Method for screening skin barrier function enhancing agent based on epidermal serine racemase and/or d-serine level, and skin barrier function evaluation method
a skin barrier and function-enhancing agent technology, applied in the direction of biological material analysis, plant/algae/fungi/lichens ingredients, peptides, etc., can solve the problems of dermatitis and allergy, skin moisture loss, and significant burden on the skin, so as to improve or enhance the skin barrier function
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example 1
Verification of Relationship Between D-Serine Content and Barrier Function in Stratum Corneum
[0069]The subjects were 57 volunteers having healthy test sites, and the test sites wetted by rinsing after cleaning by a prescribed method were allowed to stand for 30 minutes at constant temperature, constant humidity conditions (room temperature: 22° C., humidity: 45%). Next, the transepidermal water loss (TEWL) was measured with a Vapometer (Delfin Co.). Measurement was performed 3 times and the average value was subsequently used for analysis. Next, the stratum corneum at the TEWL-measured site was stripped twice using adhesive tape and the second was used for extraction of amino acids in a 95% methanol aqueous solution. The optical isomers of the extracted amino acids were analyzed by a reported method (reference: Yurika Miyoshi et al., Journal of Chromatography B, 877 (2009) 2506-2512). The results are summarized below. The extracted amino acids were subjected to fluorescent derivatiz...
example 2
Variation in D-Serine Content with Induced Differentiation of Keratinocytes
Cell Culturing and Drug Preparation
[0071]Normal human keratinocytes were seeded in a 24 well multiplate to a cell density of 2.5×104 cells / well, and cultured in KGM culture medium (Kurabo Industries, Ltd.) under conditions of 37° C., 5% CO2. After 3 days, the medium was exchanged with KGM culture medium to which 1.8 mM calcium chloride and 10 mM L-serine had been added (test group), or KGM culture medium to which 10 mM L-serine alone had been added (control group), and culturing was continued for another 2 days.
HPLC Sample Preparation and Free D-Serine Analysis by HPLC.
[0072]After rinsing cells with PBS, 500 μL of a 5% trichloroacetic acid aqueous solution was added, the cells were thoroughly dispersed and recovered, and ultrasonic treatment was performed for 30 minutes on ice, after which centrifugal separation was performed to obtain a supernatant. The amino acids in the supernatant were extracted by additi...
example 3
Screening of Candidate Drugs
Cell Culturing and Drug Preparation
[0073]Normal human keratinocytes were seeded in a 24 well multiplate to a cell density of 2.5×104 cells / well, and cultured in KGM culture medium (Kurabo Industries, Ltd.) under conditions of 37° C., 5% CO2. After 3 days, the medium was exchanged with KGM culture medium containing 1.8 mM calcium chloride, 10 mM L-serine and the candidate drug diluted solution, and culturing was continued for another 2 days. Seven drugs were used as candidate drugs, of which one was a 0.5% hydrolyzed oat protein solution.
HPLC Sample Preparation and Free D-Serine Analysis by HPLC.
[0074]After rinsing cells with PBS, 500 μL of a 5% trichloroacetic acid aqueous solution was added, the cells were thoroughly dispersed and recovered, and ultrasonic treatment was performed for 30 minutes on ice, after which centrifugal separation was performed to obtain a supernatant. The amino acids in the supernatant were extracted by addition of a 20-fold amoun...
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