Skin care cosmetic composition with whitening effect
A technology for skin care cosmetics, whitening effect, applied in the field of skin care cosmetic composition, to achieve remarkable effect of whitening effect
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Embodiment 1
[0023] Example 1: Determination of free radical scavenging
[0024] DPPH· is a stable free radical in organic solvents, and its lone pair of electrons has a strong absorption near 517nm (shows deep purple). When the organic scavenger exists, the lone pair of electrons is paired, and the absorption disappears or weakens. By measuring the degree of absorption weakening, the activity of the free radical scavenger can be evaluated.
[0025] Take 2mL of the sample solution and 2mL of the DPPH solution with a concentration of 100μmoL / L and add it to the same stoppered test tube successively, shake well; let stand at room temperature for 30min, and measure the absorbance of the sample at a wavelength of 517nm.
[0026] Inhibition rate: K%=[1-(Ai-Aj) / Ac]×100%
[0027] Ai: absorbance of 2mL DPPH solution + 2mL resveratrol solution
[0028] Aj: Absorbance of 2mL resveratrol solution + 2mL solvent
[0029] Ac: absorbance of 2mL DPPH solution + 2mL solvent
[0030] The samples of each...
Embodiment 2
[0033] Embodiment 2: Determination of anti-ultraviolet performance
[0034] Table 2 resveratrol to the absorption rate of ultraviolet rays
[0035]
[0036] In the wavelength range of 280-400nm, scan every 10nm, determine the light transmittance of the resveratrol solution at each wavelength, and calculate the average absorbance in the wavelength range. The concentration of the sample solution was 10 μg / mL.
[0037] The experimental results are shown in Table 2.
Embodiment 3
[0038] Embodiment 3: Inhibition of tyrosinase activity test
[0039] The principle of the test is that under the action of tyrosinase, L-DOPA is oxidized to brown dopachrome, and the reaction will be inhibited in the presence of inhibitors.
[0040] Table 3 The inhibitory effect of resveratrol, arbutin and ethyl Vc on tyrosinase
[0041]
[0042]
[0043] The test reaction was carried out in a test tube. 0.1mL of DMSO solution containing different mass concentrations of resveratrol and 2.8mL of the substrate solution previously incubated in a constant temperature water bath at 30°C were first added to the test tube, mixed evenly, and then 0.1mL of 600 Unit / mL tyrosinase solution, mix well, place in a 30°C water bath for 10 minutes, and immediately use a spectrophotometer to measure the absorption peak of dopachrome at 475nm. According to the measured absorbance (OD value), the inhibition rate (%) of the sample to the tyrosinase activity was calculated.
[0044] Inhibit...
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