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ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma
Materials that are able to produce free radicals have gained increasing attention for environmental and biomedical purposes. Free radicals, such as the superoxide anion (O(2)(•−)), act as secondary messengers in many physiological pathways, such as cell survival. Therefore, the production of free ra...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823868/ https://www.ncbi.nlm.nih.gov/pubmed/36615964 http://dx.doi.org/10.3390/nano13010054 |
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author | Chianese, Giovanna Fasolino, Ines Tramontano, Chiara De Stefano, Luca Imparato, Claudio Aronne, Antonio Ambrosio, Luigi Raucci, Maria Grazia Rea, Ilaria |
author_facet | Chianese, Giovanna Fasolino, Ines Tramontano, Chiara De Stefano, Luca Imparato, Claudio Aronne, Antonio Ambrosio, Luigi Raucci, Maria Grazia Rea, Ilaria |
author_sort | Chianese, Giovanna |
collection | PubMed |
description | Materials that are able to produce free radicals have gained increasing attention for environmental and biomedical purposes. Free radicals, such as the superoxide anion (O(2)(•−)), act as secondary messengers in many physiological pathways, such as cell survival. Therefore, the production of free radicals over physiological levels has been exploited in the treatment of different types of cancer, including osteosarcoma (OS). In most cases, the production of reactive oxygen species (ROS) by materials is light-induced and requires the use of chemical photosensitisers, making it difficult and expensive. Here, for the first time, we propose photoluminescent hybrid ZrO(2)-acetylacetonate nanoparticles (ZrO(2)-acac NPs) that are capable of generating O(2)(•−) without light activation as an adjuvant for the treatment of OS. To increase the uptake and ROS generation in cancer cells, we modify the surface of ZrO(2)-acac NPs with hyaluronic acid (HA), which recognizes and binds to the surface antigen CD44 overexpressed on OS cells. Since these nanoparticles emit in the visible range, their uptake into cancer cells can be followed by a label-free approach. Overall, we show that the generation of O(2)(•−) is toxic to OS cells and can be used as an adjuvant treatment to increase the efficacy of conventional drugs. |
format | Online Article Text |
id | pubmed-9823868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98238682023-01-08 ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma Chianese, Giovanna Fasolino, Ines Tramontano, Chiara De Stefano, Luca Imparato, Claudio Aronne, Antonio Ambrosio, Luigi Raucci, Maria Grazia Rea, Ilaria Nanomaterials (Basel) Article Materials that are able to produce free radicals have gained increasing attention for environmental and biomedical purposes. Free radicals, such as the superoxide anion (O(2)(•−)), act as secondary messengers in many physiological pathways, such as cell survival. Therefore, the production of free radicals over physiological levels has been exploited in the treatment of different types of cancer, including osteosarcoma (OS). In most cases, the production of reactive oxygen species (ROS) by materials is light-induced and requires the use of chemical photosensitisers, making it difficult and expensive. Here, for the first time, we propose photoluminescent hybrid ZrO(2)-acetylacetonate nanoparticles (ZrO(2)-acac NPs) that are capable of generating O(2)(•−) without light activation as an adjuvant for the treatment of OS. To increase the uptake and ROS generation in cancer cells, we modify the surface of ZrO(2)-acac NPs with hyaluronic acid (HA), which recognizes and binds to the surface antigen CD44 overexpressed on OS cells. Since these nanoparticles emit in the visible range, their uptake into cancer cells can be followed by a label-free approach. Overall, we show that the generation of O(2)(•−) is toxic to OS cells and can be used as an adjuvant treatment to increase the efficacy of conventional drugs. MDPI 2022-12-22 /pmc/articles/PMC9823868/ /pubmed/36615964 http://dx.doi.org/10.3390/nano13010054 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 Chianese, Giovanna Fasolino, Ines Tramontano, Chiara De Stefano, Luca Imparato, Claudio Aronne, Antonio Ambrosio, Luigi Raucci, Maria Grazia Rea, Ilaria ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title | ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title_full | ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title_fullStr | ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title_full_unstemmed | ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title_short | ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma |
title_sort | ros-generating hyaluronic acid-modified zirconium dioxide-acetylacetonate nanoparticles as a theranostic platform for the treatment of osteosarcoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823868/ https://www.ncbi.nlm.nih.gov/pubmed/36615964 http://dx.doi.org/10.3390/nano13010054 |
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