Anti-radiation injury repair milk
A damage repair and anti-radiation technology, applied in cosmetics, cosmetic preparations, dressing preparations, etc., can solve the problems of no obvious effect on skin repair, failure to repair damaged skin as soon as possible, and failure to satisfy consumers, so as to reduce DNA radiation damage, improve the body's self-repair function, and improve the effect of anti-lipid peroxidation
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[0039] The preparation method of above-mentioned embodiment 1~5 radiation damage repair milk comprises the following steps:
[0040] (1) Polydimethylsiloxane, cetearyl alcohol, polyglyceryl-3 methylglucose distearate, diethylhexyl carbonate, caprylic / capric triglyceride, hydrogenated polyisobutene , cyclopentasiloxane, ceramide, and tocopheryl acetate were mixed evenly, and heated to 85°C to prepare phase A;
[0041] (2) Mix glycerin, carbomer, chlorphenesin, sodium hyaluronate, dipotassium glycyrrhizinate, propylene glycol, betaine, ascorbic acid, and deionized water evenly, and heat to 85°C to prepare phase B;
[0042] (3) Add phase A to phase B, emulsify and homogenize for 4 minutes to obtain phase C;
[0043] (4) Cool phase C to 50°C, add lemon extract, alfalfa leaf protein, ganoderma lucidum polysaccharide, melittin, triethanolamine, and phenoxyethanol, stir and mix evenly, and prepare the radiation damage repair milk.
Embodiment 1
[0060] Repair milk prepared in Example 1; PierceBCA protein quantification kit: Thermo Company, USA; Diphenylpicrylic hydrazide (DPPH): Alfa Company. BP211D electronic balance: Sartorious Company of Germany; SpectraMax190 microplate reader: AD Company of the United States; constant temperature see-through water tank, Shanghai Experimental Instrument General Factory; UV-1700 spectrophotometer, Shimadzu Company of Japan.
[0061] 2. Method
[0062] 2.1 Preparation of test solution
[0063] Take the repair milk prepared in the above-mentioned Example 1, accurately weigh it, and add distilled water to prepare a 100 μg / mL test solution.
[0064] 2.2 Determination of DPPH free radical scavenging ability
[0065] Add 1mL of the test solution into clean 10mL stoppered test tubes, add 0.5mL of 0.6mmol / LDPPH methanol solution to each tube, then supplement the volume with methanol to 5mL, and measure at 517nm after reaction at room temperature for 30 minutes in the dark Absorbance val...
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