Anti-tumor active matter and its preparing method and use
A technology for anti-tumor activity and active substances, which is applied in the field of anti-tumor active substances and their preparation, and can solve problems such as no public literature reports on anti-tumor active substances.
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Embodiment 1
[0016] 1. Inoculate Monascus ruber (Monascus ruber) 3081 onto the slant of the test tube solid medium, the medium formula is wort medium, and cultivate it at 20°C for 8 days to obtain the test tube species;
[0017] 2. Inoculate the test tube seed into a solid medium in a 250ml Erlenmeyer flask (50ml per bottle). The medium formula is: 20% of Panax notoginseng fibrous root powder, 80% of water, natural pH, culture temperature 30°C, optimum 25-28 ℃, static culture for 20 days, until the hyphae are overgrown.
[0018] 3. Freeze dry the solid culture. Extract with 90% ethanol at room temperature for 2 days, concentrate under reduced pressure, and evaporate the solvent to obtain the active substance.
Embodiment 2
[0020] Basically with embodiment 1. The difference is: the temperature of the test tube solid culture is 28°C, and the time is 6 days; the formula of the solid medium is: 25% of Panax notoginseng fibrous root powder, 75% of water, the culture temperature is 25°C, and the culture is static for 18 days; % ethanol extraction at room temperature.
Embodiment 3
[0022] Basically with embodiment 1. The difference is: the temperature of the test tube solid culture is 30°C, and the time is 4 days; the formula of the solid medium is: 30% of Panax notoginseng fibrous root powder, 70% of water, the culture temperature is 20°C, and the culture is static for 15 days; % ethanol extraction at room temperature.
[0023] Two, the drug efficacy test of compound antitumor activity of the present invention
[0024] 1. Growth inhibitory effect on human tumor cells
[0025] After the cells in the logarithmic growth phase were adjusted to an appropriate concentration, they were added to a 96-well culture plate, 90ul / well. The test concentration is 100ug / ml, 3 parallel wells are set up, 10ul / well. The negative control is the same volume of culture solution, and the positive control is the anticancer drug cisplatin (DDP). At the same time, a parallel control of the corresponding concentration of DMSO solvent control and the color concentration of the...
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