Application of enilconazole in preparing drug for treating or preventing influenza virus infections
A technology for preventing influenza and virus infection, applied in the field of medicine, can solve problems such as no anti-influenza virus of enconazole, and achieve the effect of broad-spectrum antiviral activity and good safety
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Embodiment 1
[0029] Embodiment 1: Evaluation of enconazole anti-influenza virus activity
[0030] 1. Experimental Materials
[0031] 1.1 Cells, viruses and drugs
[0032] MDCK cells were purchased from American Type Culture Collection (ATCC); virus strain: A / PuertoRico / 8 / 34 (H1N1); drug: enconazole was purchased from Sigma.
[0033] 1.2 Experimental Instruments
[0034] Multilabel microplate reader (Perkin Elmer).
[0035] 2. Experimental methods and results
[0036] 2.1 Cell culture: 37°C, 5% CO 2 cultured in a humidified incubator. A DMEM medium containing 10% FBS, 100 U / mL of penicillin and streptomycin was used. Cells were subcultured after reaching 90% confluence, and the subculture ratio was 1 / 3 – 1 / 4.
[0037] 2.2 Virus culture: Take SPF chicken embryos aged 9 to 11 days, check them with an egg tester before inoculating the virus, and mark them at a position far away from the embryos, disinfect and punch holes, and inoculate 2- 4 The virus liquid with hemagglutina...
Embodiment 2
[0047] Example 2: Evaluation of broad-spectrum anti-influenza virus effect of enconazole
[0048] In this experiment, enconazole was tested against influenza A subtype H1N1 strains, influenza A virus subtype H1N1 amantadine-resistant strains, influenza A virus subtype H7N8 strains, influenza A virus subtype H9N2 strains and influenza B Antiviral activity of viruses.
[0049] 1. The virus strains used in the experiment include: 1. The virus strains used in the experiment include: A / Human / Hubei / 1 / 2009(H1N1), A / human / WSN / 33 / (H1N1,S31N), A / Duck / Hubei / 216 / 1983(H7N8), A / Chicken / Jiangsu / 1 / 2005(H9N2), B / human / Hubei / 1 / 2007.
[0050] 2. Divide MDCK cells into 1.5×10 4 Cells / well were seeded in 96-well cell culture plates, cultured in a 37°C cell culture incubator for 14-18 hours, and the cells were grown into a single layer before use. Discard the medium in the well plate, wash twice with PBS, add 100TCID 50 Each well (100 μl) was infected with virus liquid, and at the same time...
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