A kind of mixed-source terpenoid compound with hepatoprotective effect and use thereof
A technology of mixed-source terpenoids and compounds is applied in the field of mixed-source terpenoids and in the field of preparing liver-protecting and protecting drugs, which can solve the problems of little research on biological activity, no liver-protecting and liver-protecting effects, etc. The effect of good research and development prospects
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[0032] The preparation method of mixed-source terpenoids, comprises the steps:
[0033] (1) An endophytic fungus was isolated from Edgeworthia chrysantha, a traditional Chinese medicine of the genus Rupiaceae Mold Penicillium purpurogenum.
[0034] (2) Preparation of strain liquid seed liquid: the culture liquid formula is 200g of potato, 10g of yeast extract, 6g of peptone, 30g of glucose, KH 2 PO 4 2g, MgSO 4 0.5g, dilute to 1L, and adjust pH to 6.8. Dispense into 500mL conical flasks, each bottle contains about 150mL, 115℃, 68kPa, sterilize for 30 minutes. After inoculation, the cells were cultured at 28°C and 155 rpm for 3 days. Then the culture solution was diluted 100 times and used as seed solution for later use.
[0035] (3) Strain solid fermentation: 150g of rice and 180mL of purified water per 1L triangular bottle. Sterilize at 115°C, 68 kPa for 30 minutes. Add 20 mL of seed solution to each bottle and cultivate at room temperature for 40 days.
[0036] (4...
experiment example 1
[0049] Experimental Example 1: Evaluation of the protective effect of compounds on human hepatocyte injury caused by acetaminophen (APAP) in vitro
[0050] 1. Effects of compounds on the proliferation of HepG2 cells
[0051] The MTT method was used. Human hepatoma HepG2 cells (the cells better retain the characteristics of normal human hepatocytes and are often used in liver injury research) were seeded in 96-well cell culture plates, and after culturing for 24 hours, different concentrations of the samples or compounds to be tested were added. A solvent control group was set, and three parallel wells were set for each drug concentration. After the cells were treated with the drug for 48 hours, the culture medium was discarded, and 100 μL of MTT (0.5 mg / mL) solution was added to each well, and the culture was continued for 4 hours. The MTT solution was discarded, and 150 μL of DMSO was added to each well. The absorbance value was measured at the wavelength. Cell viability (...
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