Application of vaccarin for resisting oxidation and high-glucose damage
A technology of flavonoid glycosides and anti-oxidation of Wang Bu Liuxing, which is applied in the directions of medical preparations containing active ingredients, applications, organic active ingredients, etc.
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[0008] Example 1: Wang Buliu Xing flavonoid glycosides on H 2 O 2 Induces improvement of EA·hy926 cell damage
[0009] Select the cells in the logarithmic growth phase, trypsinize to prepare a cell suspension, adjust the cell concentration, inoculate 8000 cells per well in a 96-well plate, inoculate 160 μL per well, set 4 multiple wells in each group, and randomly group after 24 hours : The normal group and the model group were added with 20μL serum-free medium, and the three treatment groups were added with the corresponding concentration of the same volume of flavonoid glycosides to make the final concentration of the drug 13.76, 6.88, 3.44μmol / L, respectively. After pre-protection at 37℃ for 12h, add 20μL of H to each well in the model group and Wangbuliuxing flavonoid glycoside group 2 O 2 The final concentration is 1000μmol / L. The normal control group is added with 20μL serum-free medium and incubated at 37℃ for 2h. Cell viability is detected by SRB method. See Table 1:
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[0019] Example 2: Wangbuliu Xing's flavone glycosides improve the damage of EA·hy926 cells induced by high glucose
[0020] Select the cells in the logarithmic growth phase, trypsinize to prepare a cell suspension, adjust the cell concentration, inoculate 8000 cells per well in a 96-well plate, inoculate 160 μL per well, and randomly group after 24 hours: normal group and model group add 20 μL Serum-free medium, the three treatment groups were added with the corresponding concentration of the same volume of Wangbuluxing flavonoid glycosides to make the final drug concentrations 13.76, 6.88, and 3.44 μmol / L respectively. After pre-protection at 37°C for 12 hours, In the model group and Wang Buliu Xing flavonoid glycoside group, 20μL glucose (final concentration 180mmol / L) was added to each well, and 20μL serum-free medium was added to the normal control group. Each group had 4 multiple wells. After incubating at 37°C for 24 hours, SRB detection Cell viability. See Table 3:
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