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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:10.1088/1748-605X/aba445</dc:identifier><dc:language>eng</dc:language><dc:creator>Prieto, E.</dc:creator><dc:creator>Cardiel, M.J.</dc:creator><dc:creator>Vispe, E.</dc:creator><dc:creator>Idoipe, M.</dc:creator><dc:creator>Garcia-Martin, E.</dc:creator><dc:creator>Fraile, J.M.</dc:creator><dc:creator>Polo, V.</dc:creator><dc:creator>Mayoral, J.A.</dc:creator><dc:creator>Pablo, L.E.</dc:creator><dc:creator>Rodrigo, M.J.</dc:creator><dc:title>Dexamethasone delivery to the ocular posterior segment by sustained-release Laponite formulation</dc:title><dc:identifier>ART-2020-121787</dc:identifier><dc:description>This paper presents a novel nanoformulation for sustained-release delivery of dexamethasone (DEX) to the ocular posterior segment using a Laponite (LAP) carrier - DEX/LAP 1:10 w w-1 formulation; 10 mg ml-1. In vivo ocular feasibility and pharmacokinetics after intravitreal (IV) and suprachoroidal (SC) administration in rabbit eyes are compared against IV administration of a DEX solution (1 mg ml-1). Thirty rabbit eyes were injected with the DEX/LAP formulation (15 suprachoroid/15 intravitreous). Ophthalmological signs were monitored at day 1 and at weeks 1-4-12-24 post-administration. Three eyes per sample time point were used to quantify DEX concentration using high-performance liquid chromatography-mass spectrometry. The ocular tissues'' pharmacokinetic parameters (lens, vitreous humour, choroid-retina unit and sclera) were studied. DEX/LAP was well tolerated under both administration methods. Peak intraocular DEX levels from the DEX/LAP were detected in the vitreous humour after both deliveries soon after administration. The vitreous area under the curve was significantly greater after both DEX/LAP deliveries (IV: 205 968.47; SC: 11 442.22 ng g-1 d-1) than after IV administration of the DEX solution (317.17 ng g-1 d-1). Intravitreal DEX/LAP delivery extended higher vitreous DEX levels up to week 24 (466.32 311.15 ng g-1). With SC delivery, DEX levels were detectable in the choroid-retina unit (12.04 20.85 ng g-1) and sclera (25.46 44.09 ng g-1) up to week 24. This study demonstrated the intraocular feasibility of both SC and IV administration of the DEX/LAP formulation. The LAP increased the intraocular retention time of DEX when compared with conventional solutions. DEX/LAP could be considered a biocompatible and useful sustained-release formulation for treating posterior-pole eye diseases.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/97402</dc:source><dc:doi>10.1088/1748-605X/aba445</dc:doi><dc:identifier>http://zaguan.unizar.es/record/97402</dc:identifier><dc:identifier>oai:zaguan.unizar.es:97402</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E37-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FEDER/Construyendo Europa desde Aragón</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/M17-00213</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI12-02285</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI17-01726</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI17-01946</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-AEI-FEDER/MAT2017-83858-C2-2</dc:relation><dc:identifier.citation>Biomedical Materials 15, 6 (2020), 065021 [14 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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