Abstract

Dynamic fluorescence molecular tomography (FMT) is an attractive imaging technique for three-dimensionally resolving the metabolic process of fluorescent biomarkers in small animal. When combined with compartmental modeling, dynamic FMT can be used to obtain parametric images which can provide quantitative pharmacokinetic information for drug development and metabolic research. However, the computational burden of dynamic FMT is extremely huge due to its large data sets arising from the long measurement process and the densely sampling device. In this work, we propose to accelerate the reconstruction process of dynamic FMT based on principal component analysis (PCA). Taking advantage of the compression property of PCA, the dimension of the sub weight matrix used for solving the inverse problem is reduced by retaining only a few principal components which can retain most of the effective information of the sub weight matrix. Therefore, the reconstruction process of dynamic FMT can be accelerated by solving the smaller scale inverse problem. Numerical simulation and mouse experiment are performed to validate the performance of the proposed method. Results show that the proposed method can greatly accelerate the reconstruction of parametric images in dynamic FMT almost without degradation in image quality.

Highlights

  • Dynamic fluorescence molecular tomography (FMT) is a promising imaging technique that allows dynamically and three-dimensionally investigating the metabolic process of fluorescent biomarkers within small animals in vivo [1,2,3,4,5,6,7]

  • The proposed direct method incorporates structural priors obtained from an X-ray computed tomography (XCT) system based on Laplace regularization to mitigate the inherent ill-posedness of FMT [19, 20], which can further improve the image quality

  • The main aim of this paper is to accelerate the reconstruction process of dynamic FMT based on the data compression property of principal component analysis (PCA)

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Summary

Introduction

Dynamic fluorescence molecular tomography (FMT) is a promising imaging technique that allows dynamically and three-dimensionally investigating the metabolic process of fluorescent biomarkers within small animals in vivo [1,2,3,4,5,6,7]. The boundary measurements of dynamic FMT can be transformed into three-dimensional (3-D) images of pharmacokinetic parameters through compartmental modeling [4,5,6,7], as has been done in positron emission tomography (PET) [8,9,10] and magnetic resonance imaging (MRI) [11,12,13]. In order to obtain high-quality parametric images in dynamic FMT problem, we have proposed a novel full-direct method by applying regularization on the parametric images [7]. The proposed direct method incorporates structural priors obtained from an X-ray computed tomography (XCT) system based on Laplace regularization to mitigate the inherent ill-posedness of FMT [19, 20], which can further improve the image quality

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