Method for evaluating toxicity of cosmetic basic raw materials to infant development by using zebra fish
A basic raw material, zebrafish technology, applied in the direction of analysis of materials, material inspection products, climate change adaptation, etc., can solve the problems of long experimental period, large animal damage, and complicated experiments, and achieve reliability, high accuracy, and experimental results. Simple operation effect
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Embodiment 1
[0032] The selection of embodiment 1 basic raw material safety concentration to be tested
[0033] 1) Select the wild zebrafish AB strain embryos that have just been fertilized successfully, cultivate for 24-72h, and remove the dead embryos during the period;
[0034] 2) All remaining embryos are divided into five groups, wherein one group is the control group, and the other four groups are the treatment groups, each group has 20 embryos, and each group is set up with three repeat groups;
[0035] 3) select DMSO to dissolve phenoxyethanol, then prepare the medicinal liquid of 0, 5, 10, 20, 40 μg / mL with the culture medium, according to the size of the feeding vessel, prepare medicinal liquids of different volumes, if put into the culture dish of 6cm It is more suitable for the volume of the preparation liquid to exceed 5mL, and it is necessary to ensure that the DMSO concentration in each group is less than 1 / 1,000 to ensure that DMSO will not cause damage to the embryo;
[0...
Embodiment 2
[0039] Example 2 Detection of the effect of phenoxyethanol solution treatment on the heart rate of zebrafish embryos
[0040] 1) Select the wild zebrafish AB strain embryos that have just been fertilized successfully, cultivate for 24-72h, and remove the dead embryos during the period;
[0041] 2) All remaining embryos are divided into three groups, wherein one group is the control group, and the other two groups are the treatment groups, each group has 20 embryos, and each group is set up with three groups of repetition groups;
[0042]3) select DMSO to dissolve phenoxyethanol, and then prepare the medicinal liquid of 0, 5, and 10 μg / mL with culture medium, and wherein it is necessary to ensure that the DMSO concentration in each group is less than one thousandth to ensure that DMSO will not cause damage to the embryo;
[0043] 4) Transfer the zebrafish embryos to the prepared culture medium for exposure, and then place them in a constant temperature light-controlled incubato...
Embodiment 3
[0046] Example 3 Detection of the effect of phenoxyethanol solution treatment on the development of zebrafish
[0047] 1) Select the wild zebrafish AB strain embryos that have just been fertilized successfully, cultivate for 24-72h, and remove the dead embryos during the period;
[0048] 2) All remaining embryos are divided into three groups, wherein one group is the control group, and the other two groups are the treatment groups, each group has 20 embryos, and each group is set up with three groups of repetition groups;
[0049] 3) select DMSO to dissolve phenoxyethanol, and then prepare the medicinal liquid of 0, 5, and 10 μg / mL with nutrient solution, and wherein need to ensure that the DMSO concentration in each group is less than one thousandth;
[0050] 4) Transfer the zebrafish embryos to the prepared culture medium for exposure, and then place them in a constant temperature light-controlled incubator for cultivation, and observe once every 24 hours;
[0051] 5) After...
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