Characterizing short-wave infrared fluorescence of conventional near-infrared fluorophores

Abstract. The observed behavior of short-wave infrared (SWIR) light in tissue, characterized by relatively low scatter and subdiffuse photon transport, has generated considerable interest for the potential of SWIR imaging to produce high-resolution, subsurface images of fluorescence activity in vivo. These properties have important implications for fluorescence-guided surgery and preclinical biomedical research. Until recently, translational efforts have been impeded by the conventional understanding that fluorescence molecular imaging in the SWIR regime requires custom molecular probes that do not yet have proven safety profiles in humans. However, recent studies have shown that two readily available near-infrared (NIR-I) fluorophores produce measurable SWIR fluorescence, implying that other conventional fluorophores produce detectable fluorescence in the SWIR window. Using SWIR spectroscopy and wide-field SWIR imaging with tissue-simulating phantoms, we characterize and compare the SWIR emission properties of eight commercially available red/NIR-I fluorophores commonly used in preclinical and clinical research, in addition to a SWIR-specific fluorophore. All fluorophores produce measurable fluorescence emission in the SWIR, including shorter wavelength dyes such as Alexa Fluor 633 and methylene blue. This study is the first to report SWIR fluorescence from six of the eight conventional fluorophores and establishes an important comparative reference for developing and evaluating SWIR imaging strategies for biomedical applications.

[1]  Oliver T. Bruns,et al.  Next-generation in vivo optical imaging with short-wave infrared quantum dots , 2017, Nature Biomedical Engineering.

[2]  Jianhua Hao,et al.  Non-invasive through-skull brain vascular imaging and small tumor diagnosis based on NIR-II emissive lanthanide nanoprobes beyond 1500 nm. , 2018, Biomaterials.

[3]  Job Kievit,et al.  Intraoperative near‐infrared fluorescence imaging of parathyroid adenomas with use of low‐dose methylene blue , 2014, Head & neck.

[4]  Rui Tian,et al.  Repurposing Cyanine NIR‐I Dyes Accelerates Clinical Translation of Near‐Infrared‐II (NIR‐II) Bioimaging , 2018, Advanced materials.

[5]  Anthony J. Durkin,et al.  Review of short-wave infrared spectroscopy and imaging methods for biological tissue characterization , 2015, Journal of biomedical optics.

[6]  Joshua S Richman,et al.  Safety and Tumor Specificity of Cetuximab-IRDye800 for Surgical Navigation in Head and Neck Cancer , 2015, Clinical Cancer Research.

[7]  Laura D. Hughes,et al.  Choose Your Label Wisely: Water-Soluble Fluorophores Often Interact with Lipid Bilayers , 2014, PloS one.

[8]  Oliver T. Bruns,et al.  Absorption by water increases fluorescence image contrast of biological tissue in the shortwave infrared , 2018, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Jeffrey Wyckoff,et al.  Early tumor detection afforded by in vivo imaging of near-infrared II fluorescence. , 2017, Biomaterials.

[10]  Zhuang Liu,et al.  A route to brightly fluorescent carbon nanotubes for near-infrared imaging in mice. , 2009, Nature nanotechnology.

[11]  Zbigniew Starosolski,et al.  Indocyanine green fluorescence in second near-infrared (NIR-II) window , 2017, PloS one.

[12]  Guosong Hong,et al.  Multifunctional in vivo vascular imaging using near-infrared II fluorescence , 2012, Nature Medicine.

[13]  B. Wall,et al.  Rare-earth-doped biological composites as in vivo shortwave infrared reporters , 2013, Nature Communications.

[14]  Daniel Franke,et al.  Shortwave infrared fluorescence imaging with the clinically approved near-infrared dye indocyanine green , 2017, Proceedings of the National Academy of Sciences.