Zymolytic tuna tablet for beautifying and fighting against free radicals and preparation method of zymolytic tuna tablet
A technology of tuna and free radicals, which is applied in the direction of anti-toxic agents, pill delivery, and medical raw materials derived from fish feed, etc., can solve the problems of inapplicable antioxidants, achieve the inhibition of lipid peroxidation, less irrelevant ingredients, and the content of active ingredients high effect
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Embodiment 1
[0018] The enzymolyzed tuna beauty anti-free radical tablet and the preparation method thereof comprise using tuna blood as a raw material, wherein: in parts by weight: 15-20 parts of tuna blood enzymatic hydrolyzate dry powder; 4-8 parts of starch; 5-5 parts of dextrin 12 parts; 0.1-0.4 parts of tartaric acid; 0.2-0.4 parts of magnesium stearate. The finished product is safe and non-toxic, has strong antioxidant activity and is easy to digest and absorb, and can eliminate free radicals and inhibit lipid peroxidation. The combined use of tartaric acid and magnesium stearate has unexpectedly achieved a good effect of maintaining antioxidant components. Anti-free radical tablets also contain ethanol. Ethanol is a good solvent in the preparation of anti-free radical tablets, and it is easy to separate and relatively safe. The preparation steps of tuna blood enzyme hydrolyzate are as follows:
[0019] 1) After the tuna blood is deodorized, adjust the pH with phosphate buffer, a...
Embodiment 2
[0033](1) Take 500mL of tuna blood, add 2000mL of No. 6 light gasoline to remove the fishy smell, remove the No. 6 light gasoline, and adjust the pH to 7 with phosphoric acid buffer;
[0034] (2) Add 5g of trypsin to the above tuna dilution, enzymatically hydrolyze at 55°C for 3h, then rapidly raise the temperature to 100°C and maintain for 15min;
[0035] (3) Centrifuge the enzymatic solution at 8000r / min and 4°C for 10min, and take the supernatant;
[0036] (4) Prepare the obtained enzymatic hydrolyzate into a solution with a concentration of 20mg / mL, add it to a macroporous resin chromatography column for desalination, and then use 55% ethanol for analysis, and remove the ethanol by rotary evaporation under 40°C under low pressure, and the concentrated solution Freeze-drying is carried out to obtain dry powder of the desalted enzyme hydrolyzate.
[0037] (5) Take 20g of dry powder of enzymatic hydrolyzate, 8g of starch, 12g of dextrin, 0.4g of tartaric acid, appropriate am...
Embodiment 3
[0040] (1) Take 500mL of tuna blood, add 2000mL of No. 6 light gasoline to remove the fishy smell, remove the No. 6 light gasoline, and adjust the pH to 7 with phosphoric acid buffer;
[0041] (2) Add 5g of trypsin to the above tuna dilution, enzymatically hydrolyze at 55°C for 3h, then rapidly raise the temperature to 95°C and maintain for 10min;
[0042] (3) Centrifuge the enzymatic solution at 8000r / min and 4°C for 10min, and take the supernatant;
[0043] (4) Prepare the obtained enzymatic hydrolyzate into a solution with a concentration of 18mg / mL, add it to a macroporous resin chromatography column for desalination, and then use 45% ethanol for analysis, and remove the ethanol by rotary evaporation under 40°C under low pressure, and the concentrated solution Freeze-drying is carried out to obtain dry powder of the desalted enzyme hydrolyzate.
[0044] (5) Take 20g of dry powder of enzymatic hydrolyzate, 8g of starch, 12g of dextrin, 0.4g of tartaric acid, appropriate am...
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