Use of ganoderic acid T and ganoderic and Me in tumour growth or proliferation inhibitor
A technology of Ganoderma lucidum acid and inhibitor, which is applied in the application field of Ganoderma lucidic acid T and Ganoderma lucidum acid Me in tumor growth or proliferation inhibitors, can solve the problems such as unreported Ganoderma lucidic acid monomers, etc. The effect of less toxicity, reducing the possibility of adverse effects
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[0029] Example 1
[0030] Toxic effects of GA-T and GA-Me on HeLa cells:
[0031] Both GA-T and GA-Me are pure natural products isolated from Ganoderma lucidum mycelium produced by fermentation, with a purity greater than 99%, and diluted with DMEM culture solution to the required concentration. The thiazole blue (MTT) rapid colorimetric method was used to determine the toxic effects of GA-T and GA-Me on HeLa cells. The logarithmic growth phase cells (10 6 cell·ml -1 ) Inoculate a 96-well culture plate, 0.2ml per well, respectively add a certain concentration of GA-T and GA-Me treatment, each concentration in parallel 4 wells, the control group add an equal volume of culture medium, set 37 ℃, 5% CO 2 And 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 -1MTT 10μl, add 0.04N dimethyl sulfoxide (DMSO) to each well after incubation, 150μl per well, shake for 10min, wait unt...
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[0033] Example 2
[0034] Toxic effects of GA-T and GA-Me on 95-D cells:
[0035] Both GA-T and GA-Me are pure natural products isolated from Ganoderma lucidum mycelium produced by fermentation, with a purity greater than 99%, and diluted with RPMI-1640 culture solution to the required concentration. The rapid colorimetric method of thiazole blue (MTT) was used to determine the toxicity of GA-T and GA-Me on 95-D cells. The logarithmic growth phase cells (10 6 cell·ml -1 ) Inoculate a 96-well culture plate, 0.2ml per well, respectively add a certain concentration of GA-T and GA-Me treatment, each concentration in parallel 4 wells, the control group add the same volume of culture medium, set 37 ℃, 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 10μl, add 0.04N DMSO to each well after the incubation, 150μl per well, shake for 10min, wait until the MTT reduction ...
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[0037] Example 3
[0038] Comparison of the cytotoxicity of GA-T and GA-Me on several tumor cells and normal cell L02:
[0039] Both GA-T and GA-Me are pure natural products isolated from Ganoderma lucidum mycelium produced by fermentation, with a purity greater than 99%, and diluted with DMEM or RPMI-1640 culture solution to the required concentration. The rapid colorimetric method of thiazole blue (MTT) was used to determine the toxicity of GA-T and GA-Me on several cells. The logarithmic growth phase cells (10 6 cell·ml -1 ) Inoculate a 96-well culture plate, 0.2ml per well, respectively add a certain concentration of GA-T and GA-Me treatment, each concentration in parallel 4 wells, the control group add the same volume of culture medium, set 37 ℃, 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 10μl, after incubation, add 0.04N DMSO (dimethyl sulfoxide) to ea...
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