Application of anise plant or extract thereof in preparation of anti-animal virus medicine
A technology of plant extracts and animal viruses, applied in antiviral agents, plant raw materials, plant/algae/fungus/moss components, etc.
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Embodiment 1
[0057] Embodiment 1: preparation of star anise plant extract
[0058] Take medicinal materials, pulverize them, put them in a round bottom flask, and add 75% ethanol to reflux for extraction. For the first time, 10-12 times of 75% ethanol was refluxed for 2 hours; for the second time, 8-10 times of 75% ethanol was extracted for 2 hours. The extract was filtered, and the filtrates were combined. Use a rotary evaporator to reclaim ethanol under reduced pressure in a 45°C water bath until there is no alcohol smell, and continue to concentrate and freeze-dry to obtain the ethanol extract EEIL (yield 21.51%) and ethanol alcohol extract EEIH (yield 9.16%) ) and EEIJ (yield 13.78%)
Embodiment 2
[0059] Embodiment 2: preparation of red fennel injection
[0060] Get the ethanol extract (equivalent to 50g of the original drug), add 800ml water for injection and 20ml polysorbate 80, stir well, adjust the pH value to about 9.7 with 10% sodium hydroxide solution, add water for injection to 1000ml, Stir well, filter, pot, and sterilize to obtain red fennel injection (HHXI). Each ml contains 50mg of the original drug of red poisonous fennel.
Embodiment 3
[0061] Embodiment 3: In vitro to the killing effect of pseudorabies virus (PRV) and porcine reproductive and respiratory syndrome virus (PRRSV)
[0062] Taking the maximum safe concentration (maximum no-cytotoxic concentration, MNTC) for African green monkey kidney Vero cells and African green monkey embryonic kidney Marc-145 cells as the initial concentration, after doubling dilution with DMEM culture medium, the drug dilution with 200TCID 50 Mix equal volumes of PRV or PRRSV virus dilutions, and store at 37°C, 5% CO 2 Incubate for 2 hours in the incubator. Add 100 μL per well to a 96-well plate that has grown into a monolayer of Vero or Marc-145 cells after 24 hours of adherent culture, with 8 replicate wells. At the same time, set blank control, normal cell control and virus control. At 37°C, 5% CO 2 Culture in an incubator with shaking every 30 minutes. After incubation for 2 hours, discard the virus and drug mixture in the wells, add 100 μL of maintenance solution t...
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