Novel conjugates &lt;modified nucleoside &ndash; nanoparticle&gt; to suppress the growth of superbugs

Negrya S.; Efremenkova O.; Artemyev M.; Sizova S.; Oleinikov V.; Alexandrova L.

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2022-01-15 19:04

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NEGRYA, S., EFREMENKOVA, O., ARTEMYEV, M., SIZOVA, S., OLEINIKOV, V., ALEXANDROVA, L.. Novel conjugates <modified nucleoside – nanoparticle> to suppress the growth of superbugs. In: NANO-2019: Limits of Nanoscience and Nanotechnologies, Ed. 2019, 24-27 septembrie 2019, Chişinău. Chișinău, Republica Moldova: 2019, p. 64.

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NANO-2019: Limits of Nanoscience and Nanotechnologies 2019

Conferința "SPINTECH Summer school “S/F Hybrid Structures for Spintronics”"
2019, Chişinău, Moldova, 24-27 septembrie 2019

Novel conjugates <modified nucleoside – nanoparticle> to suppress the growth of superbugs

Pag. 64-64

Negrya S.¹, Efremenkova O.², Artemyev M.³⁴, Sizova S.³, Oleinikov V.³, Alexandrova L.¹

¹ Engelhardt Institute of Molecular Biology RAS,
² Gause Institute of New Antibiotics,
³ Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, RAS,
⁴ Research Institute for Physical Chemical Problems, Belarusian State University

Disponibil în IBN: 27 ianuarie 2020

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Nowadays practically all pathogenic bacteria and viruses have developed resistance to most clinically important medicinal preparations, hence, there is a need in new drugs acting on new targets and being active against superbugs - resistant strains of pathogens [1]. Recently we have synthesized 2’-deoxypyrimidine nucleoside derivatives bearing extended alkyloxymethyl or alkyl(1,2,3-triazol-1-yl)methyl substituents at С-5 position and demonstrated their effective bacteriostatic activity against two Mycobacterium tuberculosis strains [2] as well as against a set of Gram-positive bacteria [3]. However, the nucleosides with large hydrophobic fragments are insoluble in water, thus, limiting the biological investigations. To solve this problem, a linker group was introduced for coupling a nucleoside moiety to a nanoparticle. At the same time, we have developed fundamentally new nanostructures of the type “Plates” with both positive and negative surface charge [5] with uniquely high optical properties (narrow fluorescence peak, high extinction, high efficiency of two-photon excitation) and offered an efficient method for obtaining conjugates [nucleoside-nanoparticle]. To study the effect of nanostructures on bacterial cells were selected bacteria that differ in shape, structure and thickness of the cell wall. Herein we will present a new approach for transporting medicinal agents into bacterial cells to their targets, namely, the preparation of conjugates of biologically active nucleosides with nanoparticles.

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