A kind of phylloside and its extraction method and application
A technology of pueruloside and extraction method, applied in the field of medicine, can solve the problems of complex and diverse components of traditional Chinese medicine, and achieve the effect of good research and development prospects
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Embodiment 1
[0040] Embodiment 1 (extracting and isolating active compound from the stem and leaf of Physalis edulis)
[0041] The extracting method of lanatoside, comprises the steps:
[0042] (1) Take Physalis physalis (Physalis puscens L., an annual herb of Physalis family Solanaceae) dry stem and leaf (9.3 kg) as raw material, add 8 mass times of the raw material with a volume fraction of 75% ethanol aqueous solution, and reflux extraction 2 times, 2 hours each time, combined the extracts, recovered the solvent under reduced pressure, and obtained the total extract (1170.0g) after concentration;
[0043] (2) total extract is dispersed into the water of 4 mass times, extracts with sherwood oil of equal volume, ethyl acetate, n-butanol successively, n-butanol extract decompresses and reclaims solvent, obtains n-butanol layer extract ( 200.0g);
[0044] (3) Get the n-butanol layer extract (100g) and separate it through silica gel column chromatography. The volume ratios are: 100:1, 70:1...
Embodiment 2
[0056] Embodiment 2 (extract and isolate active compound from Physalis edulis fruit)
[0057] The extracting method of lanatoside, comprises the steps:
[0058] (1) Take Physalis physalis (Solanaceae Physalis genus Physalis puscens L.) fruit (17.5kg) as raw material, and the volume fraction of 8 mass times of raw materials added is 75% Aqueous ethanol solution, reflux extraction 2 times, each 2 hours, combined extraction solution, reclaim solvent under reduced pressure, obtain total extract (1420.0g) after concentrating;
[0059] (2) total extract is dispersed into the water of 4 mass times, extracts with sherwood oil of equal volume, ethyl acetate, n-butanol successively, n-butanol extract decompresses and reclaims solvent, obtains n-butanol layer extract ( 70.0g);
[0060] (3) The n-butanol layer extract is separated by silica gel column chromatography, and the volume ratios are: 100:0, 100:1, 90:1, 80:1, 70:1, 60:1, 50:1, 40 :1, 30:1, 20:1, 10:1 dichloromethane-methanol ...
Embodiment 3
[0065] Example 3: Activity test of compounds inhibiting the release of nitric oxide (NO) from mouse macrophage RAW 264.7.
[0066] Take mouse macrophages (ATCC, TIB-71) that are in good growth state and in the logarithmic growth phase, and the concentration is 1 × 10 6 Cells / well of mouse macrophages were seeded in 96-well plate, 100 μL per well, at 37°C, and 5% CO 2 Routine cultivation in the incubator for 24 h. The culture medium was discarded from the cell plate after 24 h of cultivation, and LPS medium containing different drug concentrations and 2 μg / mL was added, and three parallel wells were set up in each group. Add 1 group containing only LPS medium), and replicate 3 wells in parallel. The positive drug control group is hydrocortisone, and cultured at 37°C for 24h. After 24 hours, take the medium supernatant, add Griess reagent [0.1% N-naphthylethylenediamine hydrochloride (50 μ L); 1% H of p-aminobenzenesulfonamide 3 PO 4 solution (5%, 50 μL), and measure the abs...
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