Composition for removing couperose skin as well as preparation method and application thereof
A composition and capillary technology, applied in the directions of drug combinations, pharmaceutical formulations, plant raw materials, etc., can solve the problems of red capillary problems, general effects, skin irritation, etc. that cannot be fundamentally resolved, so as to enhance skin barrier and improve microcirculation. , The effect of solving the problem of red blood
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[0041] A composition for removing redness, obtained by uniformly mixing the following components: 1-6 parts of coralline algae extract, 1-5 parts of dogwood fruit extract, 0.1-10 parts of olive leaf extract; preferably, the following components Mix evenly to obtain: 2-5 parts of coralline algae extract, 2-4 parts of dogwood fruit extract, 0.5-5 parts of olive leaf extract; more preferably, the following components are mixed uniformly to obtain: 2.5 parts of coralline algae extract, 4 parts of dogwood fruit extract, 5 parts of olive leaf extract, the above-mentioned parts are by weight.
[0042] In some specific embodiments, the composition of the present invention is prepared by the following steps:
[0043](1) Take coralline algae, dry and pulverize, add 10 times the amount of ethanol to soak for 3 hours, extract by ultrasonic vibration, filter and collect the filtrate; the filtrate is concentrated under reduced pressure at a temperature of 45°C to obtain an extract; add 10 t...
experiment example 1
[0051] Experimental Example 1: Cytotoxicity Test
[0052] MTT is a yellow powder chemical reagent widely used in the detection of cytotoxicity or cell proliferation. The detection principle is that succinate dehydrogenase in the mitochondria of living cells can reduce MTT to water-insoluble blue-purple crystalline formazan and deposit it. In cells, dead cells do not have this function. Dimethyl sulfoxide (DMSO) can dissolve formazan in cells, and the number of living cells can be judged according to the measured absorbance value. The specific experimental method is as follows:
[0053] 1×10 per well in a 96-well plate 4 100 μL of DMEM medium containing 10% bovine serum and 100 μL of human immortalized epidermal cells (HaCaT) were inoculated at the density of each cell, and replaced with serum-free medium after 24 hours of cultivation; , 200 μg / mL (diluted in water) of the redness-removing composition prepared in the above-mentioned Examples 1-12 and Comparative Examples 1-3 ...
experiment example 2
[0059] Experimental example 2: Anti-inflammatory effect test
[0060] Interleukin-6 (IL-6) is a pro-inflammatory cytokine, and enzyme-linked immunosorbent assay (ELISA) can be used to measure the secretion level of IL-6 in human immortalized keratinocytes (HaCaT). The anti-inflammatory effect of the samples was evaluated. The experimental steps are as follows:
[0061] (1) Blank control group: in a 96-well plate according to 1×10 per well 4 Inoculate 100 μL of DMEM medium containing 20% bovine serum and 100 μL of HaCaT cells at a density of 1 cell, replace with serum-free medium after 24 hours of culture, collect the cell culture supernatant, and use human interleukin 6 (IL-6) ELISA detection reagent Box to detect the secretion of IL-6 in HaCat cells;
[0062] (2) Negative control group: HaCat cells were stimulated with 1 μg / ml lipopolysaccharide (LPS) for 6 hours, the cell culture supernatant was collected, and the secretion of IL-6 in HaCat cells induced by LPS was dete...
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