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Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings

In a previous attempt to achieve ileo-colonic targeting of bovine intestinal alkaline phosphatase (BIAP), we applied a pH-dependent coating, the ColoPulse coating, directly on powder bed printed (PBP) tablets. However, the high surface roughness necessitated an additional sub-coating layer [Nguyen,...

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Autores principales: Nguyen, Khanh T. T., Zillen, Daan, van Heijningen, Franca F. M., van Bommel, Kjeld J. C., van Ee, Renz J., Frijlink, Henderik W., Hinrichs, Wouter L. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537163/
https://www.ncbi.nlm.nih.gov/pubmed/37765163
http://dx.doi.org/10.3390/pharmaceutics15092193
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author Nguyen, Khanh T. T.
Zillen, Daan
van Heijningen, Franca F. M.
van Bommel, Kjeld J. C.
van Ee, Renz J.
Frijlink, Henderik W.
Hinrichs, Wouter L. J.
author_facet Nguyen, Khanh T. T.
Zillen, Daan
van Heijningen, Franca F. M.
van Bommel, Kjeld J. C.
van Ee, Renz J.
Frijlink, Henderik W.
Hinrichs, Wouter L. J.
author_sort Nguyen, Khanh T. T.
collection PubMed
description In a previous attempt to achieve ileo-colonic targeting of bovine intestinal alkaline phosphatase (BIAP), we applied a pH-dependent coating, the ColoPulse coating, directly on powder bed printed (PBP) tablets. However, the high surface roughness necessitated an additional sub-coating layer [Nguyen, K. T. T., Pharmaceutics 2022]. In this study, we aimed to find a production method for PBP tablets containing BIAP that allows the direct application of coating systems. Alterations of the printing parameters, binder content, and printing layer height, when combined, were demonstrated to create visually less rough PBP tablets. The addition of ethanol vapor treatment further improved the surface’s smoothness significantly. These changes enabled the direct application of the ColoPulse, or enteric coating, without a sub-coating. In vitro release testing showed the desired ileo-colonic release or upper-intestinal release for ColoPulse or enteric-coated tablets, respectively. Tablets containing BIAP, encapsulated within an inulin glass, maintained a high enzymatic activity (over 95%) even after 2 months of storage at 2–8 °C. Importantly, the coating process did not affect the activity of BIAP. In this study, we demonstrate, for the first time, the successful production of PBP tablets with surfaces that are directly coatable with the ColoPulse coating while preserving the stability of the encapsulated biopharmaceutical, BIAP.
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spelling pubmed-105371632023-09-29 Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings Nguyen, Khanh T. T. Zillen, Daan van Heijningen, Franca F. M. van Bommel, Kjeld J. C. van Ee, Renz J. Frijlink, Henderik W. Hinrichs, Wouter L. J. Pharmaceutics Article In a previous attempt to achieve ileo-colonic targeting of bovine intestinal alkaline phosphatase (BIAP), we applied a pH-dependent coating, the ColoPulse coating, directly on powder bed printed (PBP) tablets. However, the high surface roughness necessitated an additional sub-coating layer [Nguyen, K. T. T., Pharmaceutics 2022]. In this study, we aimed to find a production method for PBP tablets containing BIAP that allows the direct application of coating systems. Alterations of the printing parameters, binder content, and printing layer height, when combined, were demonstrated to create visually less rough PBP tablets. The addition of ethanol vapor treatment further improved the surface’s smoothness significantly. These changes enabled the direct application of the ColoPulse, or enteric coating, without a sub-coating. In vitro release testing showed the desired ileo-colonic release or upper-intestinal release for ColoPulse or enteric-coated tablets, respectively. Tablets containing BIAP, encapsulated within an inulin glass, maintained a high enzymatic activity (over 95%) even after 2 months of storage at 2–8 °C. Importantly, the coating process did not affect the activity of BIAP. In this study, we demonstrate, for the first time, the successful production of PBP tablets with surfaces that are directly coatable with the ColoPulse coating while preserving the stability of the encapsulated biopharmaceutical, BIAP. MDPI 2023-08-24 /pmc/articles/PMC10537163/ /pubmed/37765163 http://dx.doi.org/10.3390/pharmaceutics15092193 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
Nguyen, Khanh T. T.
Zillen, Daan
van Heijningen, Franca F. M.
van Bommel, Kjeld J. C.
van Ee, Renz J.
Frijlink, Henderik W.
Hinrichs, Wouter L. J.
Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title_full Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title_fullStr Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title_full_unstemmed Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title_short Surface Engineering Methods for Powder Bed Printed Tablets to Optimize External Smoothness and Facilitate the Application of Different Coatings
title_sort surface engineering methods for powder bed printed tablets to optimize external smoothness and facilitate the application of different coatings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537163/
https://www.ncbi.nlm.nih.gov/pubmed/37765163
http://dx.doi.org/10.3390/pharmaceutics15092193
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