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Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals

Gold nanoparticles (GNP) have been intensively investigated for applications in cancer imaging and therapy. Most imaging studies focused on microscopic imaging. Their potential as optical imaging probes for whole body small animal imaging has rarely been explored. Taking advantage of their surface p...

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Autores principales: Xu, Keying, Shi, Junwei, Pourmand, Ali, Udayakumar, Thirupandiyur S., Dogan, Nesrin, Zhao, Weizhao, Pollack, Alan, Yang, Yidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008467/
https://www.ncbi.nlm.nih.gov/pubmed/29921960
http://dx.doi.org/10.1038/s41598-018-27624-6
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author Xu, Keying
Shi, Junwei
Pourmand, Ali
Udayakumar, Thirupandiyur S.
Dogan, Nesrin
Zhao, Weizhao
Pollack, Alan
Yang, Yidong
author_facet Xu, Keying
Shi, Junwei
Pourmand, Ali
Udayakumar, Thirupandiyur S.
Dogan, Nesrin
Zhao, Weizhao
Pollack, Alan
Yang, Yidong
author_sort Xu, Keying
collection PubMed
description Gold nanoparticles (GNP) have been intensively investigated for applications in cancer imaging and therapy. Most imaging studies focused on microscopic imaging. Their potential as optical imaging probes for whole body small animal imaging has rarely been explored. Taking advantage of their surface plasmon resonance (SPR) properties, we aim to develop a noninvasive diffuse optical imaging method to map the distribution of a special type of GNP, gold nanorods (GNR), in small animals. We developed an integrated dual-modality imaging system capable of both x-ray computed tomography (XCT) and diffuse optical tomography (DOT). XCT provides the animal anatomy and contour required for DOT; DOT maps the distribution of GNR in the animal. This SPR enhanced optical imaging (SPROI) technique was investigated using simulation, phantom and mouse experiments. The distribution of GNR at various concentrations (0.1–100 nM, or 3.5 ug/g–3.5 mg/g) was successfully reconstructed from centimeter-scaled volumes. SPROI detected GNR at 18 μg/g concentration in the mouse breast tumor, and is 3 orders more sensitive than x-ray imaging. This study demonstrated the high sensitivity of SPROI in mapping GNR distributions in small animals. It does not require additional imaging tags other than GNR themselves. SPROI can be used to detect tumors targeted by GNR via passive targeting based on enhanced permeability and retention or via active targeting using biologically conjugated ligands.
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spelling pubmed-60084672018-06-26 Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals Xu, Keying Shi, Junwei Pourmand, Ali Udayakumar, Thirupandiyur S. Dogan, Nesrin Zhao, Weizhao Pollack, Alan Yang, Yidong Sci Rep Article Gold nanoparticles (GNP) have been intensively investigated for applications in cancer imaging and therapy. Most imaging studies focused on microscopic imaging. Their potential as optical imaging probes for whole body small animal imaging has rarely been explored. Taking advantage of their surface plasmon resonance (SPR) properties, we aim to develop a noninvasive diffuse optical imaging method to map the distribution of a special type of GNP, gold nanorods (GNR), in small animals. We developed an integrated dual-modality imaging system capable of both x-ray computed tomography (XCT) and diffuse optical tomography (DOT). XCT provides the animal anatomy and contour required for DOT; DOT maps the distribution of GNR in the animal. This SPR enhanced optical imaging (SPROI) technique was investigated using simulation, phantom and mouse experiments. The distribution of GNR at various concentrations (0.1–100 nM, or 3.5 ug/g–3.5 mg/g) was successfully reconstructed from centimeter-scaled volumes. SPROI detected GNR at 18 μg/g concentration in the mouse breast tumor, and is 3 orders more sensitive than x-ray imaging. This study demonstrated the high sensitivity of SPROI in mapping GNR distributions in small animals. It does not require additional imaging tags other than GNR themselves. SPROI can be used to detect tumors targeted by GNR via passive targeting based on enhanced permeability and retention or via active targeting using biologically conjugated ligands. Nature Publishing Group UK 2018-06-19 /pmc/articles/PMC6008467/ /pubmed/29921960 http://dx.doi.org/10.1038/s41598-018-27624-6 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Keying
Shi, Junwei
Pourmand, Ali
Udayakumar, Thirupandiyur S.
Dogan, Nesrin
Zhao, Weizhao
Pollack, Alan
Yang, Yidong
Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title_full Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title_fullStr Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title_full_unstemmed Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title_short Plasmonic Optical Imaging of Gold Nanorods Localization in Small Animals
title_sort plasmonic optical imaging of gold nanorods localization in small animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008467/
https://www.ncbi.nlm.nih.gov/pubmed/29921960
http://dx.doi.org/10.1038/s41598-018-27624-6
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