<?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>2026-05-05T13:21:57Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/41412" metadataPrefix="edm">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/41412</identifier><datestamp>2021-06-30T03:05:45Z</datestamp><setSpec>com_10324_38</setSpec><setSpec>col_10324_852</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xsi:schemaLocation="http://www.w3.org/1999/02/22-rdf-syntax-ns# http://www.europeana.eu/schemas/edm/EDM.xsd">
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<dc:contributor>Zoran Novak</dc:contributor>
<dc:contributor>Milica Pantić</dc:contributor>
<dc:contributor>Martín Martínez, Ángel</dc:contributor>
<dc:contributor>Universidad de Valladolid. Escuela de Ingenierías Industriales</dc:contributor>
<dc:creator>Rodríguez Antolín, Jorge</dc:creator>
<dc:date>2020</dc:date>
<dc:description>The following work examines the possibility of impregnating chosen model drug into&#xd;
bioaerogels to obtain final formulation with added value. The drug used in this study was&#xd;
esomeprazole, used to treat acid-related diseases.&#xd;
In the first part of the work, bioaerogels were prepared. Polysaccharide aerogels are&#xd;
lightweight biocompatible and biodegradable materials, suitable for applications in&#xd;
pharmaceutical industry. For this purpose, three different cores were prepared: pectin,&#xd;
alginate and their mixture, followed by coating with chitosan layer. The production of the&#xd;
bioaerogels follows a sol-gel synthesis and supercritical drying technique. All samples&#xd;
were characterised, and optimisation was performed based on examined properties.&#xd;
Aerogels having a pectin core and chitosan coating showed the highest surface area and&#xd;
the highest adsorption capacity.&#xd;
In the second part, the impregnation of esomeprazole was performed using two different&#xd;
methods: supercritical impregnation and diffusion via sol-gel synthesis. For supercritical&#xd;
impregnation, supercritical carbon dioxide was used as a solvent for impregnation of the&#xd;
drug. In the diffusion method, the model drug was added during sol-gel synthesis using&#xd;
ethanol as solvent. Finally, complete characterisation of prepared formulation followed&#xd;
by drug release studies was performed.&#xd;
The study showed successful impregnation of esomeprazole using either carbon dioxide&#xd;
or ethanol as a solvent. Bioaerogels proved to be promising as carriers for achieving the&#xd;
optimal release of the chosen drug</dc:description>
<dc:description>V diplomskem delu smo proučevali možnost impregnacije vzorčnega zdravila v&#xd;
bioaerogele z namenom, da dobimo učinkovito končno formulirano obliko. Kot vzorčno&#xd;
zdravilo smo uporabili esomeprazol, ki se uporablja za zdravljenje bolezni povezanih z&#xd;
želodčno kislino.&#xd;
V prvem delu diplome smo pripravili bioaerogele. Polisaharidni aerogeli so lahki&#xd;
biokompatibilni in biorazgradljivi materiali, ki so primerni za uporabo v farmacevtski&#xd;
industriji. Pektin, alginat in njuno mešanico smo uporabili za pripravo treh različnih jeder,&#xd;
ki smo jih nato prevlekli s plastjo hitozana. Bioaerogele smo sintetizirali s sol-gel sintezo&#xd;
in jih sušili s superkritičnim oglijkovim dioksidom. Opravili smo karakterizacijo in&#xd;
optimizacijo pripravljenih vzorcev. Aerogeli s pektinskim jedrom in obdani s hitozanom&#xd;
imajo največjo površino in največjo adsorpcijsko sposobnost.&#xd;
V drugem delu smo izvedli impregnacijo esomeprazola po dveh različnih metodah in&#xd;
sicer z metodo superkritične impregnacije in z metodo difuzije s sol-gel sintezo. Pri&#xd;
superkritični impregnaciji smo kot topilo uporabili superkritični ogljikov dioksid. Pri&#xd;
difuzijski metodi pa smo vzorčno zdravilo dodali med sol-gel sintezo, pri čemer smo kot&#xd;
topilo uporabili etanol. Na koncu smo izvedli popolno karakterizacijo pripravljene&#xd;
formulacije in opravili študijo sproščanja zdravila.&#xd;
Z obema metodama smo uspešno impregnirali esomeprazol ter dosegli optimalno&#xd;
sproščanje izbranega zdravila.</dc:description>
<dc:format>application/pdf</dc:format>
<dc:identifier>http://uvadoc.uva.es/handle/10324/41412</dc:identifier>
<dc:language>eng</dc:language>
<dc:subject>3302 Tecnología Bioquímica</dc:subject>
<dc:title>Bioaerogels: Promising materials for impregnation of drugs</dc:title>
<dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
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