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3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs
Fused deposition modelling (FDM) is the most extensively employed 3D-printing technique used in pharmaceutical applications, and offers fast and facile formulation development of personalized dosage forms. In the present study, mesoporous materials were incorporated into a thermoplastic filament pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308994/ https://www.ncbi.nlm.nih.gov/pubmed/34371787 http://dx.doi.org/10.3390/pharmaceutics13071096 |
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author | Katsiotis, Christos S. Åhlén, Michelle Strømme, Maria Welch, Ken |
author_facet | Katsiotis, Christos S. Åhlén, Michelle Strømme, Maria Welch, Ken |
author_sort | Katsiotis, Christos S. |
collection | PubMed |
description | Fused deposition modelling (FDM) is the most extensively employed 3D-printing technique used in pharmaceutical applications, and offers fast and facile formulation development of personalized dosage forms. In the present study, mesoporous materials were incorporated into a thermoplastic filament produced via hot-melt extrusion and used to produce oral dosage forms via FDM. Mesoporous materials are known to be highly effective for the amorphization and stabilization of poorly soluble drugs, and were therefore studied in order to determine their ability to enhance the drug-release properties in 3D-printed tablets. Celecoxib was selected as the model poorly soluble drug, and was loaded into mesoporous silica (MCM-41) or mesoporous magnesium carbonate. In vitro drug release tests showed that the printed tablets produced up to 3.6 and 1.5 times higher drug concentrations, and up to 4.4 and 1.9 times higher release percentages, compared to the crystalline drug or the corresponding plain drug-loaded mesoporous materials, respectively. This novel approach utilizing drug-loaded mesoporous materials in a printed tablet via FDM shows great promise in achieving personalized oral dosage forms for poorly soluble drugs. |
format | Online Article Text |
id | pubmed-8308994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83089942021-07-25 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs Katsiotis, Christos S. Åhlén, Michelle Strømme, Maria Welch, Ken Pharmaceutics Article Fused deposition modelling (FDM) is the most extensively employed 3D-printing technique used in pharmaceutical applications, and offers fast and facile formulation development of personalized dosage forms. In the present study, mesoporous materials were incorporated into a thermoplastic filament produced via hot-melt extrusion and used to produce oral dosage forms via FDM. Mesoporous materials are known to be highly effective for the amorphization and stabilization of poorly soluble drugs, and were therefore studied in order to determine their ability to enhance the drug-release properties in 3D-printed tablets. Celecoxib was selected as the model poorly soluble drug, and was loaded into mesoporous silica (MCM-41) or mesoporous magnesium carbonate. In vitro drug release tests showed that the printed tablets produced up to 3.6 and 1.5 times higher drug concentrations, and up to 4.4 and 1.9 times higher release percentages, compared to the crystalline drug or the corresponding plain drug-loaded mesoporous materials, respectively. This novel approach utilizing drug-loaded mesoporous materials in a printed tablet via FDM shows great promise in achieving personalized oral dosage forms for poorly soluble drugs. MDPI 2021-07-18 /pmc/articles/PMC8308994/ /pubmed/34371787 http://dx.doi.org/10.3390/pharmaceutics13071096 Text en © 2021 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 Katsiotis, Christos S. Åhlén, Michelle Strømme, Maria Welch, Ken 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title | 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title_full | 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title_fullStr | 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title_full_unstemmed | 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title_short | 3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs |
title_sort | 3d-printed mesoporous carrier system for delivery of poorly soluble drugs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308994/ https://www.ncbi.nlm.nih.gov/pubmed/34371787 http://dx.doi.org/10.3390/pharmaceutics13071096 |
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