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        <datestamp>2026-10-01T17:19:08Z</datestamp>
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          <dc:title>Fused deposition modelling three-dimensional printing of solid dosage forms</dc:title>
          <dc:creator>Sinmisola A. Oladeji (24164472)</dc:creator>
          <dc:subject>PUREID: 242864825</dc:subject>
          <dc:subject>3D printing</dc:subject>
          <dc:subject>Fused deposition modelling (FDM)</dc:subject>
          <dc:subject>gastric floating</dc:subject>
          <dc:subject>sustained release</dc:subject>
          <dc:subject>zero-order release</dc:subject>
          <dc:subject>rheology</dc:subject>
          <dc:subject>oral solid dosage forms</dc:subject>
          <dc:subject>fixed dose combinations</dc:subject>
          <dc:description>Three-dimensional printing (3DP) is a widely used technique for the design and manufacture of complex solid dosage forms with the objective of formulating personalized medicines and on-demand manufacturing. Among commercially available models, fused deposition modelling 3D-printing (FDM-3DP) has shown the potential to fabricate objects with various internal structures and the ability to introduce multiple specific functionalities. This thesis’s main aim was to understand printability in FDM-3DP and the factors influencing it, as well as to manufacture novel gastro-retentive floating drug delivery systems through FDM-3DP using pharmaceutical excipients. Hot-melt extrusion (HME) was implemented to fabricate filaments with adequate properties for FDM-3DP. Rheological, mechanical and physical characterisation of filaments were evaluated to provide information on the impact of these properties on the FDM 3DP process. Theophylline-loaded filaments, suitable for FDM-3DP, were successfully formulated using three polymeric carriers (Polyvinyl alcohol (PVA), Hydroxypropyl Cellulose (HPC), and Soluplus®). FDM-3DP enabled the manufacture of monolithic and non-monolithic floating drug delivery systems using a sandwich design. The tablet design showed the ability to achieve prolonged gastric floating (12 hours) with no floating lag time. Formulations containing Soluplus® or HPC with Eudragit RLPO provided zero-order sustained release of theophylline (THP). Fixed-dose bilayer floating tablets were also manufactured. This thesis displayed the ability of FDM-3DP to manufacture bespoke floating tablets using pharmaceutical excipients with tailored drug release profiles.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis embargoed until 31 December 2026&lt;/i&gt;.&lt;br&gt;</dc:description>
          <dc:date>2026-10-01T17:19:08Z</dc:date>
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          <dc:identifier>10.17034/32631534.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2026-12-31</dc:rights>
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