<?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>2026-04-17T02:35:19Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/175632" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/175632</identifier><datestamp>2025-11-19T10:53:46Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478917</setSpec><setSpec>col_2072_478923</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Crystal engineering of nutraceutical phytosterols: new cocrystal solid solutions?</dc:title>
   <dc:creator>Barbas Cañero, Rafael</dc:creator>
   <dc:creator>Bofill, Lídia</dc:creator>
   <dc:creator>de-Sande, Dafne</dc:creator>
   <dc:creator>Font Bardia, Ma. Mercedes</dc:creator>
   <dc:creator>Prohens López, Rafael</dc:creator>
   <dc:subject>Cristal·lografia</dc:subject>
   <dc:subject>Crystallography</dc:subject>
   <dcterms:abstract>A cocrystal screening conducted with solid solutions of three phytosterols (β-sitosterol, campesterol and stigmasterol) and a set of coformers with strong hydrogen bond donors reveals that multicomponent solid solutions are preferentially formed instead of pure cocrystals and are much enriched with β-sitosterol with respect to stigmasterol, a natural product with cytotoxicity concerns.</dcterms:abstract>
   <dcterms:issued>2021-03-23T12:48:29Z</dcterms:issued>
   <dcterms:issued>2021-06-02T05:10:26Z</dcterms:issued>
   <dcterms:issued>2020-06-02</dcterms:issued>
   <dcterms:issued>2021-03-23T12:48:29Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1039/d0ce00704h</dc:relation>
   <dc:relation>Crystengcomm, 2020, vol. 22, num. 25, p. 4210-4214</dc:relation>
   <dc:relation>https://doi.org/10.1039/d0ce00704h</dc:relation>
   <dc:rights>(c) Barbas Cañero, Rafael et al., 2020</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Royal Society of Chemistry</dc:publisher>
   <dc:source>Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)</dc:source>
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