Preparation method of active ingredients in pleurospermum plant and application thereof in preparation of anti-inflammatory drugs
A technology of active ingredients and ridges, which is applied in the field of separation and purification of active ingredients in natural plants, can solve problems such as the separation and research of phytochemical separation components of P.
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Embodiment 1
[0036] 1.1 Preparation of crude extract
[0037] Crush 3Kg of P. candollei plant, soak in 2×8L of 95% ethanol for 48h, repeat 3 times, combine the filtrates, concentrate in vacuo at 40°C to obtain 124g of crude extract, and store it at 4°C for future use.
[0038] 1.2 Screening and KD value determination of two-phase solvent system
[0039] Choosing an appropriate two-phase solvent system is the key to the successful separation of HSCCC. Several different ratios of n-hexane / ethyl acetate / methanol / water solvent systems were tested in this experiment.
[0040] Configure 10mL of n-hexane / ethyl acetate / methanol / water solvent system with different ratios, add about 2mg of crude extract, shake vigorously, and fully dissolve. Take 1 mL each of the upper and lower phases, blow dry with nitrogen, dissolve the residue in 1 mL methanol, and analyze by HPLC. According to the formula K D =A U / A L Calculate the partition coefficient K of the compound D value, where A U and A L are...
Embodiment 2
[0066] Anti-inflammatory activity assay:
[0067] The MTT assay was used to assess cytotoxicity. The macrophage Raw 264.7 cell line was obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). will total 2×10 4 cells / mL were plated in 96-well plates and incubated overnight at 37°C in DMEM containing 10% FBS. After removing the cell culture medium, Raw 264.7 cells were washed 3 times with PBS buffer. Then, the cells were treated with different concentrations of the six compounds and incubated at 37°C for an additional 24 h. At the end of each incubation period, each well was washed 3 times with PBS buffer, and 150.0 μL of fresh MTT solution (0.5 mg mL –1 ). Subsequently, remove the supernatant, add 150.0 μL DMSO, shake for 15 min, and incubate at 37 °C for 4 h. Finally, the optical density of each well was measured in triplicate at 490 nm.
[0068] The anti-inflammatory effects of the six compounds were evaluated by inhibiting LPS-induced nitric ...
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