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Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy

A promising clinical trial utilizing gold-silica core-shell nanostructures coated with polyethylene glycol (PEG) has been reported for near-infrared (NIR) photothermal therapy (PTT) of prostate cancer. The next critical step for PTT is the visualization of therapeutically relevant nanoshell (NS) con...

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Detalles Bibliográficos
Autores principales: Kadria-Vili, Yara, Neumann, Oara, Zhao, Yage, Nordlander, Peter, Martinez, Gary V., Bankson, James A., Halas, Naomi J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303993/
https://www.ncbi.nlm.nih.gov/pubmed/35858309
http://dx.doi.org/10.1073/pnas.2123527119
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author Kadria-Vili, Yara
Neumann, Oara
Zhao, Yage
Nordlander, Peter
Martinez, Gary V.
Bankson, James A.
Halas, Naomi J.
author_facet Kadria-Vili, Yara
Neumann, Oara
Zhao, Yage
Nordlander, Peter
Martinez, Gary V.
Bankson, James A.
Halas, Naomi J.
author_sort Kadria-Vili, Yara
collection PubMed
description A promising clinical trial utilizing gold-silica core-shell nanostructures coated with polyethylene glycol (PEG) has been reported for near-infrared (NIR) photothermal therapy (PTT) of prostate cancer. The next critical step for PTT is the visualization of therapeutically relevant nanoshell (NS) concentrations at the tumor site. Here we report the synthesis of PEGylated Gd(2)O(3)-mesoporous silica/gold core/shell NSs (Gd(2)O(3)-MS NSs) with NIR photothermal properties that also supply sufficient MRI contrast to be visualized at therapeutic doses (≥10(8) NSs per milliliter). The nanoparticles have r(1) relaxivities more than three times larger than those of conventional T(1) contrast agents, requiring less concentration of Gd(3+) to observe an equivalent signal enhancement in T(1)-weighted MR images. Furthermore, Gd(2)O(3)-MS NS nanoparticles have r(2) relaxivities comparable to those of existing T(2) contrast agents, observed in agarose phantoms. This highly unusual combination of simultaneous T(1) and T(2) contrast allows for MRI enhancement through different approaches. As a rudimentary example, we demonstrate T(1)/T(2) ratio MR images with sixfold contrast signal enhancement relative to its T(1) MRI and induced temperature increases of 20 to 55 °C under clinical illumination conditions. These nanoparticles facilitate MRI-guided PTT while providing real-time temperature feedback through thermal MRI mapping.
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spelling pubmed-93039932023-01-11 Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy Kadria-Vili, Yara Neumann, Oara Zhao, Yage Nordlander, Peter Martinez, Gary V. Bankson, James A. Halas, Naomi J. Proc Natl Acad Sci U S A Physical Sciences A promising clinical trial utilizing gold-silica core-shell nanostructures coated with polyethylene glycol (PEG) has been reported for near-infrared (NIR) photothermal therapy (PTT) of prostate cancer. The next critical step for PTT is the visualization of therapeutically relevant nanoshell (NS) concentrations at the tumor site. Here we report the synthesis of PEGylated Gd(2)O(3)-mesoporous silica/gold core/shell NSs (Gd(2)O(3)-MS NSs) with NIR photothermal properties that also supply sufficient MRI contrast to be visualized at therapeutic doses (≥10(8) NSs per milliliter). The nanoparticles have r(1) relaxivities more than three times larger than those of conventional T(1) contrast agents, requiring less concentration of Gd(3+) to observe an equivalent signal enhancement in T(1)-weighted MR images. Furthermore, Gd(2)O(3)-MS NS nanoparticles have r(2) relaxivities comparable to those of existing T(2) contrast agents, observed in agarose phantoms. This highly unusual combination of simultaneous T(1) and T(2) contrast allows for MRI enhancement through different approaches. As a rudimentary example, we demonstrate T(1)/T(2) ratio MR images with sixfold contrast signal enhancement relative to its T(1) MRI and induced temperature increases of 20 to 55 °C under clinical illumination conditions. These nanoparticles facilitate MRI-guided PTT while providing real-time temperature feedback through thermal MRI mapping. National Academy of Sciences 2022-07-11 2022-07-19 /pmc/articles/PMC9303993/ /pubmed/35858309 http://dx.doi.org/10.1073/pnas.2123527119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Physical Sciences
Kadria-Vili, Yara
Neumann, Oara
Zhao, Yage
Nordlander, Peter
Martinez, Gary V.
Bankson, James A.
Halas, Naomi J.
Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title_full Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title_fullStr Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title_full_unstemmed Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title_short Gd(2)O(3)-mesoporous silica/gold nanoshells: A potential dual T(1)/T(2) contrast agent for MRI-guided localized near-IR photothermal therapy
title_sort gd(2)o(3)-mesoporous silica/gold nanoshells: a potential dual t(1)/t(2) contrast agent for mri-guided localized near-ir photothermal therapy
topic Physical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303993/
https://www.ncbi.nlm.nih.gov/pubmed/35858309
http://dx.doi.org/10.1073/pnas.2123527119
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