Cyclocarya paliurus extract and application thereof in preparation of anti-coronavirus drugs
A technology of coronavirus and extract, applied in the field of Cyclocarya paliurus extract and its preparation of anti-coronavirus drugs, achieving good safety, simple preparation method, and the effect of inhibiting cell pathological changes
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Embodiment 1
[0029] Embodiment 1: the preparation of Cyclocarya paliurus leaf extract of the present invention
[0030] (1) Weigh 100 kg of Cyclocarya paliurus leaves dried in the shade at room temperature, add 80% ethanol with a solid-to-liquid ratio of 1:5 (w / w) after crushing, soak at room temperature for 4 hours, centrifuge at 4800 r / min for 10 minutes, and remove the supernatant. This step was repeated 2 times.
[0031] (2) Add water with a solid-liquid ratio of 1:4 (w / w) to the remaining precipitate after centrifugation to remove the supernatant, soak at 85°C for 4h, centrifuge at 4800r / min for 10min, and take the supernatant. This step was repeated 2 times.
[0032] (3) After concentrating the supernatant obtained in step (2), vacuum-dry at 50° C. for 24 hours to obtain 12.2 kg of powdery solid (named as extract 1).
[0033] Using ultraviolet-visible spectrophotometry ("Chinese Pharmacopoeia" 2015 edition general rule 0401), with rutin as a contrast, the content of flavonoids in t...
experiment example 1
[0039] Experimental example 1: Neutralization test of Cyclocarya paliurus leaf extract on 2019 novel coronavirus (SARS-CoV-2)
[0040] 1. Virus strains and drugs
[0041] Test virus strain: SARS-CoV-2 virus (BetaCoV / JS02 / human / 2020, virus strain isolated from clinical cases of new coronary pneumonia in Jiangsu Province).
[0042] Virus cultivation: The SARS-CoV-2 virus was isolated by culturing in the VeroE6 cell line. VeroE6 cells were seeded in 24-well cell culture plates in Dulbecco minimal essential medium (DMEM) medium containing 10% fetal bovine serum and antibiotics at 37°C, 5% CO 2 Incubate for 3-4 days until 80% of the well bottom is covered with a monolayer of cells. Inoculate 50ul of the virus stock solution into a 24-well plate and continue culturing for 3 days until the cells become lesions. The adherent monolayer VeroE6 cells were digested with 0.5% papain, and after ultrasonic disruption, they were centrifuged to remove the precipitate, and the supernatant wa...
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