Method for evaluating moisturizing effect of cosmetics
A technology for cosmetics and water replenishment, which is applied in the direction of measuring devices, material analysis through optical means, instruments, etc., can solve the problems of long detection time, high professionalism, and low accuracy, and achieve short experiment cycle, strong comparability, and low cost. low effect
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Embodiment 1
[0027] (1) Randomly select 120 melanin allele mutant translucent AL strain zebrafish 2 days after fertilization (2dpf) in a six-well plate, each well has a capacity of 3 mL, and each well is treated with 30 zebrafish, and 3.125 μL of / mL Cosmetic 1# to be tested and 9mg / mL0.9wt% sodium chloride solution, treated zebrafish for 24 hours in a water-soluble exposure mode, and established a sample group;
[0028] (2) Select zebrafish 2 days after fertilization with the same number as in step (1), without any treatment, and establish a blank control group;
[0029] (3) Select zebrafish 2 days after fertilization with the same number as in step (1), add 9mg / mL 0.9wt% sodium chloride solution, and treat zebrafish with water-soluble exposure for 24h to establish a microosmotic water-deficient model group;
[0030] (4) Add 3 mL of culture water to the experimental group, blank control group and inducer control group, respectively, and incubate at a constant temperature of 28° C. for 18 ...
Embodiment 2
[0034](1) Randomly select 120 melanin allele mutant translucent AL strain zebrafish 2 days after fertilization (2dpf) in a six-well plate, each well has a capacity of 3 mL, and each well is treated with 30 zebrafish, and 6.25 μL of / mL Cosmetic 2# to be tested and 9mg / mL0.9wt% sodium chloride solution, treated zebrafish for 24h in water-soluble exposure mode, and established a sample group;
[0035] (2) Select zebrafish 2 days after fertilization with the same number as in step (1), without any treatment, and establish a blank control group;
[0036] (3) Select zebrafish 2 days after fertilization with the same number as in step (1), add 9mg / mL 0.9wt% sodium chloride solution, and treat zebrafish with water-soluble exposure for 24h to establish a microosmotic water-deficient model group;
[0037] (4) The experimental group, the blank control group and the inducer control group were respectively added with 3 mL of breeding water, and cultured at a constant temperature at 28° C....
Embodiment 3
[0040] (1) Randomly select 120 translucent AL strain zebrafish with melanin allele mutation 2 days after fertilization (2dpf) in a six-well plate, each well has a capacity of 3 mL, and each well is treated with 30 zebrafish, adding 12.5 μL / mL Cosmetic 3# to be tested and 9mg / mL0.9wt% sodium chloride solution, treated zebrafish for 24 hours in a water-soluble exposure mode, and established a sample group;
[0041] (2) Select zebrafish 2 days after fertilization with the same number as in step (1), without any treatment, and establish a blank control group;
[0042] (3) Select zebrafish 2 days after fertilization with the same number as in step (1), add 9mg / mL 0.9wt% sodium chloride solution, and treat zebrafish with water-soluble exposure for 24h to establish a microosmotic water-deficient model group;
[0043] (4) The experimental group, the blank control group and the inducer control group were respectively added with 3 mL of breeding water, and incubated at the same tempera...
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