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  • [Efficacy of anti-neuraminidase drugs application during and after an influenza pandemic].

[Efficacy of anti-neuraminidase drugs application during and after an influenza pandemic].

Voprosy virusologii (2013-06-22)
N V Breslav, E S Shevchenko, D D Abramov, A G Prilipov, M M Zhuravleva, T A Oskerko, L V Kolobukhina, L N Merkulova, M Iu Shchelkanov, E I Burtseva, D K L'vov
摘要

The emergent 2009 A(H1N1) pandemic brought into acute focus the problem of choosing the most effective anti-influenza drugs for successive influenza infection spreading control. Oseltamivir and zanamivir, influenza virus neuraminidase inhibitors (NAIs), were recommended by the WHO experts for the treatment and prevention of influenza, including that caused by pandemic strains. A major concern regarding the use of specific antiviral compounds is the emergence of the drug-resistant strains. Oseltamivir carboxylate and zanamivir IC50 values were equal to 0.3-5.2 microM for the most of A(H1N1)pdm09 pandemic strains and 1.6-8.6 microM for the strains of influenza B virus in cell-based ELISA assay (2009-2010 season). All the studied strains of influenza A(H1N1 ) pdm09 (151) and B (22) viruses were sensitive to NAIs (2009-2011 seasons). For the first time in Russia oseltamivir-resistant A(H1N1) pdm09 influenza virus was isolated from the patient on the 5th day of a treatment course of this drug.

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Sigma-Aldrich
神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Suitable for manufacturing of diagnostic kits and reagents, Type V, lyophilized powder
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神经氨酸酶 来源于霍乱弧菌, Type III, buffered aqueous solution, 0.2 μm filtered, 1-5 units/mg protein (Lowry, using NAN-lactose)
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神经氨酸酶 来源于霍乱弧菌, Type II, buffered aqueous solution, 8-24 units/mg protein (Lowry, using NAN-lactose)
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神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Type X, lyophilized powder, ≥50 units/mg protein (using 4MU-NANA)
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α(2→3,6,8,9) 神经氨酸酶 来源于产脲节杆菌, recombinant, expressed in E. coli, buffered aqueous solution
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神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Type VIII, lyophilized powder, 10-20 units/mg protein (using 4MU-NANA), 3.5-8.0 units/mg protein (mucin)
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