Extraction method and anti-tumor application of linumusitatissimum polyphenol
An extraction method, the technology of flax, which is applied in the field of extracting active ingredients of plants, can solve the problems that the anti-tumor activity of flax polyphenols has not been seen, and achieve the effects of promoting in-depth development and effective utilization, inhibiting cancer cell proliferation, and good anti-cancer activity
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Embodiment 1
[0029] Preparation of flax polyphenols:
[0030] (1) Get 500g of flax meal and separate it into grain shape;
[0031] (2) Add distilled water at a mass ratio of 1:3, stir in a water bath at 70°C for 1 hour, let stand, filter with double gauze, and rinse;
[0032] (3) Repeat step (2) several times until there is no viscose on the surface of the flax seeds, then completely dry the degummed flax seeds in an oven at 40°C and pulverize to obtain degummed flax powder;
[0033] (4) Get 20g of degummed flax powder, dissolve it in 1600mL of 60% ethanol, and conduct ultrasonic extraction at 50°C for 50 minutes at an ultrasonic power of 400W;
[0034] (5) centrifuge the mixed material liquid obtained in step (4) at 8000×rpm for 5 minutes, discard the precipitate, centrifuge once again under the same conditions, and collect the supernatant;
[0035] (6) Degrease the supernatant obtained in step (5), add ethyl acetate at a volume ratio of 1:1, centrifuge at 11000×rpm for 10 minutes, let ...
Embodiment 2
[0039] Select the DLD1, HCT-116, SW480, SW620, HT-29, A549, HeLa, HepG2, MCF-7 cancer cells and FHC normal cells in the logarithmic growth phase respectively, make the cells into cell suspension, and count the cells every Hole 3×10 3 Inoculated into a 96-well plate at 37°C, 5% CO 2 After culturing in the incubator for 24 hours and the cells adhered to the wall, the old medium was discarded, and medium with different final concentrations of flax polyphenols (0, 0.05, 0.1, 0.3, 0.5, 0.7, 0.9 mg / mL) was added, and six chambers were set up. For parallel wells, continue to culture the culture plate for 24 hours, add 20 μL of 5.0 mg / mL MTT to each well, and incubate for another 4 hours. Remove the culture medium in the plate, add 150 μL of DMSO to each well to dissolve the formazan crystals produced by the living cells, shake on a shaker for 10 min, and measure the absorbance in each well with a microplate reader at a wavelength of 570 nm.
[0040] The flax polyphenols obtained in...
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