Application of oroxin A in preparation of medicines for treating cancer
A technology of phytoside and medicine, which is applied in the application field of phytoside A in the preparation of drugs for treating cancer, and can solve the problems such as no reports of phytoside A antitumor drug.
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Embodiment 1
[0034] Example 1 In vitro experiment of oroxylin A inhibiting the proliferation of various malignant tumor cells
[0035] (1) Experimental materials
[0036] (1) Tumor cell lines (34 strains): human breast cancer cells MCF-7, human liver cancer cell lines BEL-7402, QGY-7703, HCC-8910, mouse pre-tumor stem cells 3B5C, PMKO-102-3#, p3B11 , 2C4G2, PMKO-891-5#, human chronic myelogenous leukemia cell K562, human glioma cell SHG44, human promyelocytic leukemia cell HL-60, human cervical cancer cell Hela, human osteosarcoma cell MG-63, U- 2OS, human gastric cancer cell N87, human glioma cell A172, human myeloma cell line LP-1, human melanoma high metastatic cell line A375, human monocytic leukemia cell THP-1, human adrenal neuroblastoma cell ( Brain metastasis) KP-N-NS, human colon cancer cell line SW480, human Burkitt's lymphoma cell Raji, NAMALWA, human megakaryocyte leukemia cell Dami, human ileocecal cancer cell CCL-244, mouse tumor endothelial cell 3B11 , Human cervical cancer int...
Embodiment 2
[0051] Example 2 In vitro experiment of oroxylin A inhibiting breast cancer cell proliferation
[0052] (1) Experimental materials
[0053] (1) Tumor cell line: human breast cancer cell MCF-7 is cryopreserved in our laboratory. The cell culture medium DMEM (high sugar) is a product of Hyclone.
[0054] (2) Test drug: Oriloside A (purchased from a commercial company) was dissolved with dimethyl sulfoxide (DMSO) and diluted with DMEM (high sugar) medium to the required concentration.
[0055] (2) Experimental method
[0056] Cell culture: Cells are routinely cultured with RPMI1640 or DMEM (high glucose) medium containing 10% calf serum and 1% double antibody (anti-penicillin and anti-streptomycin). Digest with 0.25% trypsin every 48-72h, and expand the flask 1:2 to 1:4 for passage.
[0057] Alamarblue method: Take the human breast cancer cell MCF-7 in the logarithmic growth phase and adjust the cell concentration to 3×10 4 / ml, seeded on 96-well cell culture plate at 100μl / well, CO 2 Con...
Embodiment 3
[0061] Example 3 In vitro experiment of oroxylin A inducing morphological changes of tumor cells
[0062] (1) Experimental materials
[0063] (1) Tumor cell line: human breast cancer cell MCF-7 is cryopreserved in our laboratory. The cell culture medium DMEM (high sugar) is a product of Hyclone.
[0064] (2) Test drug: Oriloside A (purchased from a commercial company) was dissolved with dimethyl sulfoxide (DMSO) and diluted with DMEM (high sugar) medium to the required concentration.
[0065] (2) Experimental method
[0066] Cell culture: Cells are routinely cultured with RPMI1640 or DMEM (high glucose) medium containing 10% calf serum and 1% double antibody (anti-penicillin and anti-streptomycin). Digest with 0.25% trypsin every 48-72h, and expand the flask 1:2 to 1:4 for passage.
[0067] Rui-Ji’s staining method: take human breast cancer cells in logarithmic growth phase and adjust the cell concentration to 10 4 / Well, seeded in a 24-well culture plate. After 24 hours, complete med...
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