Application of nafronyloxalate in preparing medicine for treating or preventing influenza virus
A technology of naftifiramide oxalate and prevention of influenza, which is applied in the field of medicine, can solve the problem that naftofuramide oxalate has no anti-influenza virus, and achieve broad-spectrum antiviral activity and good safety
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Embodiment 1
[0033] Embodiment 1: the evaluation of anti-influenza virus activity of nafuramide oxalate
[0034] 1. Experimental Materials
[0035] 1.1 Cells, viruses and drugs
[0036] MDCK cells were purchased from ATCC, virus A / PuertoRico / 8 / 34 (H1N1) was amplified from chicken embryo culture, and naftofuramide oxalate was purchased from Sigma.
[0037] 1.2 Experimental Instruments
[0038] Multifunction detector PerkinElmer, inverted microscope Costar.
[0039] 2. Experimental methods and results
[0040] 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.
[0041] 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 inocu...
Embodiment 2
[0050] Embodiment 2: the evaluation of the anti-influenza virus broad-spectrum of nafuramide oxalate
[0051] This experiment detects that nafuramide oxalate is effective against influenza A subtype H1N1 strains, influenza A virus subtype H3N2 strains, influenza A virus subtype H1N1 amantadine-resistant strains, influenza A virus subtype H6N6 strains, and influenza A virus subtype H6N6 strains. Antiviral activity of influenza virus subtype H7N8 strain, influenza A virus subtype H9N2 strain and influenza B virus.
[0052] 1. The virus strains used in the experiment include: A / Human / Hubei / 1 / 2009(H1N1), A / human / Hubei / 3 / 2005(H3N2), A / WSN / S31N(H1N1), A / Duck / Hubei / 5 / 2010 (H6N6), A / Duck / Hubei / 216 / 1983 (H7N8), A / Chicken / Jiangsu / 1 / 2005 (H9N2), B / human / Huber / 1 / 2007.
[0053] 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. ...
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