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Hydnisella polysaccharides were extracted from the fruiting bodies of Hydrangea, and the crude polysaccharides of Hydatid were extracted by water extraction and alcohol precipitation. The purified polysaccharides were purified by DEAE-52 cellulose chromatography column. The Hep-G2 cells were cultured and the anticancer activity of the samples was studied by MTT assay. The results showed that the best inhibitory effect on Hep-G2 cells was 0.01 mg/mL boiled supernatant, the inhibition rate was 19.21%, and the positive control group was 29.56%. Therefore, Hydatid polysaccharide has a good inhibitory effect on hepatoma cell Hep-G2and plays an important role in drug selection in anticancer effects. Hydrangea [Sparassis crispa (Wulf.) Fr.] is also known as the flower mushroom, belonging to the non-Pleurotus, Hydrangea, Hydrangea. At present, a number of studies have confirmed that Hydatid has good anti-oxidation, improved immunity, anti-tumor activity and other effects, and the anti-tumor activity of Hydatid is mainly the polysaccharide in its fruit body. In function, mainly by stimulating the production of cytokines to fight tumors. Due to the excellent efficacy of Hydrangea, it has gradually become a research hotspot in recent years. South Korea and Japan have the most in-depth research on it, while the research on the efficacy of Hydatid in China focuses on antioxidants and immunity. Anticancer effects have rarely been reported. On the one hand, this study used the alcohol precipitation water extraction method to purify and separate it with DEAE-52 cellulose chromatography, which greatly improved the polysaccharide yield and purity. On the other hand, the anti-tumor and immunomodulatory activities of Hydatid polysaccharides were evaluated in vitro, and it is of great significance to study the anti-tumor effect and mechanism of Hydatid polysaccharides in one stepand to explore new drugs and new treatment methods for preventing and treating tumors. 1. Materials and methods 1.1 Experimental materials Hydrangea fruit body dry powder (provided by Shanghai Hexian Mushroom Biotechnology Co., Ltd.). Human hepatoma cell line HepG2. RPMI-1640 medium, cell digestive juice: 0.25% trypsin, D-Hanks solution, streptomycin solution, MTT, fluorouracil. Sevage reagent (n-butanol: chloroform = 1:4) reagents such as acetone are of analytical grade (Zhongguo Group Chemical Reagent Co., Ltd.). Centrifuge (Shanghai Anting Scientific Instrument Factory). UV-1800 UV spectrophotometer (Shimadzu Corporation, Japan). DEAE-52 cellulose chromatography column (2.6 x 40.0 cm). Electrophoresis unit (Clever Ltd., UK). 1.2 Experimental methods 1.2.1 Separation of polysaccharides from the genus Hydrangea In this paper, the alcohol-sinking water combined with the Sevage method was used to 2018 3rd International Conference on Life Sciences, Medicine, and Health (ICLSMH 2018) Copyright © (2018) Francis Academic Press, UK DOI: 10.25236/iclsmh.18.016 --67-separate and extract the polysaccharides of the genus Hydrangea. Hydrangea fruit body dry powder plus 95% ethanol, 100 ° C water bath, 1.5h. Discard the supernatant and dilute with distilled water for 3 h. The resulting solution was coarsely filtered with gauze and centrifuged (4500 rpm, 6 min) to obtain a supernatant for use. The residue was boiled with distilled water for 3 h, centrifuged, and the precipitate was discarded. The obtained supernatants were combined twice, concentrated in a water bath at 70 ° C, concentrated, cooled to room temperature, added with ethanol, and condensed in a refrigerator at 4 ° C for 12 h. The resulting solution was centrifuged (10000 rpm, 10 min), washed with absolute ethanol, acetone and diethyl ether to give a crude polysaccharide. 1.2.2 Purification of polysaccharides from the genus Hydrangea The method of separating and purifying polysaccharides from Inonotus obliquus by Dong Wenxia et al. DEAE-52 cellulose static method was used to dissolve the crude polysaccharide powder in appropriate distilled water and added to DEAE-52 cellulose chromatography column (2.6×40.0). Chromatography was carried out in cm), and elution was carried out using 0 to 2 M sodium chloride. The eluate of each gradient was collected and the polysaccharide concentration was followed by phenol sulfuric acid method to determine the elution endpoint. 1.2.3 Purity testing of polysaccharides from the genus Hydrangea In this paper, the purity of polysaccharides from the genus Hydrangea was detected by the phenol-sulfuric acid method. Take 1 ml of each sample solution in a test tube, replenish water to 2 mland allow to stand at room temperature (about 30 minutes). The solution of the standard glucose solution in a 0.00 ml tube was used as a reference solutionand the optical density OD value was measured at a maximum absorption wavelength of 490 nm. 1.2.4 SDS-polyacrylamide gel electrophoresis (SDS-PAGE) analysis SDS-PAGE gel electrophoresis: 16 μL sample was added to 5×SDS-PAGE Loading Buffer 4 μL, heated at 100 ° C for 3 min, centrifuged at 8000 rpm for 1 min at 4 ° C, the supernatant was collected, placed on iceand the whole sample was processed. Thus, 20 μL of the supernatant of the prepared sample was added to the spotting well. 1.2.5 Cell culture and counting The human hepatoma cell line HepG2, SMMC-7721 was separately cultured in a cell culture medium containing 10% fetal calf serum. All the cells in the exponential growth phase were cultured in an incubator at 5% CO2, 37 ° C and saturated humidity. When the cell fusion state reached 80% to 90%, they were digested with 0.25% trypsin and passaged. Count with a cell counting plate according to the white blood cell counting method. 1.2.6 MTT(Methyl thiazolyl tetrazolium)colorimetric analysis On the ultra clean worktable, trypsin is digested and repeatedly blown into a single-cell suspension, whose cell concentration is adjusted into 1×10/mL with fresh RPMI-1640 culture solution. Tumor cells are placed in a 96-well culture plate with a dose of 150 μL per well, which is put into incubator with 5%CO2 at 37°C under saturated humidity. 50μL sample to be tested is added into each well for processing after 24 hours. 20μLMTT is added into each well after 48 hours. After 4 hours of culture, the supernatant medium solution was carefully removed, with 150 μL dimethyl sulfoxide (DMSO) added to each hole. Then it is put into the oscillator for 10 minutes, and the absorbance is measured at a wavelength of 570nm using an enzyme marker. Cell growth inhibitory rate(%)=(1-OD value of drug group/OD value of negative control group)×100% 1.3 Data processing After three parallel trials in five groups, Origin 7.5 was used to plot the data through SPSS statistical software (SPSS 21.0, American SPSS company) and data statistics and analysis was conducted at the significance level of p=0.05.

Isolation, Purification and Anticancer Effect of Hydatid