Method for improving antioxidant activity of pueraria flavone
A technology of antioxidant activity, pueraria flavonoids, applied in the functions of food ingredients, food science, applications, etc., can solve the problems of complex products, hinder the application of modified products, etc., and achieve the effects of no toxic solvent residues and mild reaction conditions.
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Embodiment 1
[0038] Weigh 5g of Pueraria flavonoids powder, add pH5.5 citric acid-disodium hydrogen phosphate buffer solution according to the ratio of solid to liquid (g / mL) 1:5, add 5g of β-glucosidase, and hydrolyze at 40°C for 1h. After the reaction, suction filtration was performed, and the filtrate was extracted twice with 50 mL of food-grade ethyl acetate. The extract was distilled off under reduced pressure at 40°C to remove ethyl acetate, and dried under vacuum at 40°C.
[0039] The vacuum-dried sample was dissolved in ethanol to make a concentration of 5g / L, and the DPPH radical scavenging rate was determined to be 73.42%, the total reducing power was 0.375, and the hydroxyl radical scavenging rate was 12.47%.
Embodiment 2
[0041] Weigh 5g of Pueraria flavonoids powder, add pH6 citric acid-disodium hydrogen phosphate buffer solution according to the ratio of solid to liquid (g / mL) 1:5, add 5g of β-glucosidase, and hydrolyze at 30°C for 1h. After the reaction, suction filtration was performed, and the filtrate was extracted twice with 50 mL of food-grade ethyl acetate. The extract was distilled off under reduced pressure at 40°C to remove ethyl acetate, and dried under vacuum at 40°C.
[0042] The vacuum-dried sample was dissolved in ethanol to make a concentration of 5g / L, and the DPPH radical scavenging rate was determined to be 61.59%, the total reducing power was 0.268, and the hydroxyl radical scavenging rate was 9.86%.
Embodiment 3
[0044] Weigh 5g of Pueraria flavonoids powder, add pH6 citric acid-disodium hydrogen phosphate buffer solution according to the ratio of solid to liquid (g / mL) 1:5, add 5g of β-glucosidase, and hydrolyze at 45°C for 1h. After the reaction was finished, it was filtered with suction, and the filtrate was extracted twice with 50 mL of food-grade ethyl acetate. The extract was distilled off under reduced pressure at 40°C to remove ethyl acetate, and dried under vacuum at 40°C.
[0045] The vacuum-dried sample was dissolved in ethanol to make a concentration of 5g / L, and the DPPH radical scavenging rate was determined to be 85.96%, the total reducing power was 0.452, and the hydroxyl radical scavenging rate was 18.47%.
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