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Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases

The theranostics of lymph node metastasis has always been one of the major obstacles to defeating breast cancer and an important decisive factor in the prognosis of patients. Herein, we design NaGdF(4):Yb,Tm@NaLuF(4) upconversion nanoparticles with PEG and anti-HER2 monoclonal antibody (trastuzumab,...

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Autores principales: Zhang, Chuan, Zhang, Yujuan, Liang, Maolin, Shi, Xiumin, Jun, Yan, Fan, Longfei, Yang, Kai, Wang, Feng, Li, Wei, Zhu, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751193/
https://www.ncbi.nlm.nih.gov/pubmed/36532036
http://dx.doi.org/10.3389/fimmu.2022.1063678
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author Zhang, Chuan
Zhang, Yujuan
Liang, Maolin
Shi, Xiumin
Jun, Yan
Fan, Longfei
Yang, Kai
Wang, Feng
Li, Wei
Zhu, Ran
author_facet Zhang, Chuan
Zhang, Yujuan
Liang, Maolin
Shi, Xiumin
Jun, Yan
Fan, Longfei
Yang, Kai
Wang, Feng
Li, Wei
Zhu, Ran
author_sort Zhang, Chuan
collection PubMed
description The theranostics of lymph node metastasis has always been one of the major obstacles to defeating breast cancer and an important decisive factor in the prognosis of patients. Herein, we design NaGdF(4):Yb,Tm@NaLuF(4) upconversion nanoparticles with PEG and anti-HER2 monoclonal antibody (trastuzumab, Herceptin) (NP-mAb), the delivery of NP-mAb through the lymphatic system allows for effective targeting and accumulation in lymphatic metastasis. Combination of radionuclides (68)Ga and (177)Lu could be chelated by the bisphosphate groups of NP-mAb. The obtained nanoprobe (NP-mAb) and nanonuclear drug ((68)Ga-NP-mAb or (177)Lu-NP-mAb) exhibited excellent stability and show high accumulation and prolong retention in the lymph node metastasis after intratumoral injection into the foot pad by near-infrared fluorescence (NIRF), single-photon emission computed tomography (SPECT) and positron emission tomography (PET) imaging. Utilizing the β-rays released by (177)Lu, (177)Lu-NP-mAb could not only decrease the incidence of lymph node metastasis, but also significantly decrease the volumes of lymph node metastasis. Additionally, (177)Lu-NP-mAb induce no obvious toxicity to treated mice through blood routine, liver and kidney function assay. Therefore, nanoprobe and nanonuclear drug we designed could be acted as excellent theranostics agents for lymph node metastasis, providing potential alternatives diagnose and treatment option for lymph node metastasis.
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spelling pubmed-97511932022-12-16 Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases Zhang, Chuan Zhang, Yujuan Liang, Maolin Shi, Xiumin Jun, Yan Fan, Longfei Yang, Kai Wang, Feng Li, Wei Zhu, Ran Front Immunol Immunology The theranostics of lymph node metastasis has always been one of the major obstacles to defeating breast cancer and an important decisive factor in the prognosis of patients. Herein, we design NaGdF(4):Yb,Tm@NaLuF(4) upconversion nanoparticles with PEG and anti-HER2 monoclonal antibody (trastuzumab, Herceptin) (NP-mAb), the delivery of NP-mAb through the lymphatic system allows for effective targeting and accumulation in lymphatic metastasis. Combination of radionuclides (68)Ga and (177)Lu could be chelated by the bisphosphate groups of NP-mAb. The obtained nanoprobe (NP-mAb) and nanonuclear drug ((68)Ga-NP-mAb or (177)Lu-NP-mAb) exhibited excellent stability and show high accumulation and prolong retention in the lymph node metastasis after intratumoral injection into the foot pad by near-infrared fluorescence (NIRF), single-photon emission computed tomography (SPECT) and positron emission tomography (PET) imaging. Utilizing the β-rays released by (177)Lu, (177)Lu-NP-mAb could not only decrease the incidence of lymph node metastasis, but also significantly decrease the volumes of lymph node metastasis. Additionally, (177)Lu-NP-mAb induce no obvious toxicity to treated mice through blood routine, liver and kidney function assay. Therefore, nanoprobe and nanonuclear drug we designed could be acted as excellent theranostics agents for lymph node metastasis, providing potential alternatives diagnose and treatment option for lymph node metastasis. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9751193/ /pubmed/36532036 http://dx.doi.org/10.3389/fimmu.2022.1063678 Text en Copyright © 2022 Zhang, Zhang, Liang, Shi, Jun, Fan, Yang, Wang, Li and Zhu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Chuan
Zhang, Yujuan
Liang, Maolin
Shi, Xiumin
Jun, Yan
Fan, Longfei
Yang, Kai
Wang, Feng
Li, Wei
Zhu, Ran
Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title_full Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title_fullStr Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title_full_unstemmed Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title_short Near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
title_sort near-infrared upconversion multimodal nanoparticles for targeted radionuclide therapy of breast cancer lymphatic metastases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751193/
https://www.ncbi.nlm.nih.gov/pubmed/36532036
http://dx.doi.org/10.3389/fimmu.2022.1063678
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