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3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)

Niclosamide (NICLO) is a recognized antiparasitic drug being repositioned for Helicobacter pylori. The present work aimed to formulate NICLO nanocrystals (NICLO-NCRs) to produce a higher dissolution rate of the active ingredient and to incorporate these nanosystems into a floating solid dosage form...

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Autores principales: Real, Juan Pablo, Real, Daniel Andrés, Lopez-Vidal, Lucía, Barrientos, Bruno Andrés, Bolaños, Karen, Tinti, Mariano Guillermo, Litterio, Nicolás Javier, Kogan, Marcelo Javier, Palma, Santiago Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220711/
https://www.ncbi.nlm.nih.gov/pubmed/37242629
http://dx.doi.org/10.3390/pharmaceutics15051387
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author Real, Juan Pablo
Real, Daniel Andrés
Lopez-Vidal, Lucía
Barrientos, Bruno Andrés
Bolaños, Karen
Tinti, Mariano Guillermo
Litterio, Nicolás Javier
Kogan, Marcelo Javier
Palma, Santiago Daniel
author_facet Real, Juan Pablo
Real, Daniel Andrés
Lopez-Vidal, Lucía
Barrientos, Bruno Andrés
Bolaños, Karen
Tinti, Mariano Guillermo
Litterio, Nicolás Javier
Kogan, Marcelo Javier
Palma, Santiago Daniel
author_sort Real, Juan Pablo
collection PubMed
description Niclosamide (NICLO) is a recognized antiparasitic drug being repositioned for Helicobacter pylori. The present work aimed to formulate NICLO nanocrystals (NICLO-NCRs) to produce a higher dissolution rate of the active ingredient and to incorporate these nanosystems into a floating solid dosage form to release them into the stomach slowly. For this purpose, NICLO-NCRs were produced by wet-milling and included in a floating Gelucire l3D printed tablet by semi-solid extrusion, applying the Melting solidification printing process (MESO-PP) methodology. The results obtained in TGA, DSC, XRD and FT-IR analysis showed no physicochemical interactions or modifications in the crystallinity of NICLO-NCR after inclusion in Gelucire 50/13 ink. This method allowed the incorporation of NICLO-NCRs in a concentration of up to 25% w/w. It achieved a controlled release of NCRs in a simulated gastric medium. Moreover, the presence of NICLO-NCRs after redispersion of the printlets was observed by STEM. Additionally, no effects on the cell viability of the NCRs were demonstrated in the GES-1 cell line. Finally, gastroretention was demonstrated for 180 min in dogs. These findings show the potential of the MESO-PP technique in obtaining slow-release gastro-retentive oral solid dosage forms loaded with nanocrystals of a poorly soluble drug, an ideal system for treating gastric pathologies such as H. pylori.
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spelling pubmed-102207112023-05-28 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP) Real, Juan Pablo Real, Daniel Andrés Lopez-Vidal, Lucía Barrientos, Bruno Andrés Bolaños, Karen Tinti, Mariano Guillermo Litterio, Nicolás Javier Kogan, Marcelo Javier Palma, Santiago Daniel Pharmaceutics Article Niclosamide (NICLO) is a recognized antiparasitic drug being repositioned for Helicobacter pylori. The present work aimed to formulate NICLO nanocrystals (NICLO-NCRs) to produce a higher dissolution rate of the active ingredient and to incorporate these nanosystems into a floating solid dosage form to release them into the stomach slowly. For this purpose, NICLO-NCRs were produced by wet-milling and included in a floating Gelucire l3D printed tablet by semi-solid extrusion, applying the Melting solidification printing process (MESO-PP) methodology. The results obtained in TGA, DSC, XRD and FT-IR analysis showed no physicochemical interactions or modifications in the crystallinity of NICLO-NCR after inclusion in Gelucire 50/13 ink. This method allowed the incorporation of NICLO-NCRs in a concentration of up to 25% w/w. It achieved a controlled release of NCRs in a simulated gastric medium. Moreover, the presence of NICLO-NCRs after redispersion of the printlets was observed by STEM. Additionally, no effects on the cell viability of the NCRs were demonstrated in the GES-1 cell line. Finally, gastroretention was demonstrated for 180 min in dogs. These findings show the potential of the MESO-PP technique in obtaining slow-release gastro-retentive oral solid dosage forms loaded with nanocrystals of a poorly soluble drug, an ideal system for treating gastric pathologies such as H. pylori. MDPI 2023-04-30 /pmc/articles/PMC10220711/ /pubmed/37242629 http://dx.doi.org/10.3390/pharmaceutics15051387 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
Real, Juan Pablo
Real, Daniel Andrés
Lopez-Vidal, Lucía
Barrientos, Bruno Andrés
Bolaños, Karen
Tinti, Mariano Guillermo
Litterio, Nicolás Javier
Kogan, Marcelo Javier
Palma, Santiago Daniel
3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title_full 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title_fullStr 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title_full_unstemmed 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title_short 3D-Printed Gastroretentive Tablets Loaded with Niclosamide Nanocrystals by the Melting Solidification Printing Process (MESO-PP)
title_sort 3d-printed gastroretentive tablets loaded with niclosamide nanocrystals by the melting solidification printing process (meso-pp)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220711/
https://www.ncbi.nlm.nih.gov/pubmed/37242629
http://dx.doi.org/10.3390/pharmaceutics15051387
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