Composition for treating skin cell damage caused by fine dust, for strengthening skin barrier, and for Anti-aging or Anti-inflammation, containing mentha arvensis extract
A technology of skin cells and compositions, applied in skin care preparations, cosmetics, food science, etc., can solve problems such as skin discoloration and rough skin surface
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example 1
[0108] Example 1: Preparation of Peppermint Extract
[0109] Wild mint leaves and acetic acid bacteria (Acetobacter aceti) were prepared and fermented at 26° C. for 48 hours. Then, using an extraction solvent obtained by mixing purified water and ethanol (ie, 70% ethanol) at a ratio of 3:7 as an extraction solvent, the fermentation product was extracted at room temperature. After extraction at room temperature, primary filtration is performed to remove solid matter contained in the extract. Then, the extract was concentrated to remove ethanol, followed by isolation and purification. Then, the resultant was subjected to centrifugation and secondary filtration, and then dried to obtain a wild peppermint extract.
example 2
[0110] Example 2: Dust collection and extraction
[0111]Microdust was collected using a low volume air sampler (Sensidyne, Gillian, FL, U.S.A.). The filters and denuders of the filter pack were replaced at about 10:00 am on each measurement day to collect samples for about 24 hours. In Sunpung-gu, Seoul (Korea University of Foreign Studies International Research Center, the roof of the 6th floor of the dormitory building in Cheonnyeong-gu, Gyeonggi-do, Yongin-si) collects fine dust every day for 28 days. The measurement time was measured by starting a timer when the vacuum pump was turned on and recording the time of the timer when the vacuum pump was turned off. The collection flow rate was set at 16.7 L / min. The flow rate was measured with a flow meter (Model 4143, TSI Inc.) at the beginning of the measurement and again at the end of the measurement. The Teflon filters in the filter pack were weighed before and after collection. The Teflon filter was dried in a desiccat...
example 3
[0112] Example 3: Culture of Keratinocyte Line (Normal Human)
[0113] Keratinocyte cell line (normal) was purchased from Lonza Inc. (Walkersville, Maryland, USA), subcultured (subcultured), and then incubated at 37°C and 5% CO 2 under the condition of CO 2 Cultivated in an incubator. Cell culture was performed according to Lonza's guidelines. KGM-2bullet kit CC-4152 (ingredients: BPE (bovine pituitary extract)), human epidermal growth factor (human epidermal growth factor, hEGF), insulin, hydrocortisone, transferrin, adrenal Epinephrine, and KGM-2 bullet kit CC-3107 added with GA-1000 (gentamycin suflate + amphotericin-B), added to 500ml of KBM- 2CC-3103 medium to prepare medium for cell culture.
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