Investigation of oxazine and rhodamine derivatives as peripheral nerve tissue targeting contrast agent for in vivo fluorescence imaging

Accidental nerve transection or injury is a significant morbidity associated with many surgical interventions, resulting in persistent postsurgical numbness, chronic pain, and/or paralysis. Nervesparing can be a difficult task due to patient-to-patient variability and the difficulty of nerve visualization in the operating room. Fluorescence image-guided surgery to aid in the precise visualization of vital nerve structures in real time during surgery could greatly improve patient outcomes. To date, all nerve-specific contrast agents emit in the visible range. Developing a nearinfrared (NIR) nerve-specific fluorophore is poised to be a challenging task, as a NIR fluorophore must have enough “double-bonds” to reach the NIR imaging window, contradicting the requirement that a nerve-specific agent must have a relatively low molecular weight to cross the blood-nervebarrier (BNB). Herein we report our efforts to investigate the molecular characteristics for the nervespecific oxazine fluorophores, as well as their structurally analogous rhodamine fluorophores. Specifically, optical properties, physicochemical properties and their in vivo nerve specificity were evaluated herein.

[1]  F. Ling,et al.  Usefulness of intraoperative electromyographic monitoring of oculomotor and abducens nerves during skull base surgery , 2017, Acta Neurochirurgica.

[2]  Connor W. Barth,et al.  Far-Red and Near-Infrared Seminaphthofluorophores for Targeted Pancreatic Cancer Imaging , 2017, ACS omega.

[3]  F. Lombardo,et al.  Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. , 2001, Advanced drug delivery reviews.

[4]  Summer L. Gibbs,et al.  Near infrared fluorescence for image-guided surgery. , 2012, Quantitative imaging in medicine and surgery.

[5]  John V. Frangioni,et al.  Nerve-Highlighting Fluorescent Contrast Agents for Image-Guided Surgery , 2011, Molecular imaging.

[6]  Connor W. Barth,et al.  Nile Red derivatives enable improved ratiometric imaging for nerve-specific contrast , 2018, Journal of biomedical optics.

[7]  A. Gawande,et al.  Global Surgery 2030: evidence and solutions for achieving health, welfare, and economic development , 2015, The Lancet.

[8]  Juyoung Yoon,et al.  Hg2+ selective fluorescent and colorimetric sensor: its crystal structure and application to bioimaging. , 2008, Organic letters.

[9]  Connor W. Barth,et al.  Visualizing Oxazine 4 nerve-specific fluorescence ex vivo in frozen tissue sections , 2016, SPIE BiOS.

[10]  Stephen R. Johnson,et al.  Molecular properties that influence the oral bioavailability of drug candidates. , 2002, Journal of medicinal chemistry.

[11]  Summer L. Gibbs,et al.  Structure-Activity Relationship of Nerve-Highlighting Fluorophores , 2013, PloS one.

[12]  L. Ngo,et al.  The FLARE™ Intraoperative Near-Infrared Fluorescence Imaging System: A First-in-Human Clinical Trial in Breast Cancer Sentinel Lymph Node Mapping , 2009, Annals of Surgical Oncology.

[13]  David Borsook,et al.  Surgically Induced Neuropathic Pain: Understanding the Perioperative Process , 2013, Annals of surgery.

[14]  Connor W. Barth,et al.  Direct Administration of Nerve-Specific Contrast to Improve Nerve Sparing Radical Prostatectomy , 2017, Theranostics.

[15]  R. Strongin,et al.  Spiroguanidine rhodamines as fluorogenic probes for lysophosphatidic acid. , 2015, Chemical communications.

[16]  Hak Soo Choi,et al.  Prototype Nerve-Specific Near-Infrared Fluorophores , 2014, Theranostics.

[17]  B Chance,et al.  Near‐Infrared Images Using Continuous, Phase‐Modulated, and Pulsed Light with Quantitation of Blood and Blood Oxygenation a , 1998, Annals of the New York Academy of Sciences.

[18]  Connor W. Barth,et al.  Polymeric Micelles as Carriers for Nerve-Highlighting Fluorescent Probe Delivery , 2015, Molecular pharmaceutics.