Lentinan powder for preventing and/or assisting in treating tumors and extraction process thereof
A technology of lentinan and an extraction method is applied in the directions of antitumor drugs, medical raw materials derived from fungi, medical preparations containing active ingredients, etc. The effect of improving the tumor microenvironment
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Embodiment 1
[0031] The process for extracting lentinan powder for preventing tumors of the present invention comprises:
[0032] 1. Take 1kg of mushrooms (Lentinus edodes (Berk.) Sing.), add 10L of water, and extract in boiling water for 3 hours, a total of 2 extractions. Each extract was filtered and combined, heated and concentrated to a small volume, dialyzed against flowing water for 48 hours, concentrated the dialyzed liquid and centrifuged, added 30% trichloroacetic acid solution 1:1 (v / v), at 4°C React under conditions for 4 hours, add 10% NaOH solution to neutralize to about pH 7, tie a bag and dialyze against flowing water for 48 hours, concentrate the inner liquid of the dialysate and centrifuge, add 3 times the volume of 95% ethanol to the supernatant, and let it stand overnight. The precipitate was collected by centrifugation and dried at 40°C to obtain crude polysaccharide.
[0033] 2. Melt 10 g of the crude polysaccharide extracted in step 1 into 1 L of water, add 1 L of et...
Embodiment 2
[0039] Example 2: Reversal effect of lentinan LE58 extracted by the present invention on immunosuppressive cells
[0040] as attached figure 1 Shown are all flow cytometry diagrams, figure 1 Middle (a) is normal splenocytes; figure 1 Middle (b) is the proliferation peak of CD4+ T cells in splenocytes stimulated by concanavalin (ConA); figure 1 Middle (c) is immunosuppressive cells (myeloid-derived suppressor cells) inhibiting the proliferation of CD4+ T cells; figure 1 In (d) lentinan LE58 restored the proliferation of CD4+ T cells.
[0041] The splenocytes of BALB / c mice were prepared into a single cell suspension, and seeded in a 96-well cell culture plate (U-shaped bottom), the cell seeding density was 3×105 / well, and ConA and myeloid-derived suppressor cells were added in turn. For MSC2 and lentinan LE58, the concentration of ConA is 1.5 μg / well, the number of MSC2 cells is 9×103 / well, and the concentration of polysaccharide LE58 is 0.2 mg / ml. After 3 days of culture,...
Embodiment 3
[0042] Example 3: In vivo inhibitory effect of lentinan LE58 extracted by the present invention on lung cancer
[0043] as attached figure 2 As shown, the line corresponding to the diamond icon is the survival curve of the lung cancer tumor-bearing mice in the control group; the line corresponding to the rectangular icon is the survival curve of the lung cancer tumor-bearing mice in the lentinan LE58 group. LLC Lewis lung cancer cells were inoculated subcutaneously in the abdomen of C57 mice, the number of inoculated cells was 1×106 / mouse, and the subcutaneous xenograft tumor model of lung cancer was constructed. After 10 days, the tumor formed, and the intraperitoneal injection was performed with lentinan LE58 at a dose of 25 mg / kg body weight . The comparison between the two shows that the present invention has a certain inhibitory effect on the growth of lung cancer.
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