Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets

Crosslinking is an established treatment to alter the physicochemical and functional properties of polymers through the creation of bonds between the polymer chains. Polymers can be crosslinked via radiation in the presence of photo-initiator. The aim of the present study was to formulate 3D-printed...

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Autores principales: Hele Anderspuk, Laura Viidik, Kristjan Olado, Karin Kogermann, Anne Juppo, Jyrki Heinämäki, Ivo Laidmäe
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Publicado: Elsevier 2021
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spelling oai:doaj.org-article:914922e9c2c347c183df488e503e2acb2021-11-18T04:53:42ZEffects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets2666-964110.1016/j.stlm.2021.100031https://doaj.org/article/914922e9c2c347c183df488e503e2acb2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666964121000266https://doaj.org/toc/2666-9641Crosslinking is an established treatment to alter the physicochemical and functional properties of polymers through the creation of bonds between the polymer chains. Polymers can be crosslinked via radiation in the presence of photo-initiator. The aim of the present study was to formulate 3D-printed theophylline (THEO) tablets using polyethylene oxide (PEO) as a carrier polymer, and to study the influence of crosslinking on the drug release behavior. The tablets were 3D-printed using the aqueous solution of PEO and THEO (80:20 w/w) with a micro-extrusion-based printing setup. A photo-initiator (4-hydroxybenzophenone) was added into the printing solutions, and the injectability of the solutions was investigated prior to printing. The 3D-printed tablets were crosslinked after printing using ultraviolet (UV) or gamma-radiation, and crosslinking was verified by means of Fourier-transform infrared (FTIR) spectroscopy. The maximum injection force of aqueous printing solutions of PEO and THEO was close to that observed with the pure PEO solution. Increasing the number of printing layers in the 3D-printed tablets resulted in a slower drug release in vitro. Gamma-radiation in a nitrogen environment and UV-crosslinking made the carrier polymer (PEO) less water-soluble, but such crosslinking did not affect the release rate of the tablets. Surprisingly, even faster drug release behavior was found with the crosslinked 3D-printed tablets compared to that of non-crosslinked tablets. More research work is needed on the impact of 3D-printed tablet layering thickness and crosslinking for tailoring drug release behavior.Hele AnderspukLaura ViidikKristjan OladoKarin KogermannAnne JuppoJyrki HeinämäkiIvo LaidmäeElsevierarticle3D-printingUV-crosslinkingGamma-radiation crosslinkingDrug releasePolyethylene oxideTheophyllineMedical technologyR855-855.5ENAnnals of 3D Printed Medicine, Vol 4, Iss , Pp 100031- (2021)
institution DOAJ
collection DOAJ
language EN
topic 3D-printing
UV-crosslinking
Gamma-radiation crosslinking
Drug release
Polyethylene oxide
Theophylline
Medical technology
R855-855.5
spellingShingle 3D-printing
UV-crosslinking
Gamma-radiation crosslinking
Drug release
Polyethylene oxide
Theophylline
Medical technology
R855-855.5
Hele Anderspuk
Laura Viidik
Kristjan Olado
Karin Kogermann
Anne Juppo
Jyrki Heinämäki
Ivo Laidmäe
Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
description Crosslinking is an established treatment to alter the physicochemical and functional properties of polymers through the creation of bonds between the polymer chains. Polymers can be crosslinked via radiation in the presence of photo-initiator. The aim of the present study was to formulate 3D-printed theophylline (THEO) tablets using polyethylene oxide (PEO) as a carrier polymer, and to study the influence of crosslinking on the drug release behavior. The tablets were 3D-printed using the aqueous solution of PEO and THEO (80:20 w/w) with a micro-extrusion-based printing setup. A photo-initiator (4-hydroxybenzophenone) was added into the printing solutions, and the injectability of the solutions was investigated prior to printing. The 3D-printed tablets were crosslinked after printing using ultraviolet (UV) or gamma-radiation, and crosslinking was verified by means of Fourier-transform infrared (FTIR) spectroscopy. The maximum injection force of aqueous printing solutions of PEO and THEO was close to that observed with the pure PEO solution. Increasing the number of printing layers in the 3D-printed tablets resulted in a slower drug release in vitro. Gamma-radiation in a nitrogen environment and UV-crosslinking made the carrier polymer (PEO) less water-soluble, but such crosslinking did not affect the release rate of the tablets. Surprisingly, even faster drug release behavior was found with the crosslinked 3D-printed tablets compared to that of non-crosslinked tablets. More research work is needed on the impact of 3D-printed tablet layering thickness and crosslinking for tailoring drug release behavior.
format article
author Hele Anderspuk
Laura Viidik
Kristjan Olado
Karin Kogermann
Anne Juppo
Jyrki Heinämäki
Ivo Laidmäe
author_facet Hele Anderspuk
Laura Viidik
Kristjan Olado
Karin Kogermann
Anne Juppo
Jyrki Heinämäki
Ivo Laidmäe
author_sort Hele Anderspuk
title Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
title_short Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
title_full Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
title_fullStr Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
title_full_unstemmed Effects of crosslinking on the physical solid-state and dissolution properties of 3D-printed theophylline tablets
title_sort effects of crosslinking on the physical solid-state and dissolution properties of 3d-printed theophylline tablets
publisher Elsevier
publishDate 2021
url https://doaj.org/article/914922e9c2c347c183df488e503e2acb
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