Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Ping, Xin, Qian, Yang, Sheng-Tao, He, Tiantian, Huang, Yuanfang, Zeng, Guangfu, Ran, Maosheng, Tang, Xiaohai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
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
_version_ 1783250719120293888
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
work_keys_str_mv AT xieping skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT xinqian skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT yangshengtao skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT hetiantian skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT huangyuanfang skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT zengguangfu skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT ranmaosheng skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes
AT tangxiaohai skeletonlabeled13ccarbonnanoparticlesfortheimagingandquantificationintumordrainagelymphnodes