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Proceedings Paper

EGFR-directed Affibody for fluorescence-guided glioma surgery: time-dose analysis (Conference Presentation)
Author(s): Ana Luiza Ribeiro de Souza; Kayla Marra; Jason R. Gunn; Jonathan T. Elliott; Kimberley S. Samkoe; Keith D. Paulsen; Daniel R. Draney; Joachim Feldwisch

Paper Abstract

The key to fluorescence guided surgical oncology is the ability to create specific contrast between normal and glioma tissue. The blood brain barrier that limits the delivery of substances to the normal brain is broken in tumors, allowing accumulation of agents in the tumor interior. However, for a clinical success, imaging agents should be in the infiltrative edges to minimize the resection of normal brain while enable the removal of tumor. The aberrant overexpression and/or activation of EGFR is associated with many types of cancers, including glioblastoma and the injection of a fluorescent molecule targeted to these receptors would improve tumor contrast during fluorescence guided surgery. Affibody molecules have intentional medium affinity and high potential specificity, which are the desirable features of a good surgical imaging agent. The aim of this study was evaluate the brain/glioma uptake of ABY029 labeled with near-infrared dye IRDye800CW after intravenous injection. Rats were either inoculated with orthotopic implantations of U251 human glioma cell line or PBS (shams control) in the brain. The tumors were allowed to grow for 2–3 weeks before carrying out fluorescent tracer experiments. Fluorescent imaging of ex vivo brain slices from rats was acquired at different time points after infection of fluorescently labeled EGFR-specific affibody to verify which time provided maximal contrast tumor to normal brain. Although the tumor was most clearly visualized after 1h of IRDye800CW-labeled ABY029 injection, the tumor location could be identified from the background after 48h. These results suggest that the NIR-labeled affibody examined shows excellent potential to increase surgical visualization for confirmed EGFR positive tumors.

Paper Details

Date Published: 26 April 2016
PDF: 1 pages
Proc. SPIE 9696, Molecular-Guided Surgery: Molecules, Devices, and Applications II, 96960Q (26 April 2016); doi: 10.1117/12.2212858
Show Author Affiliations
Ana Luiza Ribeiro de Souza, Thayer School of Engineering at Dartmouth (United States)
CAPES Foundation (Brazil)
Kayla Marra, Thayer School of Engineering at Dartmouth (United States)
Jason R. Gunn, Thayer School of Engineering at Dartmouth (United States)
Jonathan T. Elliott, Thayer School of Engineering at Dartmouth (United States)
Kimberley S. Samkoe, Thayer School of Engineering at Dartmouth (United States)
Geisel School of Medicine (United States)
Keith D. Paulsen, Thayer School of Engineering (United States)
Geisel School of Medicine (United States)
Daniel R. Draney, LI-COR Biosciences (United States)
Joachim Feldwisch, Affibody AB (Sweden)


Published in SPIE Proceedings Vol. 9696:
Molecular-Guided Surgery: Molecules, Devices, and Applications II
Brian W. Pogue; Sylvain Gioux, Editor(s)

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