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Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents
Fullerene is a nanosized carbon structure with potential drug delivery applications. We studied the bioeffects of a water-soluble fullerene derivative, fullerenol, with 10-12 oxygen groups (F10-12); its structure was characterized by IR and XPS spectroscopy. A bioluminescent enzyme system was used t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232284/ https://www.ncbi.nlm.nih.gov/pubmed/34203700 http://dx.doi.org/10.3390/ijms22126382 |
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author | Kovel, Ekaterina S. Kicheeva, Arina G. Vnukova, Natalia G. Churilov, Grigory N. Stepin, Evsei A. Kudryasheva, Nadezhda S. |
author_facet | Kovel, Ekaterina S. Kicheeva, Arina G. Vnukova, Natalia G. Churilov, Grigory N. Stepin, Evsei A. Kudryasheva, Nadezhda S. |
author_sort | Kovel, Ekaterina S. |
collection | PubMed |
description | Fullerene is a nanosized carbon structure with potential drug delivery applications. We studied the bioeffects of a water-soluble fullerene derivative, fullerenol, with 10-12 oxygen groups (F10-12); its structure was characterized by IR and XPS spectroscopy. A bioluminescent enzyme system was used to study toxic and antioxidant effects of F10-12 at the enzymatic level. Antioxidant characteristics of F10-12 were revealed in model solutions of organic and inorganic oxidizers. Low-concentration activation of bioluminescence was validated statistically in oxidizer solutions. Toxic and antioxidant characteristics of F10-12 were compared to those of homologous fullerenols with a higher number of oxygen groups:F24-28 and F40-42. No simple dependency was found between the toxic/antioxidant characteristics and the number of oxygen groups on the fullerene’s carbon cage. Lower toxicity and higher antioxidant activity of F24-28 were identified and presumptively attributed to its higher solubility. An active role of reactive oxygen species (ROS) in the bioeffects of F10-12 was demonstrated. Correlations between toxic/antioxidant characteristics of F10-12 and ROS content were evaluated. Toxic and antioxidant effects were related to the decrease in ROS content in the enzyme solutions. Our results reveal a complexity of ROS effects in the enzymatic assay system. |
format | Online Article Text |
id | pubmed-8232284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82322842021-06-26 Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents Kovel, Ekaterina S. Kicheeva, Arina G. Vnukova, Natalia G. Churilov, Grigory N. Stepin, Evsei A. Kudryasheva, Nadezhda S. Int J Mol Sci Article Fullerene is a nanosized carbon structure with potential drug delivery applications. We studied the bioeffects of a water-soluble fullerene derivative, fullerenol, with 10-12 oxygen groups (F10-12); its structure was characterized by IR and XPS spectroscopy. A bioluminescent enzyme system was used to study toxic and antioxidant effects of F10-12 at the enzymatic level. Antioxidant characteristics of F10-12 were revealed in model solutions of organic and inorganic oxidizers. Low-concentration activation of bioluminescence was validated statistically in oxidizer solutions. Toxic and antioxidant characteristics of F10-12 were compared to those of homologous fullerenols with a higher number of oxygen groups:F24-28 and F40-42. No simple dependency was found between the toxic/antioxidant characteristics and the number of oxygen groups on the fullerene’s carbon cage. Lower toxicity and higher antioxidant activity of F24-28 were identified and presumptively attributed to its higher solubility. An active role of reactive oxygen species (ROS) in the bioeffects of F10-12 was demonstrated. Correlations between toxic/antioxidant characteristics of F10-12 and ROS content were evaluated. Toxic and antioxidant effects were related to the decrease in ROS content in the enzyme solutions. Our results reveal a complexity of ROS effects in the enzymatic assay system. MDPI 2021-06-15 /pmc/articles/PMC8232284/ /pubmed/34203700 http://dx.doi.org/10.3390/ijms22126382 Text en © 2021 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 Kovel, Ekaterina S. Kicheeva, Arina G. Vnukova, Natalia G. Churilov, Grigory N. Stepin, Evsei A. Kudryasheva, Nadezhda S. Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title | Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title_full | Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title_fullStr | Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title_full_unstemmed | Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title_short | Toxicity and Antioxidant Activity of Fullerenol C(60,70) with Low Number of Oxygen Substituents |
title_sort | toxicity and antioxidant activity of fullerenol c(60,70) with low number of oxygen substituents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232284/ https://www.ncbi.nlm.nih.gov/pubmed/34203700 http://dx.doi.org/10.3390/ijms22126382 |
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