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            <subfield code="2">doi</subfield>
            <subfield code="a">10.1186/s12989-017-0222-4</subfield>
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            <subfield code="2">sideral</subfield>
            <subfield code="a">101891</subfield>
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            <subfield code="a">ART-2017-101891</subfield>
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            <subfield code="a">eng</subfield>
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            <subfield code="a">Pérez-Hernández, Marta</subfield>
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            <subfield code="a">Multiparametric analysis of anti-proliferative and apoptotic effects of gold nanoprisms on mouse and human primary and transformed cells, biodistribution and toxicity in vivo</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2017</subfield>
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            <subfield code="a">Access copy available to the general public</subfield>
            <subfield code="f">Unrestricted</subfield>
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            <subfield code="a">Background: The special physicochemical properties of gold nanoprisms make them very useful for biomedical applications including biosensing and cancer therapy. However, it is not clear how gold nanoprisms may affect cellular physiology including viability and other critical functions. We report a multiparametric investigation on the impact of gold-nanoprisms on mice and human, transformed and primary cells as well as tissue distribution and toxicity in vivo after parental injection. Methods: Cellular uptake of the gold-nanoprisms (NPRs) and the most crucial parameters of cell fitness such as generation of reactive oxygen species (ROS), mitochondria membrane potential, cell morphology and apoptosis were systematically assayed in cells. Organ distribution and toxicity including inflammatory response were analysed in vivo in mice at 3 days or 4 months after parental administration. Results: Internalized gold-nanoprisms have a significant impact in cell morphology, mitochondrial function and ROS production, which however do not affect the potential of cells to proliferate and form colonies. In vivo NPRs were only detected in spleen and liver at 3 days and 4 months after administration, which correlated with some changes in tissue architecture. However, the main serum biochemical markers of organ damage and inflammation (TNFa and IFN¿) remained unaltered even after 4 months. In addition, animals did not show any macroscopic sign of toxicity and remained healthy during all the study period. Conclusion: Our data indicate that these gold-nanoprisms are neither cytotoxic nor cytostatic in transformed and primary cells, and suggest that extensive parameters should be analysed in different cell types to draw useful conclusions on nanomaterials safety. Moreover, although there is a tendency for the NPRs to accumulate in liver and spleen, there is no observable negative impact on animal health.</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-1-R</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/MAT2011-26851-CO2-02</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/MAT2011-26851-CO2-01</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO-FEDER/SAF2011-25390</subfield>
            <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 754609-HOTFLOW</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/754609/EU/A Photothermal Lateral Flow Test for Visual Point of Care Detection/HOTFLOW</subfield>
            <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 660228-HyHeat</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/660228/EU/Profiling gene expression in Hydra vulgaris following Gold Nanoparticle-mediated hyperthermia/HyHeat</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/EC/FP7/239931/EU/Multifunctional Magnetic Nanoparticles: Towards Smart Drugs Design/NANOPUZZLE</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/CSIC/PIE-201460I019</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-2-R</subfield>
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            <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
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            <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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            <subfield code="a">6.105</subfield>
            <subfield code="b">2017</subfield>
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            <subfield code="a">TOXICOLOGY</subfield>
            <subfield code="b">5 / 94 = 0.053</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q1</subfield>
            <subfield code="e">T1</subfield>
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            <subfield code="a">2.253</subfield>
            <subfield code="b">2017</subfield>
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        <datafield tag="593" ind1=" " ind2=" ">
            <subfield code="a">Health, Toxicology and Mutagenesis</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q1</subfield>
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        <datafield tag="593" ind1=" " ind2=" ">
            <subfield code="a">Toxicology</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="a">Medicine (miscellaneous)</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="0">(orcid)0000-0002-2861-2469</subfield>
            <subfield code="a">Moros, María</subfield>
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            <subfield code="a">Stepien, Grazyna</subfield>
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            <subfield code="a">Del Pino, Pablo</subfield>
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            <subfield code="a">Menao, Sebastián</subfield>
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            <subfield code="0">(orcid)0000-0003-3792-287X</subfield>
            <subfield code="a">Heras, Marcelo de las</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0002-9730-2210</subfield>
            <subfield code="a">Arias, Maykel</subfield>
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            <subfield code="a">Mitchell, Scott G.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Pelaz, Beatriz</subfield>
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            <subfield code="a">Gálvez, Eva M.</subfield>
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            <subfield code="a">Fuente, Jesús M. de la</subfield>
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            <subfield code="0">(orcid)0000-0003-0154-0730</subfield>
            <subfield code="a">Pardo, Julián</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Patología Animal</subfield>
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            <subfield code="c">Área Inmunología</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Química Orgánica</subfield>
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            <subfield code="g">14, 1 (2017), [20 pp]</subfield>
            <subfield code="p">Part fibre toxicol.</subfield>
            <subfield code="t">PARTICLE AND FIBRE TOXICOLOGY</subfield>
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            <subfield code="a">2019-07-09-11:51:52</subfield>
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