dc.contributor.author | Healy, Andrew V. | |
dc.contributor.author | Fuenmayor, Evert | |
dc.contributor.author | Doran, Patrick | |
dc.contributor.author | Geever, Luke M. | |
dc.contributor.author | Higginbotham, Clement L. | |
dc.contributor.author | Lyons, John G. | |
dc.date.accessioned | 2020-01-23T11:39:28Z | |
dc.date.available | 2020-01-23T11:39:28Z | |
dc.date.copyright | 2019-10 | |
dc.date.issued | 2019-12-03 | |
dc.identifier.citation | Healy, A.V., Fuenmayor, E., Doran, P., Geever, L.M, Higginbotham, C.L., Lyons, John G. (2019).Additive manufacturing dosage forms via stereolithography. Pharmaceutics 11:(12), pii: E645. doi: 10.3390/pharmaceutics11120645. | |
dc.identifier.issn | 1999-4923 | |
dc.identifier.issn | 1999-4923 | |
dc.identifier.other | Materials Research Institute AIT - Articles | en_US |
dc.identifier.uri | http://research.thea.ie/handle/20.500.12065/2961 | |
dc.description.abstract | The introduction of three-dimensional printing (3DP) has created exciting possibilities for
the fabrication of dosage forms, paving the way for personalized medicine. In this study, oral dosage
forms of two drug concentrations, namely 2.50% and 5.00%, were fabricated via stereolithography
(SLA) using a novel photopolymerizable resin formulation based on a monomer mixture that, to
date, has not been reported in the literature, with paracetamol and aspirin selected as model drugs.
In order to produce the dosage forms, the ratio of poly(ethylene glycol) diacrylate (PEGDA) to
poly(caprolactone) triol was varied with diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (Irgacure
TPO) utilized as the photoinitiator. The fabrication of 28 dosages in one print process was possible
and the printed dosage forms were characterized for their drug release properties. It was established
that both drugs displayed a sustained release over a 24-h period. The physical properties were
also investigated, illustrating that SLA accords accurate printing of dosages with some statistically
significant differences observed from the targeted dimensional range, indicating an area for future
process improvement. The work presented in this paper demonstrates that SLA has the ability to
produce small, individualized batches which may be tailored to meet patients’ specific needs or
provide for the localized production of pharmaceutical dosage forms. | en_US |
dc.format | PDF | en_US |
dc.language.iso | en | en_US |
dc.publisher | MDPI | en_US |
dc.relation.ispartof | Pharmaceutics | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Ireland | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ie/ | * |
dc.subject | Stereolithography | en_US |
dc.subject | Three-dimensional printing | en_US |
dc.subject | Additive manufacturing | en_US |
dc.subject | Personalized medicine | en_US |
dc.subject | 3D printed oral dosage forms | en_US |
dc.subject | Drug delivery | en_US |
dc.subject | Sustained drug relivery | en_US |
dc.subject | 3D printed oral dosage forms | en_US |
dc.subject | Drug delivery | en_US |
dc.subject | Sustained drug release tablets | en_US |
dc.subject | Photopolymerisation | en_US |
dc.subject | Paracetamol (acetaminophen) | en_US |
dc.subject | Aspirin (acetysalicylic acid) | en_US |
dc.title | Additive manufacturing of personalized pharmaceutical dosage forms via stereolithography. | en_US |
dc.type | Article | en_US |
dc.description.peerreview | yes | en_US |
dc.identifier.doi | doi: 10.3390/pharmaceutics11120645. | |
dc.identifier.orcid | https://orcid.org/0000-0002-9466-5964 | |
dc.identifier.orcid | ttps://orcid.org/0000-0001-8982-7845 | |
dc.identifier.orcid | https://orcid.org/0000-0001-5481-3080 | |
dc.identifier.orcid | https://orcid.org/0000-0001-8100-6276 | |
dc.identifier.orcid | https://orcid.org/0000-0003-1998-070X | |
dc.rights.access | Open Access | en_US |
dc.subject.department | Materials Research Institute - AIT | en_US |