<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Neves AR</submitter><funding>Fundação para a Ciência e a Tecnologia</funding><pagination>1256</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8401607</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(8)</volume><pubmed_abstract>Cancer gene therapy, mediated by non-viral systems, remains a major research focus. To contribute to this field, in this work we reported on the development of dendrimer drug/gene ternary complexes. This innovative approach explored the great capacity of both polyamidoamine (PAMAM)-paclitaxel (PTX) conjugate and polyethylenimine (PEI) polymers to complex a p53-encoding plasmid DNA (pDNA), highlighting the utility of considering two compacting agents. The pDNA complexation capacity has been investigated as function of the nitrogen to phosphate groups ratio (N/P), which revealed to be a tailoring parameter. The physicochemical properties of the conceived ternary complexes were revealed and were found to be promising for cellular transfection. Furthermore, the formulated co-delivery systems d</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Development of Tailor-Made Dendrimer Ternary Complexes for Drug/Gene Co-Delivery in Cancer.</pubmed_title><pmcid>PMC8401607</pmcid><funding_grant_id>2020.08310.BD; SFRH/BD/148406/2019 and SFRH/BD/148393/2019</funding_grant_id><pubmed_authors>Faria R</pubmed_authors><pubmed_authors>Biswas S</pubmed_authors><pubmed_authors>Neves AR</pubmed_authors><pubmed_authors>Paul M</pubmed_authors><pubmed_authors>Albuquerque T</pubmed_authors><pubmed_authors>Sousa A</pubmed_authors><pubmed_authors>Costa D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of Tailor-Made Dendrimer Ternary Complexes for Drug/Gene Co-Delivery in Cancer.</name><description>Cancer gene therapy, mediated by non-viral systems, remains a major research focus. To contribute to this field, in this work we reported on the development of dendrimer drug/gene ternary complexes. This innovative approach explored the great capacity of both polyamidoamine (PAMAM)-paclitaxel (PTX) conjugate and polyethylenimine (PEI) polymers to complex a p53-encoding plasmid DNA (pDNA), highlighting the utility of considering two compacting agents. The pDNA complexation capacity has been investigated as function of the nitrogen to phosphate groups ratio (N/P), which revealed to be a tailoring parameter. The physicochemical properties of the conceived ternary complexes were revealed and were found to be promising for cellular transfection. Furthermore, the formulated co-delivery systems d</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2025-04-26T17:29:43.299Z</modification><creation>2022-02-11T09:58:56.624Z</creation></dates><accession>S-EPMC8401607</accession><cross_references><pubmed>34452218</pubmed><doi>10.3390/pharmaceutics13081256</doi></cross_references></HashMap>