Whitening and repairing mask containing probiotic active extracting solution and nicotinamide
A technology of extract and nicotinamide, which is applied in the field of cosmetic formula, can solve the problems of not outstanding whitening effect and low tyrosinase inhibition rate, and achieve the effect of no cytotoxicity, broad market potential, and good moisturizing effect
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Embodiment 1
[0036] The preparation method of the fermentation activity extract of bacillus subtilis nk1 is as follows:
[0037] (1) Strain activation:
[0038] The medium used for activation is milk medium, and the formula refers to the existing technology, and the formula is as follows: 500g fresh milk, 50g sucrose, configured into 1L, and sterilized at high temperature;
[0039] The activation conditions are: 37°C shaker culture for 12 hours, the amount of bacteria after activation is 2.2×10 8 CFU / mL of seed solution.
[0040] (2) Fermentation culture:
[0041] The formula of the special liquid medium used for fermentation is as follows: 20g of glucose, 10g of peptone, 10g of yeast extract, 8g of soybean powder, 3g of nicotinamide, 3g of Antrodia camphorata extract, 3mL of Tween-80, 0.6g of MgSO 4 ·7H 2 O, 0.3g of MnSO 4 4H 2 O, 2g of K 2 HPO 4 Mix with 1000mL of distilled water, adjust the pH value to 7.0 and obtain a sterile medium after autoclaving;
[0042] Inoculate the se...
Embodiment 2
[0044] Embodiment 2 comparative example
Embodiment 3
[0050] Cytotoxicity test:
[0051] The fermentation activity extract of Bacillus subtilis nk1 obtained in Example 1 was dissolved in serum-free DMEM culture fluid, and 4 samples were prepared, with mass fractions of 0.25%, 0.5%, 1%, and 2%, respectively, and serum-free DMEM culture fluid The negative control sample group was used for MTT detection to evaluate the cytotoxicity of the fermentation activity extract of Bacillus subtilis nk1.
[0052] Inoculate L929 cells into a 96-well plate at 100 μL / well, and adjust the concentration to 1×10 5 cells / mL, at 37°C, 5% CO 2 After culturing for 24 hours in serum-free DMEM culture solution for adherence, the culture solution was discarded, and 100 μL of sample solutions with different mass fractions were added to each well. The negative control group continued to culture in serum-free DMEM for 48 hours. Add 20 μL of 5 mg / mL MTT solution and incubate for 4 h in an incubator protected from light. Discard the supernatant and add 100 μ...
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