Cosmetic compostion for preventing skin aging
A cosmetic composition and skin aging technology, which is applied in the direction of cosmetics, cosmetics, cosmetic preparations, etc., can solve the problems that are not known by people, and achieve the effects of excellent activity, excellent skin regeneration ability, and excellent anti-oxidation effect
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preparation example 1
[0034] Preparation Example 1: Preparation of Gold Nanoparticles Surface-treated with Gallic Acid and Isoflavones (GI-Au NPs)
[0035] The inventors of the present application prepared gold nanoparticles by the method described in PCT / KR / 2010 / 007516 already filed. Specifically, chloroauric acid (HAuCl 4 ) (7.8 mg, 0.02 mmol) was dissolved in 20 ml of distilled water, thereby preparing chloroauric acid. Then, a mixed solution in which 10 mg of glycoside isoflavones was dissolved in a 0.01 mol / L gallic acid solution was prepared, and then 0.3 ml of the mixed solution was added to the chloroauric acid solution and stirred for 30 minutes, thereby Gold nanoparticles were prepared.
preparation example 2
[0036] Preparation Example 2: Preparation of surface-treated gold nanoparticles (PI-Au NPs) with protocatechuic acid and isoflavones
[0037] Chlorauric acid (HAuCl 4 ) (7.8 mg, 0.02 mmol) was dissolved in 20 ml of distilled water, thereby preparing chloroauric acid. Then, prepare the mixed solution that has dissolved the isoflavones of 10mg to the protocatechuic acid solution of 0.01mol / L, afterward, this mixed solution of 0.3ml is added in the described chloroauric acid solution, and stir 30 minutes, by This produced gold nanoparticles.
Embodiment 1
[0038] Embodiment one : Cytotoxicity Assay of Gold Nanoparticles
[0039] In order to confirm the cytotoxicity of the gold nanoparticles provided by the present invention, the following test was carried out by WST-8 using L-929 cells which are a kind of muscle cells.
[0040] Specifically, the gold nanoparticles (GI-Au NPs, PI-Au NPs) of 0~50ug / ml prepared in the preparation example 1 and preparation example 2 were respectively added to the cell culture area with L-929 cells ( well), cultivated for seven days. After culturing, the absorbance at 450 nm was measured by immunoassay (ELISA), thereby confirming the cell viability. And, L-929 cells treated with 25 μg / ml and 50 μg / ml gold nanoparticles (GI-Au NPs, PI-Au NPs) were observed by scanning electron microscope and transmission electron microscope.
[0041] figure 1 Shows the survival rate of L-929 cells based on the concentration (0~50ug / ml) and days (one day, three days, five days, seven days) of the gold nanoparticle...
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