Pseudomonas aeruginosa sanitizer applicable to production of barreled drinking water and sterilization method
A Pseudomonas aeruginosa and disinfectant technology, which is applied in the field of Pseudomonas aeruginosa disinfectant and sterilization, can solve the problems of unsatisfactory killing effect of Pseudomonas aeruginosa, achieve high safety and increase sterilization speed , the effect of high lethality
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Embodiment 1
[0024] Prepare the following components:
[0025] 1. Hydrogen peroxide aqueous solution with a concentration of 0.5g / L;
[0026] 2. CuSO with a concentration of 19mmol / L 4 aqueous solution;
[0027] Stir component 1 and component 2 according to the weight ratio of 8:1 and mix evenly. It is prepared and used immediately; then take 0.5ml with a concentration of about 10 6 CFU / ml of Pseudomonas aeruginosa bacteria liquid and the mixture of the above components 1 and 2 4.5mL, injected into a sterile test tube (in the mixed solution in the test tube, Cu 2+ Concentration of 1.9mmol / L, hydrogen peroxide concentration of 0.4g / L), act for 20 seconds, and immediately perform gradient dilution to an appropriate concentration; Bacterial concentration counting; after the culture medium solidified, flip the plate, culture at 36°C for 12 hours, count and calculate the lethality.
Embodiment 2
[0029] Prepare the following components:
[0030] 1. Hydrogen peroxide aqueous solution with a concentration of 0.9g / L;
[0031] 2. ZnSO with a concentration of 21mmol / L 4 aqueous solution;
[0032] Stir component 1 and component 2 according to the weight ratio of 8:1 and mix evenly. It is prepared and used immediately; then take 0.5ml with a concentration of about 10 6 CFU / ml of Pseudomonas aeruginosa bacteria liquid and the mixture of the above components 1 and 2 4.5mL, injected into a sterile test tube (in the mixed solution in the test tube, Zn 2+ Concentration of 2.1mmol / L, hydrogen peroxide concentration of 0.72g / L), act for 20 seconds, and immediately perform gradient dilution to an appropriate concentration; then take 1mL of the diluted solution and pour it on a plate, dilute the working bacterial solution with sterile physiological saline, and make Bacterial concentration counting; after the culture medium solidified, flip the plate, culture at 36°C for 12 hours, ...
Embodiment 3
[0034] Prepare the following components:
[0035] 1. Hydrogen peroxide aqueous solution with a concentration of 0.8g / L;
[0036] 2. FeCl with a concentration of 20mmol / L 3 aqueous solution;
[0037] Stir component 1 and component 2 according to the weight ratio of 8:1 and mix evenly. It is prepared and used immediately; then take 0.5ml with a concentration of about 10 6 CFU / ml of Pseudomonas aeruginosa bacteria liquid and the mixture of the above components 1 and 2 4.5mL, injected into a sterile test tube (in the mixed solution in the test tube, Fe 3+ Concentration of 2.0mmol / L, hydrogen peroxide concentration of 0.64g / L), act for 20 seconds, and immediately perform gradient dilution to an appropriate concentration; Bacterial concentration counting; after the culture medium solidified, flip the plate, culture at 36°C for 12 hours, count and calculate the lethal rate.
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