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Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice

Radiation therapy of liver cancer is limited by low tolerance of the liver to radiation. Radiosensitizers can effectively reduce the required radiation dose. AGuIX nanoparticles are small, multifunctional gadolinium-based nanoparticles that can carry radioisotopes or fluorescent markers for single-p...

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Autores principales: Hu, Pengcheng, Cheng, Dengfeng, Huang, Tao, Banizs, Anna B., Xiao, Jie, Liu, Guobing, Chen, Quan, Wang, Yuenan, He, Jiang, Shi, Hongcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585112/
https://www.ncbi.nlm.nih.gov/pubmed/28875472
http://dx.doi.org/10.1186/s11671-017-2292-5
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author Hu, Pengcheng
Cheng, Dengfeng
Huang, Tao
Banizs, Anna B.
Xiao, Jie
Liu, Guobing
Chen, Quan
Wang, Yuenan
He, Jiang
Shi, Hongcheng
author_facet Hu, Pengcheng
Cheng, Dengfeng
Huang, Tao
Banizs, Anna B.
Xiao, Jie
Liu, Guobing
Chen, Quan
Wang, Yuenan
He, Jiang
Shi, Hongcheng
author_sort Hu, Pengcheng
collection PubMed
description Radiation therapy of liver cancer is limited by low tolerance of the liver to radiation. Radiosensitizers can effectively reduce the required radiation dose. AGuIX nanoparticles are small, multifunctional gadolinium-based nanoparticles that can carry radioisotopes or fluorescent markers for single-photon emission computed tomography (SPECT), positron emission tomography (PET), fluorescence imaging, and even multimodality imaging. In addition, due to the high atomic number of gadolinium, it can also serve as a tumor radiation sensitizer. It is critical to define the biodistribution and pharmacokinetics of these gadolinium-based nanoparticles to quantitate the magnitude and duration of their retention within the tumor microenvironment during radiotherapy. Therefore, in this study, we successfully labeled AGuIX with (64)Cu through the convenient built-in chelator. The biodistribution studies indicated that the radiotracer (64)Cu-AGuIX accumulates to high levels in the HepG2 xenograft of nude mice, suggesting that it would be a potential theranostic nanoprobe for image-guided radiotherapy in HCC. We also used a transmission electron microscope to confirm AGuIX uptake in the HepG2 cells. In radiation therapy studies, a decrease in (18)F-FDG uptake was observed in the xenografts of the nude mice irradiated with AGuIX, which was injected 1 h before. These results provide proof-of-concept that AGuIX can be used as a theranostic radiosensitizer for PET imaging to guide radiotherapy for liver cancer.
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spelling pubmed-55851122017-09-22 Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice Hu, Pengcheng Cheng, Dengfeng Huang, Tao Banizs, Anna B. Xiao, Jie Liu, Guobing Chen, Quan Wang, Yuenan He, Jiang Shi, Hongcheng Nanoscale Res Lett Nano Express Radiation therapy of liver cancer is limited by low tolerance of the liver to radiation. Radiosensitizers can effectively reduce the required radiation dose. AGuIX nanoparticles are small, multifunctional gadolinium-based nanoparticles that can carry radioisotopes or fluorescent markers for single-photon emission computed tomography (SPECT), positron emission tomography (PET), fluorescence imaging, and even multimodality imaging. In addition, due to the high atomic number of gadolinium, it can also serve as a tumor radiation sensitizer. It is critical to define the biodistribution and pharmacokinetics of these gadolinium-based nanoparticles to quantitate the magnitude and duration of their retention within the tumor microenvironment during radiotherapy. Therefore, in this study, we successfully labeled AGuIX with (64)Cu through the convenient built-in chelator. The biodistribution studies indicated that the radiotracer (64)Cu-AGuIX accumulates to high levels in the HepG2 xenograft of nude mice, suggesting that it would be a potential theranostic nanoprobe for image-guided radiotherapy in HCC. We also used a transmission electron microscope to confirm AGuIX uptake in the HepG2 cells. In radiation therapy studies, a decrease in (18)F-FDG uptake was observed in the xenografts of the nude mice irradiated with AGuIX, which was injected 1 h before. These results provide proof-of-concept that AGuIX can be used as a theranostic radiosensitizer for PET imaging to guide radiotherapy for liver cancer. Springer US 2017-09-06 /pmc/articles/PMC5585112/ /pubmed/28875472 http://dx.doi.org/10.1186/s11671-017-2292-5 Text en © The Author(s). 2017 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.
spellingShingle Nano Express
Hu, Pengcheng
Cheng, Dengfeng
Huang, Tao
Banizs, Anna B.
Xiao, Jie
Liu, Guobing
Chen, Quan
Wang, Yuenan
He, Jiang
Shi, Hongcheng
Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title_full Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title_fullStr Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title_full_unstemmed Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title_short Evaluation of Novel (64)Cu-Labeled Theranostic Gadolinium-Based Nanoprobes in HepG2 Tumor-Bearing Nude Mice
title_sort evaluation of novel (64)cu-labeled theranostic gadolinium-based nanoprobes in hepg2 tumor-bearing nude mice
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585112/
https://www.ncbi.nlm.nih.gov/pubmed/28875472
http://dx.doi.org/10.1186/s11671-017-2292-5
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