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dc.contributor.authorElbadawi, Moe
dc.contributor.authorMuñiz, Brais
dc.contributor.authorGavins, Francesca K.H.
dc.contributor.authorOng, Jun Jie
dc.contributor.authorGaisford, Simon
dc.contributor.authorPérez, Gilberto
dc.contributor.authorBasit, Abdul W
dc.contributor.authorCabalar, Pedro
dc.contributor.authorGoyanes, Álvaro
dc.date.accessioned2024-01-10T08:28:08Z
dc.date.issued2020-11
dc.identifier.citationM. Elbadawi, B. Muñiz Castro, F. K.H. Gavin, J. Jie Ong; S. Gaisford, G. Pérez, A. W. Basit, P. Cabalar, and A. Goyanes, "M3DISEEN: A novel machine learning approach for predicting the 3D printability of medicines", International Journal of Pharmaceutics, Vol. 590, 30 November 2020, doi: 10.1016/j.ijpharm.2020.119837es_ES
dc.identifier.urihttp://hdl.handle.net/2183/34788
dc.description.abstract[Abstract]: Artificial intelligence (AI) has the potential to reshape pharmaceutical formulation development through its ability to analyze and continuously monitor large datasets. Fused deposition modeling (FDM) three-dimensional printing (3DP) has made significant advancements in the field of oral drug delivery with personalized drug-loaded formulations being designed, developed and dispensed for the needs of the patient. The FDM 3DP process begins with the production of drug-loaded filaments by hot melt extrusion (HME), followed by the printing of a drug product using a FDM 3D printer. However, the optimization of the fabrication parameters is a time-consuming, empirical trial approach, requiring expert knowledge. Here, M3DISEEN, a web-based pharmaceutical software, was developed to accelerate FDM 3D printing using AI machine learning techniques (MLTs). In total, 614 drug-loaded formulations were designed from a comprehensive list of 145 different pharmaceutical excipients, 3D printed and assessed in-house. To build the predictive tool, a dataset was constructed and models were trained and tested at a ratio of 75:25. Significantly, the AI models predicted key fabrication parameters with accuracies of 76% and 67% for the printability and the filament characteristics, respectively. Furthermore, the AI models predicted the HME and FDM processing temperatures with a mean absolute error of 8.9 °C and 8.3 °C, respectively. Strikingly, the AI models achieved high levels of accuracy by solely inputting the pharmaceutical excipient trade names. Therefore, AI provides an effective holistic modeling technology and software to streamline and advance 3DP as a significant technology within drug development. M3DISEEN is available at (http://m3diseen.com/predictions/).es_ES
dc.description.sponsorshipThe authors would like to thank Dr. Atheer Awad for her support with the graphical abstract. This research was funded by the Engineering and Physical Sciences Research Council (EPSRC) UK, grant number EP/L01646X. CITIC is a Research Center of the University System of Galicia, funded by Consellería de Educación, Universidade e Formación Profesional of Xunta de Galicia and co-financed 80% by ERDF (Ref. ED431G 2019/01).es_ES
dc.description.sponsorshipReino Unido. Engineering and Physical Sciences Research Council; EP/L01646Xes_ES
dc.description.sponsorshipXunta de Galicia; ED431G 2019/01es_ES
dc.language.isoenges_ES
dc.publisherElsevier B.V.es_ES
dc.relation.urihttps://doi.org/10.1016/j.ijpharm.2020.119837es_ES
dc.rights©2020 Elsevier B.V. All rights reservedes_ES
dc.subjectAdditive manufacturinges_ES
dc.subjectFeature engineeringes_ES
dc.subjectPersonalized pharmaceuticals and medicineses_ES
dc.subjectGastrointestinal drug deliveryes_ES
dc.subject3D printed drug productses_ES
dc.subjectMaterial extrusiones_ES
dc.subjectFused filament fabricationes_ES
dc.titleM3DISEEN: A novel machine learning approach for predicting the 3D printability of medicineses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/embargoedAccesses_ES
dc.date.embargoEndDate9999-99-99es_ES
dc.date.embargoLift10007-06-07
UDC.journalTitleInternational Journal of Pharmaceuticses_ES
UDC.volume590es_ES
UDC.issue119837es_ES
dc.identifier.doi10.1016/j.ijpharm.2020.119837


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