Wheat bran polysaccharide with antitumor and immune regulation activities and extraction method thereof
A technology of wheat bran and polysaccharide, which is applied in the directions of antitumor drugs, organic active ingredients, medical preparations containing active ingredients, etc., can solve problems such as few related reports, and achieves low price, broad prospects for industrial development, and sources of rich effects
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[0035] Example 1. Extraction of wheat bran immunomodulation and anti-tumor activity polysaccharides
[0036] 1. Polysaccharide extraction: The flow chart of polysaccharide extraction is as follows figure 1 Shown.
[0037] 1) Wheat bran pretreatment
[0038] Weigh 100 g of wheat bran, disperse it in 500 mL of a dilute hydrochloric acid solution with a pH of 3.5, and soak at 25°C for 12 hours. Centrifugal separation (1500rpm, 30min), collect the precipitate; further wash the precipitate with water until the solution is clear, pass through a 200-mesh sieve, and drain the water to obtain dephytic acid and destarch wheat bran.
[0039] 2) Enzymatic hydrolysis
[0040] Disperse the dephytic acid and destarch wheat bran into 400mL water, adjust the pH of the system to 5.5, and add 0.25g xylanase (the ratio of xylanase to wheat bran is 6.25U:1g without Pretreated wheat bran), placed in a 55 ℃ heat preservation tank, stirred and extracted; after reaction for 4.0 h, the enzymatic hydrolysis pro...
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[0072] Example 2: Extraction of wheat bran immunomodulation and anti-tumor activity polysaccharides
[0073] 1. Polysaccharide extraction
[0074] 1) Wheat bran pretreatment
[0075] Weigh 1 kg of wheat bran, disperse it in 4L of dilute hydrochloric acid solution with pH 3.0, and soak overnight (10 hours) at room temperature (23°C). Centrifugal separation (1500rpm, 30min), collect the precipitate; further wash the precipitate with water until the solution is clear, pass through a 200-mesh sieve, and drain the water to obtain desphytic acid and destarch wheat bran.
[0076] 2) Enzymatic hydrolysis
[0077] Disperse the dephytic acid and destarch wheat bran into 6L water, adjust the pH of the system to 5.0, add 4.5g xylanase (the ratio of xylanase to wheat bran is 8U:1g wheat bran ), placed in a 60°C heat preservation tank, stirred and extracted; after reacting for 3.0 hours, the enzymatic hydrolysis product was obtained; the enzymatic hydrolysis product was heated to 95°C, kept for 10 ...
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[0097] Example 3. Extraction of wheat bran immunomodulation and anti-tumor activity polysaccharides
[0098] 1. Polysaccharide extraction
[0099] 1) Wheat bran pretreatment
[0100] Weigh 5 kg of wheat bran, disperse it in 20L of dilute hydrochloric acid solution with a pH of 3.0, and soak it overnight (14 hours) at room temperature (27°C). Centrifugal separation (1500rpm, 30min), collect the precipitate; further wash the precipitate with water until the solution is clear, pass through a 200-mesh sieve, and drain the water to obtain desphytic acid and destarch wheat bran.
[0101] 2) Enzymatic hydrolysis
[0102] Disperse the dephytic acid and destarch wheat bran into 35L water, adjust the pH of the system to 5.3, add 20g xylanase (the ratio of xylanase to wheat bran is 10U:1g wheat bran) , Placed in a 50°C heat preservation tank, stirred and extracted; after reaction for 2.0h, the enzymatic hydrolysis product was obtained; the enzymatic hydrolysis product was heated to 95°C, kept fo...
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