Application of soracan gum in inhibiting skin injury of ultraviolet ray
A technology for skin damage and ultraviolet rays, applied in the fields of medicine and cosmetics, can solve the problems of many chemical sunscreen additives, easy to block pores, affect the appearance and other problems, achieve excellent anti-ultraviolet function, improve survival rate, and increase the effect of tolerance
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Embodiment 1
[0021] The preparation of embodiment 1 Sola gum solution
[0022] The preparation of Sola gum solution comprises the following steps:
[0023] 1) The crude Sola gum was purified by the improved Sevag method. The purification steps are:
[0024] a. Prepare 0.5% Sola gum solution, heat (105°C, 15min), and when cooled to room temperature, 7000r / 10min, take the supernatant to remove residual bacteria.
[0025] b. Add pH4.0 acetic acid---sodium acetate solution at a ratio of 1:30 to remove DNA.
[0026] c. Mix the supernatant with phenol-chloroform solution (prepared as a mixed solution at a ratio of 1:1) according to the ratio of 1:1, shake vigorously for about 15 minutes, 7000r / 10min, and take the supernatant. Repeat this step 2-3 times to completely remove the protein.
[0027] d. Add 2 times the volume of industrial alcohol to the supernatant, the sugar flocculates into a ball, remove it, and squeeze out the alcohol.
[0028] e. Wash the precipitate with 75% alcohol for 2-...
Embodiment 2
[0031] Example 2 Sola gum to research on cell viability irradiated by ultraviolet UVA
[0032] The experimental cells were NIH3T3 mouse fibroblasts. Culture under standard experimental conditions: cells were cultured in DMEM high-glucose medium (complete medium) containing 10% calf serum and 1% penicillin and streptomycin at 37°C, 5% CO 2 In the biochemical incubator, the medium was changed every 2-3 days. Cells were digested and passaged with trypsin solution containing 0.25% trypsin-EDTA.
[0033] In the experiment, cells were treated differently, and ultraviolet UVA irradiation caused cell damage. By detecting the survival rate of cells after ultraviolet UVA irradiation, the degree of cell damage and the degree of protection of cells by Sola gum were evaluated.
[0034] NIH3T3 mouse fibroblasts in 2×10 4 Densities were seeded in 96-well plates, and the setup was divided into 6 groups of 5 wells. The experimental grouping situation is: CK, UVA, and Salecan components are...
Embodiment 3
[0035] Example 3 Sola gum to the research of mouse skin model after ultraviolet irradiation
[0036] The experimental animals were 8-week-old male C57BL / 6J mice. Raised under standard experimental conditions: 12-hour light-12-hour dark cycle, free access to water and food. All experimental mice were anesthetized by intraperitoneal injection of 10% chloral hydrate (4ml / kg). When the anesthesia was sufficient, the mice were fixed with their backs facing upward. With the back spine as the middle line, use scissors to cut off the mouse hair on the back, and the size is about 2×2cm. One week later, the mice were randomly divided into 3 groups, including CK group, UVA group and Salecan group. Among them, the CK group was the normal control group, and the UVA group was the ultraviolet UVA irradiation group. These two groups were given corresponding solvents during the experiment (ie distilled water); the Salecan group was the Sola gum solution treatment group, that is, before recei...
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