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Gold nanoparticles as multimodality imaging agents for brain gliomas

BACKGROUND: Nanoparticles can be used for targeted drug delivery, in particular for brain cancer therapy. However, this requires a detailed analysis of nanoparticles from the associated microvasculature to the tumor, not easy because of the required high spatial resolution. The objective of this stu...

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Autores principales: Lai, Sheng-Feng, Ko, Bai-Hung, Chien, Chia-Chi, Chang, Chia-Ju, Yang, Shun-Ming, Chen, Hsiang-Hsin, Petibois, Cyril, Hueng, Dueng-Yuan, Ka, Shuk-Man, Chen, Ann, Margaritondo, G., Hwu, Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654925/
https://www.ncbi.nlm.nih.gov/pubmed/26589283
http://dx.doi.org/10.1186/s12951-015-0140-2
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author Lai, Sheng-Feng
Ko, Bai-Hung
Chien, Chia-Chi
Chang, Chia-Ju
Yang, Shun-Ming
Chen, Hsiang-Hsin
Petibois, Cyril
Hueng, Dueng-Yuan
Ka, Shuk-Man
Chen, Ann
Margaritondo, G.
Hwu, Y.
author_facet Lai, Sheng-Feng
Ko, Bai-Hung
Chien, Chia-Chi
Chang, Chia-Ju
Yang, Shun-Ming
Chen, Hsiang-Hsin
Petibois, Cyril
Hueng, Dueng-Yuan
Ka, Shuk-Man
Chen, Ann
Margaritondo, G.
Hwu, Y.
author_sort Lai, Sheng-Feng
collection PubMed
description BACKGROUND: Nanoparticles can be used for targeted drug delivery, in particular for brain cancer therapy. However, this requires a detailed analysis of nanoparticles from the associated microvasculature to the tumor, not easy because of the required high spatial resolution. The objective of this study is to demonstrate an experimental solution of this problem, based in vivo and post-mortem whole organ imaging plus nanoscale 3-dimensional (3D) X-ray microscopy. RESULTS: The use of gold nanoparticles (AuNPs) as contrast agents paved the way to a detailed high-resolution three dimensional (3D) X-ray and fluorescence imaging analysis of the relation between xenografted glioma cells and the tumor-induced angiogenic microvasculature. The images of the angiogenic microvessels revealed nanoparticle leakage. Complementary tests showed that after endocytotic internalization fluorescent AuNPs allow the visible-light detection of cells. CONCLUSIONS: AuNP-loading of cells could be extended from the case presented here to other imaging techniques. In our study, they enabled us to (1) identify primary glioma cells at inoculation sites in mice brains; (2) follow the subsequent development of gliomas. (3) Detect the full details of the tumor-related microvasculature; (4) Finding leakage of AuNPs from the tumor-related vasculature, in contrast to no leakage from normal vasculature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-015-0140-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-46549252015-11-22 Gold nanoparticles as multimodality imaging agents for brain gliomas Lai, Sheng-Feng Ko, Bai-Hung Chien, Chia-Chi Chang, Chia-Ju Yang, Shun-Ming Chen, Hsiang-Hsin Petibois, Cyril Hueng, Dueng-Yuan Ka, Shuk-Man Chen, Ann Margaritondo, G. Hwu, Y. J Nanobiotechnology Research BACKGROUND: Nanoparticles can be used for targeted drug delivery, in particular for brain cancer therapy. However, this requires a detailed analysis of nanoparticles from the associated microvasculature to the tumor, not easy because of the required high spatial resolution. The objective of this study is to demonstrate an experimental solution of this problem, based in vivo and post-mortem whole organ imaging plus nanoscale 3-dimensional (3D) X-ray microscopy. RESULTS: The use of gold nanoparticles (AuNPs) as contrast agents paved the way to a detailed high-resolution three dimensional (3D) X-ray and fluorescence imaging analysis of the relation between xenografted glioma cells and the tumor-induced angiogenic microvasculature. The images of the angiogenic microvessels revealed nanoparticle leakage. Complementary tests showed that after endocytotic internalization fluorescent AuNPs allow the visible-light detection of cells. CONCLUSIONS: AuNP-loading of cells could be extended from the case presented here to other imaging techniques. In our study, they enabled us to (1) identify primary glioma cells at inoculation sites in mice brains; (2) follow the subsequent development of gliomas. (3) Detect the full details of the tumor-related microvasculature; (4) Finding leakage of AuNPs from the tumor-related vasculature, in contrast to no leakage from normal vasculature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-015-0140-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-20 /pmc/articles/PMC4654925/ /pubmed/26589283 http://dx.doi.org/10.1186/s12951-015-0140-2 Text en © Lai et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lai, Sheng-Feng
Ko, Bai-Hung
Chien, Chia-Chi
Chang, Chia-Ju
Yang, Shun-Ming
Chen, Hsiang-Hsin
Petibois, Cyril
Hueng, Dueng-Yuan
Ka, Shuk-Man
Chen, Ann
Margaritondo, G.
Hwu, Y.
Gold nanoparticles as multimodality imaging agents for brain gliomas
title Gold nanoparticles as multimodality imaging agents for brain gliomas
title_full Gold nanoparticles as multimodality imaging agents for brain gliomas
title_fullStr Gold nanoparticles as multimodality imaging agents for brain gliomas
title_full_unstemmed Gold nanoparticles as multimodality imaging agents for brain gliomas
title_short Gold nanoparticles as multimodality imaging agents for brain gliomas
title_sort gold nanoparticles as multimodality imaging agents for brain gliomas
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654925/
https://www.ncbi.nlm.nih.gov/pubmed/26589283
http://dx.doi.org/10.1186/s12951-015-0140-2
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