Antineoplastic combined medicament with enhancing and poison-reducing character
A technology with anti-tumor and anti-tumor activity, which can be used in anti-tumor drugs, medical formulations containing active ingredients, drug combinations, etc.
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Embodiment 1
[0017] Example 1 Tumor cell types and cell culture method thereof
[0018] Cell lines and cell culture: The cells used in the experiment include cervical cancer Hela cells, brain glioma SWO-38 cells, liver cancer HepG2 cells, lung cancer LAC cells and breast cancer MCF-7 cells. The culture conditions of all cells are as follows: in a carbon dioxide cell incubator (37°C, saturated humidity, CO 2 Content 5%), grown in RPMI-1640 culture medium containing 10% fetal bovine serum and 100U / mL antibiotics. Cells were passaged every 3 to 4 days.
Embodiment 2
[0019] Example 2 Inhibitory effect of dihydroartemisinin and teniposide on tumor cell growth
[0020] Drug action: Collect cells in the logarithmic growth phase and disperse them in the culture medium to contain 5×10 4 A single cell suspension of cells. The cell suspension was inoculated in 96-well cell culture plates at 100 microliters per well, and cultured in a carbon dioxide cell incubator for 24 hours. The original culture solution was discarded, and 100 microliters of culture solution containing the drug to be tested was added to each 3 wells as a detection concentration, and the culture was continued for 72 hours to observe the effect of the drug on cell growth. In the experiment, the blank control of culture medium and the control of cells without drug treatment were set up. The half inhibitory concentration of drugs on cell growth was determined by MTT method.
[0021]The basic operation of the MTT method used: After the cells in the 96-well plate were treated with...
Embodiment 3
[0031] Example 3 Synergistic or synergistic effect of dihydroartemisinin combined with teniposide in inhibiting the growth of certain tumor cells
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