Pueraria lobata extract and application thereof
A technology of kudzu root extract and medicine, which is applied in the field of kudzu root extract, can solve the problem of high price, and achieve the effect of easy industrial production and simple extraction method
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Embodiment 1
[0025] ① Take the dried kudzu root, crush it into small pieces of 1-10mm, and set aside;
[0026] ②The crushed kudzu root was refluxed with 3 times 70% ethanol to extract twice, each time for 1.5 hours, the extracts were combined, refrigerated overnight, filtered, and the filtrate was decompressed to recover ethanol to obtain ethanol extract;
[0027] ③ Add 5 times the amount of distilled water to the ethanol extract to dissolve it, and then extract it with petroleum ether, ethyl acetate, and n-butanol in sequence;
[0028] ④Recover the solvent from the ethyl acetate extract under reduced pressure to obtain extract I;
[0029] ⑤ Dissolve the extract I with 5 times the amount of 90% ethanol, refrigerate overnight, filter, and recover the ethanol from the filtrate under reduced pressure to obtain the kudzu root extract that inhibits osteoclast formation.
[0030] The extract is added to a drug carrier, mixed, granulated and dried to obtain granules. The granule can be used for...
Embodiment 2
[0032] The kudzu root extract obtained in Example 1 was used to determine its effect on osteoclast formation.
[0033] Osteoclast formation system: Multinucleated osteoclasts can be formed by culturing RAW264.7 cells in α-MEM medium for 3-5 days in the presence of RANKL. The formed osteoclasts were observed with tartrate-resistant acid phosphatase (TRAP) staining method to observe TRAP-positive multinucleated cells, and the number of TRAP-positive multinucleated cells with more than 3 nuclei under the microscope was used as an indicator of osteoclast formation.
[0034] The RAW264.7 is a mouse mononuclear / macrophage cell line, which can form into osteoclasts with bone resorption capacity in the presence of osteoclast formation factor (RANKL).
[0035] Pueraria lobata extract was dissolved in α-MEM culture medium, prepared to a certain concentration, and then added to the osteoclast formation system of RAW264.7 cells, and cultured in a cell incubator with 5% carbon dioxide and ...
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