Method for evaluating soothing efficacy of cosmetic raw materials
A technology for cosmetics and raw materials, applied in the analysis of materials, material analysis by optical means, instruments, etc., can solve the problems of high-throughput screening that cannot be efficiently, quickly and in large quantities, subjective factors in evaluation results, and long test periods, etc. Achieve objective and reliable evaluation results, meet high-throughput screening, and achieve the effect of short test period
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Embodiment 1
[0033] (1) Set up a blank control group: take zebrafish embryos fertilized for 16 hours, put them into a 96-well plate, 5 embryos per well, set 3 replicate wells in each group, add 200 μL of H-Buffer solution to each well, and culture for 1 Hour;
[0034] (2) Set up the model control group: take zebrafish embryos fertilized for 16 hours, put them into a 96-well plate, 5 embryos per well, set 3 duplicate wells for each group, add 200 μL of dodecane to each well in the form of a solution Sodium sulfonate was added at a concentration of 200 μmol / L and incubated for 1 hour. The concentration of the added sodium dodecylsulfonate solution is above the minimum percutaneous stimulation concentration.
[0035] (3) Set the sample group to be tested: take zebrafish embryos fertilized for 16 hours, put them into a 96-well plate, 5 embryos per well, set 3 duplicate wells for each group, and add 200 μL of glycyrrhizic acid to each well in the form of a solution A mixture of dipotassium and ...
Embodiment 2
[0038] (1) Set up a blank control group: take zebrafish embryos fertilized for 24 hours, put them into a 96-well plate, 5 embryos per well, set 3 replicate wells for each group, add 200 μL of H-Buffer solution to each well, and culture for 1 Hour;
[0039] (2) Set up the model control group: take zebrafish embryos fertilized for 24 hours, put them into a 96-well plate, 5 embryos per well, set 3 duplicate wells for each group, and add 200 μL of dodecane to each well in the form of a solution Sodium sulfonate was added at a concentration of 200 μmol / L and incubated for 1 hour;
[0040] (3) Set the sample group to be tested: take zebrafish embryos fertilized for 24 hours, put them into a 96-well plate, 5 embryos per well, set 3 duplicate wells for each group, add 200 μL of snow to each well in the form of a solution The mixture of glucoside and sodium dodecylsulfonate was incubated for 1 hour. The concentration of sodium dodecylsulfonate was 200 μmol / L, and the concentration of...
Embodiment 3
[0043] (1) Set up a blank control group: take zebrafish embryos fertilized for 36 hours, put them into a 96-well plate, 5 embryos per well, set 3 replicate wells for each group, add 200 μL of H-Buffer solution to each well, and culture for 1 Hour;
[0044] (2) Set up the model control group: take zebrafish embryos fertilized for 36 hours and place them in a 96-well plate, with 5 embryos per well, and set 3 duplicate wells for each group, and add 200 μL of dodecane to each well in the form of a solution Sodium sulfonate was added at a concentration of 200 μmol / L and incubated for 1 hour;
[0045] (3) Set up the sample group to be tested: take the zebrafish embryos fertilized for 36 hours, put them into a 96-well plate, and set up 3 replicate wells for each group, and add 200 μL of proanthocyanidins and The mixture of sodium dodecylsulfonate was incubated for 1 hour. The concentration of sodium dodecylsulfonate was 200 μmol / L, and the concentration of proanthocyanidins was wit...
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