White fungus composite solid beverage having anti-oxidation function and preparation method of white fungus composite solid beverage
A solid beverage and anti-oxidation technology, which is applied to the functions of food ingredients, food ingredients containing oligosaccharides, food science, etc., can solve the problems of high production cost, cumbersome process, and single form, so as to solve the cost and enhance the strength of blood vessels , easy to absorb effect
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Embodiment 1
[0043] A white fungus composite solid drink with anti-oxidation function, its raw material components include: 30-40 parts of white fungus superfine powder, 10-20 parts of fructo-oligosaccharide, 2-8 parts of inulin, rain raw red 0.02-0.08 parts of coccus, 0.02-0.08 parts of euglena, 0.02-0.08 parts of grape seed extract, 40-50 parts of sorbitol.
[0044] Said a kind of white fungus composite solid beverage with anti-oxidation function, according to the optimal weight parts, its raw material components include: 35 parts of white fungus superfine powder, 15 parts of fructooligosaccharide, 5 parts of inulin, rain raw red ball Algae 0.05 parts, Euglena 0.05 parts, grape seed extract 0.05 parts, sorbitol 44.75 parts.
[0045] The white fungus composite solid beverage with anti-oxidation function, in parts by weight, its raw material components also include 0.02-0.08 part of L-carnitine, and the optimum part by weight of L-carnitine is 0.05 part.
[0046] The white fungus composit...
Embodiment 2
[0062] In vitro antioxidant activity test of white fungus compound solid beverage:
[0063] Weigh 1g, 2g, 4g, 6g, 8g, and 10g of the product of the present invention and place them in beakers, and prepare them with 100ml of distilled water at 70-80°C to obtain concentrations of 10mg / ml, 20mg / ml, 40mg / ml, and 60mg / ml. ml, 80mg / ml, and 100mg / ml of the reconstituted solution, after leaching for 30 minutes, centrifuge to remove the supernatant, and measure the antioxidant activity of the supernatant.
[0064] The specific method is as follows:
[0065] (1) Determination method of DPPH free radical scavenging rate
[0066] Take 2ml of the sample solution into a stoppered test tube, add 2ml of 0.1mmol / l DPPH solution, mix well, react in the dark for 30min, and measure the absorbance value Ax at 517nm. At the same time, the sample liquid was replaced by the extract, and the DPPH solution was replaced by absolute ethanol as the blank group; the sample liquid was replaced by the extr...
Embodiment 3
[0088] In vivo antioxidant activity test of white fungus compound solid beverage
[0089] Select 200 twelve-month-old mice, divide them into 20 groups with 10 mice in each group, half male and half male, after adapting to the environment for 7 days, according to the body weight, the low-dose group is 0.2g / kg, the middle-dose group is 0.4g / kg, and the high-dose group is 0.4g / kg. Dosage group started administration at 1g / kg, and was given intragastric administration once a day at regular intervals. The negative control group was given normal saline, and the positive control group was given V C .
[0090] The mice were gavaged continuously for 15 days, and after 30 minutes of gavage on the 16th day, the eyeballs were removed to collect blood. After the blood coagulated, it was centrifuged at 4°C and 3000rpm for 10 minutes to prepare serum for use. The mice after blood collection were killed, the liver was taken out and washed several times with cold saline, the water was blotted w...
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