Abstract

Fluorescence diffuse optical tomography using a multi-view continuous-wave and non-contact measurement system and an algorithm incorporating the lp (0 < p ≤ 1) sparsity regularization reconstructs a localized fluorescent target in a small animal. The measurement system provides a total of 25 fluorescence surface 2D-images of an object, which are acquired by a CCD camera from five different angles of view with excitation from five different angles. Fluorescence surface emissions from five different angles of view are simultaneously imaged on the CCD sensor, thus leading to fast acquisition of the 25 images within three minutes. The distributions of the fluorophore are reconstructed by solving the inverse problem based on the photon diffusion equations. In the reconstruction process incorporating the lp sparsity regularization, the regularization term is reformulated as a differentiable function for gradient-based non-linear optimization. Numerical simulations and phantom experiments show that the use of the lp sparsity regularization improves the localization of the target and quantitativeness of the fluorophore concentration. A mouse experiment demonstrates that a localized fluorescent target in a mouse is successfully reconstructed.

Highlights

  • Fluorescence diffuse optical tomography (FDOT) is a non-invasive biomedical imaging modality [1, 2]

  • FDOT reconstructs the distributions of the concentration and properties of fluorophores, such as lifetime and quantum yield in biological media by solving an inverse problem with the input of the fluorescent light detected at the surfaces of the media

  • The objects were installed in the system, the measurements were performed in a short period of time, and the obtained multi-view surface images were used as the input measurement data for image reconstruction of FDOT

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Summary

Introduction

Fluorescence diffuse optical tomography (FDOT) is a non-invasive biomedical imaging modality [1, 2]. FDOT uses near-infrared (NIR) light propagating diffusely in biological media which strongly scatter and weakly absorb NIR light [3, 4]. FDOT reconstructs the distributions of the concentration and properties of fluorophores, such as lifetime and quantum yield in biological media by solving an inverse problem with the input of the fluorescent light detected at the surfaces of the media. One of the applications of FDOT is molecular imaging of small animals for drug developments. Delivery of drugs labeled with fluorophores in small animals can be monitored by FDOT [5]. Quantum yield and lifetime reconstructed by FDOT reflect conditions of diseased tissues and provide information useful for diagnoses [7,8]

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