Cationic effect in the formation of toxic and antiviral properties of Keggon heteropoly compounds

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The Cytotoxicity indices (IC50) of Keggin’s phosphorus-molybdenum heteropoly acids (HPCAs) and their sodium and potassium salts on dog kidney cells (MDSC) were determined. The antiviral activity of these compounds against topical strains of influenza A (H3N2 and H1N1) was revealed. The dependence of the biological properties of polyoxometalates (POMs) on the elemental composition of their molecules has been confirmed. It has been shown that when some of the molybdenum atoms are replaced by vanadium atoms, HPCA and their salts acquire higher cytotoxicities, which increase monotonically as the number of substitutions increases. For the first time, the dependence of the biological activity of HPCA and their salts on the mass of cations has been established and interpreted. In vivo (on white outbred mice) the values of semi-lethal doses (DL50) of these compounds were established. For aqueous solutions of sodium and potassium salts of GPCA in a wide range of concentrations (from 0.05 μM to 15 μM), the values of the toxicity index (It) were determined on the model of motile cells. It has been established that GPCA and their salts are classified as moderately dangerous toxic substances and have selective antiviral activity, which at low concentrations (less than 15 μM) for influenza A strains is manifested mainly by a decrease in hemagglutination activity (HA).

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F. Dalidchik

Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: domfdal@mail.ru
俄罗斯联邦, Москва

O. Lopatina

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

S. Kovalevsky

Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

E. Isaeva

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

M. Bidevkina

Erisman Federal Scientific Center of Hygiene, Federal Service for Supervision of Consumer Rights Protection and Human Welfare

Email: domfdal@mail.ru
俄罗斯联邦, Mytishchi

O. Baklanova

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

E. Gushchina

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

F. Lisitsyn

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

E. Balashov

Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences

Email: embalashov@yandex.ru
俄罗斯联邦, Moscow

M. Mezentseva

Национальный исследовательский центр эпидемиологии и микробиологии им. Н.Ф. Гамалеи

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

T. Pritchina

Gamaleya Research Institute of Epidemiology and Microbiology

Email: domfdal@mail.ru
俄罗斯联邦, Moscow

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2. Fig. 1. Visualization of a suspension of influenza A/California/07/09 virus incubated for 1 hour in an aqueous solution of H5PMo10V2O40 (100 μM): 1 - empty viral shells, 2 - intact HF.

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3. Fig. 2. Control of MDSC cells (without the use of POM). Section of the surface of an MDSC cell infected with influenza virus A/California/07/09. Arrows indicate normal HF budding from the cell surface.

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4. Fig. 3. Section of the surface of an MSDK cell infected with influenza A/California/07/09 virus after treatment with an aqueous solution of H5PMo10V2O40 (25 μM). The arrow indicates the group of defective HFs (without nucleoid).

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5. Fig. 4. Section of villi on the surface of an MDSC cell after exposure to an aqueous solution of Na5PMo10V2O40 (20 µM). The arrow indicates defective particles of influenza virus A/California/07/09 with partially destroyed and/or deformed shells.

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