Cell factor sample effect and beautifying application of nona-oligopeptide composition
A composition and oligopeptide technology, applied in the direction of medical preparations containing active ingredients, cosmetic preparations, skin care preparations, etc., can solve problems such as different effects and inconsistent content, and achieve skin problems and skin damage. The effect of perfect protection
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Embodiment 1
[0049] Preparation of oligopeptide composition
[0050] Palmitoyl Tripeptide-1, 100ppm solution, 200mL
[0051] Tripeptide-1 copper, 500ppm solution, 20mL
[0052] Palmitoyl Tripeptide-5, 1000ppm solution, 10mL
[0053] Carnosine, Powder, 0.9g
[0054] Acetyl tetrapeptide-5, 1000ppm solution, 10mL
[0055] Palmitoyl tetrapeptide-7, 50ppm solution, 200mL
[0056] Acetyl Hexapeptide-8, 500ppm solution, 30mL
[0057] Nonapeptide-1, 100ppm solution, 30mL
[0058] Nisin, 0.18g.
[0059] According to the different solubility properties of the above oligopeptides, add water to prepare a 1000 mL solution.
[0060] Use the above solution as the mother liquor, and directly prepare it and add it to the acceptable base of cream, lotion or other beauty and skin care products; you can also add 10 grams of mannitol to the solution according to the freeze-vacuum drying method, according to 1~1.5 ml / vial Subpackaging, vacuum freeze-drying, capping (sealing), and making freeze-dried pow...
Embodiment 2
[0062] Anti-wrinkle, anti-wrinkle repair program for aging skin
[0063] After the routine beauty care procedures, disinfect the skin at the wrinkled area with 70% medical alcohol, add 1~3mL of normal saline to dissolve the freeze-dried powder prepared in Example 1, apply the mixture directly to the skin, and massage until Absorbs completely. It can also be introduced with commonly used instruments and methods in cosmetology and medical cosmetology, including ultrasonic equipment, iontophoresis or microneedles, hydrolight needles, lasers, injections, etc., to help the skin absorb and achieve the best skin repair effect.
Embodiment 3
[0065] Proliferation activity test of human skin fibroblasts
[0066] Material
[0067] The raw materials of Example 1 were made into 0.3-fold, 1.0-fold, and 3.0-fold oligopeptide compositions for later use, human skin fibroblasts (Dental Research Laboratory, Hokkaido University, Japan), α-MEM medium (GIBCO), fetal bovine serum ( GIBCO) penicillin streptomycin (Invitrogen), Trypan blue solution (Sigma), 0.25% Trypsin-1mM EDTA˙4Na (Invitrogen), IMSO (Sigma), cell number determination kit WST-8 (Japan) Infinite500 automatic enzyme labeling Instrument (Tecan).
[0068] Method and Results
[0069] Human skin fibroblasts in MEM medium (containing 5% fetal bovine serum), 5% CO 2 , 95% humidity, CO at 37°C 2 Cultivate in an incubator, change the medium once every 3 days, subculture the cells after 5-6 days of culture, suck out the original culture medium, wash twice with PBS, add 0.5mL of 0.25% Trypsin-1mM EDTA˙4Na solution, and store at 37°C After 30 seconds, add 10 mL of MEM m...
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