Preparation method of Psychotria hainanensis stem extract
A technology of stem extract and extract, which is applied in the field of extraction and separation of active ingredients of natural plants, to achieve the effect of clear chemical composition, low cost, and good antibacterial activity
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Embodiment 1
[0024] Embodiment 1 The preparation of the effective part of Hainan nine-section stem
[0025] Hainan nine-section stem (10Kg) is dried and crushed in the shade, soaked in petroleum ether (60-90°C) at room temperature for 3 times, 7 days / time, combined extracts, concentrated under reduced pressure to obtain petroleum ether-dissolved part extract (78g); After evaporating the residual petroleum ether, soak it in ethyl acetate at room temperature for 3 times, 7 days / time, combine the extracts, concentrate under reduced pressure to obtain the part of the extract dissolved in ethyl acetate (150g); , using ethanol aqueous solution (50-70%) to soak at room temperature for 3 times, 7 days / time, combine the extracts, concentrate under reduced pressure to obtain ethanol-dissolved partial extracts (180g).
[0026] The petroleum ether dissolved part is chromatographed on a silica gel column, and petroleum ether is used to elute to remove small polar mixtures such as long-chain grease wax ...
Embodiment 2
[0028] Example 2 Study on the Antibacterial Activity of Different Solvent Dissolved Parts and Monomer Compounds of Hainan Nine-section Stem
[0029] 1. Experimental method: 5 cultured strains of human pathogenic bacteria (tetrazyme, bacillus cereus, bacillus subtilis, staphylococcus albus, staphylococcus aureus) were mixed with 1:500-1:1000 Dilute the drug in DMSO to make 1 mg / mL for use, add 10 μL of the stock solution to each well of the first row of the 96-well plate, and put ciprofloxacin in a separate well as a positive control; then take 190 μL of the diluted strain solution , add to the first row of 96-well plate, mix well, then take 100 μL from the first row and add it to the second row, and so on until the 100 μL diluted bacterial solution from the last row is taken out and discarded; finally add 100 μL diluted bacterial solution to each well, The final volume of the well is 200 μL; incubate in a 37°C incubator for 8-10 hours, and observe the turbidity in the well wit...
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