Composition for ameliorating, preventing or treating muscle atrophy comprising potentilla chinensis extract or polygonum tinctorium extract
A technology of muscle atrophy and extract, which is applied in the composition for preventing or treating muscle atrophy, and in the field of improvement, which can solve problems such as muscle atrophy and diabetes, and achieve the effect of improving muscle atrophy, strengthening muscles, and increasing size
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Embodiment 1
[0045] Embodiment 1: Preparation Potentilla extract
[0046] Add 10 times (volume) of extraction solvent (70% ethanol) based on the weight of the whole herb of Potentilla japonicus, at a temperature of 50-70° C., after soaking for 22-26 hours, obtain the extract at room temperature, and The Potentilla extract was extracted by applying ultrasonic waves for about 3 hours. This process can be repeated 2 to 3 times. Then, the extract was filtered, concentrated under reduced pressure, and dried to obtain a 70% ethanol extract.
Embodiment 2
[0047] Embodiment 2: preparation Polygonum indigo extract
[0048] By taking the weight of the whole plant of Polygonum indigo as a basis, adding 10 times (volume) of extraction solvent (70% ethanol), at a temperature of 50-70 ° C, after soaking for 22-26 hours, the extract was obtained at room temperature, and The indigo extract was extracted by applying ultrasonic waves for about 3 hours. This process can be repeated 2 to 3 times. Then, the extract was filtered, concentrated under reduced pressure, and dried to obtain a 70% ethanol extract.
experiment example 1
[0049] Experimental Example 1: Evaluation of Potentilla extract or Polygonum indigo extract for improving muscle atrophy
[0050] In this Experimental Example, the following experiment was conducted to confirm whether muscle atrophy was improved when treated with Potentilla extract (Example 1) or Polygonum indigo extract (Example 2).
[0051] 1) Cell culture and induction into myotube cells
[0052] L6 mouse myoblasts (myoblast) were obtained from ATCC (American Type Culture Collection, Manassa (Manassa), Virginia (VA), U.S. (USA)) and stored in DMEM (Du Baker's Modified Eagle's medium (Dulbecco's Modified Eagle's medium) added 10% FBS and 0.5% antibiotic-antimycotic (antibiotic-antimycotic) medium, at a temperature of 37 ° C, in 5% CO 2 cultured in a constant temperature reactor. To differentiate myoblasts into myotubes, the DMEM differentiation medium containing 2% horse serum was replaced every 2 days for cells in a confluent state of 100%. After 5-7 days, the formation ...
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