JoVE Logo
Authors
Contact Us

Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes a new intraoperative imaging technique that uses a ruthenium complex as a source of chemiluminescent light emission, thereby producing high signal-to-noise ratios during in vivo imaging. Intraoperative imaging is an expanding field that could revolutionize the way that surgical procedures are performed.

Abstract

Intraoperative imaging techniques have the potential to make surgical interventions safer and more effective; for these reasons, such techniques are quickly moving into the operating room. Here, we present a new approach that utilizes a technique not yet explored for intraoperative imaging: chemiluminescent imaging. This method employs a ruthenium-based chemiluminescent reporter along with a custom-built nebulizing system to produce ex vivo or in vivo images with high signal-to-noise ratios. The ruthenium-based reporter produces light following exposure to an aqueous oxidizing solution and re-reduction within the surrounding tissue. This method has allowed us to detect reporter concentrations as low as 6.9 pmol/cm2. In this work, we present a visual guide to our proof-of-concept in vivo studies involving subdermal and intravenous injections in mice. The results suggest that this technology is a promising candidate for further preclinical research and might ultimately become a useful tool in the operating room.

Introduction

In recent decades, imaging technologies have revolutionized the way that physicians diagnose and monitor disease. These imaging technologies, however, have been largely limited to whole body imaging systems, such as positron emission tomography (PET), single photon-emission computed tomography (SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). Particular attention has been paid to cancer, and technological imaging breakthroughs have greatly improved the way that this disease is diagnosed and treated. Despite these advances, there is one place where these imaging technologies just don't fit: the operating room. While whole body imaging techniques can help in surgical planning, they typically lack spatial resolutions high enough to help physicians determine in real-time whether all of the tumor tissue has been removed or residual tumor tissue remains hidden at the surgical margins1. Making sure that no infiltrative tumor margins are left behind is one of the most important surgical goals, and surgeons must walk a tight-rope between rigorous and cautious tissue resection. If too much is removed, unwanted side effects for the patient are exacerbated; if too little is removed, recurrence rates are increased2,3. Therefore, it is crucial to delineate accurate tumor margins, and we believe that chemiluminescent intraoperative imaging can help to improve the accuracy of the identification of tumor margins by helping surgeons to visualize malignant tissue that could otherwise remain undetected with established techniques.

There are many imaging technologies currently being investigated for their possible utility as intraoperative imaging systems. These include β- and γ-radiation-emitting probes4, optical fluorescence5, Raman spectroscopy6,7, and Cherenkov luminescence8,9. To date, however, none of these have become established as standard clinical tools. Optical fluorescence imaging has so far proven to be the most promising of these techniques and is therefore the most explored. While it has already been shown to be a valuable tool for many applications, it is not without its limitations. Indeed, its principal drawback is the background fluorescence generated by inherently autofluorescent biological tissue. This background autofluorescent signal is a product of the excitation of the surrounding tissue, in addition to the fluorophore, by the external light source needed for the generation of a fluorescent signal. From a practical perspective, this autofluorescence can potentially lead to low signal-to-noise ratios, which can limit the utility of this technology in the operating room.

The principal advantage of chemiluminescence imaging over fluorescence imaging is that no excitation light is necessary. As a result, there is no background autofluorescence. In chemiluminescence imaging, the excitation energy is instead generated chemically. This process produces no unintended background signal and therefore can result in higher signal-to-noise ratios. This could ultimately result in the more precise and accurate detection of surgical margins. Somewhat surprisingly, the utility of this approach as an intraoperative imaging technique has remained unexplored10. Indeed, the closest example to this technique is the oxidation of luminol by myeloperoxidase in mice11,12,13. Chemiluminescent biomedical imaging is therefore a rather unexplored area of research that could offer the following advantages: (1) minimal autofluorescence resulting in a low background signal with higher signal-to-noise ratios; (2) tunable wavelengths of chemiluminescent emissions ranging from the visible to the near-infrared; and (3) functionalizable chemiluminescent complexes that, when combined with linker technologies and targeted biomolecules that already exist, provide access to whole libraries of targeted molecular imaging probes14.

This proof-of-principle study illustrates the potential utility of chemiluminescent imaging in the biomedical setting using a ruthenium-based imaging agent. The chemiluminescent properties of this compound are well studied, with investigations dating back to the mid-1960s15. Upon chemical activation, the agent produces light at around 600 nm16, which is well suited for medical imaging purposes. The activation energy is provided by a redox reaction that leads to an excited state-which has a lifetime of 650 ns in water17-followed by the generation of photons upon relaxation of this excited state. Through the use of a specially-designed remote nebulizer, we were able to detect the compound both ex vivo and in vivo. The results of initial experiments are very promising, suggesting further investigation of this technology.

Protocol

Ethics statement: All of the in vivo animal experiments described were performed according to an approved protocol and under the ethical guidelines of the Memorial Sloan Kettering Cancer Center (MSK) Institutional Animal Care and Use Committee (IACUC).

1. Construction of a Nebulizing Device

  1. Attach wood part A (12.5 x 2.5 x 1.8 cm3) upright in the center of part B (12.7 x 10.7 x 1.8 cm3) using two screws (4 x 25 mm2). Attach wood part C (11 × 2.5 × 1.8 cm3) to the middle of part A (12.5 x 2.5 x 1.8 cm3) using one screw, such that part C (11 x 2.5 x 1.8 cm3) can still be moved. See Figure 1.
  2. Drill two holes through the lower tip of the spray bottle trigger of a plastic 3 oz mini sprayer (D) and push a stainless steel rod (10 cm of 1/16" steel) (E) through to form two loops, one on either side of the trigger.
  3. Wrap the bottom part of the spray bottle with duct tape (F) to prevent the cable ties from slipping off. Attach the spray bottle to wood part C (11 x 2.5 x 1.8 cm3) using the two plastic cable ties (28 cm) (G).
  4. Cut off the 011 servo motor (I) and reconnect it with the loose cables of the servo control (H). Then, attach the servo motor to the top of wood part A (12.5 x 2.5 x 1.8 cm3) using duct tape.
  5. Attach a pencil (J) to the servo motor lever using the paper clip (K). Tightly connect the outermost parts of the pencil to the steel rod loops using plastic covered twist wires (L) and secure the ends on the pencil with duct tape.
  6. Cut off the servo motor control unit's magnetic cable connector (M) and reattach it to the speaker cable (N). Then, tape the servo motor control unit to wood part B (12.7 x 10.7 x 1.8 cm3). Cut a w1 cable with magnetic connectors in half and attach one part to the loose end of the copper speaker cable (1 m). Connect the (magnetic) i2 toggle switch and p1 power to the available w1 cable and a 9V battery.

2. Sensitivity Determination of the Method

  1. In a 1.5 mL microcentrifuge tube, prepare solutions of [Ru(bpy)3]Cl2 in reverse osmosis water (100 µL) in amounts of 260 µg (347 nmol), 52 µg (69 nmol), 26 µg (34 nmol), 5 µg (6.9 nmol), 3 µg (3.5 nmol), 520 ng (694 pmol), 260 ng (347 pmol), 52 ng (69 pmol), 26 ng (34 pmol), 5 ng (6.9 pmol), and 3 ng (3.5 pmol).
  2. Mix 100 µL of each [Ru(bpy)3]Cl2 solution with 100 µL of an aqueous solution of ammonium cerium nitrate ((NH4)2Ce(NO3)6) in water (25 mM) on a microscope slide.
  3. Set up the acquisition in the bioluminescence reader by initializing the imaging software.
    1. Sign in to the user profile and look for the acquisition control panel. Click on "Initialize" and wait until the instrument is ready.
    2. Look for "Imaging Mode" and make sure "Luminescent" and "Photograph" are checked and that "Fluorescent" is unchecked.
    3. Change "Exposure Time" setting for "Luminescent" to 20 s. Set the remaining settings for "Luminescent" as follows: "Binning": Medium; "F/stop": 1; and "Emission Filter": Open.
      NOTE: The exposure times might need to be adapted according to the instrumentation and experimental setting used, if different from the presented setup.
    4. For "Photograph," use the following settings: "Exposure Time": Auto; "Binning": Medium; and "F/stop": 8. Adjust the "Subject Height" according to imaging target.Look for the "Field of View" dropdown menu. The initial setting is "C." Change to "B" (14 cm distance between the camera and sample stage).
  4. Set up the nebulizer by placing a microscopic slide on a sheet of black construction paper on the floor of the imaging chamber to protect it from the oxidizing agent. Mix a 100 µLdroplet of [Ru(bpy)3]Cl2-solution with 100 µL of an aqueous solution of (NH4)2Ce(NO3)6. Observe the green box crosshair.
    1. Place the imaging subject on the black construction paper, such that the area of interest is in the center of the green light box crosshair displayed on the sample stage. Prepare the nebulizer by detaching the plastic spray bottle from the wooden support. Fill a solution of triethylamine (1:3 in water/ethanol) into its plastic reservoir and reattach it to the wooden support.
    2. Place the nebulizer inside the bioluminescence reader and make sure that the power cord is disconnected from the nebulizer cord. Ensure that the power switch is on, the toggle switch is off, and the red LED is lit. Place the nebulizer such that the spray flow is pointed towards the area of interest on the imaging subject, while minimizing the view obstruction from the camera towards the imaging subject by the spray nozzle head.
    3. Place small, black pieces of construction paper over any potential hot spots (e.g., white marks on microscopic slides or injection sites) to shield them from spray. Place at least 40 cm of the nebulizer remote cord inside the imaging chamber, such that it does not interfere with the imaging subject, the nebulizer, or the magnetic door latch. Close the imaging system door.
      NOTE: The crosshair will change size based on the "Field of View" setting in "Living Image;" make sure that this is set to "B".
  5. Acquire an image by initiating the imaging sequence. Click "Acquire" in the "Acquisition Control Panel." On the first imaging sequence, enable autosaving if desired (recommended) and choose a data folder. Ignore the "Edit Imaging Labels" dialog until the end of the sequence.
    NOTE: The control software displays the instrument's actions step-by-step in real time. After preparing the measurement and moving the sample stage to the right position, it opens the camera shutter and counts the measurement time. The shutter opening can also be heard by a click sound generated by the machine.
  6. As the shutter opens, spray three bursts of a solution of triethylamine (1:3 in water/ethanol, 0.24 ± 0.04 mL per spray burst) by switching the toggle switch three times to generate chemiluminescence.
    NOTE: The sample stage will move during the measurement. Leave enough (minimum 40 cm) cable inside the instrument to allow this. Make sure that the solution to be sprayed by the nebulizer can be aspired by the ascending pipe and that there are no air bubbles in the pipe. Have several spare batteries for the nebulizer ready in case needed.

3. In Vivo Imaging After Systemic Intravenous Injection

  1. In a 1.5 mL microcentrifuge tube, prepare 100 µL of phosphate-buffered saline (PBS) solution containing between 8 and 33 nmol of [Ru(bpy)3]Cl2. Prepare an aqueous solution of (NH4)2Ce(NO3)6 in water (25 mM) at the same time.
  2. Intravenously inject 100 µL of [Ru(bpy)3]Cl2 into the tail vein of healthy mice (n = 5).
  3. Euthanize the mice 10 min after injection via CO2 asphyxiation.
    1. Remove the skin with a Y-cut from the torso, then remove the costal arch in a U-shape to expose the heart and lungs. Perfuse the mice by cutting an outlet in the right atrium and injecting 20 mL of PBS through a 24 gauge needle into the left ventricle18. Carefully cut through the belly skin and expose the kidney and liver. Cut longitudinally through the organs to create a visible cut.
  4. Set up the acquisition as described in steps 2.3-2.6, with the following changes.
    1. After thoroughly washing the nebulizer plastic reservoir, fill it with a solution of (NH4)2Ce(NO3)6 in water (25 mM) instead of triethylamine.
      NOTE: It is important to thoroughly rinse the nebulizer nozzle after every use, since crystallizing (NH4)2Ce(NO3)6 may destroy the spray nozzle after several uses.
  5. Use the whole animal or organ samples for imaging.
    1. For whole abdomen imaging, position the mouse carcass with the open abdomen facing the camera and the head pointing to the back of the instrument. Center the organ to be imaged (e.g., liver or kidney) in the green light box crosshair.
    2. For individual organ imaging and quantification, remove the mouse from the imaging instrument and pin it down. Starting from the already-opened body cavity, excise the inner organs (e.g., kidney, liver, lung, muscle, spleen, brain, and heart). Cut through the hind leg skin to excise muscle tissue. Carefully open the skull with a scalpel to excise the brain.
      1. If the organ of interest is liver, kidney or spleen, cut all organs in half longitudinally, place each organ on a petri dish or piece of black construction paper.
    3. Follow the procedure described in steps 2.3-2.6 to establish the relative emission of the chemiluminescent tracer for single organs.

4. In Vivo Imaging of Lymph Nodes

  1. Prepare 10 µL of a PBS solution containing 80 nmol of [Ru(bpy)3]Cl2. Prepare an aqueous solution of (NH4)2Ce(NO3)6 in water (25 mM) at the same time.
  2. Inject 10 µL of the solution subdermally into the hind paw of healthy mice (n = 5). As a negative control, inject the contralateral paw with 10 µL of pure PBS. Sacrifice the mice via CO2 asphyxiation 15 min after the injection. Remove the skin on both hind legs to expose the lymph canals up to the popliteal lymph nodes.
  3. Set up the acquisition as described in step 3.4.
  4. Remove the popliteal lymph nodes from both hind legs, cut them in half, and spray them with oxidant on a Petri dish, as described before (step 3.5.3), for the purpose of quantification.

Results

The nebulizer system described in protocol section 1 can be constructed from easily-available materials at a low cost. It is intended to be an inset for remote-triggered spraying of the reducing/oxidizing agent inside a bioluminescent reader (Figure 1). Our design allows for the safe operation of the nebulizer within the bioluminescence reader at a 14 cm distance from the lens. No fogging or blurring of the lens was observed during the operation. We selected the commercia...

Discussion

Here, we have presented a technology that is capable of optically delineating tissue via the emission of photons created by a chemiluminescent reporter. In contrast to other, more established, technologies4,5,6,7,8,9, this chemiluminescent reporter system employs an imaging probe that is non-radioactive and facilitates detect...

Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank Prof. Jan Grimm and Mr. Travis Shaffer for their helpful discussions and Mr. David Gregory for editing the manuscript. Technical services provided by the MSK Animal Imaging Core Facility, supported in part by NIH Cancer Center Support Grant P30CA008748-48, are gratefully acknowledged. The authors thank the NIH (K25 EB016673 and R21 CA191679, T.R. and 4R00CA178205-02, B.M.Z.), the MSK Center for Molecular Imaging and Nanotechnology (T.R.), the Tow Foundation (B.C.), and the National Science Foundation Integrative Graduate Education and Research Traineeship (IGERT 0965983 at Hunter College for B.C. and T.M.S.) for their generous support. The research reported in this publication was supported by funding from the King Abdullah University of Science and Technology.

Materials

NameCompanyCatalog NumberComments
Wood part A (12.5 × 2.5 × 1.8 cm) Woodcraft131404Cut from a 3/4” x 24” x 30” birch plywood sheet
Wood part B (12.7 × 10.7 × 1.8 cm)Woodcraft131404Cut from a 3/4” x 24” x 30” birch plywood sheet
Wood part C (11 × 2.5 × 1.8 cm)Woodcraft131404Cut from a 3/4” x 24” x 30” birch plywood sheet
Screws (4 × 25 mm)Screwfix79939
Harmon Face Values 3 oz mini sprayerBed, Bath and Beyond
stainless steel rod (10 cm of 1/16” steel)Metals Depot Int. Inc.2192
Pencil Classic HBPapermate58592
Paper clipOffice Depot221720
speaker cableRCA Inc.AH1650SN
Energizer 9V alkaline batteryEnergizer Holdings Inc.EN22
Hitech HS-82MG Micro Servo Motor, 3.4 kg/cm output torque @ 6VHitech RCD USA Inc.32082S
NameCompanyCatalog NumberComments
28 cm plastic cable tiesGeneral Electric Inc.50725
Duct tape3M Inc.3939
littleBits w1 wirelittleBits Inc.w1 wire
littleBits p1 powerlittleBits Inc.p1 power
littleBits i2 toggle switchlittleBits Inc.i2 toggle switch
littleBits 011 servolittleBits Inc.011 servo
20 cm plastic covered wire twist tiesFour Star Plastics71TIE8000
Tris(2,2′-bipyridyl)dichlororuthenium(II) hexahydrateSigma-Aldrich Inc.224758
Ammonium cerium(IV) nitrateSigma-Aldrich Inc.22249
IsofluoraneBaxter Healthcare1001936060
PBSSigma-AldrichPBS1
EthanolSigma-Aldrich2854
TriethylamineSigma-Aldrich Inc.T0886
WaterWater was purified using a Milipore Mili-Q (R ≥ 18 MΩ)
Female nude (outbred) miceJackson Laboratories1929age 5 - 6 weeks
Strain C57BL/6J  
NU/J male mice at Jackson Laboratories2019age 6 – 8 weeks
IVIS 200 bioluminescence readerCaliper Live Science
Live Image 4.2 softwarePerkin-Elmer128165
Microscope slidesThermoScientific4951PLUS4

References

  1. Fong, Y., Giulianotti, P. C., Lewis, J., Koerkamp, B. G., Reiner, T. . Imaging and Visualization in The Modern Operating Room: A Comprehensive Guide for Physicians. , (2015).
  2. Nguyen, Q. T., Tsien, R. Y. Fluorescence-guided surgery with live molecular navigation - a new cutting edge. Nat. Rev. Cancer. 13 (9), 653-662 (2013).
  3. Weissleder, R., Pittet, M. J. Imaging in the era of molecular oncology. Nature. 452, 580-589 (2008).
  4. Heller, S., Zanzonico, P. Nuclear probes and intraoperative gamma cameras. Semin. Nucl. Med. 41 (3), 166-181 (2011).
  5. van Dam, G. M., et al. Intraoperative tumor-specific fluorescence imaging in ovarian cancer by folate receptor-α targeting: first in-human results. Nat. Med. 17 (10), 1315-1319 (2011).
  6. Zavaleta, C. L., et al. A Raman-based endoscopic strategy for multiplexed molecular imaging. Proc. Natl. Acad. Sci. U S A. 110 (25), E2288-E2297 (2013).
  7. Harmsen, S., Bedics, M. A., Wall, M. A., Huang, R., Detty, M. R., Kircher, M. F. Rational design of a chalcogenopyrylium-based surface-enhanced resonance Raman scattering nanoprobe with attomolar sensitivity. Nat. Commun. 6, 1-9 (2015).
  8. Thorek, D. L., et al. Positron Lymphography: Multimodal, High-Resolution, Dynamic Mapping and Resection of Lymph Nodes After Intradermal Injection of 18F-FDG. Nucl. Med. 53 (9), 1438-1445 (2012).
  9. Thorek, D. L. J., Riedl, C. C., Grimm, J. Clinical Cerenkov Luminescence Imaging of 18F-FDG. Nucl. Med. 55 (1), 95-98 (2014).
  10. Gross, S., et al. Bioluminescence imaging of myeloperoxidase activity in vivo. Nat. Med. 15 (4), 455-461 (2009).
  11. Lee, J. -. J., White, A. G., Rice, D. R., Smith, B. D. In vivo imaging using polymeric nanoparticles stained with near-infrared chemiluminescent and fluorescent squaraine catenane endoperoxide. Chem. Commun. 49 (29), 3016-3018 (2013).
  12. Lee, D., et al. In vivo imaging of hydrogen peroxide with chemiluminescent nanoparticles. Nat. Mater. 6 (10), 765-769 (2007).
  13. Baumes, J. M., et al. thermally activated, near-infrared chemiluminescent dyes and dye-stained microparticles for optical imaging. Nat. Chem. 2 (12), 1025-1030 (2010).
  14. Siraj, N., et al. Fluorescence, Phosphorescence, and Chemiluminescence. Anal. Chem. 88 (1), 170-202 (2016).
  15. Hercules, D. M., Lytle, F. E. Chemiluminescence from Reduction Reactions. Am. Chem. Soc. 88 (20), 4745-4746 (1966).
  16. Kerr, E. Annihilation electrogenerated chemiluminescence of mixed metal chelates in solution: modulating emission colour by manipulating the energetics. Chem. Sci. 6, 472-479 (2015).
  17. Montalti, M., Credi, A., Prodi, L., Gandolfi, M. T. . Handbook of Photochemistry 3rd Ed. , 379-404 (2006).
  18. Gage, G. J., Kipke, D. R., Shain, W. Whole Animal Perfusion Fixation for Rhodents. J. Vis. Exp. (65), e3564 (2012).
  19. Büchel, G. E., et al. Near-infrared intraoperative chemiluminescent imaging. ChemMedChem. , (2016).
  20. Ntziachristos, V., Ripoll, J., Wang, L. V., Weissleder, R. Looking and Listening to Light: the Evolution of Whole-Body Photonic Imaging. Nat. Biotechnol. 23, 313-320 (2005).
  21. Koch, J. H., Gyarfas, E. C., Dwyer, F. P. Biological Activity of Complex Ions Mechanism of Inhibition of Acetylcholinesterase. Austral. J. Biol. Sci. 9 (3), 371-381 (1956).
  22. Juris, A., Balzani, V., Barigelletti, F., Campagna, S., Belser, P., Zelewsky, A. V. Ru(II) polypyridine complexes: photophysics, photochemistry, electrochemistry, and chemiluminescence. Coord. Chem. Rev. 84, 85-277 (1988).
  23. Knoll, J. D., Turro, C. Control and utilization of ruthenium and rhodium metal complex excited states for photoactivated cancer therapy. Coord. Chem. Rev. 282, 110-126 (2015).
  24. Haley, T. J. Pharmacology and toxicology of the rare earth elements. J. Pharm. Sci. 54 (5), 663-670 (1965).
  25. Siekierski, S., Mioduski, T., Salomon, M. . IUPAC Commission on Solubility Data. Solubility Data Series. Vol 13. Scandium, Yttrium, Lanthanum, and Lanthanide Nitrates. , (1983).
  26. Reiner, T., Jantke, D., Marziale, A. N., Raba, A., Eppinger, J. Metal-Conjugated Affinity Labels: A New Concept to Create Enantioselective Artificial Metalloenzymes. ChemistryOpen. 2, 50-54 (2013).
  27. Zanarini, S., et al. Synthesis and Electrochemiluminescence of a Ru(bpy)3-Labeled Coupling Adduct Produced on a Self-Assembled Monolayer. J. Phys. Chem. C. 112 (8), 2949-2957 (2008).
  28. Liu, R., Lv, Y., Hou, X., Yang, L., Mester, Z. Protein Quantitation Using Ru-NHS Ester Tagging and Isotope Dilution High-Pressure Liquid Chromatography-Inductively Coupled Plasma Mass Spectrometry Determination. Anal. Chem. 84 (6), 2769-2775 (2012).
  29. Jantke, D., et al. Synthetic strategies for efficient conjugation of organometallic complexes with pendant protein reactive markers. J. Organomet. Chem. 744, 82-91 (2013).
  30. Aoki, Y., et al. An experimental xenograft mouse model of diffuse pontine glioma designed for therapeutic testing. J Neurooncol. 108 (1), 29-35 (2012).
  31. Forster, R. J., Bertoncello, P., Keyes, T. E. Electrogenerated Chemiluminescence. Annual Rev. Anal. Chem. 2, 359-385 (2009).
  32. Connell, T. U., James, J. L., White, A. R., Donnelly, P. S. Protein Labelling with Versatile Phosphorescent Metal Complexes for Live Cell Luminescence Imaging. Chem. Eur. J. 21 (40), 14146-14155 (2015).
  33. Zhou, X., et al. Synthesis, labeling and bioanalytical applications of a tris(2,2′-bipyridyl)ruthenium(II)-based electrochemiluminescence probe. Nat. Protoc. 9 (5), 1146-1159 (2014).
  34. Bœuf, G., et al. Encapsulated Ruthenium(II) Complexes in Biocompatible Poly(d,l-lactide-co-glycolide) Nanoparticles for Application in Photodynamic Therapy. ChemPlusChem. 79 (1), 171-180 (2014).
  35. Loizidou, M., Seifalian, A. M. Nanotechnology and its applications in surgery. Brit. J. Surgery. 97 (4), 463-465 (2010).
  36. Barry, N. P. E., Sadler, P. J. Challenges for Metals in Medicine: How Nanotechnology May Help To Shape the Future. ACS Nano. 7, 5654-5659 (2013).
  37. Hasan, K., Bansal, A. K., Samuel, I. D. W., Roldán-Carmona, C., Bolink, H. J., Zysman-Colman, E. Tuning the Emission of Cationic Iridium (III) Complexes Towards the Red Through Methoxy Substitution of the Cyclometalating Ligand. Nat.Sci. Rep. 5, 1-15 (2015).
  38. Truong, J., et al. Chemiluminescence detection with water-soluble iridium(III) complexes containing a sulfonate-functionalised ancillary ligand. Analyst. 139 (22), 6028-6035 (2014).

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Explore More Articles

ChemiluminescenceBiological ImagingInteroperativeHigh Signal to noise RatioTris bypiridine ruthenium II chlorideAmmonium Cerium NitrateNebulizerTriethylaminePreclinical

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Contact Us

Recommend to library

JoVE NEWSLETTERS

Research

Education

Authors

Librarians

ABOUT JoVE

Copyright © 2025 MyJoVE Corporation. All rights reserved