<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T07:30:43Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/108013" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/108013</identifier><datestamp>2025-03-18T14:39:19Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Interaction between acetylsalicylic acid and a cationic amphiphile model: an experimental approach using surface techniques</dc:title>
   <dc:creator>Flores-Sánchez, R.</dc:creator>
   <dc:creator>Bigorra-Mir, M.</dc:creator>
   <dc:creator>Gámez, F.</dc:creator>
   <dc:creator>Lopes-Costa, T.</dc:creator>
   <dc:creator>Argudo, P. G.</dc:creator>
   <dc:creator>Martín-Romero, M. T.</dc:creator>
   <dc:creator>Camacho, L.</dc:creator>
   <dc:creator>Pedrosa, J. M.</dc:creator>
   <dc:subject>544</dc:subject>
   <dc:subject>Drug–lipid interaction</dc:subject>
   <dc:subject>Langmuir monolayer</dc:subject>
   <dc:subject>Brewster angle microscopy</dc:subject>
   <dc:subject>Reflection spectroscopy</dc:subject>
   <dc:subject>Química física (Química)</dc:subject>
   <dc:subject>2307 Química Física</dc:subject>
   <dc:description>Mechanical and morphological effects of monolayers of octadecylamine upon aspirin adsorption are monitored by Langmuir isotherms measurements and Brewster angle microscopy. Aspirin induced a notable expansion of the corresponding isotherms and a concentration-dependence of the mechanical stability of the films as a consequence of the subtle balance between the solubility of the amine and the monolayer stabilization induced by the ion-pairs, as corroborated by Brewster Angle Microscopy images. The incorporation of the aspirin into the interface was confirmed by UV–vis reflection spectroscopy. Some comments on the feasibility of using aliphatic amines for drug delivery of anionic species are presented.</dc:description>
   <dc:description>Depto. de Química Física</dc:description>
   <dc:description>Fac. de Ciencias Químicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:description>APC financiada por la UCM</dc:description>
   <dc:date>2024-09-09T10:20:18Z</dc:date>
   <dc:date>2024-09-09T10:20:18Z</dc:date>
   <dc:date>2023</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/108013</dc:identifier>
   <dc:identifier>0009-2614</dc:identifier>
   <dc:identifier>10.1016/j.cplett.2023.140450</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>R. Flores-Sánchez, M. Bigorra-Mir, F. Gámez, T. Lopes-Costa, P.G. Argudo, M.T. Martín-Romero, L. Camacho, J.M. Pedrosa, Interaction between acetylsalicylic acid and a cationic amphiphile model: An experimental approach using surface techniques, Chemical Physics Letters, Volume 819, 2023, 140450, ISSN 0009-2614, https://doi.org/10.1016/j.cplett.2023.140450.</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>