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Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide

Niclosamide (NCS) is a drug that has been used as an anthelmintic and anti-parasitic drug for about 40 years. Recently, some studies have highlighted its potential in treating various tumors, allowing a repositioning of this drug. Despite its potential, NCS is a Biopharmaceutical Classification Syst...

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Autores principales: Pistone, Monica, Racaniello, Giuseppe Francesco, Arduino, Ilaria, Laquintana, Valentino, Lopalco, Antonio, Cutrignelli, Annalisa, Rizzi, Rosanna, Franco, Massimo, Lopedota, Angela, Denora, Nunzio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242976/
https://www.ncbi.nlm.nih.gov/pubmed/35138629
http://dx.doi.org/10.1007/s13346-022-01124-7
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author Pistone, Monica
Racaniello, Giuseppe Francesco
Arduino, Ilaria
Laquintana, Valentino
Lopalco, Antonio
Cutrignelli, Annalisa
Rizzi, Rosanna
Franco, Massimo
Lopedota, Angela
Denora, Nunzio
author_facet Pistone, Monica
Racaniello, Giuseppe Francesco
Arduino, Ilaria
Laquintana, Valentino
Lopalco, Antonio
Cutrignelli, Annalisa
Rizzi, Rosanna
Franco, Massimo
Lopedota, Angela
Denora, Nunzio
author_sort Pistone, Monica
collection PubMed
description Niclosamide (NCS) is a drug that has been used as an anthelmintic and anti-parasitic drug for about 40 years. Recently, some studies have highlighted its potential in treating various tumors, allowing a repositioning of this drug. Despite its potential, NCS is a Biopharmaceutical Classification System (BCS) Class II drug and is consequently characterized by low aqueous solubility, poor dissolution rate and reduced bioavailability, which limits its applicability. In this work, we utilize a very novel technique, direct powder extrusion (DPE) 3D printing, which overcomes the limitations of previously used techniques (fused deposition modelling, FDM) to achieve direct extrusion of powder mixtures consisting of NCS, hydroxypropyl methylcellulose (HPMC, Affinisol 15 LV), hydroxypropyl-β-cyclodextrin (HP-β-CD) and polyethylene glycol (PEG) 6000. For the first time, direct printing of powder blends containing HP-β-CD was conducted. For all tablets, in vitro dissolution studies showed sustained drug release over 48 h, but for tablets containing HP-β-CD, the release was faster. Solid-state characterization studies showed that during extrusion, the drug lost its crystal structure and was evenly distributed within the polymer matrix. All printed tablets have exhibited good mechanical and physical features and a stability of the drug content for up to 3 months. This innovative printing technique has demonstrated the possibility to produce personalized pharmaceutical forms directly from powders, avoiding the use of filament used by FDM. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13346-022-01124-7.
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spelling pubmed-92429762022-07-01 Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide Pistone, Monica Racaniello, Giuseppe Francesco Arduino, Ilaria Laquintana, Valentino Lopalco, Antonio Cutrignelli, Annalisa Rizzi, Rosanna Franco, Massimo Lopedota, Angela Denora, Nunzio Drug Deliv Transl Res Original Article Niclosamide (NCS) is a drug that has been used as an anthelmintic and anti-parasitic drug for about 40 years. Recently, some studies have highlighted its potential in treating various tumors, allowing a repositioning of this drug. Despite its potential, NCS is a Biopharmaceutical Classification System (BCS) Class II drug and is consequently characterized by low aqueous solubility, poor dissolution rate and reduced bioavailability, which limits its applicability. In this work, we utilize a very novel technique, direct powder extrusion (DPE) 3D printing, which overcomes the limitations of previously used techniques (fused deposition modelling, FDM) to achieve direct extrusion of powder mixtures consisting of NCS, hydroxypropyl methylcellulose (HPMC, Affinisol 15 LV), hydroxypropyl-β-cyclodextrin (HP-β-CD) and polyethylene glycol (PEG) 6000. For the first time, direct printing of powder blends containing HP-β-CD was conducted. For all tablets, in vitro dissolution studies showed sustained drug release over 48 h, but for tablets containing HP-β-CD, the release was faster. Solid-state characterization studies showed that during extrusion, the drug lost its crystal structure and was evenly distributed within the polymer matrix. All printed tablets have exhibited good mechanical and physical features and a stability of the drug content for up to 3 months. This innovative printing technique has demonstrated the possibility to produce personalized pharmaceutical forms directly from powders, avoiding the use of filament used by FDM. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13346-022-01124-7. Springer US 2022-02-09 2022 /pmc/articles/PMC9242976/ /pubmed/35138629 http://dx.doi.org/10.1007/s13346-022-01124-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Pistone, Monica
Racaniello, Giuseppe Francesco
Arduino, Ilaria
Laquintana, Valentino
Lopalco, Antonio
Cutrignelli, Annalisa
Rizzi, Rosanna
Franco, Massimo
Lopedota, Angela
Denora, Nunzio
Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title_full Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title_fullStr Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title_full_unstemmed Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title_short Direct cyclodextrin-based powder extrusion 3D printing for one-step production of the BCS class II model drug niclosamide
title_sort direct cyclodextrin-based powder extrusion 3d printing for one-step production of the bcs class ii model drug niclosamide
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242976/
https://www.ncbi.nlm.nih.gov/pubmed/35138629
http://dx.doi.org/10.1007/s13346-022-01124-7
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