GATG Dendrimers and PEGylated Block Copolymers: from Synthesis to Bioapplications

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Molecularesgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorSousa Hervés, Ana
dc.contributor.authorNovoa Carballal, Ramón
dc.contributor.authorRiguera Vega, Ricardo
dc.contributor.authorFernández Megía, Eduardo
dc.date.accessioned2018-07-05T12:28:26Z
dc.date.available2018-07-05T12:28:26Z
dc.date.issued2014
dc.descriptionThis is a post-peer-review, pre-copyedit version of an article published in The AAPS Journal. The final authenticated version is available online at: https://doi.org/10.1208/s12248-014-9642-3gl
dc.description.abstractDendrimers are synthetic macromolecules composed of repetitive layers of branching units that emerge from a central core. They are characterized by a tunable size and precise number of peripheral groups which determine their physicochemical properties and function. Their high multivalency, functional surface, and globular architecture with diameters in the nanometer scale makes them ideal candidates for a wide range of applications. Gallic acid-triethylene glycol (GATG) dendrimers have attracted our attention as a promising platform in the biomedical field because of their high tunability and versatility. The presence of terminal azides in GATG dendrimers and poly(ethylene glycol) (PEG)-dendritic block copolymers allows their efficient functionalization with a variety of ligands of biomedical relevance including anionic and cationic groups, carbohydrates, peptides, or imaging agents. The resulting functionalized dendrimers have found application in drug and gene delivery, as antiviral agents and for the treatment of neurodegenerative diseases, in diagnosis and as tools to study multivalent carbohydrate recognition and dendrimer dynamics. Herein, we present an account on the preparation and recent applications of GATG dendrimers in these fieldsgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThe authors wish to acknowledge past and present lab members who have contributed to the development of dendrimers in our group. This work was financially supported by the Spanish Government (CTQ2009-10963, CTQ2012-34790, CTQ2009-14146-C02-02, CTQ2012-33436) and the Xunta de Galicia (10CSA209021PR and CN2011/037)gl
dc.identifier.citationSousa-Herves, A., Novoa-Carballal, R., Riguera, R. et al. AAPS J (2014) 16: 948. https://doi.org/10.1208/s12248-014-9642-3gl
dc.identifier.doi10.1208/s12248-014-9642-3
dc.identifier.essn1550-7416
dc.identifier.urihttp://hdl.handle.net/10347/16967
dc.language.isoenggl
dc.publisherSpringergl
dc.relation.publisherversionhttps://doi.org/10.1208/s12248-014-9642-3gl
dc.rights© American Association of Pharmaceutical Scientists 2014gl
dc.rights.accessRightsopen accessgl
dc.subjectBlock copolymergl
dc.subjectDendrimergl
dc.subjectDrug deliverygl
dc.subjectMultivalencygl
dc.subjectNMRgl
dc.titleGATG Dendrimers and PEGylated Block Copolymers: from Synthesis to Bioapplicationsgl
dc.typejournal articlegl
dc.type.hasVersionAMgl
dspace.entity.typePublication
relation.isAuthorOfPublication0f51f559-1806-45ca-945e-f4c12c3cefb9
relation.isAuthorOfPublicationfe5ace22-ce25-4507-aacf-a74fa1010319
relation.isAuthorOfPublication.latestForDiscovery0f51f559-1806-45ca-945e-f4c12c3cefb9

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