Dandruff removing cosmetic containing propionibacterium
A technology for propionic acid bacteria and cosmetics, applied in the field of daily chemicals, can solve the problems of inability to stay on the scalp and fundamentally prevent dandruff, etc., and achieve the effect of broad application prospects.
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Embodiment 1
[0022] An anti-dandruff shampoo containing propionibacterium, the preparation method of the anti-dandruff shampoo comprises the following steps: making dodecyltrimethylammonium chloride, sodium phosphate, germ oil, Dipsacus polysaccharide ultraviolet For sterilization, add 19 parts of dodecyltrimethylammonium chloride to 50 parts of sterile water at 70°C, stir to dissolve and add 4 parts of sodium phosphate and 2.5 parts of germ oil; when the temperature drops to 50°C, add 1.5 parts of Dipsacus polysaccharide moisturizer; stir for 40 minutes and let it stand at room temperature, adjust the pH to 6.4 with propionic acid, add 0.1 parts of the pre-configured concentration under sterile conditions to 1.9×10 2 cfu / ml Propionibacterium suspension, stir well and store at 5°C.
Embodiment 2
[0024] An anti-dandruff shampoo spray containing propionibacterium, the preparation method of the anti-dandruff shampoo spray comprises the following steps: ultraviolet sterilizing alkanol polyoxyethylene ether, myristic acid, avocado oil, and genus polysaccharide Bacteria, add 8 parts of alkyl alcohol polyoxyethylene ether to 60 parts of sterile water at 75 ℃, stir to dissolve and add 0.1 part of myristic acid and 0.1 part of avocado oil; when the temperature drops to 53 ℃, add 0.1 part of Shenjincao Polysaccharide, stirred for 30 minutes and allowed to stand at room temperature, adjusted the pH to 5.5 with succinic acid, and added 0.25 parts of pre-configured concentration to 4×10 under sterile conditions 2 cfu / ml Propionibacterium suspension, stir well and store at 8°C.
Embodiment 3
[0026] An anti-dandruff shampoo containing propionibacterium, the preparation method of the anti-dandruff shampoo comprises the following steps: sterilizing trehalose lipid, guar gum, silk peptide, and lemon polysaccharide by ultraviolet light, at 40 parts at 80°C Add 30 parts of trehalose lipid in sterile water, stir to dissolve and add 8 parts of guar gum and 5 parts of silk peptide; add 3 parts of lemon polysaccharide when the temperature drops to 55°C; stir for 50 minutes and let it stand at room temperature, adjust the pH with lactic acid To 7.3, under aseptic conditions, add 0.5 parts of a pre-prepared propionibacterium suspension with a concentration of 0.2 cfu / ml, stir evenly and store at 2°C.
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