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Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission
Significantly reduced photon scattering and minimal tissue autofluorescence levels in the second biological transparency window (NIR-II; 1000-1700 nm) facilitate higher resolution in vivo biological imaging compared to tradition NIR fluorophores (~700-900 nm). However, the existing palette of NIR-II...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096392/ https://www.ncbi.nlm.nih.gov/pubmed/30128042 http://dx.doi.org/10.7150/thno.27995 |
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author | Zhu, Shoujun Yung, Bryant C. Chandra, Swati Niu, Gang Antaris, Alexander L. Chen, Xiaoyuan |
author_facet | Zhu, Shoujun Yung, Bryant C. Chandra, Swati Niu, Gang Antaris, Alexander L. Chen, Xiaoyuan |
author_sort | Zhu, Shoujun |
collection | PubMed |
description | Significantly reduced photon scattering and minimal tissue autofluorescence levels in the second biological transparency window (NIR-II; 1000-1700 nm) facilitate higher resolution in vivo biological imaging compared to tradition NIR fluorophores (~700-900 nm). However, the existing palette of NIR-II fluorescent agents including semiconducting inorganic nanomaterials and recently introduced small-molecule organic dyes face significant technical and regulatory hurdles prior to clinical translation. Fortunately, recent spectroscopic characterization of NIR-I dyes (e.g., indocyanine green (ICG), IRDye800CW and IR-12N3) revealed long non-negligible emission tails reaching past 1500 nm. Repurposing the most widely used NIR dye in medicine, in addition to those in the midst of clinical trials creates an accelerated pathway for NIR-II clinical translation. This review focuses on the significant advantage of imaging past 1000 nm with NIR-I fluorophores from both a basic and clinical viewpoint. We further discuss optimizing NIR-I dyes around their NIR-II/shortwave infrared (SWIR) emission, NIR-II emission tail characteristics and prospects of NIR-II imaging with clinically available and commercially available dyes. |
format | Online Article Text |
id | pubmed-6096392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-60963922018-08-20 Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission Zhu, Shoujun Yung, Bryant C. Chandra, Swati Niu, Gang Antaris, Alexander L. Chen, Xiaoyuan Theranostics Review Significantly reduced photon scattering and minimal tissue autofluorescence levels in the second biological transparency window (NIR-II; 1000-1700 nm) facilitate higher resolution in vivo biological imaging compared to tradition NIR fluorophores (~700-900 nm). However, the existing palette of NIR-II fluorescent agents including semiconducting inorganic nanomaterials and recently introduced small-molecule organic dyes face significant technical and regulatory hurdles prior to clinical translation. Fortunately, recent spectroscopic characterization of NIR-I dyes (e.g., indocyanine green (ICG), IRDye800CW and IR-12N3) revealed long non-negligible emission tails reaching past 1500 nm. Repurposing the most widely used NIR dye in medicine, in addition to those in the midst of clinical trials creates an accelerated pathway for NIR-II clinical translation. This review focuses on the significant advantage of imaging past 1000 nm with NIR-I fluorophores from both a basic and clinical viewpoint. We further discuss optimizing NIR-I dyes around their NIR-II/shortwave infrared (SWIR) emission, NIR-II emission tail characteristics and prospects of NIR-II imaging with clinically available and commercially available dyes. Ivyspring International Publisher 2018-07-16 /pmc/articles/PMC6096392/ /pubmed/30128042 http://dx.doi.org/10.7150/thno.27995 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Zhu, Shoujun Yung, Bryant C. Chandra, Swati Niu, Gang Antaris, Alexander L. Chen, Xiaoyuan Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title | Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title_full | Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title_fullStr | Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title_full_unstemmed | Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title_short | Near-Infrared-II (NIR-II) Bioimaging via Off-Peak NIR-I Fluorescence Emission |
title_sort | near-infrared-ii (nir-ii) bioimaging via off-peak nir-i fluorescence emission |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096392/ https://www.ncbi.nlm.nih.gov/pubmed/30128042 http://dx.doi.org/10.7150/thno.27995 |
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