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    <subfield code="a">10.1021/acsami.1c02338</subfield>
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    <subfield code="a">Beola, L.</subfield>
    <subfield code="0">(orcid)0000-0003-4516-8694</subfield>
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    <subfield code="a">Critical Parameters to Improve Pancreatic Cancer Treatment Using Magnetic Hyperthermia: Field Conditions, Immune Response, and Particle Biodistribution</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">Magnetic hyperthermia (MH) was used to treat a murine model of pancreatic cancer. This type of cancer is generally characterized by the presence of dense stroma that acts as a barrier for chemotherapeutic treatments. Several alternating magnetic field (AMF) conditions were evaluated using three-dimensional (3D) cell culture models loaded with magnetic nanoparticles (MNPs) to determine which conditions were producing a strong effect on the cell viability. Once the optimal AMF conditions were selected, in vivo experiments were carried out using similar frequency and field amplitude parameters. A marker of the immune response activation, calreticulin (CALR), was evaluated in cells from a xenograft tumor model after the MH treatment. Moreover, the distribution of nanoparticles within the tumor tissue was assessed by histological analysis of tumor sections, observing that the exposure to the alternating magnetic field resulted in the migration of particles toward the inner parts of the tumor. Finally, a relationship between an inadequate body biodistribution of the particles after their intratumoral injection and a significant decrease in the effectiveness of the MH treatment was found. Animals in which most of the particles remained in the tumor area after injection showed higher reductions in the tumor volume growth in comparison with those animals in which part of the particles were found also in the liver and spleen. Therefore, our results point out several factors that should be considered to improve the treatment effectiveness of pancreatic cancer by magnetic hyperthermia.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/PGC2018-096016-B-I00</subfield>
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    <subfield code="b">23 / 108 = 0.213</subfield>
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    <subfield code="a">Materials Science (miscellaneous)</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Grazu, V.</subfield>
    <subfield code="0">(orcid)0000-0001-6170-4237</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Fernandez-Afonso, Y.</subfield>
    <subfield code="0">(orcid)0000-0002-0970-1917</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Fratila, R.M.</subfield>
    <subfield code="0">(orcid)0000-0001-5559-8757</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">De Las Heras, M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3792-287X</subfield>
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    <subfield code="a">De La Fuente, J.M.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gutierrez, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-2366-3598</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Asin, L.</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">2009</subfield>
    <subfield code="2">750</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Analítica</subfield>
    <subfield code="c">Área Química Analítica</subfield>
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    <subfield code="1">1009</subfield>
    <subfield code="2">773</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Patología Animal</subfield>
    <subfield code="c">Área Sanidad Animal</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">13, 11 (2021), 12982–12996</subfield>
    <subfield code="p">ACS appl. mater. interfaces</subfield>
    <subfield code="t">ACS applied materials &amp; interfaces</subfield>
    <subfield code="x">1944-8244</subfield>
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