Application of cuphea hossipifolia kunth extractives in cosmetics and medicines
A technology of Calyx chinensis and its extract, which is applied in the field of cosmetics and medical supplies, and can solve the problems of moisturizing, whitening and anti-oxidation that have not been seen
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Embodiment 1
[0044] Plant material and extraction method:
[0045] 4.4 kg Cuphea hossipifolia Kunth dried in the sun, crushed, soaked in ethanol three to four times at room temperature, filtered, and the ethanol solution was concentrated under reduced pressure to obtain an extract (292.5 grams). After adding an appropriate amount of water to 20 g of the extract, extract with ethyl acetate to obtain ethyl acetate (9.23 g) and water components. The aqueous layer was passed through a D101 macroporous resin column, and the column was eluted with water, 25% methanol-water, 50% methanol-water, 75% methanol-water and methanol to obtain different fractions, water (11.68 grams), 25% methanol - water (0.32 g), 50% methanol-water (0.18 g), 75% methanol-water (0.34 g) and methanol (0.09 g) (see figure 1 ). The silica gel column chromatography of the ethyl acetate fraction was eluted with petroleum ether, 25% acetone-petroleum ether, 50% acetone-petroleum ether, 75% acetone-petroleum ether, acetone a...
Embodiment 2
[0064] Toxic activity test on B16 cells:
[0065]On a 96-well cell culture plate, mix B16 cells with different concentrations of the drug solution to be tested, set up 8 replicate wells, and set a blank control without drug at the same time, 37 ° C, 5% CO 2 After culturing for 24 hours, the cytotoxicity was detected by the MTS colorimetric method, and the OD value was measured by a microplate reader at a wavelength of 490 nm. Calculated to get CC 50 The value (50% cytotoxic concentration) is the concentration of the drug that produces toxicity to 50% of B16 cells.
[0066] Table 1 The results of the toxic effect of samples on B16 cells
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Embodiment 3
[0071] In vitro antioxidant activity test:
[0072] Mix and react the drug to be tested with DPPH (final concentration: 100 μM), set up 3 replicate wells, and set a blank control without drug and Trolox positive control at the same time, at 30°C for 1 h, measure the OD value with a microplate reader, and the detection wavelength is 515nm. Calculate the antioxidant rate.
[0073] Table 2 In vitro antioxidant activity results of samples
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