Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/25185
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dc.contributor.authorPanraksa, P-
dc.contributor.authorZhang, B-
dc.contributor.authorRachtanapun, P-
dc.contributor.authorJantanasakulwong, K-
dc.contributor.authorQi, S-
dc.contributor.authorJantrawut, P-
dc.date.accessioned2022-09-10T15:02:44Z-
dc.date.available2022-02-18-
dc.date.available2022-09-10T15:02:44Z-
dc.date.issued2022-02-18-
dc.identifier443-
dc.identifier.citationPanraksa, P. et al. (2022) '‘Tablet-in-Syringe’: A Novel Dosing Mechanism for Dysphagic Patients Containing Fast-Disintegrating Tablets Fabricated Using Semisolid Extrusion 3D Printing', Pharmaceutics, 14 (2), 443, pp. 1-18. doi: 10.3390/pharmaceutics14020443.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/25185-
dc.descriptionSupplementary Materials: The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/pharmaceutics14020443/s1, Figure S1: Disintegrating behavior of 3D-printed FDT with polymer:drug ratio (w/w) of 1:30 and extrusion rates of 3.5 L/s in syringe at different time interval 15 s (a), 30 s (b), 45 s (c), 60 s (d).en_US
dc.description.abstractCopyright: © 2022 by the authors. With the ability to fabricate personalized dosage forms and considerably shorter manufacturing time, semisolid extrusion (SSE) 3D printing has rapidly grown in popularity in recent years as a novel, versatile manufacturing method that powers a wide range of applications in the pharmaceutical field. In this work, the feasibility of using SSE 3D printing to fabricate fast-disintegrating tablets (FDTs) that are pre-filled in dosing syringes was evaluated. The novel design approach, ‘tablet-in-syringe’, was aimed to ease the oral drug administration and improve the dosing accuracy for dysphagic patients. The effect of varying polymer (hydroxypropyl methylcellulose E15) concentrations and printing parameters (e.g., extrusion rate) on dimensional accuracy, physicochemical properties, disintegration time, and content uniformity of 3D-printed FDTs was studied. An overall comparison of results demonstrated that the best FDT formulation among those developed was with a polymer:drug ratio (w/w) of 1:30, printed at extrusion rate of 3.5 μL/s. The diameter of printed filaments of this formulation was observed to be similar to the nozzle diameter (22G), proving that good printing accuracy was achieved. This FDTs also had the fastest disintegration time (0.81 ± 0.14 min) and a drug (phenytoin sodium, as the model drug) content uniformity that met pharmacopeial specifications. Although the flow characteristics of the dissolved formulation still need improvement, our findings suggested that the novel ‘tablet-in-syringe’ could potentially be considered as a promising fast-disintegrating drug delivery system that can be personalized and manufactured at—or close to—the point of care for dysphagic patients using SSE.en_US
dc.description.sponsorshipNational Research Council of Thailand (NRCT): NRCT5-RGJ63004-079; partial funding from Chiang Mai University.en_US
dc.format.extent1 - 18-
dc.format.mediumElectronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherMDPI AGen_US
dc.rightsCopyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject3D printingen_US
dc.subjectextrusion-based 3D printingen_US
dc.subjectsemisolid extrusion 3D printingen_US
dc.subjectdysphagiaen_US
dc.subjectfast-disintegrating tabletsen_US
dc.subjectphenytoin sodiumen_US
dc.title‘Tablet-in-Syringe’: A Novel Dosing Mechanism for Dysphagic Patients Containing Fast-Disintegrating Tablets Fabricated Using Semisolid Extrusion 3D Printingen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3390/pharmaceutics14020443-
dc.relation.isPartOfPharmaceutics-
pubs.issue2-
pubs.publication-statusPublished-
pubs.volume14-
dc.identifier.eissn1999-4923-
dc.rights.holderThe authors-
Appears in Collections:Dept of Mechanical and Aerospace Engineering Research Papers

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