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    <subfield code="2">doi</subfield>
    <subfield code="a">10.3390/gels12030231</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">148680</subfield>
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    <subfield code="a">ART-2026-148680</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Salto-Girón, Carmen</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Protein-directed nucleation and stabilization of ultrasmall silver nanoparticles within BSA hydrogels</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2026</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Biocompatible nanocomposite hydrogels are emerging as versatile platforms in nanomedicine, particularly when natural proteins are used as both structural and chemical components. In this work, we report a green, simple, and rapid in situ synthesis of ultrasmall silver nanoparticles (uAgNPs) within a bovine serum albumin (BSA) hydrogel, in which albumin simultaneously acts as the reducing agent and three-dimensional scaffold. The confined reaction environment generated uniformly dispersed Ag nanostructures with diameters in the 4–40 nm range, as confirmed by DLS and TEM. High-resolution TEM revealed clear Face-Centered Cubic (FCC, 111) lattice fringes, demonstrating the crystalline nature of the embedded uAgNPs. Quantitative image analysis showed narrow size distributions and high circularities, consistent with cluster stabilization through protein–metal interactions. Rheological measurements further indicated that the incorporation of uAgNPs enhanced hydrogel stiffness and delayed yielding, reflecting a reinforcement effect mediated by the nanoparticles acting as additional cross-linking points. Moreover, when very small embedded uAgNPs are formed, the presence of emissive silver nanoclusters was found using fluorescence emission spectroscopy. Overall, our results show that BSA hydrogels provide an effective matrix for directing green uAgNP nucleation, ensuring high stability, controlled growth in less than 2 min, and improved mechanical properties. The resulting protein–nanoparticle composite constitutes a promising soft material for imaging, sensing, and other biomedical applications requiring stable, biocompatible nanoscale architectures.</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/AEI/CEX2023-001286-S</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/UZ-DGA/T57-23R</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
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    <subfield code="u">https://creativecommons.org/licenses/by/4.0/deed.es</subfield>
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    <subfield code="a">González-García, M. Carmen</subfield>
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    <subfield code="a">Mañas-Torres, Mari C.</subfield>
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    <subfield code="a">López-López, Modesto T.</subfield>
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    <subfield code="a">Álvarez de Cienfuegos, Luis</subfield>
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    <subfield code="a">Hueso, José L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-4546-4111</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Orte, Angel</subfield>
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    <subfield code="a">García-Fernández, Emilio</subfield>
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    <subfield code="1">5005</subfield>
    <subfield code="2">790</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ing.Quím.Tecnol.Med.Amb.</subfield>
    <subfield code="c">Área Tecnologi. Medio Ambiente</subfield>
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    <subfield code="g">12, 3 (2026), 231</subfield>
    <subfield code="p">Gels</subfield>
    <subfield code="t">Gels</subfield>
    <subfield code="x">2310-2861</subfield>
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    <subfield code="t">Material suplementario</subfield>
    <subfield code="w">https://www.mdpi.com/article/10.3390/gels12030231/s1</subfield>
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    <subfield code="a">2026-03-26-14:31:52</subfield>
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