Cosmetic composition for skin improvement comprising green barley extract
A technology for cosmetic compositions and extracts, which can be applied to cosmetics, medical preparations containing active ingredients, drug combinations, etc., can solve problems such as difficult to expect improvement in skin function, negligible effects, and limit usage, and achieve excellent skin barrier enhancement. , Excellent skin moisturizing, high utilization effect
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preparation example 1
[0090] Preparation example 1. Preparation of samples such as green barley extract
[0091] 1-1. Preparation of green wheat extract by seedling cultivation machine (cultivation for two weeks)
[0092]In a house made of glass or plastic, there is provided a plurality of trays with small holes through which the roots of the seedlings can descend, under each of these trays, and consisting of a waterway that circulates water or a culture solution Culture plates and stacking tables (supporting tables) that can be stacked into multiple layers. Next, a culture solution circulator that circulates water or culture solution on the above-mentioned culture plate is provided; a water tank that stores water or culture solution supplied to the above-mentioned culture plate by the above-mentioned culture solution circulator; water is delivered from the above-mentioned water tank to the above-mentioned culture plate Or the first delivery pipe of the culture solution; and the second deliver...
preparation example 2
[0101] Preparation example 2. Preparation according to saponin during cultivation
[0102] As saponin used in the experiment, 10 mg of saponin purchased from EXTRASYNTHESE was dissolved in autoclaved distilled water, filtered through a 0.2 μM syringe filter, diluted with cell culture and treated to cells.
[0103] Saponin HPLC Analysis Conditions
[0104] -Column: C18
[0105] -Column Temperature: 30°C
[0106] -Injection Volume: 5μL
[0107] -Flow rate: 1.0mL / min
[0108] -Mobile phase: A: (5% acetic acid in water) 80%
[0109] D: Methanol 20%
[0110] - Gradient: None. From 0 minutes A 80%, D 20%
[0111] -Detector: UV 270nm
[0112] According to the analysis results, it was confirmed that the saponin content of the green wheat extract cultivated according to the above-mentioned Preparation Example 1 was higher ( figure 2 ).
preparation example 3
[0113] Preparation example 3. Preparation of saponarin, luteolin and apigenin
[0114] The green wheat extract prepared in Preparation Example 1 above was prepared to 5,000 ppm and used for analysis. A standard foam mixture was prepared to 1,000 ppm using a MeOH / pyridine mixed solvent, and the above standard foam mixture was diluted to 0.5-100 ppm and used for analysis.
[0115] HPLC conditions
[0116] - Instrument: Agilent Technologies 6410 triple quadrupole (LC-MS / MS)
[0117] -Column: Chromasil C18 (3.0mm×150mm, 3.0μm)
[0118] - Solvents: A; 0.1% formic acid in water, B; 0.1% formic acid in acetonitrile
[0119] -Flow rate: 0.4mL / min
[0120] -Injection volume: 5μL
[0121] -gradient:
[0122] - time (minutes) B% 1 0 5 2 30 100 3 32 100
[0123] MS conditions
[0124] -Ionization Mode: ESI, scan mode
[0125] -Gas temp. (°C): 350
[0126] -Capillary volt. (V): 4000
[0127] - Atomizer (psig): 40
[0128] - Cracking volta...
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