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Fluorescence molecular tomography has become a promising technique for in vivo small animal imaging, and has many potential applications. Due to the ill-posed and the ill-conditioned nature of the problem, Tikhonov regularization is generally adopted to stabilize the solution. However, the result is usually over-smoothed. In this study, the sparsity of the fluorescent source is used as a priori information. We replace Tikhonov method with an iteratively reweighted scheme. By dynamically updating the weight matrix, L0- or L1-norm regularization can be approximated which can promote the sparsity of the solution. Simulation study shows that this method can preserve the sparsity of the fluorescent source within heterogeneous medium, even with very limited measurement data.

The purpose of this study was to noninvasively monitor the therapeutic efficacy of cyclophosphamide (CTX) in a mouse model by dual-modality molecular imaging: positron emission tomography (PET) and bioluminescence imaging (BLI). Firefly luciferase (fLuc) transfected HCC-LM3-fLuc human hepatocellular carcinoma cells were injected subcutaneously into BALB/c nude mice to establish the experimental tumor model. Two groups of HCC-LM3-fLuc tumor-bearing mice (n = 7 per group) were treated with saline or CTX (100 mg/kg on days 0, 2, 5, and 7). BLI and (18)F-fluorodeoxyglucose ((18)F-FDG) PET scans were done to evaluate the treatment efficacy. CTX induced a 25.25 ± 13.13% and 35.91 ± 25.85% tumor growth inhibition rate on days 9 and 12 posttreatment, respectively, as determined by BLI. A good linear correlation was found between the tumor sizes measured by caliper and the BLI signals determined by optical imaging (R(2) = .9216). (18)F-FDG imaging revealed a significant uptake reduction in the tumors of the CTX-treated group compared to that in the saline control group (5.30 ± 1.97 vs 3.00 ± 2.11% ID/g) on day 16 after CTX treatment. Dual-modality molecular imaging using BLI and small-animal PET can play important roles in the process of chemotherapy and will provide noninvasive and reliable monitoring of the therapeutic response.

In non-equality optical field, we use the RO model, which is based on the theory of geometric optics, the optical trapping force which is in Y axes way on the micro sphere particles in the Mie scattering field is calculated quantitatively. The simulation results under given parameters are described. According to the simulation results, the relations between the optical trapping force and the main parameters of the system, including focus corset radius and the laser wave-length are discussed.