Composition containing extracts of cichorium intybus and poncirus trifoliata for strengthening skin barrier
A skin barrier and composition technology, which is applied in the field of skin barrier strengthening compositions, can solve problems such as bad skin effects, skin irritation, difficulty in manufacturing, etc., so as to increase moisture retention, strengthen skin barrier, prevent and improve atopy effect of dermatitis
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Embodiment 1
[0040] Embodiment 1: the manufacture of chicory (Cichorium intybus), citrus orange (Poncirus trifoliata RAFIN), chicory (Cichorium intybus) and citrus orange (Poncirus trifoliata RAFIN) mixed extract
[0041] 50 g of dried chicory (Cichorium intybus) (Daiko Pharmaceutical) and citrus (Poncirus trifoliata RAFIN) (Daiko Pharmaceutical) were made into powder using a pulverizer, and extracted with 1 L of 70% ethanol at room temperature 3 hours, and then filtered with Whatman NO.4 filter paper and Advantec NO.5C filter paper. After concentrating the filtrate with a vacuum rotary concentrator, the yield of chicory was 21.76%, and the yield of Hovenia was 14.06%. For the chicory + citrus mixture, the two natural powders were mixed at a ratio of 1:1, and the extract was made by the above method.
experiment example 1
[0042] Experimental Example 1: Cell Culture
[0043] [Sebocyte, SZ95]
[0044] Use added 10% fetal bovine serum (Fetal bovine serum (FBS)), 5ng / ml human epidermal growth factor (human epidermal growth factor), 1mM CaCl 2 Dulbecco's modified eagle medium (DMEM) / F12 (1:1) in CO 2 Incubator (37°C, 5% CO 2 ) in which SZ95 cells were cultured, and the medium was replaced every 2-3 days.
[0045] [Fibroblast, CCD-986SK]
[0046] Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) was used in CO 2 Incubator (37°C, 5% CO 2 CCD-986 or cells were cultured in ), and the medium was changed every 2-3 days.
experiment example 2
[0047] Experimental Example 2: Cytotoxicity Evaluation (MTT assay)
[0048] In order to evaluate the cytotoxicity of the mixture extracts of Cichorium intybus, Poncirus trifoliata RAFIN, Cichorium intybus and Poncirus trifoliata RAFIN produced in Example 1, MTT assay was carried out. confirmed.
[0049] SZ95 and CCD-986SK cells were separately planted into 96-well plates at a concentration of 1×105 cells / ml, and incubated at 37°C, 5% CO 2Cultured in an incubator for 24 hours. After the culture, all the medium was removed, and 100 ul of the sample diluted to an appropriate concentration (25 ug / ml to 200 ug / ml) in a medium not containing serum was treated in each well, and cultured for 24 hours. After culturing for 24 hours, the MTT reagent was dissolved in PBS at a concentration of 5 mg / ml, and 20 μl each was added to culture for 4 hours. Remove all the medium containing MTT reagents and samples, add 100ul of acid isopropanol to each well, and stir in a shaker for 10-15 minu...
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