Application of tegaserod maleate in preparation of antitumor drug
A technology of tegaserod maleate and anti-tumor drugs, which is applied in the field of tumor treatment and prevention, and can solve problems such as lack of research
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Embodiment 1
[0026] Embodiment 1: Cytotoxicity experiment
[0027] Experimental process: KYSE 150 cells were seeded in 96-well plates at 8,000 per well and cultured with 1640 medium, KYSE450 cells were inoculated at 12,000 per well in 96-well plates and cultured with DMEM medium (37°C, 5% CO 2 ), after 16-18 hours, the final concentration of 50 mM tegaserod maleate plus DMSO solution was gradiently diluted to 0, 3.125, 6.25, 12.5, 25 mM, and the drug-containing medium was prepared according to 1:1000, so that The drug concentration of tegaserod maleate in the medium reached 0, 3.125, 6.25, 12.5, 25, 50 μM, added the above-mentioned drug-containing medium, cultured for 24 hours and 48 hours respectively, and then treated with 4% paraformaldehyde Fix the cells at 100 μL per well, then add DAPI staining solution (DAPI stock solution: 1×PBS=1:5000 dilution, Beijing Suolaibao Technology Co., Ltd.), 100 μL per well, and incubate at 37°C for at least 20 min After staining, put the 96-well plate ...
Embodiment 2
[0029] Embodiment 2: cell proliferation experiment
[0030] Experimental process: KYSE 150 cells were seeded in 96-well plates at 2000 per well and cultured with 1640 medium, KYSE450 cells were seeded at 4000 per well in 96-well plates and cultured with DMEM medium (37°C, 5% CO 2), after 16-18 hours, replace the fresh medium (KYSE 150 cells use 1640 medium; KYSE 450 cells use DMEM medium), and add different amounts of tegaserod maleate (0, 0.25, 0.5, 1, 2.5 μM is the final concentration), after culturing for 0, 24, 48, 72, and 96 hours respectively, fix the cells with 4% paraformaldehyde at 100 μL per well, and then prepare DAPI staining solution (DAPI stock solution) at 1:5000 : 1×PBS=1:5000 dilution, Beijing Soleibao Technology Co., Ltd.), 100 μL per well, incubate at 37°C for at least 20 minutes for staining, and finally put the 96-well plate into IN Cell Analyzer 3000, take pictures and count.
[0031] Experimental results such as figure 1 B, figure 2 Shown in B. It ...
Embodiment 3
[0032] Embodiment 3: soft agar colony formation experiment
[0033] Experimental process: Spread 3 ml of drug-containing medium in each well of a 6-well plate (KYSE 150 cells use 1640 medium; KYSE450 cells use DMEM medium), so that the final concentration of tegaserod maleate reaches 0, 0.25, 0.5, 1, 2.5 μM, after solidification, spread into the upper layer gel with 8000 esophageal cancer cells KYSE 150 or KYSE 450 suspended (the upper layer gel composition: 40% 2×BME; 40% Agar glue; 10% FBS; 9% Sterile water; 1% glutamine; 0.1% gentamicin), put it into the incubator (37°C, 5% CO 2 ) culture, choose an appropriate time to terminate the culture according to the colony formation, and use IN Cell Analyzer 3000 to take pictures and count and analyze.
[0034] Experimental results such as figure 1 C, figure 2 C shown. It can be found that as the concentration of tegaserod maleate increases, the number of clones gradually decreases, indicating that at low toxic concentrations, ...
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