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Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers
Published on: July 17, 2012
Fluorescence diffuse optical tomographic (fDOT) system for small animal studies
1CEA-LETI Minatec, DTBS/STD, 17 rue des Martyrs, 38054 Grenoble cedex France. anne.koenig@cea.fr
Summary
A new fluorescence diffuse optical tomography (fDOT) system reconstructs fluorescence yield in challenging tissues without immersion. This enables effective biological studies in small animals, including tumor development tracking.
Area of Science:
- Biomedical Optics
- Medical Imaging
- Optical Tomography
Background:
- Fluorescence diffuse optical tomography (fDOT) is crucial for in vivo imaging.
- Imaging in heterogeneous and highly attenuating tissues presents significant challenges.
- Current methods often require sample immersion in index-matching fluids.
Purpose of the Study:
- To introduce a novel fDOT system and reconstruction algorithm.
- To enable fluorescence yield reconstruction in complex biological tissues.
- To facilitate small animal imaging without immersion media.
Main Methods:
- Development of a new fDOT system.
- Implementation of an advanced reconstruction algorithm for heterogeneous media.
- Phantom studies for system characterization and validation.
- In vivo mice study focusing on lung tumor development.
Main Results:
- The fDOT system successfully reconstructs fluorescence yield in heterogeneous and attenuating regions.
- The method allows for mouse imaging without optical index matching liquid (Intralipid and ink).
- Phantom experiments validated the system's performance in complex media.
- A mice study demonstrated effective follow-up of lung tumor development.
Conclusions:
- The developed fDOT system and reconstruction method are effective for imaging challenging biological tissues.
- The system eliminates the need for immersion media, simplifying small animal studies.
- This technology is validated for biological applications, particularly in tracking tumor progression in vivo.

