2004
DOI: 10.1364/josaa.21.001035
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Fluorescence optical diffusion tomography using multiple-frequency data

Abstract: A method is presented for fluorescence optical diffusion tomography in turbid media using multiple-frequency data. The method uses a frequency-domain diffusion equation model to reconstruct the fluorescent yield and lifetime by means of a Bayesian framework and an efficient, nonlinear optimizer. The method is demonstrated by using simulations and laboratory experiments to show that reconstruction quality can be improved in certain problems through the use of more than one frequency. A broadly applicable mutual… Show more

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Cited by 85 publications
(68 citation statements)
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“…Given N s sources and N d detectors, the measurement Γ i,j of the jth detector due to ith source is given as follows [1],…”
Section: Fdot Imaging Problemmentioning
confidence: 99%
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“…Given N s sources and N d detectors, the measurement Γ i,j of the jth detector due to ith source is given as follows [1],…”
Section: Fdot Imaging Problemmentioning
confidence: 99%
“…The inverse problem of fluorescence diffusse optical tomography (FDOT) requires reconstruction of 2D or 3D fluorophore map inside the imaging domain using boundary measurements obtained at the emission and excitation wavelengths [1]. However, the number of measurements available is usually insufficient.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…This work uses an exponential curve model for compartmental modeling and a linear time-invariant fluorescence light propagation model derived based on authors' prior work in [26] and [27]. The reconstruction of pharmacokinetic-rate images is addressed based on the maximum a posteriori (MAP) estimation together with a parametric iterative coordinate descent optimization technique similar to the approach reported in [13].…”
Section: B Related Work and The Advantages Of Our Approachmentioning
confidence: 99%
“…This model is given as (27) where , are the indices of the voxels in the neighborhood of the th voxel; , are the spatial weighting coefficients, which may be different for each pharmacokinetic-rate or volume fraction image; and , is a zero-mean Gaussian process with , . The weighting coefficients may be spatially varying and can be chosen based on a variety of physiological information, i.e., tumor location, size, or shape.…”
Section: A a Priori Model For Pharmacokinetic Rates And Volume Fractmentioning
confidence: 99%