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Title: Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green

Abstract

Fluorescence imaging is a method of real-time molecular tracking in vivo that has enabled many clinical technologies. Imaging in the shortwave IR (SWIR; 1,000–2,000 nm) promises higher contrast, sensitivity, and penetration depths compared with conventional visible and near-IR (NIR) fluorescence imaging. However, adoption of SWIR imaging in clinical settings has been limited, partially due to the absence of US Food and Drug Administration (FDA)-approved fluorophores with peak emission in the SWIR. Here, we show that commercially available NIR dyes, including the FDA-approved contrast agent indocyanine green (ICG), exhibit optical properties suitable for in vivo SWIR fluorescence imaging. Even though their emission spectra peak in the NIR, these dyes outperform commercial SWIR fluorophores and can be imaged in the SWIR, even beyond 1,500 nm. We show real-time fluorescence imaging using ICG at clinically relevant doses, including intravital microscopy, noninvasive imaging in blood and lymph vessels, and imaging of hepatobiliary clearance, and show increased contrast compared with NIR fluorescence imaging. Furthermore, we show tumor-targeted SWIR imaging with IRDye 800CW-labeled trastuzumab, an NIR dye being tested in multiple clinical trials. Our findings suggest that high-contrast SWIR fluorescence imaging can be implemented alongside existing imaging modalities by switching the detection of conventional NIR fluorescencemore » systems from silicon-based NIR cameras to emerging indium gallium arsenide-based SWIR cameras. Using ICG in particular opens the possibility of translating SWIR fluorescence imaging to human clinical applications. Furthermore, our findings suggest that emerging SWIR-fluorescent in vivo contrast agents should be benchmarked against the SWIR emission of ICG in blood.« less

Authors:
ORCiD logo [1];  [1]; ORCiD logo [1];  [1];  [1];  [2];  [3];  [2];  [2];  [1];  [1]
  1. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139,
  2. Edwin L. Steele Labs for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital, MGH Research Institute and Harvard Medical School, Boston, MA 02114,
  3. Edwin L. Steele Labs for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital, MGH Research Institute and Harvard Medical School, Boston, MA 02114,, Department of Chemical and Biological Engineering, Tufts University, Medford, MA 02155
Publication Date:
Research Org.:
Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
Sponsoring Org.:
USDOE Office of Science (SC)
OSTI Identifier:
1432122
Alternate Identifier(s):
OSTI ID: 1540274
Grant/Contract Number:  
FG02-07ER46454
Resource Type:
Published Article
Journal Name:
Proceedings of the National Academy of Sciences of the United States of America
Additional Journal Information:
Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Volume: 115 Journal Issue: 17; Journal ID: ISSN 0027-8424
Publisher:
Proceedings of the National Academy of Sciences
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Science & Technology; Other Topics; shortwave infrared; biomedical imaging; fluorescence imaging; near infrared; indocyanine green

Citation Formats

Carr, Jessica A., Franke, Daniel, Caram, Justin R., Perkinson, Collin F., Saif, Mari, Askoxylakis, Vasileios, Datta, Meenal, Fukumura, Dai, Jain, Rakesh K., Bawendi, Moungi G., and Bruns, Oliver T. Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green. United States: N. p., 2018. Web. doi:10.1073/pnas.1718917115.
Carr, Jessica A., Franke, Daniel, Caram, Justin R., Perkinson, Collin F., Saif, Mari, Askoxylakis, Vasileios, Datta, Meenal, Fukumura, Dai, Jain, Rakesh K., Bawendi, Moungi G., & Bruns, Oliver T. Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green. United States. https://doi.org/10.1073/pnas.1718917115
Carr, Jessica A., Franke, Daniel, Caram, Justin R., Perkinson, Collin F., Saif, Mari, Askoxylakis, Vasileios, Datta, Meenal, Fukumura, Dai, Jain, Rakesh K., Bawendi, Moungi G., and Bruns, Oliver T. Fri . "Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green". United States. https://doi.org/10.1073/pnas.1718917115.
@article{osti_1432122,
title = {Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green},
author = {Carr, Jessica A. and Franke, Daniel and Caram, Justin R. and Perkinson, Collin F. and Saif, Mari and Askoxylakis, Vasileios and Datta, Meenal and Fukumura, Dai and Jain, Rakesh K. and Bawendi, Moungi G. and Bruns, Oliver T.},
abstractNote = {Fluorescence imaging is a method of real-time molecular tracking in vivo that has enabled many clinical technologies. Imaging in the shortwave IR (SWIR; 1,000–2,000 nm) promises higher contrast, sensitivity, and penetration depths compared with conventional visible and near-IR (NIR) fluorescence imaging. However, adoption of SWIR imaging in clinical settings has been limited, partially due to the absence of US Food and Drug Administration (FDA)-approved fluorophores with peak emission in the SWIR. Here, we show that commercially available NIR dyes, including the FDA-approved contrast agent indocyanine green (ICG), exhibit optical properties suitable for in vivo SWIR fluorescence imaging. Even though their emission spectra peak in the NIR, these dyes outperform commercial SWIR fluorophores and can be imaged in the SWIR, even beyond 1,500 nm. We show real-time fluorescence imaging using ICG at clinically relevant doses, including intravital microscopy, noninvasive imaging in blood and lymph vessels, and imaging of hepatobiliary clearance, and show increased contrast compared with NIR fluorescence imaging. Furthermore, we show tumor-targeted SWIR imaging with IRDye 800CW-labeled trastuzumab, an NIR dye being tested in multiple clinical trials. Our findings suggest that high-contrast SWIR fluorescence imaging can be implemented alongside existing imaging modalities by switching the detection of conventional NIR fluorescence systems from silicon-based NIR cameras to emerging indium gallium arsenide-based SWIR cameras. Using ICG in particular opens the possibility of translating SWIR fluorescence imaging to human clinical applications. Furthermore, our findings suggest that emerging SWIR-fluorescent in vivo contrast agents should be benchmarked against the SWIR emission of ICG in blood.},
doi = {10.1073/pnas.1718917115},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
number = 17,
volume = 115,
place = {United States},
year = {Fri Apr 06 00:00:00 EDT 2018},
month = {Fri Apr 06 00:00:00 EDT 2018}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1073/pnas.1718917115

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