Application of ganoderic acid Me in tumoral growth or propagation inhibitor
A technology of ganoderma acid and inhibitors, applied in the field of application of ganoderma acid Me in tumor growth or proliferation inhibitors, can solve the problems such as no reports of ganoderma acid monomers, and achieve the ability to curb infinite proliferation, low cytotoxicity, and inhibition The effect of tumor cell proliferation
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Embodiment 1
[0032] Toxic effects of GA-T and GA-Me on HeLa cells:
[0033] Both GA-T and GA-Me are pure natural products isolated from the mycelium of Ganoderma lucidum produced by fermentation, with a purity greater than 99%, and are diluted with DMEM culture solution to the required concentration. Toxic effects of GA-T and GA-Me on HeLa cells were determined by thiazolium blue (MTT) rapid colorimetric method. Cells in logarithmic growth phase (10 6 cell ml -1 ) was inoculated in a 96-well culture plate, 0.2ml per well, and treated with a certain concentration of GA-T and GA-Me respectively, and each concentration was paralleled to 4 wells, and the control group was added with an equal volume of culture solution, placed at 37 ° C, 5% CO 2Incubate in an incubator with saturated humidity for 1-4 days, add 5mg·ml to each well 4 hours before the end of the experiment -1 MTT 10 μl, add 0.04 N dimethyl sulfoxide (DMSO) to each well after the culture, 150 μl per well, shake for 10 minutes, ...
Embodiment 2
[0036] Toxic effects of GA-T and GA-Me on 95-D cells:
[0037] Both GA-T and GA-Me are pure natural products isolated from the mycelium of Ganoderma lucidum produced by fermentation, with a purity greater than 99%, and are diluted with RPMI-1640 culture solution to the required concentration. The toxic effects of GA-T and GA-Me on 95-D cells were determined by rapid colorimetric method of thiazolium blue (MTT). Cells in logarithmic growth phase (10 6 cell ml -1 ) was inoculated in a 96-well culture plate, 0.2ml per well, and treated with a certain concentration of GA-T and GA-Me respectively, and each concentration was paralleled to 4 wells, and the control group was added with an equal volume of culture solution, placed at 37 ° C, 5% CO 2 Incubate in an incubator with saturated humidity for 1-4 days, add 5mgml to each well 4 hours before the end of the experiment -1 MTT 10 μl, add 0.04 N DMSO to each well after the culture, 150 μl per well, shake for 10 minutes, wait unti...
Embodiment 3
[0040] Cytotoxicity comparison of GA-T and GA-Me on several tumor cells and normal cell L02:
[0041] Both GA-T and GA-Me are pure natural products isolated from the mycelium of Ganoderma lucidum produced by fermentation, with a purity greater than 99%, and are diluted with DMEM or RPMI-1640 culture solution to the desired concentration. The toxic effects of GA-T and GA-Me on several kinds of cells were determined by rapid colorimetric method of thiazolium blue (MTT). Cells in logarithmic growth phase (10 6 cell ml -1 ) was inoculated in a 96-well culture plate, 0.2ml per well, and treated with a certain concentration of GA-T and GA-Me respectively, and each concentration was paralleled to 4 wells, and the control group was added with an equal volume of culture solution, placed at 37 ° C, 5% CO 2 Incubate in an incubator with saturated humidity for 1-4 days, add 5mg ml to each well 4 hours before the end of the experiment -1 MTT 10 μl, add 0.04 N DMSO (dimethyl sulfoxide) ...
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