<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-08T10:16:13Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/11487" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/11487</identifier><datestamp>2026-03-24T01:05:39Z</datestamp><setSpec>com_10259_4313</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_4314</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">Listeria monocytogenes is a major foodborne pathogen associated with listeriosis, with a mortality rate of up to 30 %. Conventional detection methods are often time-consuming and require sophisticated equipment or complementary techniques to ensure sensitivity and specificity. This study presents a smart chromogenic polymeric sensor for the rapid detection of L. monocytogenes based on the activity of phosphatidylinositol-specific phospholipase C (PI-PLC). Six hydrophilic polymer films with identical compositions but different surface properties were developed, incorporating a chromogenic substrate that produces a visible colour change upon enzymatic hydrolysis, allowing the direct visual identification of L. monocytogenes. The sensitivity and specificity were assessed against a panel of foodborne bacteria, with detection limits of 104 CFUs/mL. Among the tested materials, NC2sf, Ff, and Sf showed the highest sensitivity and limited cross-reactivity with L. ivanovii, Staphylococcus aureus, and Bacillus cereus. Biocompatibility assays in HepG2 cells confirmed acceptable cytocompatibility, underscoring the importance of substrate selection for minimising adverse cellular effects. A proof-of-concept test on chicken breast slices and fresh-cut melon demonstrated the specific detection of L. monocytogenes and clear discrimination from non-pathogenic L. innocua, confirming the robustness and selectivity of the system. Finally, a Life Cycle Assessment highlighted the environmental impact of the sensing materials and provided insights into their potential pre-industrial scalability.</subfield>
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<subfield code="a">10.1016/j.snb.2025.139378</subfield>
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<subfield code="a">Naked-eye detection of Listeria monocytogenes using smart chromogenic polymers with tuneable surface morphologies</subfield>
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