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Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations

For the last 40 years, praziquantel has been the standard treatment for schistosomiasis, a neglected parasitic disease affecting more than 250 million people worldwide. However, there is no suitable paediatric formulation on the market, leading to off-label use and the splitting of commercial tablet...

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Autores principales: Boniatti, Janine, Januskaite, Patricija, da Fonseca, Laís B., Viçosa, Alessandra L., Amendoeira, Fábio C., Tuleu, Catherine, Basit, Abdul W., Goyanes, Alvaro, Ré, Maria-Inês
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398999/
https://www.ncbi.nlm.nih.gov/pubmed/34452075
http://dx.doi.org/10.3390/pharmaceutics13081114
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author Boniatti, Janine
Januskaite, Patricija
da Fonseca, Laís B.
Viçosa, Alessandra L.
Amendoeira, Fábio C.
Tuleu, Catherine
Basit, Abdul W.
Goyanes, Alvaro
Ré, Maria-Inês
author_facet Boniatti, Janine
Januskaite, Patricija
da Fonseca, Laís B.
Viçosa, Alessandra L.
Amendoeira, Fábio C.
Tuleu, Catherine
Basit, Abdul W.
Goyanes, Alvaro
Ré, Maria-Inês
author_sort Boniatti, Janine
collection PubMed
description For the last 40 years, praziquantel has been the standard treatment for schistosomiasis, a neglected parasitic disease affecting more than 250 million people worldwide. However, there is no suitable paediatric formulation on the market, leading to off-label use and the splitting of commercial tablets for adults. In this study, we use a recently available technology, direct powder extrusion (DPE) three-dimensional printing (3DP), to prepare paediatric Printlets™ (3D printed tablets) of amorphous solid dispersions of praziquantel with Kollidon(®) VA 64 and surfactants (Span™ 20 or Kolliphor(®) SLS). Printlets were successfully printed from both pellets and powders obtained from extrudates by hot melt extrusion (HME). In vitro dissolution studies showed a greater than four-fold increase in praziquantel release, due to the formation of amorphous solid dispersions. In vitro palatability data indicated that the printlets were in the range of praziquantel tolerability, highlighting the taste masking capabilities of this technology without the need for additional taste masking excipients. This work has demonstrated the possibility of 3D printing tablets using pellets or powder forms obtained by HME, avoiding the use of filaments in fused deposition modelling 3DP. Moreover, the main formulation hurdles of praziquantel, such as low drug solubility, inadequate taste, and high and variable dose requirements, can be overcome using this technology.
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spelling pubmed-83989992021-08-29 Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations Boniatti, Janine Januskaite, Patricija da Fonseca, Laís B. Viçosa, Alessandra L. Amendoeira, Fábio C. Tuleu, Catherine Basit, Abdul W. Goyanes, Alvaro Ré, Maria-Inês Pharmaceutics Article For the last 40 years, praziquantel has been the standard treatment for schistosomiasis, a neglected parasitic disease affecting more than 250 million people worldwide. However, there is no suitable paediatric formulation on the market, leading to off-label use and the splitting of commercial tablets for adults. In this study, we use a recently available technology, direct powder extrusion (DPE) three-dimensional printing (3DP), to prepare paediatric Printlets™ (3D printed tablets) of amorphous solid dispersions of praziquantel with Kollidon(®) VA 64 and surfactants (Span™ 20 or Kolliphor(®) SLS). Printlets were successfully printed from both pellets and powders obtained from extrudates by hot melt extrusion (HME). In vitro dissolution studies showed a greater than four-fold increase in praziquantel release, due to the formation of amorphous solid dispersions. In vitro palatability data indicated that the printlets were in the range of praziquantel tolerability, highlighting the taste masking capabilities of this technology without the need for additional taste masking excipients. This work has demonstrated the possibility of 3D printing tablets using pellets or powder forms obtained by HME, avoiding the use of filaments in fused deposition modelling 3DP. Moreover, the main formulation hurdles of praziquantel, such as low drug solubility, inadequate taste, and high and variable dose requirements, can be overcome using this technology. MDPI 2021-07-21 /pmc/articles/PMC8398999/ /pubmed/34452075 http://dx.doi.org/10.3390/pharmaceutics13081114 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
Boniatti, Janine
Januskaite, Patricija
da Fonseca, Laís B.
Viçosa, Alessandra L.
Amendoeira, Fábio C.
Tuleu, Catherine
Basit, Abdul W.
Goyanes, Alvaro
Ré, Maria-Inês
Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title_full Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title_fullStr Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title_full_unstemmed Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title_short Direct Powder Extrusion 3D Printing of Praziquantel to Overcome Neglected Disease Formulation Challenges in Paediatric Populations
title_sort direct powder extrusion 3d printing of praziquantel to overcome neglected disease formulation challenges in paediatric populations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398999/
https://www.ncbi.nlm.nih.gov/pubmed/34452075
http://dx.doi.org/10.3390/pharmaceutics13081114
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