, and O. The 20 values of the characteristic diffraction peaks of the sample measured by X-ray diffraction are 38.2', 44.4', 64.5', 77.5' in turn, and the displayed diffraction crystal planes are (111), (200), (220) and (311) respectively Compared with the standard crystalline silver card (PDFg04-...
Embodiment 3
[0033] In this embodiment, Escherichia coli and Staphylococcus aureus are selected as representatives of Gram-negative bacteria and positive bacteria, and the bacteriostatic test of Example 1 is carried out.
[0034] The operation steps of the inhibition zone test are as follows: sterilize and dissolve the LB agar solid medium and pour it into a sterilized petri dish. Spread it evenly with a sterile coating stick, then use sterile tweezers to pick up the Oxford cup, gently place it in the middle of the plate, and then let it stand for a while so that it can be fixed on the plate. Then pipette 2mL of nano-silver hydrogel solution into the Oxford cup, and use sterile water as a blank control, and make three parallel samples for each bacterium. The medium was cultured in an incubator at 37°C for 24 hours, and then the diameters of the inhibition zones were measured with a ruler, and the average value was taken. After checking the nano silver hydrogel has obvious antibacterial ef...
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