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A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer

Nanobubble (NB), a newly developed nanoscaled ultrasound contrast agent (UCA) for molecular imaging, has been widely researched for these years. Targeting it with functional molecule, nanobubble can adhere selectively to cellular epitopes and receptors outside the vasculature via enhanced permeabili...

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Autores principales: Lv, Wei, Shen, Yamei, Yang, Hengli, Yang, Rui, Cai, Wenbin, Zhang, Jian, Yuan, Lijun, Duan, Yunyou, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944285/
https://www.ncbi.nlm.nih.gov/pubmed/29854844
http://dx.doi.org/10.1155/2018/6202876
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author Lv, Wei
Shen, Yamei
Yang, Hengli
Yang, Rui
Cai, Wenbin
Zhang, Jian
Yuan, Lijun
Duan, Yunyou
Zhang, Li
author_facet Lv, Wei
Shen, Yamei
Yang, Hengli
Yang, Rui
Cai, Wenbin
Zhang, Jian
Yuan, Lijun
Duan, Yunyou
Zhang, Li
author_sort Lv, Wei
collection PubMed
description Nanobubble (NB), a newly developed nanoscaled ultrasound contrast agent (UCA) for molecular imaging, has been widely researched for these years. Targeting it with functional molecule, nanobubble can adhere selectively to cellular epitopes and receptors outside the vasculature via enhanced permeability and retention (EPR) effect of tumor blood vessel. To enhance the targeting rate of our previous prepared NBs-Affibody for HER2 (+) breast cancer imaging, we introduced a near-infrared fluorescent (NIRF) dye, IR783, in this study to enhance tumor-specific targeting rate and provide a promising modality for dual-mode imaging. The prepared IR783-NBs-Affibody presented a uniform nanoscale size around 482.7 ± 54.3 nm, good biosecurity, and stability over time. The encapsulation efficiency (EE) of IR-783 was 15.09% in the conjugates leading to a successful NIR fluorescence and ultrasound enhancement imaging ex vivo. IR783-NBs-Affibody was able to automatically accumulate on BT474 cells with a highly increased targeting rate of 85.4% compared with previous NBs-Affibody of 26.6%, while Affibody-guided HER2 binding was only found in HER2-positive cell lines (BT474 and T-47D). The newly developed IR783-NBs-Affibody is characterized with favorable HER2 targeting ability and bimodal imaging capability for breast cancer. Thus, IR783-NBs-Affibody holds great potential in molecular diagnosis for patients with breast cancer.
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spelling pubmed-59442852018-05-31 A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer Lv, Wei Shen, Yamei Yang, Hengli Yang, Rui Cai, Wenbin Zhang, Jian Yuan, Lijun Duan, Yunyou Zhang, Li J Immunol Res Research Article Nanobubble (NB), a newly developed nanoscaled ultrasound contrast agent (UCA) for molecular imaging, has been widely researched for these years. Targeting it with functional molecule, nanobubble can adhere selectively to cellular epitopes and receptors outside the vasculature via enhanced permeability and retention (EPR) effect of tumor blood vessel. To enhance the targeting rate of our previous prepared NBs-Affibody for HER2 (+) breast cancer imaging, we introduced a near-infrared fluorescent (NIRF) dye, IR783, in this study to enhance tumor-specific targeting rate and provide a promising modality for dual-mode imaging. The prepared IR783-NBs-Affibody presented a uniform nanoscale size around 482.7 ± 54.3 nm, good biosecurity, and stability over time. The encapsulation efficiency (EE) of IR-783 was 15.09% in the conjugates leading to a successful NIR fluorescence and ultrasound enhancement imaging ex vivo. IR783-NBs-Affibody was able to automatically accumulate on BT474 cells with a highly increased targeting rate of 85.4% compared with previous NBs-Affibody of 26.6%, while Affibody-guided HER2 binding was only found in HER2-positive cell lines (BT474 and T-47D). The newly developed IR783-NBs-Affibody is characterized with favorable HER2 targeting ability and bimodal imaging capability for breast cancer. Thus, IR783-NBs-Affibody holds great potential in molecular diagnosis for patients with breast cancer. Hindawi 2018-03-06 /pmc/articles/PMC5944285/ /pubmed/29854844 http://dx.doi.org/10.1155/2018/6202876 Text en Copyright © 2018 Wei Lv et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lv, Wei
Shen, Yamei
Yang, Hengli
Yang, Rui
Cai, Wenbin
Zhang, Jian
Yuan, Lijun
Duan, Yunyou
Zhang, Li
A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title_full A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title_fullStr A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title_full_unstemmed A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title_short A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer
title_sort novel bimodal imaging agent targeting her2 molecule of breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944285/
https://www.ncbi.nlm.nih.gov/pubmed/29854844
http://dx.doi.org/10.1155/2018/6202876
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