Application of sodium oxamate in preparing drugs for radiotherapy sensitization
The technology of sodium oxalate and drug is applied in the application field of preparing radiotherapy sensitization drugs, which can solve the problems such as no reports on radiotherapy sensitization of sodium oxamate, and achieve the effect of improving radiotherapy sensitivity.
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Embodiment 1
[0017] (1) Cell culture: The cells were cultured in DMEM medium containing 10% calf serum, glutamine and 1 million U / L penicillin and streptomycin. Cells were placed in 5% CO 2 , cultured in an incubator at 37°C, passaged once every 2-3 days, and cells in logarithmic growth phase were used for experiments.
[0018] (2) CCK-8 colorimetric method: cells in logarithmic growth phase (5×10 24 hours before drug treatment) 4 / mL) were inoculated into 96-well plates, and 6 parallel wells were set for each concentration. Different concentrations of sodium oxamate were added to continue the incubation for 12, 24 or 48 hours. Add 10 μL of CCK-8 reagent to the cell culture medium and continue to culture for 1-4 hours. The absorbance at 450 nm was measured using a microplate reader. Finally, the cell viability was calculated by the formula of cell viability=value of drug-added group / value of control group×100%.
[0019] The result is as figure 1 As shown, the results showed that sodi...
Embodiment 2
[0021] (1) cell culture is with embodiment one;
[0022] (2) Cell clone formation method: take cells in logarithmic growth phase, and inoculate different numbers of cells into 60 mm culture dishes according to different irradiation dose requirements (the number of cells inoculated at 0, 2, 4, 6, and 8 Gy doses is 400, respectively. , 2000, 6000, 1000 and 15000). After 24 hours, the combined sodium oxalate and radiation group were treated with 0.75 μmol / L sodium oxalate for 24 hours, and the control group was treated with the same amount of absolute ethanol as a negative control. The cells in the two groups received different doses (0-8Gy) of γ-ray irradiation at the same time, and continued to culture for 24 hours after the irradiation. Both groups were replaced with ordinary medium, and the culture was continued until obvious cell clones appeared in the culture dish. . The culture medium was discarded, washed twice with PBS, fixed with anhydrous methanol for 30 minutes, sta...
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