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基于 L1-范数原始加速近端梯度的荧光分子断层重建方法。

Reconstruction method for fluorescence molecular tomography based on L1-norm primal accelerated proximal gradient.

机构信息

Beijing Jiaotong University, School of Computer and Information Technology, Haidian District, Beijin, China.

Institute of Automation, CAS Key Laboratory of Molecular Imaging, Chinese Academy of Sciences, Beiji, China.

出版信息

J Biomed Opt. 2018 Aug;23(8):1-11. doi: 10.1117/1.JBO.23.8.085002.

Abstract

Fluorescence molecular tomography (FMT) has been widely used in preclinical tumor imaging, which enables three-dimensional imaging of the distribution of fluorescent probes in small animal bodies via image reconstruction method. However, the reconstruction results are usually unsatisfactory in the term of robustness and efficiency because of the ill-posed and ill-conditioned of FMT problem. In this study, an FMT reconstruction method based on primal accelerated proximal gradient (PAPG) descent and L1-norm regularized projection (L1RP) is proposed. The proposed method utilizes the current and previous iterations to obtain a search point at each iteration. To achieve fast convergence, the PAPG method is applied to efficiently solve the search point, and then L1RP is performed to obtain the robust and accurate reconstruction. To verify the performance of the proposed method, simulation experiments are conducted. The comparative results revealed that it held advantages of robustness, accuracy, and efficiency in FMT reconstructions. Furthermore, a phantom experiment and an in vivo mouse experiment were also performed, which proved the potential and feasibility of the proposed method for practical applications.

摘要

荧光分子断层成像(FMT)已广泛应用于临床前肿瘤成像,它可以通过图像重建方法实现小动物体内荧光探针分布的三维成像。然而,由于 FMT 问题的不适定性和病态性,重建结果通常在稳健性和效率方面不尽如人意。在这项研究中,提出了一种基于原始加速近端梯度(PAPG)下降和 L1-范数正则化投影(L1RP)的 FMT 重建方法。该方法利用当前和前几次迭代来获得每次迭代的搜索点。为了实现快速收敛,应用 PAPG 方法来有效地求解搜索点,然后进行 L1RP 以获得稳健且准确的重建。为了验证所提出方法的性能,进行了模拟实验。比较结果表明,它在 FMT 重建中具有稳健性、准确性和效率方面的优势。此外,还进行了一项体模实验和一项体内小鼠实验,证明了该方法在实际应用中的潜力和可行性。

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