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Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes
Carbon nanoparticles (CNPs) have been widely used in tumor drainage lymph node (TDLN) imaging, drug delivery, photothermal therapy, and so on. However, during the theranostic applications, the accumulation efficiency of CNPs in target organs is unknown yet, which largely hinders the extension of CNP...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513824/ https://www.ncbi.nlm.nih.gov/pubmed/28744123 http://dx.doi.org/10.2147/IJN.S134493 |
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author | Xie, Ping Xin, Qian Yang, Sheng-Tao He, Tiantian Huang, Yuanfang Zeng, Guangfu Ran, Maosheng Tang, Xiaohai |
author_facet | Xie, Ping Xin, Qian Yang, Sheng-Tao He, Tiantian Huang, Yuanfang Zeng, Guangfu Ran, Maosheng Tang, Xiaohai |
author_sort | Xie, Ping |
collection | PubMed |
description | Carbon nanoparticles (CNPs) have been widely used in tumor drainage lymph node (TDLN) imaging, drug delivery, photothermal therapy, and so on. However, during the theranostic applications, the accumulation efficiency of CNPs in target organs is unknown yet, which largely hinders the extension of CNPs into clinical uses. Herein, we prepared skeleton-labeled (13)C-CNPs that had identical properties to commercial CNPs suspension injection (CNSI) for the imaging and quantification in TDLN. (13)C-CNPs were prepared by arc discharge method, followed by homogenization with polyvinylpyrrolidone. The size distribution and morphology of (13)C-CNPs were nearly the same as those of CNSI under transmission electron microscope. The hydrodynamic radii of both (13)C-CNPs and CNSI were similar, too. According to X-ray photoelectron spectroscopy and infrared spectroscopy analyses, the chemical compositions and chemical states of elements were also nearly identical for both labeled and commercial forms. The skeleton labeling of (13)C was reflected by the shift of G-band toward lower frequency in Raman spectra. (13)C-CNPs showed competitive performance in TDLN imaging, where the three lymph nodes (popliteal lymph node, common iliac artery lymph node, and paraaortic lymph node) were stained black upon the injection into the hind extremity of mice. The direct quantification of (13)C-CNPs indicated that 877 μg/g of (13)C-CNPs accumulated in the first station of TDLN (popliteal lymph node). The second station of TDLN (common iliac artery lymph node) had even higher accumulation level (1,062 μg/g), suggesting that (13)C-CNPs migrated efficiently along lymphatic vessel. The value decreased to 405 μg/g in the third station of TDLN (paraaortic lymph node). Therefore, the (13)C-CNPs provided quantitative approach to image and quantify CNSI in biological systems. The implication in biomedical applications and biosafety evaluations of CNSI is discussed. |
format | Online Article Text |
id | pubmed-5513824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55138242017-07-25 Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes Xie, Ping Xin, Qian Yang, Sheng-Tao He, Tiantian Huang, Yuanfang Zeng, Guangfu Ran, Maosheng Tang, Xiaohai Int J Nanomedicine Original Research Carbon nanoparticles (CNPs) have been widely used in tumor drainage lymph node (TDLN) imaging, drug delivery, photothermal therapy, and so on. However, during the theranostic applications, the accumulation efficiency of CNPs in target organs is unknown yet, which largely hinders the extension of CNPs into clinical uses. Herein, we prepared skeleton-labeled (13)C-CNPs that had identical properties to commercial CNPs suspension injection (CNSI) for the imaging and quantification in TDLN. (13)C-CNPs were prepared by arc discharge method, followed by homogenization with polyvinylpyrrolidone. The size distribution and morphology of (13)C-CNPs were nearly the same as those of CNSI under transmission electron microscope. The hydrodynamic radii of both (13)C-CNPs and CNSI were similar, too. According to X-ray photoelectron spectroscopy and infrared spectroscopy analyses, the chemical compositions and chemical states of elements were also nearly identical for both labeled and commercial forms. The skeleton labeling of (13)C was reflected by the shift of G-band toward lower frequency in Raman spectra. (13)C-CNPs showed competitive performance in TDLN imaging, where the three lymph nodes (popliteal lymph node, common iliac artery lymph node, and paraaortic lymph node) were stained black upon the injection into the hind extremity of mice. The direct quantification of (13)C-CNPs indicated that 877 μg/g of (13)C-CNPs accumulated in the first station of TDLN (popliteal lymph node). The second station of TDLN (common iliac artery lymph node) had even higher accumulation level (1,062 μg/g), suggesting that (13)C-CNPs migrated efficiently along lymphatic vessel. The value decreased to 405 μg/g in the third station of TDLN (paraaortic lymph node). Therefore, the (13)C-CNPs provided quantitative approach to image and quantify CNSI in biological systems. The implication in biomedical applications and biosafety evaluations of CNSI is discussed. Dove Medical Press 2017-07-11 /pmc/articles/PMC5513824/ /pubmed/28744123 http://dx.doi.org/10.2147/IJN.S134493 Text en © 2017 Xie 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 Xie, Ping Xin, Qian Yang, Sheng-Tao He, Tiantian Huang, Yuanfang Zeng, Guangfu Ran, Maosheng Tang, Xiaohai Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title | Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title_full | Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title_fullStr | Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title_full_unstemmed | Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title_short | Skeleton labeled (13)C-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
title_sort | skeleton labeled (13)c-carbon nanoparticles for the imaging and quantification in tumor drainage lymph nodes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513824/ https://www.ncbi.nlm.nih.gov/pubmed/28744123 http://dx.doi.org/10.2147/IJN.S134493 |
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