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New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity

Nanosized systems of DOX with antitumor activity on the base of micelle-like particles of amphiphilic thermosensitive copolymers of N-vinylpyrrolidone (VP) with triethylene glycol dimethacrylate (TEGDM), and N-vinylpyrrolidone and methacrylic acid (MAA) with TEGDM were explored. They were investigat...

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Autores principales: Kurmaz, Svetlana V., Ignatiev, Vladislav M., Emel’yanova, Nina S., Kurmaz, Vladimir A., Konev, Dmitry V., Balakina, Anastasiya A., Terentyev, Alexey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784683/
https://www.ncbi.nlm.nih.gov/pubmed/36559068
http://dx.doi.org/10.3390/pharmaceutics14122572
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author Kurmaz, Svetlana V.
Ignatiev, Vladislav M.
Emel’yanova, Nina S.
Kurmaz, Vladimir A.
Konev, Dmitry V.
Balakina, Anastasiya A.
Terentyev, Alexey A.
author_facet Kurmaz, Svetlana V.
Ignatiev, Vladislav M.
Emel’yanova, Nina S.
Kurmaz, Vladimir A.
Konev, Dmitry V.
Balakina, Anastasiya A.
Terentyev, Alexey A.
author_sort Kurmaz, Svetlana V.
collection PubMed
description Nanosized systems of DOX with antitumor activity on the base of micelle-like particles of amphiphilic thermosensitive copolymers of N-vinylpyrrolidone (VP) with triethylene glycol dimethacrylate (TEGDM), and N-vinylpyrrolidone and methacrylic acid (MAA) with TEGDM were explored. They were investigated in aqueous solutions by electron absorption spectroscopy, dynamic light scattering and cyclic voltammetry. Experimental data and quantum-chemical modeling indicated the formation of a hydrogen bond between oxygen-containing groups of monomer units of the copolymers and H-atoms of OH and NH(2) groups of DOX; the energies and H-bond lengths in the considered structures were calculated. A simulation of TDDFT spectra of DOX and its complexes with the VP and TEGDM units was carried out. Electrochemical studies in PBS have demonstrated that the oxidation of encapsulated DOX appeared to be easier than that of the free one, and its reduction was somewhat more difficult. The cytotoxicity of VP-TEGDM copolymer compositions containing 1, 5 and 15 wt% DOX was studied in vitro on HeLa cells, and the values of IC(50) doses were determined at 24 and 72 h of exposure. The copolymer compositions containing 5 and 15 wt% DOX accumulated actively in cell nuclei and did not cause visual changes in cell morphology.
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spelling pubmed-97846832022-12-24 New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity Kurmaz, Svetlana V. Ignatiev, Vladislav M. Emel’yanova, Nina S. Kurmaz, Vladimir A. Konev, Dmitry V. Balakina, Anastasiya A. Terentyev, Alexey A. Pharmaceutics Article Nanosized systems of DOX with antitumor activity on the base of micelle-like particles of amphiphilic thermosensitive copolymers of N-vinylpyrrolidone (VP) with triethylene glycol dimethacrylate (TEGDM), and N-vinylpyrrolidone and methacrylic acid (MAA) with TEGDM were explored. They were investigated in aqueous solutions by electron absorption spectroscopy, dynamic light scattering and cyclic voltammetry. Experimental data and quantum-chemical modeling indicated the formation of a hydrogen bond between oxygen-containing groups of monomer units of the copolymers and H-atoms of OH and NH(2) groups of DOX; the energies and H-bond lengths in the considered structures were calculated. A simulation of TDDFT spectra of DOX and its complexes with the VP and TEGDM units was carried out. Electrochemical studies in PBS have demonstrated that the oxidation of encapsulated DOX appeared to be easier than that of the free one, and its reduction was somewhat more difficult. The cytotoxicity of VP-TEGDM copolymer compositions containing 1, 5 and 15 wt% DOX was studied in vitro on HeLa cells, and the values of IC(50) doses were determined at 24 and 72 h of exposure. The copolymer compositions containing 5 and 15 wt% DOX accumulated actively in cell nuclei and did not cause visual changes in cell morphology. MDPI 2022-11-23 /pmc/articles/PMC9784683/ /pubmed/36559068 http://dx.doi.org/10.3390/pharmaceutics14122572 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kurmaz, Svetlana V.
Ignatiev, Vladislav M.
Emel’yanova, Nina S.
Kurmaz, Vladimir A.
Konev, Dmitry V.
Balakina, Anastasiya A.
Terentyev, Alexey A.
New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title_full New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title_fullStr New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title_full_unstemmed New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title_short New Nanosized Systems Doxorubicin—Amphiphilic Copolymers of N-Vinylpyrrolidone and (Di)methacrylates with Antitumor Activity
title_sort new nanosized systems doxorubicin—amphiphilic copolymers of n-vinylpyrrolidone and (di)methacrylates with antitumor activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784683/
https://www.ncbi.nlm.nih.gov/pubmed/36559068
http://dx.doi.org/10.3390/pharmaceutics14122572
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