Application of raspberry extract in the preparation of drugs for the prevention and treatment of retinal damage diseases
A retinal injury, raspberry technology, applied in the direction of drug combination, sensory disease, cardiovascular system disease, etc., to achieve the effect of strong protective effect, strong protective effect and high drug efficacy
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Embodiment 1
[0044] Example 1 Raspberry Extract
[0045] (1) Extraction process, such as figure 1
[0046] Take 400g raspberries, grind them into powder, and extract twice with 3200mL and 2400mL of 70% ethanol under reflux, each time for 1.5h, combine the extracts, recover the ethanol under reduced pressure, and obtain 370mL extracts, and transfer the obtained 370mL extracts into a large Carry out chromatographic separation on a porous adsorption resin column, elute with 95% ethanol, and recover the ethanol solvent from the obtained eluate under reduced pressure to obtain 24.49 g ethanol eluate (FPZ-Z).
[0047] The 15.00g ethanol eluate (FPZ-Z) was separated by ODS column chromatography, and eluted with 20% methanol aqueous solution, 40% methanol aqueous solution, 70% methanol aqueous solution and 100% methanol respectively to obtain 20% methanol aqueous solution elution 4.33 g of the product was designated as FPZ-20, 5.66 g of the product eluted with 40% methanol aqueous solution was d...
Embodiment 2
[0057] (1) H 2 o 2 Establishment of induced retinal-associated cell (ARPE-19, RGC5, Muller) damage model
[0058] ARPE-19 cells were subcultured according to 2×10 5 cell / ml drop plate, 100ul / well. After 24h, different concentrations of H 2 o 2 (0mM, 0.5mM, 1mM, 1.5mM, 2mM) acted on ARPE-19 cells for 24h respectively. Coloring: Add 20ul of MTT solution to each well and continue to incubate for 2-4h. Colorimetry: Select a wavelength of 490nm, measure the light absorption value of each well on an enzyme-linked immunosorbent monitor, record the results, and use different concentrations of H 2 o 2 The cell growth curve is drawn as the abscissa and the absorbance value as the ordinate. When the cell viability was around 50%, the H 2 o 2 The concentration was used as the modeling concentration of the oxidative damage model.
[0059] Figure 3A different concentrations of hydrogen peroxide (H 2 o 2 ) to establish the ARPE-19 cell model. Depend on Figure 3A It can be s...
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