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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:10.1016/j.biomaterials.2025.123867</dc:identifier><dc:language>eng</dc:language><dc:creator>Conejos-Sánchez, Inmaculada</dc:creator><dc:creator>Melnyk, Tetiana</dc:creator><dc:creator>Masiá, Esther</dc:creator><dc:creator>Morelló-Bolumar, Daniel</dc:creator><dc:creator>Tortajada-Comeche, Luz</dc:creator><dc:creator>Dolz-Pérez, Irene</dc:creator><dc:creator>Torrijos-Saiz, Lucía Inés</dc:creator><dc:creator>Tenhaeff, Paula</dc:creator><dc:creator>Roosz, Julia</dc:creator><dc:creator>Moruzzi, Alessia</dc:creator><dc:creator>Sogorb, Gloria</dc:creator><dc:creator>Medel, Maria</dc:creator><dc:creator>Loskill, Peter</dc:creator><dc:creator>Roselló, Esther</dc:creator><dc:creator>Sebastian, Victor</dc:creator><dc:creator>Florindo, Helena</dc:creator><dc:creator>Felip-León, Carles</dc:creator><dc:creator>Nebot, Vicent J.</dc:creator><dc:creator>Herranz-Pérez, Vicente</dc:creator><dc:creator>García-Vedugo, José Manuel</dc:creator><dc:creator>Vicent, María J.</dc:creator><dc:title>A rationally designed polypeptide-based hybrid platform for targeted intranasal brain drug delivery</dc:title><dc:identifier>ART-2025-147912</dc:identifier><dc:description>Intranasal administration represents a safe and non-invasive route for drug delivery to the brain; however, clinical translation remains limited due to anatomical and physiological barriers. We present a modular hybrid biomaterial platform (NanoInBrain) that bypasses the blood-brain barrier via the olfactory route and enables central nervous system (CNS) drug delivery. The platform integrates a rationally designed polypeptide-based nanocarrier with a depot-forming hydrogel vehicle - a hyaluronic acid–poly-L-glutamate crosspolymer (HA-CP, Yalic®) - adapted from dermatological applications to enhance nasal mucosal retention and brain uptake. We engineered the nanocarrier system using star-shaped poly-L-glutamate (StPGA) architectures and systematically tuned physicochemical properties to optimize mucosal interaction and CNS diffusion. We introduced mucoadhesive and mucodiffusive functionalities via C-terminal odorranalectin (OL) conjugation, which improved nasal epithelium permeation through receptor-mediated mechanisms. Redox-responsive disulfide crosslinking (StPGA-CL-SS) further enhanced mucosal transport by enabling thiol-mediated anchoring to mucin glycoproteins, outperforming inert click-crosslinked variants. Ex vivo Franz diffusion studies and a nasal-mucosa-on-chip model demonstrated robust permeation, with in vivo imaging confirming brain distribution and intracellular uptake in neurons and microglia. Incorporation of HA-CP prolonged nasal residence (∼4 h) and increased total brain accumulation while being well-tolerated. This new platform combines architectural tunability, bioresponsive surface chemistry, and depot-mediated delivery in a scalable, biocompatible nose-to-brain delivery system with potential for treating neurological disorders.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/168458</dc:source><dc:doi>10.1016/j.biomaterials.2025.123867</dc:doi><dc:identifier>http://zaguan.unizar.es/record/168458</dc:identifier><dc:identifier>oai:zaguan.unizar.es:168458</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2021-127847OB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICIU/CEX2023-001286-S</dc:relation><dc:identifier.citation>Biomaterials 328 (2025), 123867 [19 pp.]</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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