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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Embodiment 1
[0008] Embodiment 1: the effect of flavonoid glycosides of wangbuliuxing on H 2 o 2 Induced EA·hy926 cell injury improvement
[0009] Select cells in logarithmic growth phase, trypsinize to make cell suspension, adjust cell concentration, inoculate 8000 cells per well in 96-well plate, inoculate 160 μL in each well, set 4 duplicate wells in each group, and randomly group them after 24 hours : The normal group and the model group were added with 20 μL of serum-free medium, and the three drug groups were respectively added with the corresponding concentration and equal volume of flavonoid glucoside liquid, so that the final concentrations of the drug were 13.76, 6.88, and 3.44 μmol / L respectively. After pre-protection incubation at 37°C for 12 hours, 20 μL of H 2 o 2 , the final concentration of which was 1000 μmol / L. The normal control group was added with 20 μL of serum-free medium, incubated at 37°C for 2 hours, and the cell viability was detected by SRB method. See Table...
Embodiment 2
[0019] Example 2: Improvement of high glucose-induced EA·hy926 cell damage by flavonoid glycosides
[0020] Select cells in the logarithmic growth phase, trypsinize to make cell suspension, adjust the cell concentration, inoculate 8000 cells per well in a 96-well plate, inoculate 160 μL in each well, and randomly divide into groups after 24 hours: normal group and model group add 20 μL In the serum-free medium, the 3 administration groups were respectively added with the corresponding concentration and equal volume of flavonoid glucoside liquid, so that the final concentration of the drug was 13.76, 6.88, and 3.44 μmol / L respectively, and incubated at 37°C for 12 hours after pre-protection, Add 20 μL of glucose (final concentration: 180 mmol / L) to each well of the model group and the blancillin group, add 20 μL of serum-free medium to the normal control group, set up 4 duplicate wells in each group, incubate at 37°C for 24 hours, and detect with SRB method cell viability. See...
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