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Fused Deposition Modeling as a Possible Approach for the Preparation of Orodispersible Tablets

dc.contributor.authorTranova, Thao
dc.contributor.authorPyteraf, Jolanta
dc.contributor.authorKurek, Mateusz
dc.contributor.authorJamroz, Witold
dc.contributor.authorBrniak, Witold
dc.contributor.authorSpalovska, Dita
dc.contributor.authorLoskot, Jan
dc.contributor.authorJurkiewicz, Karolina
dc.contributor.authorGrelska, Joanna
dc.contributor.authorKramarczyk, Daniel
dc.contributor.authorMuzikova, Jitka
dc.contributor.authorPaluch, Marian
dc.contributor.authorJachowicz, Renata
dc.date.accessioned2025-12-05T10:47:22Z
dc.date.available2025-12-05T10:47:22Z
dc.date.issued2022
dc.description.abstractAdditive manufacturing technologies are considered as a potential way to support individualized pharmacotherapy due to the possibility of the production of small batches of customized tablets characterized by complex structures. We designed five different shapes and analyzed the effect of the surface/mass ratio, the influence of excipients, and storage conditions on the disintegration time of tablets printed using the fused deposition modeling method. As model pharmaceutical active ingredients (APIs), we used paracetamol and domperidone, characterized by different thermal properties, classified into the various Biopharmaceutical Classification System groups. We found that the high surface/mass ratio of the designed tablet shapes together with the addition of mannitol and controlled humidity storage conditions turned out to be crucial for fast tablet's disintegration. As a result, mean disintegration time was reduced from 5 min 46 s to 2 min 22 s, and from 11 min 43 s to 2 min 25 s for paracetamol- and domperidone-loaded tablets, respectively, fulfilling the European Pharmacopeia requirement for orodispersible tablets (ODTs). The tablet's immediate release characteristics were confirmed during the dissolution study: over 80% of APIs were released from printlets within 15 min. Thus, this study proved the possibility of using fused deposition modeling for the preparation of ODTs.eng
dc.formatp. &quot;Article Number: 69&quot;
dc.identifier.doi10.3390/ph15010069
dc.identifier.issn1424-8247
dc.identifier.obd43878587
dc.identifier.urihttp://hdl.handle.net/20.500.12603/1421
dc.identifier.wos000748828200001
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherMDPI
dc.relation.ispartofPHARMACEUTICALS, volume 15, issue: 1eng
dc.relation.publisherversionhttps://www.mdpi.com/1424-8247/15/1/69
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://www.mdpi.com/1424-8247/15/1/69
dc.subjectfused deposition modelingeng
dc.subject3D printingeng
dc.subjecthot-melt extrusioneng
dc.subjectsolid dosage formseng
dc.subjectorodispersible tabletseng
dc.subjectparacetamoleng
dc.subjectdomperidoneeng
dc.subjectdisintegration timeeng
dc.titleFused Deposition Modeling as a Possible Approach for the Preparation of Orodispersible Tabletseng
dc.typearticle

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Fused_Deposition_Modeling_as_a_Possible_Approach_for_thePreparation_of_Orodispersible_Tablets.pdf
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