Abstract:Abstract:We have performed modeling of fluorescence signals from inclusions inside turbid media to investigate the influence of a limited fluorescence contrast and how accurately the depth can be determined by using the spectral information. The depth was determined by forming a ratio of simulated fluorescence intensities at two wavelengths. The results show that it is important to consider the background autofluorescence in determining the depth of a fluorescent inclusion. It is also necessary to know the opt… Show more
“…To retrieve the spatially varying regularization parameter, or regularization map, the fluorescence emission from the inclusion itself can be used. It has previously been reported that the intensity ratio of the fluorescence emission at two wavelengths, here denoted λ m1 and λ m2 , from a fluorescent inclusion detected at the boundary of the tissue is dependent on the depth of the inclusion [15,16]. This effect is due to the difference in bulk tissue attenuation, mainly absorption i.e.…”
Section: Spatial Priors Based On Fluorescence Emissionmentioning
Abstract:Fluorescence molecular tomography suffers from being mathematically ill-conditioned resulting in non-unique solutions to the reconstruction problem. In an attempt to reduce the number of possible solutions in the underdetermined system of equations in the reconstruction, we present a method to retrieve a spatially varying regularization map outlining the feasible inclusion position. This approach can be made very simple by including a few multispectral recordings from only one source position. The results retrieved through tissue phantom experiments imply that initial reconstructions with spatially varying priors reduces artifacts and show slightly more accurate reconstruction results compared to reconstructions using no priors.
“…To retrieve the spatially varying regularization parameter, or regularization map, the fluorescence emission from the inclusion itself can be used. It has previously been reported that the intensity ratio of the fluorescence emission at two wavelengths, here denoted λ m1 and λ m2 , from a fluorescent inclusion detected at the boundary of the tissue is dependent on the depth of the inclusion [15,16]. This effect is due to the difference in bulk tissue attenuation, mainly absorption i.e.…”
Section: Spatial Priors Based On Fluorescence Emissionmentioning
Abstract:Fluorescence molecular tomography suffers from being mathematically ill-conditioned resulting in non-unique solutions to the reconstruction problem. In an attempt to reduce the number of possible solutions in the underdetermined system of equations in the reconstruction, we present a method to retrieve a spatially varying regularization map outlining the feasible inclusion position. This approach can be made very simple by including a few multispectral recordings from only one source position. The results retrieved through tissue phantom experiments imply that initial reconstructions with spatially varying priors reduces artifacts and show slightly more accurate reconstruction results compared to reconstructions using no priors.
“…In the visible part of the spectrum this is due to the difference in bulk tissue attenuation, mainly influenced by the blood absorption 8 . This is experimentally shown in Fig.…”
Fluorescence molecular tomography (FMT) suffers from inherent ill-posedness due to the vast number of possible solutions to the reconstruction problem. To increase the robustness of such a problem one need prior information. We present here a method for rendering a priori information of the position of a fluorescent inclusion inside turbid media. The method utilizes solely two spectral bands within the fluorescence spectrum emitted from the fluorophore. The method is presented and verified using experimental data from a tissue phantom. The confinement is also used to impose weights onto the voxels before the inversion of the linear set of equations describing the FMT problem.
“…The multispectral information provided in fluorescence measurements of lesions located at a certain depth in tissue would, in addition to the diagnostic information that there exist a lesion, also provide depth information useful for reconstruction of fluorescent inclusions in tissue [15,16]. This is one possible concept to improving the robustness and accuracy of the fluorescence tomography reconstructions.…”
Section: Time-of-flight Laser Spectroscopy In Biomedical Diagnosticsmentioning
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