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PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging
BACKGROUND: Radioactive isotope-labeled gold nanomaterials have potential biomedical applications. Here, we report the synthesis and characterization of PEGylated crushed gold shell-radioactive iodide-124-labeled gold core nanoballs (PEG-(124)I-Au@AuCBs) for in vivo tumor imaging applications throug...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907375/ https://www.ncbi.nlm.nih.gov/pubmed/29669544 http://dx.doi.org/10.1186/s12951-018-0366-x |
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author | Lee, Sang Bong Kumar, Dinesh Li, Yinghua Lee, In-Kyu Cho, Sung Jin Kim, Sang Kyoon Lee, Sang-Woo Jeong, Shin Young Lee, Jaetae Jeon, Yong Hyun |
author_facet | Lee, Sang Bong Kumar, Dinesh Li, Yinghua Lee, In-Kyu Cho, Sung Jin Kim, Sang Kyoon Lee, Sang-Woo Jeong, Shin Young Lee, Jaetae Jeon, Yong Hyun |
author_sort | Lee, Sang Bong |
collection | PubMed |
description | BACKGROUND: Radioactive isotope-labeled gold nanomaterials have potential biomedical applications. Here, we report the synthesis and characterization of PEGylated crushed gold shell-radioactive iodide-124-labeled gold core nanoballs (PEG-(124)I-Au@AuCBs) for in vivo tumor imaging applications through combined positron emission tomography and Cerenkov luminescent imaging (PET/CLI). RESULTS: PEG-(124)I-Au@AuCBs showed high stability and sensitivity in various pH solutions, serum, and in vivo conditions and were not toxic to tested cells. Combined PET/CLI clearly revealed tumor lesions at 1 h after injection of particles, and both signals remained visible in tumor lesions at 24 h, consistent with the biodistribution results. CONCLUSION: Taken together, the data provided strong evidence for the application of PEG-(124)I-Au@AuCBs as promising imaging agents in nuclear medicine imaging of various biological systems, particularly in cancer diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0366-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5907375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59073752018-04-30 PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging Lee, Sang Bong Kumar, Dinesh Li, Yinghua Lee, In-Kyu Cho, Sung Jin Kim, Sang Kyoon Lee, Sang-Woo Jeong, Shin Young Lee, Jaetae Jeon, Yong Hyun J Nanobiotechnology Research BACKGROUND: Radioactive isotope-labeled gold nanomaterials have potential biomedical applications. Here, we report the synthesis and characterization of PEGylated crushed gold shell-radioactive iodide-124-labeled gold core nanoballs (PEG-(124)I-Au@AuCBs) for in vivo tumor imaging applications through combined positron emission tomography and Cerenkov luminescent imaging (PET/CLI). RESULTS: PEG-(124)I-Au@AuCBs showed high stability and sensitivity in various pH solutions, serum, and in vivo conditions and were not toxic to tested cells. Combined PET/CLI clearly revealed tumor lesions at 1 h after injection of particles, and both signals remained visible in tumor lesions at 24 h, consistent with the biodistribution results. CONCLUSION: Taken together, the data provided strong evidence for the application of PEG-(124)I-Au@AuCBs as promising imaging agents in nuclear medicine imaging of various biological systems, particularly in cancer diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0366-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-18 /pmc/articles/PMC5907375/ /pubmed/29669544 http://dx.doi.org/10.1186/s12951-018-0366-x Text en © The Author(s) 2018 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 Lee, Sang Bong Kumar, Dinesh Li, Yinghua Lee, In-Kyu Cho, Sung Jin Kim, Sang Kyoon Lee, Sang-Woo Jeong, Shin Young Lee, Jaetae Jeon, Yong Hyun PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title | PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title_full | PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title_fullStr | PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title_full_unstemmed | PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title_short | PEGylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and Cerenkov luminescent imaging |
title_sort | pegylated crushed gold shell-radiolabeled core nanoballs for in vivo tumor imaging with dual positron emission tomography and cerenkov luminescent imaging |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907375/ https://www.ncbi.nlm.nih.gov/pubmed/29669544 http://dx.doi.org/10.1186/s12951-018-0366-x |
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