<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>2448-5691</journal-id>
<journal-title><![CDATA[Mundo nano. Revista interdisciplinaria en nanociencias y nanotecnología]]></journal-title>
<abbrev-journal-title><![CDATA[Mundo nano]]></abbrev-journal-title>
<issn>2448-5691</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Instituto de Ciencias Aplicadas y Tecnología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2448-56912025000200105</article-id>
<article-id pub-id-type="doi">10.22201/ceiich.24485691e.2025.35.69845</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Nanopartículas viromiméticas para la entrega de ácidos nucleicos en el estudio del parásito Trypanosoma cruzi]]></article-title>
<article-title xml:lang="en"><![CDATA[Viromimetic nanoparticles for nucleic acid delivery in the study of parasite Trypanosoma cruzi]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cárdenas-Guerra]]></surname>
<given-names><![CDATA[R. E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moreno-Gutiérrez]]></surname>
<given-names><![CDATA[D. S.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández-García]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Química Laboratorio de Ingeniería Biomolecular y Bionanotecnología]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de California Departamento de Química y Bioquímica ]]></institution>
<addr-line><![CDATA[Los Ángeles ]]></addr-line>
<country>USA</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<volume>18</volume>
<numero>35</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2448-56912025000200105&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2448-56912025000200105&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2448-56912025000200105&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: La enfermedad de Chagas, causada por el parásito Trypanosoma cruzi, sigue siendo una patología desatendida con altas tasas de subdiagnóstico y opciones terapéuticas limitadas, especialmente en la fase crónica. A pesar de los avances en biología molecular, el estudio funcional de genes en T. cruzi enfrenta grandes desafíos debido a su diversidad genética y a la falta de herramientas eficientes para la entrega de ácidos nucleicos. En este contexto, las nanopartículas viromiméticas (NPVM) se perfilan como plataformas bioinspiradas, las cuales imitan propiedades estructurales y funcionales de los virus, permitiendo una entrega segura, dirigida y poco inmunogénica de material genético. Se abordan los principios de diseño, características funcionales y aplicaciones biomédicas de las NPVM. Se destaca el caso del sistema viromimético C4BK12 como ejemplo de entrega de oligonucleótidos antisentido en T. cruzi, evidenciado el potencial de estas plataformas como herramientas emergentes para la investigación funcional y el desarrollo de nuevas estrategias terapéuticas dirigidas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: Chagas disease, caused by the parasite Trypanosoma cruzi, remains a neglected illness with high rates of underdiagnosis and limited therapeutic options, especially in the chronic phase. Despite advances in molecular biology, the functional study of genes in T. cruzi faces significant challenges due to its genetic diversity and the lack of efficient nucleic acid delivery tools. In this context, viromimetic nanoparticles (VNPs) emerge as bioinspired platforms that mimic the structural and functional properties of viruses, enabling safe, targeted, and minimally immunogenic delivery of genetic material. This work explores the design principles, functional characteristics, and biomedical applications of VNPs. The viromimetic system C4BK12 is highlighted as an example of antisense oligonucleotide delivery in T. cruzi, demonstrating the potential of these platforms as emerging tools for functional research and the development of new targeted therapeutic strategies.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Chagas disease]]></kwd>
<kwd lng="en"><![CDATA[Trypanosoma cruzi]]></kwd>
<kwd lng="en"><![CDATA[viromimetic nanoparticles]]></kwd>
<kwd lng="en"><![CDATA[antisense oligonucleotides]]></kwd>
<kwd lng="en"><![CDATA[gene therapy]]></kwd>
<kwd lng="es"><![CDATA[enfermedad de Chagas]]></kwd>
<kwd lng="es"><![CDATA[Trypanosoma cruzi]]></kwd>
<kwd lng="es"><![CDATA[nanopartículas viromiméticas]]></kwd>
<kwd lng="es"><![CDATA[oligonucleótidos antisentido]]></kwd>
<kwd lng="es"><![CDATA[terapia génica]]></kwd>
</kwd-group>
</article-meta>
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