Application of puer tea for eliminating formaldehyde biological damage
A technology for eliminating formaldehyde and Pu'er tea, applied in the field of Pu'er tea, can solve the problem that the biological hazard of formaldehyde in Pu'er tea has not been discovered, and achieve the effect of avoiding biological toxicity
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Embodiment 1
[0038] Inoculate 1x10 5 -1x10 6 Put mouse embryonic fibroblasts on glass slides in six-well cell culture plates, use DMEM+10% FBS medium, and culture them in a 37°C, 5% CO2, 3% O2 incubator for 12 to 24 hours. Pu-erh tea with a final concentration of 0.05 mg / ml was added for co-cultivation for 6 hours, and the blank control was co-cultivated without Pu-erh tea. Then, add 100-300 μmol / L formaldehyde to the cells of Pu'er tea protection group and blank control group respectively. At four time points of 30min, 1hr, 3hr, and 5hr, the morphological changes of cells were observed by differential interference imaging (DIC) microscopy, and Annexin V fluorescent staining was performed.
Embodiment 2
[0040] Inoculate 1x10 5 -1x10 6Put mouse embryonic fibroblasts on glass slides in a six-well cell culture plate, use DMEM+10% FBS medium, and culture in a 37°C, 5% CO2, 3% O2 incubator for 12-24 hours, Pu-erh tea with a final concentration of 0.25 mg / ml was added for co-cultivation for 6 hours, and the blank control was co-cultivated without Pu-erh tea. Then, add 100-300 μmol / L formaldehyde to the cells of Pu'er tea protection group and blank control group respectively. At four time points of 30min, 1hr, 3hr, and 5hr, the morphological changes of cells were observed by differential interference imaging (DIC) microscopy, and Annexin V fluorescent staining was performed.
Embodiment 3
[0042] Inoculate 1x10 5 -1x10 6 Put mouse embryonic fibroblasts on glass slides in six-well cell culture plates, use DMEM+10% FBS medium, and culture them in a 37°C, 5% CO2, 3% O2 incubator for 12 to 24 hours. Pu-erh tea with a final concentration of 0.05 mg / ml was added for co-cultivation for 24 hours, and the blank control was co-cultivated without Pu-erh tea. Then, add 100-300 μmol / L formaldehyde to the cells of Pu'er tea protection group and blank control group respectively. At four time points of 30min, 1hr, 3hr, and 5hr, the morphological changes of cells were observed by differential interference imaging (DIC) microscopy, and Annexin V fluorescent staining was performed.
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