Application of clooxine in preparation of medicine for treating or preventing influenza virus infection
A technology for preventing influenza and virus infection, applied in the field of medicine, can solve problems such as no reports of chloroxacin being anti-influenza virus, and achieve the effect of broad-spectrum anti-influenza virus activity and good safety
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Embodiment 1
[0031] Embodiment 1: Evaluation of clooxine anti-influenza virus activity
[0032] 1. Experimental Materials
[0033] 1.1 Cells, viruses and drugs
[0034] MDCK cells were purchased from American Type Culture Collection (ATCC); virus strain: A / PuertoRico / 8 / 34 (H1N1); drug: chloroxine was purchased from Sigma.
[0035] 1.2 Experimental Instruments
[0036] Multilabel microplate reader (PerkinElmer).
[0037] 2. Experimental methods and results
[0038] 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.
[0039] 2.2 Virus culture: Take SPF chicken embryos aged 9 to 11 days, check them with an egg tester before inoculating the virus, mark them at a position far away from the embryos, disinfect and punch holes, and inoculate 2- 4 The virus liquid with hemagglutination titer was sea...
Embodiment 2
[0049] Embodiment 2: Evaluation of broad-spectrum anti-influenza virus effect of clooxine
[0050] In this experiment, clooxine was tested against influenza A subtype H1N1 strain, influenza A virus subtype H3N2 strain, influenza A virus subtype H1N1 amantadine-resistant strain, influenza A virus subtype H6N6 strain, influenza A virus Antiviral activity of virus subtype H7N8 strain, influenza A virus subtype H9N2 strain and influenza B virus.
[0051] 1. The virus strains used in the experiment include: A / Human / Hubei / 1 / 2009(H1N1), A / human / Hubei / 3 / 2005(H3N2), A / human / WSN / 33 / (H1N1, S31N), A / Duck / Hubei / 5 / 2010(H6N6), A / Duck / Hubei / 216 / 1983(H7N8), A / Chicken / Jiangsu / 1 / 2005(H9N2), B / human / Hubei / 1 / 2007.
[0052] 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 100TCI...
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