Spleen strengthening and appetite promoting fructus crataegi and snow pear juice and method for preparing same
A technology of invigorating the spleen and appetizing pear juice, which is applied in the fields of juice extraction, food forming, food science, etc., can solve the problems of low shelf life of products, increase of acidity in the stomach, and destruction of nutritional components, and achieve the improvement of sterilization and anti-oxidation efficiency, Enhance the effect of immune regulation and strengthen nutrition
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Embodiment 1
[0048] A spleen-invigorating and appetizing hawthorn pear juice and a preparation method thereof comprises mixing 50 parts of hawthorn juice and 100 parts of pear juice and homogenizing for 30 minutes at a pressure of 20-30 MPa and a temperature of 20-30°C. The homogenized hawthorn pear juice is continuously deoxygenated by a vacuum degasser at a vacuum degree of 0.09MPa and a temperature of 25-30°C to prevent the oxidation of nutrients such as vitamins. PEF non-thermal sterilization is adopted, and the parameters of PEF non-thermal sterilization are: electric field frequency 200Hz, electric field strength 35-50kv / cm, processing time 240μs, temperature 30℃-40℃, which can avoid non-enzymatic browning and flavor caused by thermal sterilization material loss.
[0049] The preparation method of hawthorn juice comprises the steps:
[0050] ① Hawthorn pretreatment: select fresh hawthorns that are fully mature and bright red in color, soak them in a salicylic acid solution for 5 min...
Embodiment 2
[0063] Add 8 parts of stomach-nourishing porous prebiotic balls to the raw materials of Example 1, mix them with hawthorn juice and pear juice, homogenize, degas, sterilize, fill and pack.
[0064] The preparation method of the stomach-nourishing porous probiotic ball is:
[0065] ①Preparation of Bifidobacteria culture solution: B. Longum bacteria solution was inoculated in MRS medium, cultured anaerobically at 37°C for 12h after nitrogen filling, and centrifuged at 4°C and 6000r / min for 10min. After decanting the supernatant, the cell pellet was washed twice with 0.85% normal saline and resuspended in normal saline, and the cell concentration was adjusted to 2×10 9 CFU ml.
[0066] ②Preparation of bacterial complex solution: 6 parts of bifidobacterium culture solution, 1 part of lactococcus oligosaccharides (mainly including stachyose and raffinose), 2 parts of soybean oligosaccharides, 1 part of konjac gum hydrolyzate, 1 part of liver juice , 1 part of coconut milk, 2 part...
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