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Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor

Diagnostic approaches based on multimodal imaging of clinical noninvasive imaging (eg. MRI/CT scanner) are highly developed in recent years for accurate selection of the therapeutic regimens in critical diseases. Therefore, it is highly demanded in the development of appropriate all-in-one multimoda...

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Autores principales: Wang, Guannan, Gao, Wei, Zhang, Xuanjun, Mei, Xifan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911575/
https://www.ncbi.nlm.nih.gov/pubmed/27312564
http://dx.doi.org/10.1038/srep28258
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author Wang, Guannan
Gao, Wei
Zhang, Xuanjun
Mei, Xifan
author_facet Wang, Guannan
Gao, Wei
Zhang, Xuanjun
Mei, Xifan
author_sort Wang, Guannan
collection PubMed
description Diagnostic approaches based on multimodal imaging of clinical noninvasive imaging (eg. MRI/CT scanner) are highly developed in recent years for accurate selection of the therapeutic regimens in critical diseases. Therefore, it is highly demanded in the development of appropriate all-in-one multimodal contrast agents (MCAs) for the MRI/CT multimodal imaging. Here a novel ideal MCAs (F-AuNC@Fe(3)O(4)) were engineered by assemble Au nanocages (Au NC) and ultra-small iron oxide nanoparticles (Fe(3)O(4)) for simultaneous T(1)–T(2)dual MRI and CT contrast imaging. In this system, the Au nanocages offer facile thiol modification and strong X-ray attenuation property for CT imaging. The ultra-small Fe(3)O(4) nanoparticles, as excellent contrast agent, is able to provide great enhanced signal of T(1)- and T(2)-weighted MRI (r(1) = 6.263 mM(−1) s(−1), r(2) = 28.117 mM(−1) s(−1)) due to their ultra-refined size. After functionalization, the present MCAs nanoparticles exhibited small average size, low aggregation and excellent biocompatible. In vitro and In vivo studies revealed that the MCAs show long-term circulation time, renal clearance properties and outstanding capability of selective accumulation in tumor tissues for simultaneous CT imaging and T(1)- and T(2)-weighted MRI. Taken together, these results show that as-prepared MCAs are excellent candidates as MRI/CT multimodal imaging contrast agents.
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spelling pubmed-49115752016-06-17 Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor Wang, Guannan Gao, Wei Zhang, Xuanjun Mei, Xifan Sci Rep Article Diagnostic approaches based on multimodal imaging of clinical noninvasive imaging (eg. MRI/CT scanner) are highly developed in recent years for accurate selection of the therapeutic regimens in critical diseases. Therefore, it is highly demanded in the development of appropriate all-in-one multimodal contrast agents (MCAs) for the MRI/CT multimodal imaging. Here a novel ideal MCAs (F-AuNC@Fe(3)O(4)) were engineered by assemble Au nanocages (Au NC) and ultra-small iron oxide nanoparticles (Fe(3)O(4)) for simultaneous T(1)–T(2)dual MRI and CT contrast imaging. In this system, the Au nanocages offer facile thiol modification and strong X-ray attenuation property for CT imaging. The ultra-small Fe(3)O(4) nanoparticles, as excellent contrast agent, is able to provide great enhanced signal of T(1)- and T(2)-weighted MRI (r(1) = 6.263 mM(−1) s(−1), r(2) = 28.117 mM(−1) s(−1)) due to their ultra-refined size. After functionalization, the present MCAs nanoparticles exhibited small average size, low aggregation and excellent biocompatible. In vitro and In vivo studies revealed that the MCAs show long-term circulation time, renal clearance properties and outstanding capability of selective accumulation in tumor tissues for simultaneous CT imaging and T(1)- and T(2)-weighted MRI. Taken together, these results show that as-prepared MCAs are excellent candidates as MRI/CT multimodal imaging contrast agents. Nature Publishing Group 2016-06-17 /pmc/articles/PMC4911575/ /pubmed/27312564 http://dx.doi.org/10.1038/srep28258 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Guannan
Gao, Wei
Zhang, Xuanjun
Mei, Xifan
Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title_full Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title_fullStr Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title_full_unstemmed Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title_short Au Nanocage Functionalized with Ultra-small Fe(3)O(4) Nanoparticles for Targeting T(1)–T(2)Dual MRI and CT Imaging of Tumor
title_sort au nanocage functionalized with ultra-small fe(3)o(4) nanoparticles for targeting t(1)–t(2)dual mri and ct imaging of tumor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911575/
https://www.ncbi.nlm.nih.gov/pubmed/27312564
http://dx.doi.org/10.1038/srep28258
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