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    <subfield code="a">10.1038/s41598-023-33487-3</subfield>
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    <subfield code="a">Sarreshtehdari, Amirhossein</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Preliminary evaluation of the safety and efficacy of glucose solution infusion through the hepatic artery on irreversible electroporation focusing</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2023</subfield>
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    <subfield code="a">Due to electrical features of the tissue, such as impedance, which have a significant impact on irreversible electroporation (IRE) function, the administration of glucose solution 5% (GS5%) through the hepatic artery would focus IRE on scattered liver tumors. By creating a differential impedance between healthy and tumor tissue. This study aimed to determine the effects of the GS5% protocol on healthy liver tissue and its safety. 21 male Athymic nude rats Hsd: RH-Foxn1mu were used in the study. Animals were split into two groups. In group 1, a continuous infusion through the gastroduodenal artery of GS5% was performed to measure the impedance with a dose of 0.008 mL/g for 16 min. In group 2, the animals were divided into two subgroups for infusions of GS5%. Group 2.1, at 0.008 mL/g for 16 min. Group 2.2 at 0.03 mL/g for 4 min. Blood samples were collected after anesthesia has been induced. The second sample, after catheterization of the artery, and the third after the GS5% infusion. All the animals were sacrificed to collect histological samples. The survival rate during the experiment was 100%. A considerable impact on the impedance of the tissue was noticed, on average up to 4.31 times more than the baseline, and no side effects were observed after GS5% infusion. In conclusion, impedance alteration by Glucose solution infusion may focus IRE on tumor tissue and decrease IRE’s effects on healthy tissue.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/ISCIII/PI21-00440</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RTI2018-094357-B-C21</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RTI2018-094357-B-C22</subfield>
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    <subfield code="a">MULTIDISCIPLINARY SCIENCES</subfield>
    <subfield code="b">25 / 134 = 0.187</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Multidisciplinary</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Burdio, Fernando</subfield>
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    <subfield code="a">López-Alonso, Borja</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-2848-170X</subfield>
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    <subfield code="a">Lucía, Óscar</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1284-9007</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Burdio, José Miguel</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-9655-5531</subfield>
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    <subfield code="a">Villamonte, María</subfield>
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    <subfield code="a">Andaluz, A.</subfield>
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    <subfield code="a">García-Arnas, F.</subfield>
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    <subfield code="a">Berjano, E.</subfield>
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    <subfield code="1">5008</subfield>
    <subfield code="2">785</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ingeniería Electrón.Com.</subfield>
    <subfield code="c">Área Tecnología Electrónica</subfield>
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    <subfield code="g">13 (2023), 7120 [9 pp.]</subfield>
    <subfield code="p">Sci. rep. (Nat. Publ. Group)</subfield>
    <subfield code="t">Scientific reports (Nature Publishing Group)</subfield>
    <subfield code="x">2045-2322</subfield>
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