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dc.contributor.authorEbrahimi, Farnoosh
dc.contributor.authorXu, Han
dc.contributor.authorFuenmayor, Evert
dc.contributor.authorMajor, Ian
dc.date.accessioned2025-01-08T14:22:33Z
dc.date.available2025-01-08T14:22:33Z
dc.date.copyright2024
dc.date.issued2024-07-10
dc.identifier.citationEbrahimi, F., Xu, H., Fuenmayor, E. and Major, I. (2024) 'Material compatibility and processing challenges in droplet deposition modelling additive manufacturing: A study on pharmaceutical excipients Polyvinylpyrrolidone/vinyl acetate (PVP/VA) and Polycaprolactone (PCL)', European Journal of Pharmaceutical Sciences, 200, 106850. Available at: https://doi.org/10.1016/j.ejps.2024.106850en_US
dc.identifier.issn0928-0987
dc.identifier.urihttps://research.thea.ie/handle/20.500.12065/4882
dc.description.abstractAdditive manufacturing (AM) enables the production of complex, lightweight, and customized components with superior quality. Selecting the right materials considering their thermal properties, printability, and layer adhesion is crucial in melting-based AM techniques. This study investigates Droplet Deposition Modelling (DDM), an innovative material extrusion process that utilizes thermoplastic granules. DDM is distinguished by its shorter manufacturing times and a wider range of materials, setting it apart from traditional material extrusion methods such as fused filament fabrication. We investigated the printability and part quality in DDM using two common pharmaceutical excipients: Polyvinylpyrrolidone/vinyl acetate 6:4 (PVP/VA), which is highly brittle, and Polycaprolactone (PCL), known for its low solubility and role in controlled drug release. Different ratios of PVP/VA and PCL were compounded via hot melt extrusion (HME) and used in DDM to study the impact of ingredient content on printability and part quality, employing geometrical models to assess material compatibility and printability. The study revealed that increasing PVP/VA content leads to higher viscosity, reduced flowability, and uneven deposition, with formulations of 80 % and 100 % PVP/VA showing poor processability. In contrast, formulations with 60 % and 40 % PVP/VA exhibited smooth processing and compatibility with DDM. We identified processing temperature and Drop Aspect Ratio (DAR) as key factors influencing material printability and part quality. Elevated processing temperatures and reduced DAR were found to increase interface temperatures, reduce diffusion, and potentially cause the 'elephant feet' issue. Additionally, smaller droplet sizes and material characteristics, such as higher interfacial tension in PCL, could lead to coalescence. Our findings highlight the complexities in optimizing DDM processing parameters and material blends, underscoring the need for careful formulation design to achieve high-quality 3D printed products.en_US
dc.formatapplication/pdfen_US
dc.language.isoengen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofEuropean Journal of Pharmaceutical Sciencesen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectDroplet deposition modellingen_US
dc.subjectMaterial selectionen_US
dc.subjectPharmaceutical manufacturingen_US
dc.subjectPlastic freeformingen_US
dc.subjectPolymer blendsen_US
dc.titleMaterial compatibility and processing challenges in droplet deposition modelling additive manufacturing: A study on pharmaceutical excipients Polyvinylpyrrolidone/vinyl acetate (PVP/VA) and Polycaprolactone (PCL)en_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.contributor.affiliationTechnological University of the Shannon: Midlands Midwesten_US
dc.description.peerreviewyesen_US
dc.identifier.doi10.1016/j.ejps.2024.106850en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0538-9786en_US
dc.identifier.startpage106850en_US
dc.identifier.volume200en_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentPRISM Research Instituteen_US
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as Attribution 4.0 International