Preparation method and application of hosta plantaginea root animal-origin-fungi-resistant effective parts
An animal-derived, white-flowered technology, applied in the field of ethnic medicine, can solve the problems of large differences in active ingredients and unpredictable antifungal activity of hosta roots.
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Embodiment 1
[0023] Preparation method of each effective part:
[0024] 1) Total extract extraction
[0025] Take 300g of dried white hosta roots, dry, and crush. Soak the powder of hosta roots with 10 times the amount of 70% ethanol for half an hour.
[0026] 2) Reflux extraction
[0027] Reflux and extract twice at 70-80°C for two hours each time, filter, collect the filtrate, and concentrate to 200 mL.
[0028] 3) Gradient extraction
[0029] The diluted concentrate was extracted with petroleum ether, chloroform, ethyl acetate, and n-butanol in turn, combined the same organic phases, and concentrated under reduced pressure to obtain petroleum ether fraction (0.2074 g, extraction rate: 0.0691%) and chloroform fraction (1.5708 g , Extraction rate: 0.524%), ethyl acetate fraction (0.8724 g, extraction rate: 0.291%), n-butanol fraction (20.5678 g, extraction rate: 6.86%) and water fraction (42.0368 g, extraction rate: 14%) .
Embodiment 2
[0031] The Ethanol Extract from the Root of Hosta White Flower and Its Different Polar Parts' Antifungal Effects on Animal Origin
[0032] 1) Resuscitation of strains: Inoculate Microsporum canis, Trichophyton mentagrophytes, and Microsporum gypsum stored in a refrigerator at 4°C into PDA medium, and place it in a fungus constant temperature incubator at 27°C for 7 days to activate. , Pick the mycelium around the activated colony and inoculate it into the PDA medium, and place it in a fungus incubator at 25°C for 7 days to restore the fungus to normal growth.
[0033] 2) Determination of the antifungal activity of the ethanol extract from the roots of Hosta white flower and its different polar parts: the ethanol extract and the four polar parts in Example 1 were dissolved in 500 μL of sterile distilled water and then diluted with distilled water to 50 mg / mL. In the ultra-clean workbench, after the aqueous solution is filtered through a microporous membrane (0.22 μm), add the melted...
Embodiment 3
[0038] MIC Determination of Ethanol Extracts from the Roots of Hosta White Flower and Its Different Polar Parts against Animal-derived Fungi
[0039] In a 96-well plate, add 100 μL of freshly prepared PDB medium to wells 1 to 6, add 100 μL (20 mg / mL) of the prepared drug solution to well 1, and use the multiple dilution method to dilute the drug in wells 2 to 6 . Add 100 μL of freshly prepared bacterial solution to wells 1~6 (10 6 CFU / mL). Add only 200 μL of bacterial solution to the 9th well, 200 μL of liquid medium to the 10th well, 100 μL of LPDB medium and 100 μL of bacterial to the 11th hole, and 100 μL of LPDB medium and 100 μL of medicine to the 12th hole. Solution, respectively, as controls. After placing each plate in a 35°C incubator for 48 hours, compare with the control group to observe the inhibitory effect of the drug on the growth of the tested bacteria.
[0040] See the results of the experiment Figure 4-Figure 8 .
[0041] See the results of MIC determination of...
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