Preparation method of mulberry polysaccharide-iron chelate with anti-oxidation activity
A technology of antioxidant activity, mulberry polysaccharide, applied in the directions of antitoxin, drug combination, blood diseases, etc., can solve the problems of insufficient preparation and purification of polysaccharide, high cost of ethanol production, and inability to eliminate influence, etc., to achieve mass production, cost Low, improved absorption effect
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Embodiment 1
[0035]The preparation method of Sevage reagent described in step (2) in embodiment 1, embodiment 2 and embodiment 3 is that chloroform, n-butanol are mixed by volume ratio 4: 1, and the method of Sevage method deproteinization is polysaccharide and Sevage reagent Mix at a volume ratio of 1:4, shake for 20 minutes, centrifuge at 5000r / min for 5 minutes, take out the polysaccharide solution in the upper layer, and repeat the above steps for 10 to 13 times until the protein is completely removed.
[0036] Example 1
[0037] (1) Extraction of mulberry polysaccharides: After 500 g of mulberries were dried naturally, they were refluxed with 95% ethanol at 70° C. for 4 hours to remove small molecular impurities such as lipids and pigments. Extract in a water bath at 90° C. for 2 hours, twice in total. After concentrating the water extract, add 80% ethanol for alcohol precipitation to obtain crude polysaccharide.
[0038] (2) Separation of mulberry polysaccharides: After removing pro...
Embodiment 2
[0043] (1) Extraction of mulberry polysaccharides: After 500 g of mulberries were dried naturally, they were refluxed with 95% ethanol at 70° C. for 4 hours to remove small molecular impurities such as lipids and pigments. Extract in a water bath at 90° C. for 2 hours, twice in total. After concentrating the water extract, add 80% ethanol for alcohol precipitation to obtain crude polysaccharide.
[0044] (2) Separation of mulberry polysaccharides: After removing protein from mulberry polysaccharides by Sevage method, the macroporous resin AB-8 was used to decolorize the polysaccharides by static adsorption, and the solution was clarified by shaking at 400 rpm at room temperature. The supernatant was concentrated and dialyzed against distilled water for 72h. Finally, 40% ethanol was added for ethanol precipitation, 5000r / min, centrifuged for 5min, the supernatant was discarded, the precipitate was dissolved in distilled water, and the obtained solution was freeze-dried to obtai...
Embodiment 3
[0050] (1) Extraction of mulberry polysaccharides: After 500 g of mulberries were dried naturally, they were refluxed with 90% ethanol at 90° C. for 5 hours to remove small molecular impurities such as lipids and pigments. The water bath was extracted at 70° C. for 4 hours, twice in total. After the water extract was concentrated, 40% ethanol was added for alcohol precipitation to obtain the crude polysaccharide.
[0051] (2) Separation of mulberry polysaccharides: After the mulberry polysaccharides were deproteinized by the Sevage method, the macroporous resin AB-8 was used to decolorize the polysaccharides by static adsorption, and the solution was clarified by shaking at room temperature at 500 rpm. The supernatant was concentrated and dialyzed against distilled water for 48 h. Finally, 20% ethanol was added for ethanol precipitation, 4500r / min, centrifuged for 10min, the supernatant was discarded, the precipitate was dissolved in distilled water, and the obtained solution ...
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