Effects of Artemisinin B on Inhibiting Migration and Invasion of A549 Cells
A cell migration, artemisinin technology, applied in the field of medicine, can solve problems such as toxicity
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Embodiment 1
[0018] Example 1: Effect of artemisinin B on A549 cell clone formation
[0019] Take the monolayer cultured cells in the logarithmic growth phase, and prepare a cell suspension of 100 cells / mL. Cells were seeded in 6-well plates, 2 mL / well, 37°C, 5% CO 2 Incubate overnight in an incubator. Dosing culture: Discard the supernatant in the well, add artemisinin B liquid (0.625, 1.25, 2.5 and 5 μM) 2 mL / well, set 3 replicate wells for each concentration. The experiment set up a drug-dosing group and a negative control group, at 37°C, 5% CO 2 Continue culturing for 14 days under the same conditions, observe the cloning situation, and change the medium once during the period. After culturing for 14 days, the old culture medium in the culture plate was discarded, washed twice with PBS, and the cells were fixed with methanol for 30 min. Crystal violet staining was carried out for 30 min, and the excess staining solution was rinsed by soaking in tap water. Place the 6-well plate on...
Embodiment 2
[0021] Example 2: Effect of Artemisinin B on A549 Cell Adhesion
[0022] Take monolayer cultured cells in the logarithmic growth phase, and prepare 10 5 cells / mL of cell suspension. Artemisinin B solutions were prepared with cell suspension, and the final concentrations were 40, 20, 10, and 5 μM, respectively. B cell suspensions containing different concentrations of artemisinin were inoculated in 6-well plates, 2 ml / well, with 3 replicate wells for each concentration. The experiment consisted of a dosing group and a negative control group. 37°C, 5% CO 2 After culturing for 2.5 h in an incubator, gently wash twice with PBS to remove unattached cells. Fix with methanol for 1 h, stain with crystal violet for 1 h, soak in tap water to rinse excess staining solution, take pictures and count.
[0023] The results showed that when the concentration of artemisinin B was 20 μM and 40 μM, the number of adhered cells was significantly less than that of the control group, and the in...
Embodiment 3
[0024] Example 3: Effect of Artemisinin B on A549 Cell Migration
[0025] ① Scratch healing experiment: draw a line on the bottom of the 6-well plate with a ruler and a marker pen, and divide the wells into 3 parts. Prepare 5×10 5 Cells / mL cell suspension, seeded in 6-well plate, 2 mL / well, confluent overnight. Scratch: Use a 10 μL pipette tip to make a scratch, the scratch passes through the three lines at the bottom, wash the cells twice with PBS, remove the scratched cells, and take pictures. Dosing culture: prepare 4 different concentrations of artemisinin B solutions (ie 40, 20, 10, 5 μM), 2 mL / well, 3 replicate wells for each concentration, and set the dosing group and negative control group in the experiment. 37°C, 5% CO 2 Observed and photographed after 24 h in the incubator.
[0026] ② Transwell migration experiment: prepare 8×10 4 cells / 200 μl of cell suspension, the cell suspension was used to prepare different concentrations of artemisinin B solutions (0, 5, 1...
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