<?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>2026-04-18T04:31:17Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2117/411771" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2117/411771</identifier><datestamp>2026-01-16T09:54:39Z</datestamp><setSpec>com_2072_1033</setSpec><setSpec>col_2072_452950</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>Application of ultrasound-assisted compression and 3D-printing semi-solid extrusion techniques to the development of sustained-release drug delivery systems based on a novel biodegradable aliphatic copolyester</dc:title>
   <dc:creator>Ferrero, Carmen</dc:creator>
   <dc:creator>Urpí Garriga, Lourdes</dc:creator>
   <dc:creator>Aguilar de Leiva, Angela</dc:creator>
   <dc:creator>Linares, V</dc:creator>
   <dc:creator>Mora Castaño, Gloria</dc:creator>
   <dc:creator>Millán Jiménez, Mónica</dc:creator>
   <dc:creator>Martínez de Ilarduya Sáez de Asteasu, Domingo Antxon</dc:creator>
   <dc:creator>Caraballo Rodríguez, Isidoro</dc:creator>
   <dc:contributor>Universitat Politècnica de Catalunya. Departament d'Enginyeria Química</dc:contributor>
   <dc:contributor>Universitat Politècnica de Catalunya. POL - Polímers Industrials Avançats i Biopolímers Tecnològics</dc:contributor>
   <dc:subject>Àrees temàtiques de la UPC::Enginyeria química</dc:subject>
   <dc:subject>Polymers -- Biodegradation</dc:subject>
   <dc:subject>Polymers in medicine</dc:subject>
   <dc:subject>Aliphatic copolyester</dc:subject>
   <dc:subject>Ultrasound-assisted compression</dc:subject>
   <dc:subject>3D-printing semi-solid extrusion</dc:subject>
   <dc:subject>Metronidazole</dc:subject>
   <dc:subject>Drug delivery systems</dc:subject>
   <dc:subject>Sustained-release</dc:subject>
   <dc:subject>Polímers -- Biodegradació</dc:subject>
   <dc:subject>Polímers en medicina</dc:subject>
   <dc:description>The purpose of this study was to investigate the ability of two advanced hot-processing technologies, Ultrasound-Assisted Compression (USAC) and 3D-printing Semi-solid Extrusion (SSE), to manufacture sustained-release drug delivery systems based on a novel biodegradable aliphatic copolyester. The copolymer was synthesized from ¿-pentadecalactone (PDL), 1,4-cyclohexanedimethanol (CHDM) and dimethyl succinate (DMS) (monomer ratio PDL/CHDM/DMS 70/30/30) by enzymatic ring opening polymerization and two-step melt polycondensation processes and has a random microstructure, a high molecular weight (107,100 g mol-1) and a relatively low melting point (~65 °C). The antibacterial agent metronidazole (MTZ) was chosen as model drug and binary physical mixtures copolymer:drug were prepared at 90:10 and 70:30 w/w ratios. Thermal analysis studies evidenced that the formulations could be processed below their degradation temperatures. Drug delivery devices with dense and meshed structures were manufactured using USAC and SSE techniques, respectively, with USAC devices exhibiting more reproducible physical properties than the SSE systems. Powder X-ray diffraction and scanning electron microscopy studies showed a partial sintering of the copolyester during USAC processing while MTZ remained mostly crystalline. In contrast, the copolymer melted and the drug underwent some amorphization when processed using SSE. In vitro drug release studies in phosphate buffer (pH 6.8) showed that, after an initial burst release of metronidazole, USAC and SSE devices exhibited a prolonged and/or sustained drug release over 20 days. The initial burst release was dependent on the manufacturing technique and the drug/polymer ratio, being minimized for SSE devices containing 10 wt% MTZ. The whole drug release profiles fitted well to the Peppas-Sahlin model, being drug diffusion the predominant release mechanism. After the burst release, the sustained release period of USAC and SSE devices containing 10 wt% MTZ showed a good fit to the zero-order kinetic model, with faster drug release from the SSE devices due to the larger surface area of their meshed structure. In conclusion, this work demonstrates that processing the aliphatic copolyester by both USAC and SSE technologies provides an attractive strategy to manufacture biodegradable drug delivery systems for long-term release of metronidazole.</dc:description>
   <dc:description>This work was part of the project RTI2018-095041-BC31 and was supported by MCIN/AEI/10.13039/501100011033 and by ERDF A way of making Europe.</dc:description>
   <dc:description>Peer Reviewed</dc:description>
   <dc:description>Postprint (published version)</dc:description>
   <dc:date>2024-05</dc:date>
   <dc:type>Article</dc:type>
   <dc:identifier>Ferrero, C. [et al.]. Application of ultrasound-assisted compression and 3D-printing semi-solid extrusion techniques to the development of sustained-release drug delivery systems based on a novel biodegradable aliphatic copolyester. "Journal of drug delivery science and technology", Maig 2024, vol. 95, núm. article 105652.</dc:identifier>
   <dc:identifier>1773-2247</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2117/411771</dc:identifier>
   <dc:identifier>10.1016/j.jddst.2024.105652</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>https://www.sciencedirect.com/science/article/pii/S1773224724003216?via%3Dihub</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-095041-B-C31/ES/SISTEMAS DE LIBERACION DE FARMACOS BASADOS EN MATERIALES POLIMERICOS AVANZADOS PARA EL TRATAMIENTO DE ENFERMEDADES DEL TRACTO GASTRO-INTESTINAL/</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>Open Access</dc:rights>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:format>application/pdf</dc:format>
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