Cargando…

Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery

Cryogels consisting of polyvinyl alcohol and iron (II, III) oxide magnetic nanoparticles coated with a model drug—acetaminophen, were developed as a tunable platform for thermally triggered drug release, based on shape-selective heat transfer. Two different shapes of cryogels; discs and spherical ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Perera, Ayomi S., Jackson, Richard J., Bristow, Reece M. D., White, Chinyere A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187744/
https://www.ncbi.nlm.nih.gov/pubmed/35688935
http://dx.doi.org/10.1038/s41598-022-13572-9
_version_ 1784725233225170944
author Perera, Ayomi S.
Jackson, Richard J.
Bristow, Reece M. D.
White, Chinyere A.
author_facet Perera, Ayomi S.
Jackson, Richard J.
Bristow, Reece M. D.
White, Chinyere A.
author_sort Perera, Ayomi S.
collection PubMed
description Cryogels consisting of polyvinyl alcohol and iron (II, III) oxide magnetic nanoparticles coated with a model drug—acetaminophen, were developed as a tunable platform for thermally triggered drug release, based on shape-selective heat transfer. Two different shapes of cryogels; discs and spherical caps, were formed via adding polymer-nanoparticle-drug mixtures into 3D printed molds, followed by freeze-thawing five times. No additional chemical crosslinking agents were used for gel formation and the iron oxide nanoparticles were coated with acetaminophen using only citric acid as a hydrogen-bonding linker. The two gel shapes displayed varying levels of acetaminophen release within 42–50 °C, which are ideal temperatures for hyperthermia induced drug delivery. The amount and time of drug-release were shown to be tunable by changing the temperature of the medium and the shape of the gels, while keeping all other factors (ex. gel volume, surface area, polymer/nanoparticle concentrations and drug-loading) constant. The discs displayed higher drug release at all temperatures while being particularly effective at lower temperatures (42–46 °C), in contrast to the spherical caps, which were more effective at higher temperatures (48–50 °C). Magnetic hyperthermia-mediated thermal imaging and temperature profiling studies revealed starkly different heat transfer behavior from the two shapes of gels. The disc gels retained their structural integrity up to 51 °C, while the spherical caps were stable up to 59 °C, demonstrating shape-dependent robustness. The highly customizable physicochemical features, facile synthesis, biocompatibility and tunable drug release ability of these cryogels offer potential for their application as a low cost, safe and effective platform for hyperthermia-mediated drug delivery, for external applications such as wound care/muscle repair or internal applications such as melanoma treatment.
format Online
Article
Text
id pubmed-9187744
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-91877442022-06-12 Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery Perera, Ayomi S. Jackson, Richard J. Bristow, Reece M. D. White, Chinyere A. Sci Rep Article Cryogels consisting of polyvinyl alcohol and iron (II, III) oxide magnetic nanoparticles coated with a model drug—acetaminophen, were developed as a tunable platform for thermally triggered drug release, based on shape-selective heat transfer. Two different shapes of cryogels; discs and spherical caps, were formed via adding polymer-nanoparticle-drug mixtures into 3D printed molds, followed by freeze-thawing five times. No additional chemical crosslinking agents were used for gel formation and the iron oxide nanoparticles were coated with acetaminophen using only citric acid as a hydrogen-bonding linker. The two gel shapes displayed varying levels of acetaminophen release within 42–50 °C, which are ideal temperatures for hyperthermia induced drug delivery. The amount and time of drug-release were shown to be tunable by changing the temperature of the medium and the shape of the gels, while keeping all other factors (ex. gel volume, surface area, polymer/nanoparticle concentrations and drug-loading) constant. The discs displayed higher drug release at all temperatures while being particularly effective at lower temperatures (42–46 °C), in contrast to the spherical caps, which were more effective at higher temperatures (48–50 °C). Magnetic hyperthermia-mediated thermal imaging and temperature profiling studies revealed starkly different heat transfer behavior from the two shapes of gels. The disc gels retained their structural integrity up to 51 °C, while the spherical caps were stable up to 59 °C, demonstrating shape-dependent robustness. The highly customizable physicochemical features, facile synthesis, biocompatibility and tunable drug release ability of these cryogels offer potential for their application as a low cost, safe and effective platform for hyperthermia-mediated drug delivery, for external applications such as wound care/muscle repair or internal applications such as melanoma treatment. Nature Publishing Group UK 2022-06-10 /pmc/articles/PMC9187744/ /pubmed/35688935 http://dx.doi.org/10.1038/s41598-022-13572-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Article
Perera, Ayomi S.
Jackson, Richard J.
Bristow, Reece M. D.
White, Chinyere A.
Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title_full Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title_fullStr Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title_full_unstemmed Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title_short Magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
title_sort magnetic cryogels as a shape-selective and customizable platform for hyperthermia-mediated drug delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187744/
https://www.ncbi.nlm.nih.gov/pubmed/35688935
http://dx.doi.org/10.1038/s41598-022-13572-9
work_keys_str_mv AT pereraayomis magneticcryogelsasashapeselectiveandcustomizableplatformforhyperthermiamediateddrugdelivery
AT jacksonrichardj magneticcryogelsasashapeselectiveandcustomizableplatformforhyperthermiamediateddrugdelivery
AT bristowreecemd magneticcryogelsasashapeselectiveandcustomizableplatformforhyperthermiamediateddrugdelivery
AT whitechinyerea magneticcryogelsasashapeselectiveandcustomizableplatformforhyperthermiamediateddrugdelivery