Antibacterial composition and application of antibacterial composition in acidifying agent preparation
A composition, caprylic acid technology, applied in the application, animal feed, additional food elements and other directions, can solve the problems of feed attracting influence, high use cost, poor antibacterial performance, etc., achieve good bacteriostatic effect, small dosage, reduce cost effect
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Embodiment 1
[0020] Caprylic acid, carvacrol, capric acid, cinnamaldehyde, eugenol and hexanoic acid are mixed according to the mass ratio of 2:1:1:5:2:2 to form an antibacterial composition, and then dissolved in 0.5% (v / v) Add absolute ethanol, then add sterile liquid containing 0.5% (w / v) Tween-80, configure the antibacterial composition to a concentration of 0.5% (w / w), stir while pouring, and shake evenly. A sterile liquid containing 0.5% (v / v) ethanol and 0.5% (w / v) Tween-80 was used as a control (the above control has been proved to have no bacteriostasis through preliminary experiments). Aspirate 100 μL10 7 The CFU / mL bacterial suspension is placed in a nutrient agar petri dish, spread evenly, and placed for 4-6 hours, so that the bacteria can stably attach to the surface of the solid medium. Divide the petri dish into 4 areas on average, punch a hole in the center of each area with a sterile pipette tip with a diameter of 8 mm, seal the small holes with the flame of an alcohol la...
Embodiment 2
[0022] Caprylic acid, carvacrol, capric acid, cinnamaldehyde, eugenol, and caproic acid are mixed in a mass ratio of 2:3:4:5:1:2 to form an antibacterial composition, and then dissolved in 0.5% (v / v) Add absolute ethanol, then add sterile liquid containing 0.5% (w / v) Tween-80, configure the antibacterial composition to a concentration of 0.5% (w / w), stir while pouring, and shake evenly. A sterile liquid containing 0.5% (v / v) ethanol and 0.5% (w / v) Tween-80 was used as a control (the above control has been proved to have no bacteriostasis through preliminary experiments). Aspirate 100 μL 10 7 The CFU / mL bacterial suspension is placed in a nutrient agar petri dish, spread evenly, and placed for 4-6 hours, so that the bacteria can stably attach to the surface of the solid medium. Divide the petri dish into 4 areas on average, punch a hole in the center of each area with a sterile pipette tip with a diameter of 8 mm, seal the small holes with the flame of an alcohol lamp, and the...
Embodiment 3
[0026] Embodiment 3 medium-chain fatty acid, plant essential oil and embodiment 1 and 2 to the MIC of three kinds of indicator bacteria
[0027] With reference to NCCLS with slight changes, the agar plate dilution method is adopted: take the single medium-chain fatty acid, plant essential oil, bacteriostatic composition and flavomycin in Table 2 respectively, and 10 mL of the above-mentioned substances of different concentrations (also dissolved in 0.5% (v / v) absolute ethanol, then add sterile liquid containing 0.5% (w / v) Tween-80), then add the quantitative (10mL) beef extract peptone solid medium that has been melted and cooled to about 50°C, shake Pour the plate evenly and quickly to make a sample plate with different decreasing concentrations. Use a sterile inoculator to inoculate the indicator bacteria, and the final number of bacteria per point is about 10 4 CFU, forming plaques with a diameter of 5-8mm. After the inoculation, place it statically on the ultra-clean wo...
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