Application of traditional Chinese medicine composition in treating diseases caused by mucosal injury
A mucosal injury and composition technology, applied in the field of medicine, can solve the problems of unproven gastric mucosal repair effect, achieve the effect of shortening the recovery time, less toxic and side effects, and accelerating mucosal repair
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Embodiment 1
[0032] Atractylodes 80g, Chenpi 80g, Magnolia officinalis (made from ginger) 80g, Angelica dahurica 120g, Poria cocos 120g, Dabupi 120g, raw pinellia 80g, licorice extract 10g, patchouli oil 0.8ml, perilla leaf oil 0.4ml.
[0033] The Magnolia officinalis of formula quantity is refluxed and extracted with ethanol to obtain the ethanol extract of Magnolia officinalis; The atractylodes atractylodis of formula quantity, the described tangerine peel and the said Angelica dahurica are distilled and extracted with water as medium to obtain a distillation extraction mixture; The above-mentioned amount of Poria cocos is decocted with water and filtered to obtain a decoction of Poria cocos; after boiling the Poria cocos in the formula amount as a medium, it is cooled to 70-90° C. to fully infiltrate and filtered to obtain Poria cocos. Soaking solution: take the raw pinellia of the formula and fully soak it in water medium to obtain the pinellia soaking liquid; and take dried ginger equi...
experiment example 1
[0035] Experimental example 1 Human gastric mucosal epithelial cell line GES-1
[0036] 1. Experimental steps
[0037] When carrying out subculture in sub-discs, the solution (filtered and sterilized) obtained in Example 1 was added to the culture solution of experimental group 1, and the addition amount was 0.05ml / 1ml medium; Solution (filtered and sterilized), the addition amount is 0.025ml / 1ml culture medium; ultrapure water is added to the culture solution of the control group, the addition amount is 0.05ml / 1ml culture medium. The above three mediums were used to culture the human gastric mucosal epithelial cell line GES-1 cells, and the growth of the cells was observed before and after 2 days of culture, and photographed and counted.
[0038] 2. Experimental results
[0039]
[0040]
[0041] The growth of the cell number of the experimental group 1 and the experimental group 2 is significantly higher than that of the control group. Therefore, the pharmaceutical c...
experiment example 2
[0042] Experimental Example 2 Human normal colorectal mucosal cell line FHC
[0043] 1. Experimental steps
[0044] When carrying out subculture in sub-discs, the solution (filtered and sterilized) obtained in Example 1 was added to the culture solution of experimental group 1, and the addition amount was 0.05ml / 1ml medium; Solution (filtered and sterilized), the addition amount is 0.025ml / 1ml culture medium; ultrapure water is added to the culture solution of the control group, the addition amount is 0.05ml / 1ml culture medium. The above three mediums were used to culture the human normal colorectal mucosal cell line FHC cells, and the growth of the cells was observed after 2 days, and the cells were photographed and counted.
[0045] 2. Experimental results
[0046] group
[0047] The growth of the cell number of the experimental group 1 and the experimental group 2 is significantly higher than that of the control group, therefore, the pharmaceutical composition o...
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