Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783321804245303296 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5944285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lvwei anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT shenyamei anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yanghengli anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yangrui anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT caiwenbin anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT zhangjian anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yuanlijun anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT duanyunyou anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT zhangli anovelbimodalimagingagenttargetingher2moleculeofbreastcancer AT lvwei novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT shenyamei novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yanghengli novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yangrui novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT caiwenbin novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT zhangjian novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT yuanlijun novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT duanyunyou novelbimodalimagingagenttargetingher2moleculeofbreastcancer AT zhangli novelbimodalimagingagenttargetingher2moleculeofbreastcancer |