Application of jerusalem artichoke extract in preparing anti-tumor medicine or anti-tumor health care product
A technology of anti-tumor drugs and extracts, applied in the field of application of Jerusalem artichoke leaf extracts in the preparation of anti-tumor drugs, to achieve the effects of being beneficial to environmental and ecological governance, increasing farmers' income, and enriching natural drug resources
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Embodiment 1
[0021] Example 1 The inhibitory effect of Jerusalem artichoke leaf ethyl acetate extract on small cell lung cancer cell line A549
[0022] Preparation of Jerusalem artichoke leaf ethyl acetate extract: dry and crush the Jerusalem artichoke leaf, weigh it quantitatively, mix the Jerusalem artichoke leaf with ethyl acetate at a ratio of 1g:10ml, soak for 24 hours, filter, and concentrate under reduced pressure to extract; During the experiment, the required concentration was prepared with complete medium.
[0023] Small cell lung cancer cell line A549, with containing 10% newborn bovine serum (volume ratio), the sodium pyruvate of 1.0mM, penicillin 100,000 units / liter, the MEM (Eagle) medium of streptomycin 100,000 μg / liter at 37 °C, 5% CO 2 Cultivate in the incubator of (volume ratio); During the experiment, get the logarithmic growth phase cell, digest with 0.25% trypsin digestion solution, adjust the cell concentration to be 10 5 1 / mL, add 100 μL / well in 96-well plate, and ...
Embodiment 2
[0027] Example 2 The inhibitory effect of Jerusalem artichoke leaf ethyl acetate extract on breast cancer cell line MCF-7
[0028] The preparation of the ethyl acetate extract of Jerusalem artichoke leaves is the same as in Example 1. When doing pharmacological experiments, prepare the required concentration with complete medium.
[0029] Breast cancer cell line MCF-7 was cultivated in an incubator at 37°C and 5% CO2 with RPMI1640 medium containing 10% newborn calf serum, 100,000 units / liter of penicillin, and 100,000 μg / liter of streptomycin; Take cells in the logarithmic growth phase, digest with 0.25% trypsin digestion solution, and adjust the cell concentration to 10 5 1 / mL, add 100 μL / well in 96-well plate, and cultivate overnight; add 100 μL of ethyl acetate extracts of Jerusalem artichoke leaves prepared in four different concentrations to each well, and continue to cultivate for 24 hours. The growth inhibition rate was detected by MTT method, and the IC was calculated...
Embodiment 3
[0032] Example 3 The inhibitory effect of Jerusalem artichoke leaf ethyl acetate extract on cervical cancer cell line Hela
[0033] The preparation of the ethyl acetate extract of Jerusalem artichoke leaves is the same as in Example 1. When doing pharmacological experiments, prepare the required concentration with complete medium.
[0034] Cervical cancer cell line Hela was cultured in RPMI1640 medium containing 10% newborn bovine serum, 100,000 units / liter of penicillin, and 100,000 μg / liter of streptomycin in an incubator at 37°C and 5% CO2; Count the cells in the growth phase, digest with 0.25% trypsin digestion solution, and adjust the cell concentration to 10 5 1 / mL, add 100 μL / well in 96-well plate, and cultivate overnight; add 100 μL of ethyl acetate extracts of Jerusalem artichoke leaves prepared in four different concentrations to each well, and continue to cultivate for 24 hours. The growth inhibition rate was detected by MTT method, and the IC was calculated. 50 v...
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