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Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine

Cancer still poses a global threat, since a lot of tumors remain untreatable despite all the available chemotherapeutic drugs, whose side effects, it must also be noted, still raise concerns. The antitumoral properties of marine seaweeds make them a potential source of new, less toxic, and more acti...

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Autores principales: González-Ballesteros, Noelia, Maietta, Immacolata, Rey-Méndez, Raquel, Rodríguez-Argüelles, M. Carmen, Lastra-Valdor, Mariano, Cavazza, Antonella, Grimaldi, Maria, Bigi, Franca, Simón-Vázquez, Rosana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865996/
https://www.ncbi.nlm.nih.gov/pubmed/36662193
http://dx.doi.org/10.3390/md21010020
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author González-Ballesteros, Noelia
Maietta, Immacolata
Rey-Méndez, Raquel
Rodríguez-Argüelles, M. Carmen
Lastra-Valdor, Mariano
Cavazza, Antonella
Grimaldi, Maria
Bigi, Franca
Simón-Vázquez, Rosana
author_facet González-Ballesteros, Noelia
Maietta, Immacolata
Rey-Méndez, Raquel
Rodríguez-Argüelles, M. Carmen
Lastra-Valdor, Mariano
Cavazza, Antonella
Grimaldi, Maria
Bigi, Franca
Simón-Vázquez, Rosana
author_sort González-Ballesteros, Noelia
collection PubMed
description Cancer still poses a global threat, since a lot of tumors remain untreatable despite all the available chemotherapeutic drugs, whose side effects, it must also be noted, still raise concerns. The antitumoral properties of marine seaweeds make them a potential source of new, less toxic, and more active antitumoral agents. Furthermore, these natural extracts can be combined with nanotechnology to increase their efficacy and improve targeting. In this work, a Codium tomentosum (CT) aqueous extract was employed for the green synthesis of gold nanoparticles (Au@CT). The complete characterization of Au@CT was performed by UV-Vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Zeta potential, electron microscopy, X-ray powder diffraction (XRD), high-performance steric exclusion chromatography (HPSEC), and by the determination of their antioxidant capacity. The antiproliferative activity of Au@CT was then tested in hepatic (HEPG-2) and pancreatic (BxPC-3) cell lines. Their potential capacity as enhancers of gemcitabine, a drug frequently used to treat both types of tumors, was also tested. The activity of Au@CT was compared to the activity of the CT extract alone. A synergistic effect with gemcitabine was proven for HEPG-2. Our results showed that gold nanoparticles synthesized from seaweed extracts with antitumoral activity could be a good gemcitabine enhancer.
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spelling pubmed-98659962023-01-22 Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine González-Ballesteros, Noelia Maietta, Immacolata Rey-Méndez, Raquel Rodríguez-Argüelles, M. Carmen Lastra-Valdor, Mariano Cavazza, Antonella Grimaldi, Maria Bigi, Franca Simón-Vázquez, Rosana Mar Drugs Article Cancer still poses a global threat, since a lot of tumors remain untreatable despite all the available chemotherapeutic drugs, whose side effects, it must also be noted, still raise concerns. The antitumoral properties of marine seaweeds make them a potential source of new, less toxic, and more active antitumoral agents. Furthermore, these natural extracts can be combined with nanotechnology to increase their efficacy and improve targeting. In this work, a Codium tomentosum (CT) aqueous extract was employed for the green synthesis of gold nanoparticles (Au@CT). The complete characterization of Au@CT was performed by UV-Vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Zeta potential, electron microscopy, X-ray powder diffraction (XRD), high-performance steric exclusion chromatography (HPSEC), and by the determination of their antioxidant capacity. The antiproliferative activity of Au@CT was then tested in hepatic (HEPG-2) and pancreatic (BxPC-3) cell lines. Their potential capacity as enhancers of gemcitabine, a drug frequently used to treat both types of tumors, was also tested. The activity of Au@CT was compared to the activity of the CT extract alone. A synergistic effect with gemcitabine was proven for HEPG-2. Our results showed that gold nanoparticles synthesized from seaweed extracts with antitumoral activity could be a good gemcitabine enhancer. MDPI 2022-12-27 /pmc/articles/PMC9865996/ /pubmed/36662193 http://dx.doi.org/10.3390/md21010020 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
González-Ballesteros, Noelia
Maietta, Immacolata
Rey-Méndez, Raquel
Rodríguez-Argüelles, M. Carmen
Lastra-Valdor, Mariano
Cavazza, Antonella
Grimaldi, Maria
Bigi, Franca
Simón-Vázquez, Rosana
Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title_full Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title_fullStr Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title_full_unstemmed Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title_short Gold Nanoparticles Synthesized by an Aqueous Extract of Codium tomentosum as Potential Antitumoral Enhancers of Gemcitabine
title_sort gold nanoparticles synthesized by an aqueous extract of codium tomentosum as potential antitumoral enhancers of gemcitabine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865996/
https://www.ncbi.nlm.nih.gov/pubmed/36662193
http://dx.doi.org/10.3390/md21010020
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