<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kober M</submitter><funding>Generalitat de Catalunya</funding><funding>H2020 Marie Sklodowska-Curie Actions</funding><funding>Instituto de Salud Carlos III</funding><funding>Horizon 2020 Framework Programme</funding><funding>Agencia Estatal de Investigación</funding><funding>Ministerio de Educación, Cultura y Deporte</funding><funding>European Regional Development Fund</funding><pagination>354-364</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12801183</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Delivering plasmid DNA (pDNA) into cells is essential for numerous biotechnological and biomedical applications. Among available nanocarriers, nonviral lipid-based vesicles are particularly promising for transfecting mammalian cells. Nevertheless, further development is required to create delivery systems that are both broadly effective across cell types and scalable for clinical use. Here, we explore stable nanovesicles composed of the sterol derivative cholesteryl &lt;i>N&lt;/i>-(2-dimethylaminoethyl)carbamate (DC-CHOL) and myristalkonium chloride (MKC) as a platform for pDNA delivery. These nanovesicles, previously shown to efficiently deliver small RNAs to neuroblastoma cells, exhibit favorable physicochemical properties, such as high morphological uniformity and long-term colloidal stabilit</pubmed_abstract><journal>ACS biomaterials science &amp; engineering</journal><pubmed_title>Plasmid DNA Delivery Using a Stable Nanovesicle Platform: A Design-of-Experiments-Guided Investigation.</pubmed_title><pmcid>PMC12801183</pmcid><funding_grant_id>712949</funding_grant_id><funding_grant_id>CEX2019-000917-S</funding_grant_id><funding_grant_id>PI23/01144</funding_grant_id><funding_grant_id>FORT23/00034</funding_grant_id><funding_grant_id>PID2022-137332OB-I00</funding_grant_id><funding_grant_id>ICI21000/76</funding_grant_id><funding_grant_id>CB06/01/0033</funding_grant_id><funding_grant_id>2021-SGR-00438</funding_grant_id><funding_grant_id>2021-SGR-00638</funding_grant_id><funding_grant_id>FPU16/02555</funding_grant_id><funding_grant_id>FPU15/03577</funding_grant_id><funding_grant_id>953110</funding_grant_id><funding_grant_id>CEX2023-001263-S</funding_grant_id><pubmed_authors>Ventosa N</pubmed_authors><pubmed_authors>Gonzalez-Dominguez I</pubmed_authors><pubmed_authors>Puente-Massaguer E</pubmed_authors><pubmed_authors>Aviles-Dominguez L</pubmed_authors><pubmed_authors>Segura MF</pubmed_authors><pubmed_authors>Kober M</pubmed_authors><pubmed_authors>Boloix A</pubmed_authors><pubmed_authors>Godia F</pubmed_authors><pubmed_authors>Valdospinos D</pubmed_authors><pubmed_authors>Pique-Ponti J</pubmed_authors><pubmed_authors>Pina D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasmid DNA Delivery Using a Stable Nanovesicle Platform: A Design-of-Experiments-Guided Investigation.</name><description>Delivering plasmid DNA (pDNA) into cells is essential for numerous biotechnological and biomedical applications. Among available nanocarriers, nonviral lipid-based vesicles are particularly promising for transfecting mammalian cells. Nevertheless, further development is required to create delivery systems that are both broadly effective across cell types and scalable for clinical use. Here, we explore stable nanovesicles composed of the sterol derivative cholesteryl &lt;i>N&lt;/i>-(2-dimethylaminoethyl)carbamate (DC-CHOL) and myristalkonium chloride (MKC) as a platform for pDNA delivery. These nanovesicles, previously shown to efficiently deliver small RNAs to neuroblastoma cells, exhibit favorable physicochemical properties, such as high morphological uniformity and long-term colloidal stabilit</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T15:17:42.669Z</modification><creation>2026-06-01T03:11:03.465Z</creation></dates><accession>S-EPMC12801183</accession><cross_references><pubmed>41347866</pubmed><doi>10.1021/acsbiomaterials.5c01328</doi></cross_references></HashMap>