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Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development

Mesoporous silica nanoparticles (MSNs) have shown great potential in improving drug delivery of poorly water soluble (BCS class II, IV) and poorly permeable (BCS class III, IV) drugs, as well as facilitating successful delivery of unstable compounds. The nanoparticle technology would allow improved...

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Autores principales: Wickström, Henrika, Hilgert, Ellen, Nyman, Johan O., Desai, Diti, Şen Karaman, Didem, de Beer, Thomas, Sandler, Niklas, Rosenholm, Jessica M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150386/
https://www.ncbi.nlm.nih.gov/pubmed/29160839
http://dx.doi.org/10.3390/molecules22112020
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author Wickström, Henrika
Hilgert, Ellen
Nyman, Johan O.
Desai, Diti
Şen Karaman, Didem
de Beer, Thomas
Sandler, Niklas
Rosenholm, Jessica M.
author_facet Wickström, Henrika
Hilgert, Ellen
Nyman, Johan O.
Desai, Diti
Şen Karaman, Didem
de Beer, Thomas
Sandler, Niklas
Rosenholm, Jessica M.
author_sort Wickström, Henrika
collection PubMed
description Mesoporous silica nanoparticles (MSNs) have shown great potential in improving drug delivery of poorly water soluble (BCS class II, IV) and poorly permeable (BCS class III, IV) drugs, as well as facilitating successful delivery of unstable compounds. The nanoparticle technology would allow improved treatment by reducing adverse reactions of currently approved drugs and possibly reintroducing previously discarded compounds from the drug development pipeline. This study aims to highlight important aspects in mesoporous silica nanoparticle (MSN) ink formulation development for digital inkjet printing technology and to advice on choosing a method (2D/3D) for nanoparticle print deposit characterization. The results show that both unfunctionalized and polyethyeleneimine (PEI) surface functionalized MSNs, as well as drug-free and drug-loaded MSN–PEI suspensions, can be successfully inkjet-printed. Furthermore, the model BCS class IV drug remained incorporated in the MSNs and the suspension remained physically stable during the processing time and steps. This proof-of-concept study suggests that inkjet printing technology would be a flexible deposition method of pharmaceutical MSN suspensions to generate patterns according to predefined designs. The concept could be utilized as a versatile drug screening platform in the future due to the possibility of accurately depositing controlled volumes of MSN suspensions on various materials.
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spelling pubmed-61503862018-11-13 Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development Wickström, Henrika Hilgert, Ellen Nyman, Johan O. Desai, Diti Şen Karaman, Didem de Beer, Thomas Sandler, Niklas Rosenholm, Jessica M. Molecules Article Mesoporous silica nanoparticles (MSNs) have shown great potential in improving drug delivery of poorly water soluble (BCS class II, IV) and poorly permeable (BCS class III, IV) drugs, as well as facilitating successful delivery of unstable compounds. The nanoparticle technology would allow improved treatment by reducing adverse reactions of currently approved drugs and possibly reintroducing previously discarded compounds from the drug development pipeline. This study aims to highlight important aspects in mesoporous silica nanoparticle (MSN) ink formulation development for digital inkjet printing technology and to advice on choosing a method (2D/3D) for nanoparticle print deposit characterization. The results show that both unfunctionalized and polyethyeleneimine (PEI) surface functionalized MSNs, as well as drug-free and drug-loaded MSN–PEI suspensions, can be successfully inkjet-printed. Furthermore, the model BCS class IV drug remained incorporated in the MSNs and the suspension remained physically stable during the processing time and steps. This proof-of-concept study suggests that inkjet printing technology would be a flexible deposition method of pharmaceutical MSN suspensions to generate patterns according to predefined designs. The concept could be utilized as a versatile drug screening platform in the future due to the possibility of accurately depositing controlled volumes of MSN suspensions on various materials. MDPI 2017-11-21 /pmc/articles/PMC6150386/ /pubmed/29160839 http://dx.doi.org/10.3390/molecules22112020 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wickström, Henrika
Hilgert, Ellen
Nyman, Johan O.
Desai, Diti
Şen Karaman, Didem
de Beer, Thomas
Sandler, Niklas
Rosenholm, Jessica M.
Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title_full Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title_fullStr Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title_full_unstemmed Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title_short Inkjet Printing of Drug-Loaded Mesoporous Silica Nanoparticles—A Platform for Drug Development
title_sort inkjet printing of drug-loaded mesoporous silica nanoparticles—a platform for drug development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150386/
https://www.ncbi.nlm.nih.gov/pubmed/29160839
http://dx.doi.org/10.3390/molecules22112020
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