Use of icaritin in preparation of drugs for treating GP80 related diseases
A kind of technology of Acradine and usage, which is applied in the field of medicine to achieve the effect of good pharmaceutical effect
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Embodiment 1
[0032] Preparation of Alcoradine
[0033] Acradine, also known as icariin, is extracted and separated from the traditional Chinese medicine Epimedium.
[0034] The preparation method of Epimedium is disclosed in the patent whose publication number is CN 101302548. In the method, icariin is used as a raw material, hydrolyzed by β-glucosidase, the precipitate obtained by centrifuging the hydrolyzed product is dissolved in acetone, and the supernatant is obtained by centrifuging and filtering. Then the supernatant liquid obtained by centrifugation is recrystallized with water to obtain the pure Epimedium. The icariin in the present invention was purchased from Shaanxi Jiahe Plant Chemical Co., Ltd., with a purity of 90%.
Embodiment 2
[0036] Detect the inhibitory effects of alcoladine on hepatocarcinoma PLC / PRF / 5 cells.
[0037] Experimental steps: cell culture: first, the PLC / PRF / 5 liver cancer cells are cultured to a cell density of 80% in an amino acid and glucose medium (i.e., DMEM medium) containing a volume concentration of 10% fetal bovine serum; The cells were divided into a phenol red-free medium containing activated carbon-treated fetal bovine serum at a volume concentration of 2.5% by volume, and cultured for 24 hours.
[0038] Add dimethyl sulfoxide (DMSO) and alcradine: add DMSO control (i.e. DMSO solution not containing alcradine) and 5 μM alcradine DMSO solution respectively in the culture system, and make each reaction system The final volume concentration of DMSO in the medium was 0.1%.
[0039] The cells were harvested at 12, 24 and 48 hours respectively, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) antibody and GP80 (IL-6R) antibody were added to the cells for western blot detect...
Embodiment 3
[0042] To detect the inhibitory effects of alcoladine on liver cancer cells HUH-7.
[0043] Experimental steps: cell culture: first, HUH-7 cells were cultured in an amino acid and glucose medium (i.e. DMEM medium) containing 10% volume concentration of fetal bovine serum to a cell density of about 80%; then the cultured cells were divided into Cultured for 24 hours in a phenol red-free medium containing activated carbon-treated fetal bovine serum at a volume concentration of 2.5%.
[0044] Add dimethyl sulfoxide (DMSO) and alcradine: add DMSO control (that is, the DMSO solution that does not contain alcradine) and the alcladine DMSO solution of 5 μ M concentration respectively in the culture system, and make each The final volume concentration of DMSO in the reaction system was 0.1%.
[0045] The cells were harvested at 12, 24 and 48 hours respectively, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and GP80 antibodies were added to the cells for western blot detection....
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