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    Título
    Antineoplastic behavior of polydopamine nanoparticles prepared in different water/alcohol media
    Autor(es)
    Nieto Jiménez, CeliaUSAL authority ORCID
    Marcelo, Gema
    Vega Moreno, Milena AmparoUSAL authority ORCID
    Martín del Valle, Eva MaríaUSAL authority
    Palabras clave
    Polydopamine nanoparticles
    Alcohols
    Size
    Iron adsorption capacity
    Cytotoxicity
    Fecha de publicación
    2021
    Editor
    Elsevier
    Citación
    Celia Nieto, Gema Marcelo, Milena Vega, Eva M. Martín del Valle, Antineoplastic behavior of polydopamine nanoparticles prepared in different water/alcohol media, Colloids and Surfaces B: Biointerfaces, Volume 199, 2021, 111506, ISSN 0927-7765, https://doi.org/10.1016/j.colsurfb.2020.111506. (https://www.sciencedirect.com/science/article/pii/S0927776520308626)
    Resumen
    [EN]Polydopamine nanoparticles (PD NPs) have been synthesized in the present work through the oxidative polymerization of dopamine in aqueous media containing five different types of alcohol in a constant solvent volume ratio. We have shown that the type of alcohol, along with the ammonium hydroxide concentration used in the synthesis process, conditions particle size. Additionally, it has been found that the type of alcohol employed influences the well-known capacity of polydopamine nanoparticles to adsorb iron. As a consequence, since a ferroptosis-like mechanism may account for the cytotoxicity of these nanoparticles, the type of alcohol could also have a determining role in their antineoplastic activity. Here, the existence of a correlation between the ability of polydopamine nanoparticles to load Fe3+ and their toxic effect on breast cancer cells has been proven. For instance, nanoparticles synthesized using 2-propanol adsorbed more Fe3+ and had the greatest capacity to reduce breast tumor cell viability. Moreover, none of the nanoparticle synthesized with the different alcohols significantly decreased normal cell survival. Cancer cells present greater iron-dependence than healthy cells and this fact may explain why polydopamine nanoparticles toxicity, in which Fenton chemistry could be implicated, seems tumor-specific.
    URI
    https://hdl.handle.net/10366/168899
    ISSN
    0927-7765
    DOI
    10.1016/j.colsurfb.2020.111506
    Versión del editor
    https://doi.org/10.1016/j.colsurfb.2020.111506
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