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Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green

Tissue necrosis commonly accompanies the development of a wide range of serious diseases. Therefore, highly sensitive detection and precise boundary delineation of necrotic tissue via effective imaging techniques are crucial for clinical treatments; however, no imaging modalities have achieved satis...

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Autores principales: Fang, Cheng, Wang, Kun, Zeng, Chaoting, Chi, Chongwei, Shang, Wenting, Ye, Jinzuo, Mao, Yamin, Fan, Yingfang, Yang, Jian, Xiang, Nan, Zeng, Ning, Zhu, Wen, Fang, Chihua, Tian, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749996/
https://www.ncbi.nlm.nih.gov/pubmed/26864116
http://dx.doi.org/10.1038/srep21013
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author Fang, Cheng
Wang, Kun
Zeng, Chaoting
Chi, Chongwei
Shang, Wenting
Ye, Jinzuo
Mao, Yamin
Fan, Yingfang
Yang, Jian
Xiang, Nan
Zeng, Ning
Zhu, Wen
Fang, Chihua
Tian, Jie
author_facet Fang, Cheng
Wang, Kun
Zeng, Chaoting
Chi, Chongwei
Shang, Wenting
Ye, Jinzuo
Mao, Yamin
Fan, Yingfang
Yang, Jian
Xiang, Nan
Zeng, Ning
Zhu, Wen
Fang, Chihua
Tian, Jie
author_sort Fang, Cheng
collection PubMed
description Tissue necrosis commonly accompanies the development of a wide range of serious diseases. Therefore, highly sensitive detection and precise boundary delineation of necrotic tissue via effective imaging techniques are crucial for clinical treatments; however, no imaging modalities have achieved satisfactory results to date. Although fluorescence molecular imaging (FMI) shows potential in this regard, no effective necrosis-avid fluorescent probe has been developed for clinical applications. Here, we demonstrate that indocyanine green (ICG) can achieve high avidity of necrotic tissue owing to its interaction with lipoprotein (LP) and phospholipids. The mechanism was explored at the cellular and molecular levels through a series of in vitro studies. Detection of necrotic tissue and real-time image-guided surgery were successfully achieved in different organs of different animal models with the help of FMI using in house-designed imaging devices. The results indicated that necrotic tissue with a 0.6 mm diameter could be effectively detected with precise boundary definition. We believe that the new discovery and the associated imaging techniques will improve personalized and precise surgery in the near future.
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spelling pubmed-47499962016-02-18 Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green Fang, Cheng Wang, Kun Zeng, Chaoting Chi, Chongwei Shang, Wenting Ye, Jinzuo Mao, Yamin Fan, Yingfang Yang, Jian Xiang, Nan Zeng, Ning Zhu, Wen Fang, Chihua Tian, Jie Sci Rep Article Tissue necrosis commonly accompanies the development of a wide range of serious diseases. Therefore, highly sensitive detection and precise boundary delineation of necrotic tissue via effective imaging techniques are crucial for clinical treatments; however, no imaging modalities have achieved satisfactory results to date. Although fluorescence molecular imaging (FMI) shows potential in this regard, no effective necrosis-avid fluorescent probe has been developed for clinical applications. Here, we demonstrate that indocyanine green (ICG) can achieve high avidity of necrotic tissue owing to its interaction with lipoprotein (LP) and phospholipids. The mechanism was explored at the cellular and molecular levels through a series of in vitro studies. Detection of necrotic tissue and real-time image-guided surgery were successfully achieved in different organs of different animal models with the help of FMI using in house-designed imaging devices. The results indicated that necrotic tissue with a 0.6 mm diameter could be effectively detected with precise boundary definition. We believe that the new discovery and the associated imaging techniques will improve personalized and precise surgery in the near future. Nature Publishing Group 2016-02-11 /pmc/articles/PMC4749996/ /pubmed/26864116 http://dx.doi.org/10.1038/srep21013 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Fang, Cheng
Wang, Kun
Zeng, Chaoting
Chi, Chongwei
Shang, Wenting
Ye, Jinzuo
Mao, Yamin
Fan, Yingfang
Yang, Jian
Xiang, Nan
Zeng, Ning
Zhu, Wen
Fang, Chihua
Tian, Jie
Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title_full Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title_fullStr Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title_full_unstemmed Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title_short Illuminating necrosis: From mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
title_sort illuminating necrosis: from mechanistic exploration to preclinical application using fluorescence molecular imaging with indocyanine green
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749996/
https://www.ncbi.nlm.nih.gov/pubmed/26864116
http://dx.doi.org/10.1038/srep21013
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