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Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing

Graphene Oxide (GO) has recently attracted substantial attention in biomedical field as an effective platform for biological sensing, tissue scaffolds and in vitro fluorescence imaging. However, the targeting modality and the capability of its in vivo detection have not been explored. To enhance the...

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Detalles Bibliográficos
Autores principales: Gonzalez-Rodriguez, Roberto, Campbell, Elizabeth, Naumov, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553710/
https://www.ncbi.nlm.nih.gov/pubmed/31170197
http://dx.doi.org/10.1371/journal.pone.0217072
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author Gonzalez-Rodriguez, Roberto
Campbell, Elizabeth
Naumov, Anton
author_facet Gonzalez-Rodriguez, Roberto
Campbell, Elizabeth
Naumov, Anton
author_sort Gonzalez-Rodriguez, Roberto
collection PubMed
description Graphene Oxide (GO) has recently attracted substantial attention in biomedical field as an effective platform for biological sensing, tissue scaffolds and in vitro fluorescence imaging. However, the targeting modality and the capability of its in vivo detection have not been explored. To enhance the functionality of GO, we combine it with superparamagnetic iron oxide nanoparticles (Fe(3)O(4) NPs) serving as a biocompatible magnetic drug delivery addends and magnetic resonance contrast agent for MRI. Synthesized GO-Fe(3)O(4) conjugates have an average size of 260 nm and show low cytotoxicity comparable to that of GO. Fe(3)O(4) nanoparticles provide superparamagnetic properties for magnetic targeted drug delivery allowing simple manipulation by the magnetic field and magnetic resonance imaging with high r(2)/r(1) relaxivity ratios of ~10.7. GO-Fe(3)O(4) retains pH-sensing capabilities of GO used in this work to detect cancer versus healthy environments in vitro and exhibits fluorescence in the visible for bioimaging. As a drug delivery platform GO-Fe(3)O(4) shows successful fluorescence-tracked transport of hydrophobic doxorubicin non-covalently conjugated to GO with substantial loading and 2.5-fold improved efficacy. As a result, we propose GO-Fe(3)O(4) nanoparticles as a novel multifunctional magnetic targeted platform for high efficacy drug delivery traced in vitro by GO fluorescence and in vivo via MRI capable of optical cancer detection.
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spelling pubmed-65537102019-06-17 Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing Gonzalez-Rodriguez, Roberto Campbell, Elizabeth Naumov, Anton PLoS One Research Article Graphene Oxide (GO) has recently attracted substantial attention in biomedical field as an effective platform for biological sensing, tissue scaffolds and in vitro fluorescence imaging. However, the targeting modality and the capability of its in vivo detection have not been explored. To enhance the functionality of GO, we combine it with superparamagnetic iron oxide nanoparticles (Fe(3)O(4) NPs) serving as a biocompatible magnetic drug delivery addends and magnetic resonance contrast agent for MRI. Synthesized GO-Fe(3)O(4) conjugates have an average size of 260 nm and show low cytotoxicity comparable to that of GO. Fe(3)O(4) nanoparticles provide superparamagnetic properties for magnetic targeted drug delivery allowing simple manipulation by the magnetic field and magnetic resonance imaging with high r(2)/r(1) relaxivity ratios of ~10.7. GO-Fe(3)O(4) retains pH-sensing capabilities of GO used in this work to detect cancer versus healthy environments in vitro and exhibits fluorescence in the visible for bioimaging. As a drug delivery platform GO-Fe(3)O(4) shows successful fluorescence-tracked transport of hydrophobic doxorubicin non-covalently conjugated to GO with substantial loading and 2.5-fold improved efficacy. As a result, we propose GO-Fe(3)O(4) nanoparticles as a novel multifunctional magnetic targeted platform for high efficacy drug delivery traced in vitro by GO fluorescence and in vivo via MRI capable of optical cancer detection. Public Library of Science 2019-06-06 /pmc/articles/PMC6553710/ /pubmed/31170197 http://dx.doi.org/10.1371/journal.pone.0217072 Text en © 2019 Gonzalez-Rodriguez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gonzalez-Rodriguez, Roberto
Campbell, Elizabeth
Naumov, Anton
Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title_full Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title_fullStr Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title_full_unstemmed Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title_short Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
title_sort multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553710/
https://www.ncbi.nlm.nih.gov/pubmed/31170197
http://dx.doi.org/10.1371/journal.pone.0217072
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