<?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>2026-06-14T03:44:53Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18061" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18061</identifier><datestamp>2024-11-28T15:31:10Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16938</setSpec><setSpec>col_20.500.12105_16927</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Paris, Juan L.</subfield>
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      <subfield code="a">Vallet-Regí, María</subfield>
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      <subfield code="c">2020-06-08</subfield>
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      <subfield code="a">Mesoporous silica nanoparticles have attracted much attention in recent years as drug and gene delivery systems for biomedical applications. Among their most beneficial features for biomedicine, we can highlight their biocompatibility and their outstanding textural properties, which provide a great loading capacity for many types of cargos. In the context of cancer nanomedicine, combination therapy and gene transfection/silencing have recently been highlighted as two of its most promising fields. In this review, we aim to provide an overview of the different small molecule drug-nucleic acid co-delivery combinations that have been developed using mesoporous silica nanoparticles as carriers. By carefully selecting the chemotherapeutic drug and nucleic acid cargos to be co-delivered by mesoporous silica nanoparticles, different therapeutic goals can be achieved by overcoming resistance mechanisms, combining different cytotoxic mechanisms, or providing an additional antiangiogenic effect. The examples here presented highlight the great promise of this type of strategies for the development of future therapeutics.</subfield>
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      <subfield code="a">10.3390/pharmaceutics12060526</subfield>
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      <subfield code="a">Pharmaceutics</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18061</subfield>
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      <subfield code="a">Mesoporous silica nanoparticles</subfield>
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      <subfield code="a">Co-delivery</subfield>
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      <subfield code="a">Drug delivery</subfield>
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      <subfield code="a">Nucleic acids</subfield>
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      <subfield code="a">Gene transfection</subfield>
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      <subfield code="a">Dióxido de silicio</subfield>
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      <subfield code="a">Nanopartículas</subfield>
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      <subfield code="a">Sistemas de liberación de medicamentos</subfield>
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      <subfield code="a">Ácidos nucleicos</subfield>
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      <subfield code="a">Nanomedicina</subfield>
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      <subfield code="a">Mesoporous Silica Nanoparticles for Co-Delivery of Drugs and Nucleic Acids in Oncology: A Review</subfield>
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