Tyrosinase inhibitor composition, skin brightening essence and preparation method of skin brightening essence
A tyrosinase and inhibitor technology, applied in the field of daily chemicals, can solve the problems of easy discoloration of kojic acid, skin irritation, skin irritation, etc. Effect
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Embodiment 2-6
[0053] Dilute the extract of Phyllostachys antarctica with ultrapure water to obtain 5 groups of test solutions with different concentrations (final concentrations). When performing the test for inhibiting tyrosinase activity, the concentrations of the extracts of Phyllostachys antarctica are shown in Table 1 below.
[0054] Inhibition of tyrosinase activity by extracts from Phyllostachys antarctica. The tyrosinase activity is measured by the tyrosinase activity that catalyzes the production of dopaquinone from L-dopa. Specifically: Take 6 test tubes, add 0 μl, 50 μl, 100 μl, 200 μl, 300 μl, 400 μl of Plexiglas antarctica extract respectively, fill up to 1ml with phosphate buffer (0.5mM, PH=6.8), and then add 500μl tyrosine Acidase (50U / ml), water bath at 23°C for 10min, add 500μl L-DOPA (2.5mM) after the reaction, and measure the absorbance at a wavelength of 450nm with a UV spectrophotometer, denoted as A.
[0055] Take 6 test tubes, add 0 μl, 50 μl, 100 μl, 200 μl, 300 μl...
Embodiment 7-13
[0066] Take Plexiglas antarctica extract and Resurrection Grass extract as tyrosinase inhibitors. The Antarctica Antarctica extract and the resurrection grass extract are in a mass ratio of 1:9 (Example 7), 2:8 (Example 8), 2:3 (Example 9), 4:1 (Example 10) , 3:2 (Example 11), 8:2 (Example 12), and 9:1 (Example 13) were mixed to obtain a tyrosinase inhibitory composition with a total concentration of 10%. Determination of the inhibition of tyrosinase by the combination of the extracts of Phyllostachys antarctica and the extracts of P.
[0067] Take 10 test tubes, add 0μl, 0μl, 20μl, 40μl, 80μl, 100μl, 120μl, 160μl, 180μl, 200μl of P. , 20μl, 0μl Resurrection Grass extract, and make up to 1ml with phosphate buffer (0.5mM PH=6.8), then add 500μl tyrosinase (50U / ml), water bath at 23°C for 10min, add 500μl L- For DOPA (2.5mM), the absorbance was detected at a wavelength of 450nm by an ultraviolet spectrophotometer, and it was recorded as X.
[0068] Take 6 test tubes, add 0 μl...
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