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Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site
Photoacoustic technology in combination with molecular imaging is a highly effective method for accurately diagnosing brain glioma. For glioma detection at a deeper site, contrast agents with higher photoacoustic imaging sensitivity are needed. Herein, we report a MoS(2)–ICG hybrid with indocyanine...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199097/ https://www.ncbi.nlm.nih.gov/pubmed/30393697 http://dx.doi.org/10.1007/s40820-018-0202-8 |
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author | Liu, Chengbo Chen, Jingqin Zhu, Ying Gong, Xiaojing Zheng, Rongqin Chen, Ningbo Chen, Dong Yan, Huixiang Zhang, Peng Zheng, Hairong Sheng, Zonghai Song, Liang |
author_facet | Liu, Chengbo Chen, Jingqin Zhu, Ying Gong, Xiaojing Zheng, Rongqin Chen, Ningbo Chen, Dong Yan, Huixiang Zhang, Peng Zheng, Hairong Sheng, Zonghai Song, Liang |
author_sort | Liu, Chengbo |
collection | PubMed |
description | Photoacoustic technology in combination with molecular imaging is a highly effective method for accurately diagnosing brain glioma. For glioma detection at a deeper site, contrast agents with higher photoacoustic imaging sensitivity are needed. Herein, we report a MoS(2)–ICG hybrid with indocyanine green (ICG) conjugated to the surface of MoS(2) nanosheets. The hybrid significantly enhanced photoacoustic imaging sensitivity compared to MoS(2) nanosheets. This conjugation results in remarkably high optical absorbance across a broad near-infrared spectrum, redshifting of the ICG absorption peak and photothermal/photoacoustic conversion efficiency enhancement of ICG. A tumor mass of 3.5 mm beneath the mouse scalp was clearly visualized by using MoS(2)–ICG as a contrast agent for the in vivo photoacoustic imaging of orthotopic glioma, which is nearly twofold deeper than the tumors imaged in our previous report using MoS(2) nanosheet. Thus, combined with its good stability and high biocompatibility, the MoS(2)–ICG hybrid developed in this study has a great potential for high-efficiency tumor molecular imaging in translational medicine. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40820-018-0202-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6199097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-61990972018-11-02 Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site Liu, Chengbo Chen, Jingqin Zhu, Ying Gong, Xiaojing Zheng, Rongqin Chen, Ningbo Chen, Dong Yan, Huixiang Zhang, Peng Zheng, Hairong Sheng, Zonghai Song, Liang Nanomicro Lett Article Photoacoustic technology in combination with molecular imaging is a highly effective method for accurately diagnosing brain glioma. For glioma detection at a deeper site, contrast agents with higher photoacoustic imaging sensitivity are needed. Herein, we report a MoS(2)–ICG hybrid with indocyanine green (ICG) conjugated to the surface of MoS(2) nanosheets. The hybrid significantly enhanced photoacoustic imaging sensitivity compared to MoS(2) nanosheets. This conjugation results in remarkably high optical absorbance across a broad near-infrared spectrum, redshifting of the ICG absorption peak and photothermal/photoacoustic conversion efficiency enhancement of ICG. A tumor mass of 3.5 mm beneath the mouse scalp was clearly visualized by using MoS(2)–ICG as a contrast agent for the in vivo photoacoustic imaging of orthotopic glioma, which is nearly twofold deeper than the tumors imaged in our previous report using MoS(2) nanosheet. Thus, combined with its good stability and high biocompatibility, the MoS(2)–ICG hybrid developed in this study has a great potential for high-efficiency tumor molecular imaging in translational medicine. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40820-018-0202-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-04-23 /pmc/articles/PMC6199097/ /pubmed/30393697 http://dx.doi.org/10.1007/s40820-018-0202-8 Text en © The Author(s) 2018 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 | Article Liu, Chengbo Chen, Jingqin Zhu, Ying Gong, Xiaojing Zheng, Rongqin Chen, Ningbo Chen, Dong Yan, Huixiang Zhang, Peng Zheng, Hairong Sheng, Zonghai Song, Liang Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title | Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title_full | Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title_fullStr | Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title_full_unstemmed | Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title_short | Highly Sensitive MoS(2)–Indocyanine Green Hybrid for Photoacoustic Imaging of Orthotopic Brain Glioma at Deep Site |
title_sort | highly sensitive mos(2)–indocyanine green hybrid for photoacoustic imaging of orthotopic brain glioma at deep site |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199097/ https://www.ncbi.nlm.nih.gov/pubmed/30393697 http://dx.doi.org/10.1007/s40820-018-0202-8 |
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