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Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction

IR820, an analog of FDA-approved indocyanine green, is a promising second near-infrared window (NIR-II) fluorescence probe with better NIR-II fluorescence stability and great clinical transformation potential. Moreover, its fluorescence can be further remarkably enhanced by the interaction with albu...

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Detalles Bibliográficos
Autores principales: Feng, Xinyu, Cao, Yuan, Zhuang, Pengrui, Cheng, Ran, Zhang, Xuejun, Liu, Hong, Wang, Guohe, Sun, Shao-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023119/
https://www.ncbi.nlm.nih.gov/pubmed/35481109
http://dx.doi.org/10.1039/d2ra00449f
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author Feng, Xinyu
Cao, Yuan
Zhuang, Pengrui
Cheng, Ran
Zhang, Xuejun
Liu, Hong
Wang, Guohe
Sun, Shao-Kai
author_facet Feng, Xinyu
Cao, Yuan
Zhuang, Pengrui
Cheng, Ran
Zhang, Xuejun
Liu, Hong
Wang, Guohe
Sun, Shao-Kai
author_sort Feng, Xinyu
collection PubMed
description IR820, an analog of FDA-approved indocyanine green, is a promising second near-infrared window (NIR-II) fluorescence probe with better NIR-II fluorescence stability and great clinical transformation potential. Moreover, its fluorescence can be further remarkably enhanced by the interaction with albumin. Therefore, it is significant to flexibly design IR820–albumin complex using endogenous or exogenetic albumin to meet the requirements of different biological applications. Herein, we show the rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction. We compared the NIR-II fluorescence imaging ability of IR820 pre-incubated with albumin or not to visualize tumors and the gastrointestinal tract in vivo and found that the formation of IR820–albumin was essential for the intense NIR-II fluorescence. For imaging-guided tumor treatment, after intravenous injection of free IR820, IR820–albumin complex can be formed in vivo due to the presence of plenty of albumin in the blood. For imaging-guided gastrointestinal obstruction removal, IR820–albumin complex should be synthesized in vitro before oral administration. NIR-II fluorescence imaging-guided surgeries were successfully realized in both tumor resection and gastrointestinal obstruction removal. Besides, toxicity assessments in vitro and in vivo confirmed the good biocompatibility of IR820. Our study provides a flexible paradigm for IR820-based NIR-II fluorescence imaging and surgical navigation towards different diseases.
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spelling pubmed-90231192022-04-26 Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction Feng, Xinyu Cao, Yuan Zhuang, Pengrui Cheng, Ran Zhang, Xuejun Liu, Hong Wang, Guohe Sun, Shao-Kai RSC Adv Chemistry IR820, an analog of FDA-approved indocyanine green, is a promising second near-infrared window (NIR-II) fluorescence probe with better NIR-II fluorescence stability and great clinical transformation potential. Moreover, its fluorescence can be further remarkably enhanced by the interaction with albumin. Therefore, it is significant to flexibly design IR820–albumin complex using endogenous or exogenetic albumin to meet the requirements of different biological applications. Herein, we show the rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction. We compared the NIR-II fluorescence imaging ability of IR820 pre-incubated with albumin or not to visualize tumors and the gastrointestinal tract in vivo and found that the formation of IR820–albumin was essential for the intense NIR-II fluorescence. For imaging-guided tumor treatment, after intravenous injection of free IR820, IR820–albumin complex can be formed in vivo due to the presence of plenty of albumin in the blood. For imaging-guided gastrointestinal obstruction removal, IR820–albumin complex should be synthesized in vitro before oral administration. NIR-II fluorescence imaging-guided surgeries were successfully realized in both tumor resection and gastrointestinal obstruction removal. Besides, toxicity assessments in vitro and in vivo confirmed the good biocompatibility of IR820. Our study provides a flexible paradigm for IR820-based NIR-II fluorescence imaging and surgical navigation towards different diseases. The Royal Society of Chemistry 2022-04-21 /pmc/articles/PMC9023119/ /pubmed/35481109 http://dx.doi.org/10.1039/d2ra00449f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Feng, Xinyu
Cao, Yuan
Zhuang, Pengrui
Cheng, Ran
Zhang, Xuejun
Liu, Hong
Wang, Guohe
Sun, Shao-Kai
Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title_full Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title_fullStr Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title_full_unstemmed Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title_short Rational synthesis of IR820–albumin complex for NIR-II fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
title_sort rational synthesis of ir820–albumin complex for nir-ii fluorescence imaging-guided surgical treatment of tumors and gastrointestinal obstruction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023119/
https://www.ncbi.nlm.nih.gov/pubmed/35481109
http://dx.doi.org/10.1039/d2ra00449f
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