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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/polym13050684</dc:identifier><dc:language>eng</dc:language><dc:creator>Abad, Miriam</dc:creator><dc:creator>Martínez-Bueno, Alejandro</dc:creator><dc:creator>Mendoza, Gracia</dc:creator><dc:creator>Arruebo, Manuel</dc:creator><dc:creator>Oriol, Luis</dc:creator><dc:creator>Sebastián, Víctor</dc:creator><dc:creator>Piñol, Milagros</dc:creator><dc:title>Supramolecular functionalizable linear–dendritic block copolymers for the preparation of nanocarriers by microfluidics</dc:title><dc:identifier>ART-2021-124115</dc:identifier><dc:description>Hybrid linear–dendritic block copolymers (LDBCs) having dendrons with a precise number of peripheral groups that are able to supramolecular bind functional moieties are challenging materials as versatile polymeric platforms for the preparation of functional polymeric nanocarriers. PEG2k-b-dxDAP LDBCs that are based on polyethylene glycol (PEG) as hydrophilic blocks and dendrons derived from bis-MPA having 2, 6-diacylaminopyridine (DAP) units have been efficiently synthesized by the click coupling of preformed blocks, as was demonstrated by spectroscopic techniques and mass spectrometry. Self-assembly ability was first checked by nanoprecipitation. A re-producible and fast synthesis of aggregates was accomplished by microfluidics optimizing the total flow rate and phase ratio to achieve spherical micelles and/or vesicles depending on dendron generation and experimental parameters. The morphology and size of the self-assemblies were studied by TEM, Cryogenic Transmission Electron Microscopy (cryo-TEM), and Dynamic Light Scattering (DLS). The cytotoxicity of aggregates synthesized by microfluidics and the influence on apoptosis and cell cycle evaluation was studied on four cell lines. The self-assemblies are not cytotoxic at doses below 0.4 mg mL–1. Supramolecular functionalization using thymine derivatives was explored for reversibly cross-linking the hydrophobic blocks. The results open new possibilities for their use as drug nanocarriers with a dynamic cross-linking to improve nanocarrier stability but without hindering disassembly to release molecular cargoes.</dc:description><dc:date>2021</dc:date><dc:source>http://zaguan.unizar.es/record/101641</dc:source><dc:doi>10.3390/polym13050684</dc:doi><dc:identifier>http://zaguan.unizar.es/record/101641</dc:identifier><dc:identifier>oai:zaguan.unizar.es:101641</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FEDER/E47-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII-IIS/MS19-00092</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/RTI2018-099019-A-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/MAT2017-84838-P</dc:relation><dc:identifier.citation>Polymers 13, 5 (2021), 684 [27 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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