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Nano-graphene oxide composite for in vivo imaging
INTRODUCTION: Positron emission tomography (PET) tracers has the potential to revolutionize cancer imaging and diagnosis. PET tracers offer non-invasive quantitative imaging in biotechnology and biomedical applications, but it requires radioisotopes as radioactive imaging tracers or radiopharmaceuti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757201/ https://www.ncbi.nlm.nih.gov/pubmed/29379283 http://dx.doi.org/10.2147/IJN.S148211 |
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author | Jang, Sung-Chan Kang, Sung-Min Lee, Jun Young Oh, Seo Yeong Vilian, AT Ezhil Lee, Ilsong Han, Young-Kyu Park, Jeong Hoon Cho, Wan-Seob Roh, Changhyun Huh, Yun Suk |
author_facet | Jang, Sung-Chan Kang, Sung-Min Lee, Jun Young Oh, Seo Yeong Vilian, AT Ezhil Lee, Ilsong Han, Young-Kyu Park, Jeong Hoon Cho, Wan-Seob Roh, Changhyun Huh, Yun Suk |
author_sort | Jang, Sung-Chan |
collection | PubMed |
description | INTRODUCTION: Positron emission tomography (PET) tracers has the potential to revolutionize cancer imaging and diagnosis. PET tracers offer non-invasive quantitative imaging in biotechnology and biomedical applications, but it requires radioisotopes as radioactive imaging tracers or radiopharmaceuticals. METHOD: This paper reports the synthesis of (18)F-nGO-PEG by covalently functionalizing PEG with nano-graphene oxide, and its excellent stability in physiological solutions. Using a green synthesis route, nGO is then functionalized with a biocompatible PEG polymer to acquire high stability in PBS and DMEM. RESULTS AND DISCUSSION: The radiochemical safety of (18)F-nGO-PEG was measured by a reactive oxygen species and cell viability test. The biodistribution of (18)F-nGO-PEG could be observed easily by PET, which suggested the significantly high sensitivity tumor uptake of (18)F-nGO-PEG and in a tumor bearing CT-26 mouse compared to the control. (18)F-nGO-PEG was applied successfully as an efficient radiotracer or drug agent in vivo using PET imaging. This article is expected to assist many researchers in the fabrication of (18)F-labeled graphene-based bio-conjugates with high reproducibility for applications in the biomedicine field. |
format | Online Article Text |
id | pubmed-5757201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57572012018-01-29 Nano-graphene oxide composite for in vivo imaging Jang, Sung-Chan Kang, Sung-Min Lee, Jun Young Oh, Seo Yeong Vilian, AT Ezhil Lee, Ilsong Han, Young-Kyu Park, Jeong Hoon Cho, Wan-Seob Roh, Changhyun Huh, Yun Suk Int J Nanomedicine Original Research INTRODUCTION: Positron emission tomography (PET) tracers has the potential to revolutionize cancer imaging and diagnosis. PET tracers offer non-invasive quantitative imaging in biotechnology and biomedical applications, but it requires radioisotopes as radioactive imaging tracers or radiopharmaceuticals. METHOD: This paper reports the synthesis of (18)F-nGO-PEG by covalently functionalizing PEG with nano-graphene oxide, and its excellent stability in physiological solutions. Using a green synthesis route, nGO is then functionalized with a biocompatible PEG polymer to acquire high stability in PBS and DMEM. RESULTS AND DISCUSSION: The radiochemical safety of (18)F-nGO-PEG was measured by a reactive oxygen species and cell viability test. The biodistribution of (18)F-nGO-PEG could be observed easily by PET, which suggested the significantly high sensitivity tumor uptake of (18)F-nGO-PEG and in a tumor bearing CT-26 mouse compared to the control. (18)F-nGO-PEG was applied successfully as an efficient radiotracer or drug agent in vivo using PET imaging. This article is expected to assist many researchers in the fabrication of (18)F-labeled graphene-based bio-conjugates with high reproducibility for applications in the biomedicine field. Dove Medical Press 2018-01-03 /pmc/articles/PMC5757201/ /pubmed/29379283 http://dx.doi.org/10.2147/IJN.S148211 Text en © 2018 Jang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Jang, Sung-Chan Kang, Sung-Min Lee, Jun Young Oh, Seo Yeong Vilian, AT Ezhil Lee, Ilsong Han, Young-Kyu Park, Jeong Hoon Cho, Wan-Seob Roh, Changhyun Huh, Yun Suk Nano-graphene oxide composite for in vivo imaging |
title | Nano-graphene oxide composite for in vivo imaging |
title_full | Nano-graphene oxide composite for in vivo imaging |
title_fullStr | Nano-graphene oxide composite for in vivo imaging |
title_full_unstemmed | Nano-graphene oxide composite for in vivo imaging |
title_short | Nano-graphene oxide composite for in vivo imaging |
title_sort | nano-graphene oxide composite for in vivo imaging |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757201/ https://www.ncbi.nlm.nih.gov/pubmed/29379283 http://dx.doi.org/10.2147/IJN.S148211 |
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