4.5 Article

Noncontact optical imaging in mice with full angular coverage and automatic surface extraction

Journal

APPLIED OPTICS
Volume 46, Issue 17, Pages 3617-3627

Publisher

OPTICAL SOC AMER
DOI: 10.1364/AO.46.003617

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Funding

  1. MRC [MC_U117512796] Funding Source: UKRI
  2. Medical Research Council [MC_U117512796] Funding Source: researchfish
  3. Medical Research Council [MC_U117512796] Funding Source: Medline
  4. NCI NIH HHS [R33-CA91807] Funding Source: Medline
  5. NIBIB NIH HHS [R01 EB000750-1] Funding Source: Medline

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During the past decade, optical imaging combined with tomographic approaches has proved its potential in offering quantitative three-dimensional spatial maps of chromophore or fluorophore concentration in vivo. Due to its direct application in biology and biomedicine, diffuse optical tomography (DOT) and its fluorescence counterpart, fluorescence molecular tomography (FMT), have benefited from an increase in devoted research and new experimental and theoretical developments, giving rise to a new imaging modality. The most recent advances in FMT and DOT are based on the capability of collecting large data sets by using CCDs as detectors, and on the ability to include multiple projections through recently developed noncontact approaches. For these to be implemented, we have developed an imaging setup that enables three-dimensional imaging of arbitrary shapes in fluorescence or absorption mode that is appropriate for small animal imaging. This is achieved by implementing a noncontact approach both for sources and detectors and coregistering surface geometry measurements using the same CCD camera. A thresholded shadowgrammetry approach is applied to the geometry measurements to retrieve the surface mesh. We present the evaluation of the system and method in recovering three-dimensional surfaces from phantom data and live mice. The approach is used to map the measured in vivo fluorescence data onto the tissue surface by making use of the free-space propagation equations, as well as to reconstruct fluorescence concentrations inside highly scattering tissuelike phantom samples. Finally, the potential use of this setup for in vivo small animal imaging and its impact on biomedical research is discussed. (C) 2007 Optical Society of America.

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