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Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors
Theranostic nanoparticles offer the potential for mixing and matching disparate diagnostic and therapeutic functionalities within a single nanoparticle for the personalized treatment of diseases. In this article, we present composite iron oxide-gadolinium-containing Prussian blue nanoparticles (Fe(3...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592912/ https://www.ncbi.nlm.nih.gov/pubmed/28919744 http://dx.doi.org/10.2147/IJN.S144515 |
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author | Kale, Shraddha S Burga, Rachel A Sweeney, Elizabeth E Zun, Zungho Sze, Raymond W Tuesca, Anthony Subramony, J Anand Fernandes, Rohan |
author_facet | Kale, Shraddha S Burga, Rachel A Sweeney, Elizabeth E Zun, Zungho Sze, Raymond W Tuesca, Anthony Subramony, J Anand Fernandes, Rohan |
author_sort | Kale, Shraddha S |
collection | PubMed |
description | Theranostic nanoparticles offer the potential for mixing and matching disparate diagnostic and therapeutic functionalities within a single nanoparticle for the personalized treatment of diseases. In this article, we present composite iron oxide-gadolinium-containing Prussian blue nanoparticles (Fe(3)O(4)@GdPB) as a novel theranostic agent for T(1)-weighted magnetic resonance imaging (MRI) and photothermal therapy (PTT) of tumors. These particles combine the well-described properties and safety profiles of the constituent Fe(3)O(4) nanoparticles and gadolinium-containing Prussian blue nanoparticles. The Fe(3)O(4)@GdPB nanoparticles function both as effective MRI contrast agents and PTT agents as determined by characterizing studies performed in vitro and retain their properties in the presence of cells. Importantly, the Fe(3)O(4)@GdPB nanoparticles function as effective MRI contrast agents in vivo by increasing signal:noise ratios in T(1)-weighted scans of tumors and as effective PTT agents in vivo by decreasing tumor growth rates and increasing survival in an animal model of neuroblastoma. These findings demonstrate the potential of the Fe(3)O(4)@GdPB nanoparticles to function as effective theranostic agents. |
format | Online Article Text |
id | pubmed-5592912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55929122017-09-15 Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors Kale, Shraddha S Burga, Rachel A Sweeney, Elizabeth E Zun, Zungho Sze, Raymond W Tuesca, Anthony Subramony, J Anand Fernandes, Rohan Int J Nanomedicine Original Research Theranostic nanoparticles offer the potential for mixing and matching disparate diagnostic and therapeutic functionalities within a single nanoparticle for the personalized treatment of diseases. In this article, we present composite iron oxide-gadolinium-containing Prussian blue nanoparticles (Fe(3)O(4)@GdPB) as a novel theranostic agent for T(1)-weighted magnetic resonance imaging (MRI) and photothermal therapy (PTT) of tumors. These particles combine the well-described properties and safety profiles of the constituent Fe(3)O(4) nanoparticles and gadolinium-containing Prussian blue nanoparticles. The Fe(3)O(4)@GdPB nanoparticles function both as effective MRI contrast agents and PTT agents as determined by characterizing studies performed in vitro and retain their properties in the presence of cells. Importantly, the Fe(3)O(4)@GdPB nanoparticles function as effective MRI contrast agents in vivo by increasing signal:noise ratios in T(1)-weighted scans of tumors and as effective PTT agents in vivo by decreasing tumor growth rates and increasing survival in an animal model of neuroblastoma. These findings demonstrate the potential of the Fe(3)O(4)@GdPB nanoparticles to function as effective theranostic agents. Dove Medical Press 2017-09-05 /pmc/articles/PMC5592912/ /pubmed/28919744 http://dx.doi.org/10.2147/IJN.S144515 Text en © 2017 Kale et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kale, Shraddha S Burga, Rachel A Sweeney, Elizabeth E Zun, Zungho Sze, Raymond W Tuesca, Anthony Subramony, J Anand Fernandes, Rohan Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title | Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title_full | Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title_fullStr | Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title_full_unstemmed | Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title_short | Composite iron oxide–Prussian blue nanoparticles for magnetically guided T(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
title_sort | composite iron oxide–prussian blue nanoparticles for magnetically guided t(1)-weighted magnetic resonance imaging and photothermal therapy of tumors |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592912/ https://www.ncbi.nlm.nih.gov/pubmed/28919744 http://dx.doi.org/10.2147/IJN.S144515 |
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