Simple method for preparing nano silver from bacterial fermentation solution
A technology of bacterial fermentation and nano-silver, applied in the biological field, can solve the problems of relatively high preparation technology requirements, and achieve the effects of strong operability, simple and easy preparation method, and low cost
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Embodiment 1
[0015] Inoculate Staphylococcus aureus into 100ml of sterilized MH medium, mix thoroughly, place in a constant temperature water bath shaker at 37°C for 24 hours, add the culture solution to a centrifuge tube and centrifuge at 5000rpm for 5 minutes. The bacterial pellet was separated from the supernatant (bacterial suspension). Add 200 μl of 0.1M silver nitrate solution to 20ml of supernatant to make the concentration of silver ions 1mM, place on a water bath shaker at 37°C for 24 hours, and then ultrasonically crush the shaken solution in an ice bath, and output The power is 150 watts, ultrasound is 30s, interval is 30s, repeat 6 times. The ultrasonicated solution was filtered with a 0.22 μm filter membrane to obtain a clear nano-silver solution. The electron microscope picture of this nano-silver solution is as follows: figure 1 shown, from figure 1 It can be seen that the nano-silver solution in this embodiment is indeed a nano-silver solution.
Embodiment 2
[0017] Inoculate Staphylococcus aureus into 100ml of sterilized MH medium, mix thoroughly, place in a constant temperature water bath shaker at 37°C for 24 hours, add the culture solution to a centrifuge tube and centrifuge at 5000rpm for 5 minutes. The bacterial pellet was separated from the supernatant (bacterial suspension). Add 1ml of 0.1M silver nitrate solution to 20ml of the supernatant to make the concentration of silver ions 5mM, place it on a water bath shaker at 37°C for 24 hours, and then ultrasonically break the shaken solution under ice bath conditions, output The power is 200 watts, 30s of ultrasound, 30s of rest, repeated 6 times. The ultrasonicated solution was filtered with a 0.22 μm filter membrane to obtain a clear nano-silver solution. The electron microscope picture of this nano-silver solution is as follows: figure 2 shown, from figure 2 It can be seen that the nano-silver solution in this embodiment is indeed a nano-silver solution.
Embodiment 3
[0019] Inoculate Staphylococcus aureus into 100ml of sterilized MH medium, mix thoroughly, place in a constant temperature water bath shaker at 37°C for 24 hours, add the culture solution to a centrifuge tube and centrifuge at 5000rpm for 5 minutes. The bacterial pellet was separated from the supernatant (bacterial suspension). Add 2ml of 0.1M silver nitrate solution to 20ml of the supernatant to make the concentration of silver ions 10mM, place it on a water bath shaker at 37°C for 5h, and then ultrasonically crush the shaken solution in an ice bath, and output The power is 200 watts, 30s of ultrasound, 30s of rest, repeated 10 times. The ultrasonicated solution was filtered with a 0.22 μm filter membrane to obtain a clear nano-silver solution. The electron microscope picture of this nano-silver solution is as follows: image 3 shown, from image 3 It can be seen that the nano-silver solution in this embodiment is indeed a nano-silver solution.
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