Medical applications of stringy stonecrop ethamol soluble extractive
A technology for the alcohol extract of Cercis chinensis, which is applied in the field of medical application of the alcohol extract of C. cycle effect
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Embodiment 1
[0017] Embodiment 1: the preparation of weeping pot grass ethanol extract
[0018] Soak 500g of syringa hay in 5000mL of 95% ethanol for 5 days, filter with gauze, and collect the liquid medicine. Repeat 2 times, combine the liquid medicines, centrifuge to take the supernatant, evaporate the obtained supernatant under reduced pressure to remove the solvent, extract with 1000mL of petroleum ether to remove the lipid, evaporate the petroleum ether, then dissolve it with 100mL of methanol, and evaporate to dryness under reduced pressure. Dry to obtain alcohol extract.
Embodiment 2
[0019] Example 2: Inhibitory effect of ethanol extract on the proliferation of liver cancer cells
[0020] The ethanol extract was dissolved in DMSO and diluted with RPMI1640 medium to make the final concentration of DMSO 0.1%, and sterilized through a sterile filter for use. Human liver cancer cell line HepG2 was placed in RPMI1640 culture medium containing 10% calf serum at 37°C and 5% CO 2 cultured in an incubator. The tumor cells were cultured to the logarithmic growth phase, and the cell concentration was adjusted to 1×10 4 cells / ml, inoculated in 96-well plates, 100 μl / well, after 4 hours of adherence, added alcohol extracts to make the final concentrations of 25, 50, 100, and 200 μg / ml respectively, and set up a negative control group (RPMI1640 medium) And 0.1% DMSO solvent control group, set 6 parallel wells for each group, continue to culture for 24, 48, 72 hours, and detect the proliferation results by MTT method.
[0021] The effect of each dose group on HepG2 is...
Embodiment 3
[0025] Example 3: Cell cycle detection by flow cytometry:
[0026] 1×10 HepG2 cells were collected from the control group and the HepG2 cells after each dose of ethanol extract for 48 hours. 6 1, PI staining, cell cycle analysis by flow cytometry, the results are shown in Figure 1. Flow cytometry analysis showed that the ethanol extract could arrest liver cancer cells in G0 / G1 phase, thereby inhibiting its proliferative activity.
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