Eye repair composition as well as preparation method and application thereof
A composition and eye technology, applied in skin care preparations, pharmaceutical formulas, cosmetic preparations, etc., can solve problems such as safety considerations, side effects, and increased eye burden, so as to improve bags under the eyes, Effective in reducing puffiness around the eyes and dark circles
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preparation example Construction
[0031] The preparation method of the whitening plant extract composition is as follows: (1) dry the required plant parts, crush them, weigh them according to the required number, and mix them evenly; (2) add 25-40 times the amount of deionized water to extract, extract The temperature is 75-95°C, the extraction time is 2-4h, the number of extractions is 2-3 times, and the extracts are combined; (3) Cool the extract obtained in step (2) to 30°C or below, and use a 100-200 mesh Filtrate with gauze, filter twice, collect the filtrate to obtain the first filtrate, and let the first filtrate stand naturally for 24 hours; (4) centrifuge the solution after step (3) standing for 0.5-1 hour, the rotating speed is 2000-10000rpm, and the aperture is 0.1 -1.0 μm filter membrane is filtered, and the filtrate is collected to obtain the secondary filtrate; (5) the secondary filtrate obtained in step (4) is concentrated under reduced pressure, added polyhydric alcohol, and mixed; (6) the obtai...
experiment example 1
[0038] Experimental Example 1: Cytotoxicity Test
[0039] 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:
[0040] 1×10 per well in a 96-well plate 4 Each 100 μL of DMEM medium containing 10% bovine serum and human immortalized epidermal cells (HaCaT) were inoculated at a density of 1 cell, and replaced with serum-free medium after 24 hours of cultivation; 12 and the eye repair composition prepared in Comparative Example 1-3 were treated and incubated for 24 hours; the culture medium was removed and treate...
experiment example 2
[0046] Experimental Example 2: Determination of Inhibition of Tyrosinase Activity
[0047] As shown in Table 3, add the phosphate buffer solution with a pH of 6.8, the eye repair composition prepared in Examples 1-12 and Comparative Examples 1-3, and the tyrosine solution to the test tube in sequence, and bathe in water at 35°C for 10 minutes. Then add tyrosinase solution, mix well, incubate at 35°C for 30 minutes, quickly transfer to a cuvette, and measure the absorbance value at 475nm. The experimental group, negative control, and positive control were adjusted to zero with blank control 1, blank control 2, and blank control 3, respectively.
[0048] The concentrations of the eye repair composition and the arbutin solution used in the experiment were both 1 mg / mL.
[0049] Tyrosinase inhibition rate=[(A-B) / A]×100%, A is the absorbance value of the negative control, B is the absorbance value of the experimental group or the positive control.
[0050] table 3
[0051]
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