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Additive Manufacturing of an Extended-Release Tablet of Tacrolimus
An extended-release tablet of tacrolimus as once-daily dosing was fabricated using 3D printing technology. It was developed by combining two 3D-printing methods in parallel. Indeed, an optimized mixture of PVA, sorbitol, and magnesium stearate as a shell compartment was printed through a hot-melt ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381679/ https://www.ncbi.nlm.nih.gov/pubmed/37512202 http://dx.doi.org/10.3390/ma16144927 |
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author | Abdollahi, Azin Ansari, Zahra Akrami, Mohammad Haririan, Ismaeil Dashti-Khavidaki, Simin Irani, Mohammad Kamankesh, Mojtaba Ghobadi, Emad |
author_facet | Abdollahi, Azin Ansari, Zahra Akrami, Mohammad Haririan, Ismaeil Dashti-Khavidaki, Simin Irani, Mohammad Kamankesh, Mojtaba Ghobadi, Emad |
author_sort | Abdollahi, Azin |
collection | PubMed |
description | An extended-release tablet of tacrolimus as once-daily dosing was fabricated using 3D printing technology. It was developed by combining two 3D-printing methods in parallel. Indeed, an optimized mixture of PVA, sorbitol, and magnesium stearate as a shell compartment was printed through a hot-melt extrusion (HME) nozzle while an HPMC gel mixture of the drug in the core compartment was printed by a pressure-assisted micro-syringe (PAM). A 3D-printed tablet with an infill of 90% was selected as an optimized formula upon the desired dissolution profile, releasing 86% of the drug at 12 h, similar to the commercial one. The weight variation, friability, hardness, assay, and content uniformity determination met USP requirements. A microbial evaluation showed that the 3D-printed tablet does not support microbial growth. SEM analysis showed smooth surfaces with multiple deposited layers. No peak interference appeared based on FTIR analysis. No decomposition of the polymer and drug was observed in the printing temperature, and no change in tacrolimus crystallinity was detected based on TGA and DSC analyses, respectively. The novel, sTable 3D-printed tablet, fabricated using controllable additive manufacturing, can quickly provide tailored dosing with specific kinetic release for personalized medicine at the point-of-care. |
format | Online Article Text |
id | pubmed-10381679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103816792023-07-29 Additive Manufacturing of an Extended-Release Tablet of Tacrolimus Abdollahi, Azin Ansari, Zahra Akrami, Mohammad Haririan, Ismaeil Dashti-Khavidaki, Simin Irani, Mohammad Kamankesh, Mojtaba Ghobadi, Emad Materials (Basel) Article An extended-release tablet of tacrolimus as once-daily dosing was fabricated using 3D printing technology. It was developed by combining two 3D-printing methods in parallel. Indeed, an optimized mixture of PVA, sorbitol, and magnesium stearate as a shell compartment was printed through a hot-melt extrusion (HME) nozzle while an HPMC gel mixture of the drug in the core compartment was printed by a pressure-assisted micro-syringe (PAM). A 3D-printed tablet with an infill of 90% was selected as an optimized formula upon the desired dissolution profile, releasing 86% of the drug at 12 h, similar to the commercial one. The weight variation, friability, hardness, assay, and content uniformity determination met USP requirements. A microbial evaluation showed that the 3D-printed tablet does not support microbial growth. SEM analysis showed smooth surfaces with multiple deposited layers. No peak interference appeared based on FTIR analysis. No decomposition of the polymer and drug was observed in the printing temperature, and no change in tacrolimus crystallinity was detected based on TGA and DSC analyses, respectively. The novel, sTable 3D-printed tablet, fabricated using controllable additive manufacturing, can quickly provide tailored dosing with specific kinetic release for personalized medicine at the point-of-care. MDPI 2023-07-10 /pmc/articles/PMC10381679/ /pubmed/37512202 http://dx.doi.org/10.3390/ma16144927 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Abdollahi, Azin Ansari, Zahra Akrami, Mohammad Haririan, Ismaeil Dashti-Khavidaki, Simin Irani, Mohammad Kamankesh, Mojtaba Ghobadi, Emad Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title | Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title_full | Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title_fullStr | Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title_full_unstemmed | Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title_short | Additive Manufacturing of an Extended-Release Tablet of Tacrolimus |
title_sort | additive manufacturing of an extended-release tablet of tacrolimus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381679/ https://www.ncbi.nlm.nih.gov/pubmed/37512202 http://dx.doi.org/10.3390/ma16144927 |
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