Medicinal liquor and preparation method thereof
A technology for medicinal wine and liquor, which is applied in the preparation of alcoholic beverages, pharmaceutical formulations, antibacterial drugs, etc., can solve the problems of not being able to exert the best medicinal properties of medicinal wine, unreasonable proportions, single raw materials, etc. The effect of promoting secretion
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specific Embodiment 1
[0028] Such as figure 1 Shown, a kind of medicated wine and the technological process of preparation thereof are as follows:
[0029] SP1: Choose Moringa leaves, cloves, sealwort and dandelion as the raw materials to be processed into medicinal wine. Choose white wine or red wine as the base wine. The raw materials must be accurately weighed and proportioned. Moringa leaves account for 55%, cloves and sealwort Both dandelion and dandelion account for 15%. Moringa leaves are the main ingredient, cloves, dandelion and sealwort are auxiliary ingredients, and then the impurities and sludge contained on the surface of the raw materials are cleaned. All raw materials need to be purchased from regular pharmacies.
[0030] People with yin deficiency and body heat are forbidden to take the medicinal wine after adding cloves, as it will aggravate the phenomenon of internal heat in the body.
[0031] SP2: Quickly dry the cleaned Moringa leaves, cloves, sealwort, and dandelion to keep th...
specific Embodiment 2
[0040] SP1: dose design, set multiple dose groups, respectively according to 1u+100ul culture solution, 3u1+100ul culture solution, 9ul+100ul culture solution, 27ul+100ul culture solution 4 groups, calculated according to the concentration, roughly equal to 1%, 3 %, 8% and 21% liquid concentration;
[0041] SP2: Cell recovery and subculture preparation, take out the cryopreservation tube storing L-929 cells from the liquid nitrogen tank, and put it into a small bucket filled with liquid nitrogen prepared in advance;
[0042] SP3: centrifuge at 300g for 3 minutes, discard the supernatant, resuspend the cells with MEM medium, inoculate them in a culture flask, and place the cells in a 37°C incubator containing 5% carbon dioxide;
[0043] SP4: The next day, check the growth status of the cells under an inverted microscope. If necessary, replace the culture medium with a new medium to continue the culture. If the number of cells grows to 80%, it should be passaged in time;
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