Whitening, freckle and anti-glycation fermented product cosmetics
A whitening, freckle-removing and anti-glycation technology, which is applied to cosmetics, cosmetic preparations, cosmetic preparations, etc., to achieve the effects of wide application, obvious anti-glycation and whitening effects, and convenient use.
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Embodiment 1
[0023] A whitening, freckle-removing, and anti-glycation plant fermented composition is characterized in that its preparation method is as follows:
[0024] (1) Under sterile conditions, inoculate 1v / v% of preserved Lactobacillus crispatus CGMCC No.6364 in MRS medium, and cultivate it at 35°C and 200rpm for 12 hours, and the resulting culture is used as the seed liquid for fermentation culture , the final concentration is 6*10 7 cfu / ml;
[0025] (2) (2) The Lactobacillus crispatus CGMCC No.6364 seed solution was inoculated in the liquid medium according to the inoculum size 10v / v%, and cultured on a shaking table at 30°C for 24 hours at 200rpm;
[0026] The liquid medium preparation method: the curcumin of 0.3g, the Cortex Morus alba extract of 50ml, the glucose of 25g, the peptone of 8g, the yeast extract of 7g, the beef extract of 8g, the sodium acetate of 5g, the citric acid of 2g Ammonium, 2 mL of Tween-80, 0.6 g of MgSO 4 ·7H 2 O, 0.3g of MnSO 4 4H 2 O, 2g of K 2 H...
Embodiment 2
[0028] Embodiment 2 comparative example
[0029] The R&D team found that curcumin and Morus alba can synergistically increase the antioxidant, whitening and anti-glycation properties of fermented extracts.
Embodiment 3
[0039] Cytotoxicity test:
[0040]The plant fermentation composition obtained in Example 1 was dissolved in serum-free DMEM culture fluid, and 4 samples were prepared respectively, with mass fractions of 0.25%, 0.5%, 1%, and 2%, respectively, and serum-free DMEM culture fluid was used as a negative MTT test was carried out in the same group to evaluate the cytotoxicity of the whitening, freckle-removing and anti-glycation plant fermentation composition.
[0041] 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 supernata...
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