Application of silktree albizia bark water extract in preparation of anti-tumor medicaments
An anti-tumor drug, the technology of Albizia Julibrissin, applied in the direction of anti-tumor drugs, drug combinations, pharmaceutical formulas, etc.
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Embodiment 1
[0022] Example 1: Preparation of Albizia Julibrissin Water Extract and Preparation of Medicinal Solution
[0023] Crush the dried bark of Albizia Julibrissin, accurately weigh 50g of the powder, boil it twice with 1000ml of distilled water for 1.5 hours each time, filter it roughly with gauze, combine the two medicinal solutions, centrifuge at 8000rpm / min for 10min, and take the supernatant for vacuum Suction filtration, the filtrate was concentrated under reduced pressure with a rotary evaporator, and finally the concentrated components were freeze-dried with a freeze dryer, and the obtained dry matter was the water extract of Albizia juliensis bark, with a yield of 10.6%.
[0024] Preparation of Albizia Julibrissin Medicinal Solution: Accurately weigh 0.1 g of dried Albizia Julibrissin aqueous extract, dissolve it in 10 mL of autoclaved PBS buffer, and after fully dissolving, it becomes 10 mg / mL Albizia Julibrissin Medicinal Solution. Sterilize by filtration with a microporo...
Embodiment 2
[0025] Example 2: Effect of Albizia Julibrissin Water Extract on the Proliferation Activity of C6 Cells
[0026] Experimental process: After the rat brain glioma C6 cell line in the logarithmic growth phase was digested with 0.25% Trypsin-0.02%Na2EDTA, it was seeded in a 96-well cell culture plate at a density of 2×105 / mL, and each well was 200 μL, put in the cell incubator for culture. After the cells were completely attached to the wall, the cell culture plate was taken out, and the pre-prepared Albizia juniper solution was added, 20 μL / well, so that the final concentrations were 0, 50, 100, 150, 200, 250, 300, and 350 μg / mL. Each group has 6 replicate wells. After reaching the time required for the experiment (24h, 48h, 72h), take out the cell culture plate, add MTT solution (5mg / mL), 20μL / well, put it in the incubator to continue the culture, and stop the culture after 4h. Carefully aspirate and discard the culture medium in the wells, add 150 μL DMSO to each well, shake...
Embodiment 3
[0032] Example 3: Apoptosis-inducing effect of Albizia Julibrissin on C6 cells
[0033] Experimental process: the Annexin V-FITC cell apoptosis detection kit produced by Nanjing Kaiji Biotechnology Co., Ltd. was used. After digesting the rat brain glioma cell line C6 in the logarithmic growth phase with EDTA-free cell hydrolysis solution, inoculate it in a 60mm cell culture dish at a density of 1.0×105 / mL, 4 mL per plate, and release the cells Incubator cultivation. After the cells were completely adhered to the wall, the culture dish was taken out, the old medium was discarded, and the pre-prepared fresh medium containing the aqueous extract of Albizia juliensis at a concentration of 0, 200, and 250 μg / mL was added, and the culture was continued for 24 hours in the incubator. Digest and collect the cells of each experimental group and control group, wash the cells twice with PBS, add 500 μL Binding Buffer to suspend the cells; add 5 μL Annexin V-FITC, flick gently, add 5 μL ...
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