Alcohol-relieving medicine composition and preparation method thereof
A composition and anti-alcoholic technology, which is applied in the direction of drug combination, anti-drug, pharmaceutical formula, etc., can solve the problems of lack of products, accelerated ethanol metabolism, and single effect, so as to protect the liver, promote alcohol metabolism and excretion, and prevent drunkenness Effect
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specific Embodiment 1
[0047] The preparation of specific embodiment 1 extract dry powder
[0048] Pueraria japonica, Hovenia dulcis, hawthorn, Poria skin, reed root, tangerine peel, Schisandra chinensis, safflower, the raw materials are removed from the sundries and set aside. Take 4-8g of kudzu flower, 4-8g of Hovenia dulcis, 3-5g of hawthorn, 1-2.5g of poria cocos skin, 1-5g of reed root, 2-4g of tangerine peel, 3-5g of schisandra, and 0.1-0.25g of safflower. cook. For the first decoction, the soaking time of medicinal materials is 0.5-1.5 hours, the amount of water added is 8-12 times, and the extraction time is 1.0-2.0 hours. For the second decoction, add 6 to 10 times the amount of water, and the extraction time is 0.5 to 1.5 hours. Collect and combine the extracts that have been decocted for the second time, and the material-liquid specific gravity of the extracts is 1-2. Perform spray drying. The drying air inlet temperature is 180°C-210°C, the outlet air temperature is 80°C-110°C, the s...
specific Embodiment 2
[0049] The preparation of specific embodiment 2 granules
[0050] The dry powder obtained by spray-drying the extract of Example 1, adding an appropriate amount of absolute ethanol to granulate, passing through a 10-20 mesh sieve, drying in a constant temperature drying oven at 40-60°C for 3-4 hours, and then drying with a 10-20 mesh The granules are sieved to obtain granules, and the total flavonoids contained in the granules are not less than 1.5%.
specific Embodiment 3
[0051] The preparation of specific embodiment 3 buccal tablet
[0052] Spray-dry the obtained dry powder of the extract of Example 1, add magnesium stearate according to 2% of the dry powder mass, mix evenly, compress into tablets, and the pressure is 5-12KN to make buccal tablets, with a tablet weight of 0.5g, buccal tablets Containing total flavonoids is not less than 0.5%.
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