Application of terminalia bellerica extract and terminalia bellerica polyphenol
An extract and drug technology, applied in the field of medicine, can solve the problems of difficult radical cure, prolonged disease course, damage, intestinal perforation and even intestinal cancer, etc., to achieve the effect of treating enteritis and relieving inflammatory reaction.
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Embodiment 1
[0045] 1. Pulverize the medicinal material of myrobalan, use 10 times the amount of water-containing organic solvent 90% ethanol to extract 3 times, each time for 10 hours, filter and recover and concentrate under reduced pressure at -0.08~-0.09MPa, 45°C.
[0046] 2. Collect the above extracts, add 2 times of water to dilute and centrifuge at 3000rpm / min for 30min, then use macroporous resin column to absorb and elute, -0.08~-0.09MPa, recover under reduced pressure at 45°C, concentrate and dry, which is Maohe sub-extract.
Embodiment 2
[0047] Embodiment 2 enteritis model construction and treatment
[0048] Fifteen male C57BL / 6 mice of 4-5 weeks were divided into 3 groups: negative control group, model group, and treatment group with chebula extract, 5 mice in each group.
[0049] The experimental animals in the model group and the treatment group of Myrobalan extract were induced by the chemical medium dextran sodium sulfate (DSS) to establish the IBD model: after the mice were weighed, they were given 4% DSS solution in exchange for normal drinking water, and the mice were observed daily. Rat feces were shaped and collected for occult blood test detection. After 5 days, if there is bloody stool, weight loss, granulocyte infiltration or strong positive occult blood test, the modeling is successful. HE staining and DAI scoring are performed to observe the inflammatory damage of the colonic mucosa and then used in the experiment.
[0050] The experimental animals depending on the treatment group of myrobalan ...
Embodiment 3
[0052] Example 3 Enteritis Model Dendritic Cell Extraction
[0053] Male 4-5 week old C57BL / 6 mice or IBD model mice were sacrificed and soaked in 75% alcohol for 10 minutes. The femur and tibia were dissected out, and the bone marrow cavity was washed repeatedly with RMPI1640 medium until the bone turned white. After centrifugation, the middle buffy coat was taken, and the cells were resuspended with the complete medium of bone marrow-derived dendritic cells (RMPI1640 medium containing 500 U / ml rmGM-CSG and rmIL-4), and the cells were mixed in 2×10 6 The density of each well was divided into 6-well plates. Change the medium every other day, add the same concentration of cytokines, and keep the suspended cells as much as possible. On day 6, all suspension cells were collected, and the expression of CD11C, a molecule on the surface of dendritic cells, was detected by flow cytometry to evaluate the purity of BMDC dendritic cells and used for experiments. Flow cytometry results...
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