Preparation method of probiotic and aloe mask
A technology of probiotics and compound probiotics, applied in the field of preparation of probiotics aloe facial mask, can solve the problems of single effect, hidden safety hazards, high price, etc.
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Embodiment 1
[0028] Embodiment 1: the fermentation condition of aloe probiotic fermented liquid is determined:
[0029] 1. Preparation of aloe vera juice: select fresh, plump, and fleshy Aloe vera leaves, and remove leaves with diseased spots and soft rot. The average weight of the leaves is about 300-400 g. Wipe the leaf surface with alcohol to remove the epidermis, use a juicer to squeeze the mesophyll into aloe vera juice, subpackage, centrifuge at 6000 rpm / min for 10 min, and take the supernatant. The original aloe juice was sterilized by pasteurization, bathed in water at 55°C for 30 minutes, cooled and stored in a refrigerator at 4°C for future use.
[0030] 2. Fermentation: 6 kinds of probiotics after secondary activation were selected and mixed according to the ratio of 1:1 to prepare a composite probiotic suspension, which was added to the original juice of aloe vera according to the inoculation amount of 5%, supplemented with glucose, and carried out co-fermentation.
[0031] 3....
Embodiment 2
[0032] Embodiment 2: Determination and evaluation of antioxidant index
[0033] 1. Reagents: 0.2 mmol / L DPPH ethanol; 150 mmol / L pH 8.0 Tris-Hcl; 1.2 mmol / L pyrogallol; 0.4% FeSO4: FeSO47H2O; 1% ascorbic acid; 0.2 mol / L sodium hydroxide; 10 % trichloroacetic acid; 0.1% o-phenanthroline; pH 6.6 phosphate buffer; 0.1% ferric chloride.
[0034] 2. After determining the optimum conditions for the aloe fermented liquid, carry out fermentation under the optimum conditions, and store it in a refrigerator at 4°C after fermentation.
[0035] 3. Determination of Antioxidant Index
[0036] 1. Determination of DPPH free radical scavenging ability
[0037] Take 2ml of aloe fermented liquid, add 2ml of 0.2mol / LDPPH ethanol solution, react at room temperature in the dark for 30min, then extract with an equal volume of chloroform, take the supernatant to measure OD at 517nm, the control is deionized water plus DPPH solution.
[0038] 2. Determination of hydroxyl radical scavenging ability ...
Embodiment 3
[0047] Embodiment 3: antibacterial test
[0048] Experimental materials: probiotics, typhoid fever, Salmonella enteritidis, Shiga flexneri, E. coli O157, ATCC, Shiga 301, Staphylococcus aureus cowan1, Aloe vera, LB medium, Oxford cup.
[0049] Experimental steps:
[0050] A Activate probiotics and pathogenic bacteria and culture them overnight.
[0051] B Adjust the concentration of pathogenic bacteria to 10 8 About CFU / mL, take 100 μL of the bacterial solution and spread it on the LB plate.
[0052] C After the bacteria liquid is dried, carefully put a sterile Oxford cup on the plate; add the aloe vera probiotic fermentation liquid to the Oxford cup.
[0053] D Incubate at 37°C for 6-8 h, observe every 2-3 h.
[0054] E Measure the diameter of the inhibition zone in the plate and take a picture.
[0055] The results of Example 1 showed that after fermentation at 37°C, pH=7 for 48 h, and centrifugation at 10,000 rpm / min for 10, the fermentation broth was clear and transl...
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