Email bio-eu@licor.com
Applications for the Pearl Imaging System
IMPORTANT: IRDye 680LT dye products should not be used for small animal in vivo imaging.
Imaging of targeting agents in the vascular and lymphatic systems is a specialized type of biodistribution study.
Tumor vasculature commonly displays enhanced permeability and retention. The vascular endothelium in the tumor microenvironment is often discontinuous, allowing molecules to diffuse into surrounding tissue.1,2 Lymphatic drainage in these regions is also poor.3
These properties cause larger molecules to accumulate in tumors
Can be exploited for molecular imaging of cancer
Figure 1 [ABOVE] Dorsal view of athymic male nu/nu mouse, with A431 subcutaneous tumor on the right flank. IV injection of IRDye 800CW PEG was administered ~1 hr prior to image capture with the Pearl Imager. Increased vasculature is seen in the tumor region.
1 Vasey, PA, et al. 1999. Clin. Cancer Res. 5:83-94.
2 Matsumura, Y and H Maeda. 1986. Cancer Res 46:6387-6392.
3 Seymour, LW. 1992. Crit. Rev. Ther. Drug Carrier Syst. 9(2):135-187.
IRDye 800CW PEG Contrast Agent exploits the unique vascular properties of tumors for molecular imaging of cancer.
IRDye 800CW is conjugated to polyethylene glycol (PEG; a soluble synthetic polymer) to create a non-specific contrast agent for vascular imaging.
Agent is administered by intravenous (IV) injection
Highlights surface vasculature for ~0.5 hour after intravenous injection (Figure 1; requires appropriate mouse model* )
Retention of agent is visible in the tumor ~4 hr post-injection (Figure 2)
By 9 hours post-injection, the tumor is well defined (Figure 3)
Use of IRDye 800CW near-infrared fluorophore minimizes interfering autofluorescence, to improve image quality and resolution.
* Success of vascular imaging depends on the mouse model used. Vessels may be less visible in mice that are obese or have hair.
Images were captured with the Pearl® Imaging System.
Figure 1. Athymic male nu/nu mouse (~5-6 wks old), 0.5 hr after injection of IRDye 800CW PEG (1 nmole). Surface blood vessels are visible. Note: ability to visualize vasculature is dependent on mouse model used.
Figure 2a. Athymic male nu/nu mouse, ~4 hr after injection of IRDye 800CW PEG (1 nmole). Large blood vessels and tumor are visible.
Figure 2b. High resolution (85 µm) image of the tumor region shows large blood vessels recruited to feed the tumor. Sequestration of contrast agent in tumor is likely due to enhanced permeability and retention.
Figure 3. Athymic male nu/nu mouse, ~ 9 hr after injection of IRDye 800CW PEG (1 nmole). Tumor is clearly defined.
IRDye 800CW PEG is an effective lymph tracking agent (Figure 4).
Administer by intradermal injection
Other contrast agents labeled with IRDye 800CW have been used for intraoperative identification of lymphatic branches and small sentinel lymph nodes, and outperformed NIR quantum dots.1
The new Pearl Imager Impulse permits rapid time-lapse imaging of vasculature and lymphatics. Watch a two-minute video about Impulse here.
Image captured with the Pearl® Imaging System.
Figure 4. Athymic male nu/nu mouse, minutes after receiving IRDye 800CW PEG (~0.1 nmole) intradermally on the tail (right side). Image highlights use of IRDye PEG as a lymph imaging agent.
1. Tanaka, E et al. 2006. Ann Surg Oncol. 13(12):1672-81.
Why image in the near-infrared
Adams, KE et al.
Comparison of Visible and near-infrared wavelength-excitable fluorescent dyes for molecular imaging of cancer.
J Biomed Opt. 12(2):024017 (2007)
Kovar, J et al.
A systematic approach to the development of fluorescent contrast agents for optical imaging of mouse cancer models.
Anal Biochem. 367(1):1-12 (2007)
Osterman, H and Schutz-Geschwender, A.
Seeing beyond the visible with IRDye infrared dyes
LI-COR Biosciences (2007)
Olive, DM.
Near infrared technology and optical agents for molecular imaging
LI-COR Biosciences (2006)
Developing Imaging agents
Kovar, J et al.
A systematic approach to the development of fluorescent contrast agents for optical imaging of mouse cancer models.
Anal Biochem. 367(1):1-12 (2007)
Kovar, J et al.
Purification method directly influences effectiveness of an epidermal growth factor-coupled targeting agent for noninvasive tumor detection in mice.
Anal Biochem. 361(1):47-54 (2007)
Kovar, J. et al.
EGF-IRDye 800CW: in vitro and in vivo characterization as a biomarker for optical fluorescent imaging of tumor growth kinetics.
Poster presentation, SMI Annual Meeting (2005)
Vascular and lymphatic imaging
Kovar, JL et al.
Imaging Lymphatics With A Variety of Near-Infrared-Labeled Optical Agents.
Poster Presentation, World Molecular Imaging Annual Meeting (2009)
Tanaka, E et al.
Image-guided oncologic surgery using invisible light: completed pre-clinical development for sentinel lymph node mapping.
Ann Surg Oncol. 13(12):1671-81 (2006).
Parungo, CP et al.
In vivo optical imaging of pleural space drainage to lymph nodes of prognostic significance.
Ann Surg Oncol. 11:1085–92 (2004)
Why Image in the NIR?
“Advances in In Vivo Imaging: Near-Infrared Optical Imaging of Mice”
Jeff Harford, LI-COR
“Instrumentation and Imaging Considerations”
Eva Sevick-Muraca, Baylor College of Medicine
“In vivo imaging of prostate cancer using an IRDye 800CW EGF Optical Probe”
Melanie Simpson, University of Nebraska – Lincoln
“Comparison of visible and near-infrared wavelength-excitable fluorescent dyes for molecular imaging of cancer”
Eva Sevick-Muraca and Shi Ke, Baylor College of Medicine
Development of imaging agents
“Systematic Evaluation and Use of Targeted IRDye labeled Optical Contrast Agents”
Mike Olive, LI-COR
“Systematic Evaluation of Targeted IRDye Labeled Optical Imaging Agents”
Joy Kovar, LI-COR
“Near Infrared Fluorescent Approaches to Cell-Based Assays and Small Animal Imaging”
Amy Geschwender, LI-COR
See Small Animal Imaging application page for more related webinars.