Objective.Fluorescence molecular tomography (FMT) holds promise for early tumor detection by mapping fluorescent agents in three dimensions non-invasively with low cost. However, since ill-posedness and ill-condition due to strong scattering effects in biotissues and limited measurable data, current FMT reconstruction is still up against unsatisfactory accuracy, including location prediction and morphological preservation.Approach.To strike the above challenges, we propose a novel Sparse-Laplace hybrid graph manifold (SLHGM) model. This model integrates a hybrid Laplace norm-based graph manifold learning term, facilitating a trade-off between sparsity and preservation of morphological features. To address the non-convexity of the hybrid objective function, a fixed-point equation is designed, which employs two successive resolvent operators and a forward operator to find a converged solution.Main results.Through numerical simulations andin vivoexperiments, we demonstrate that the SLHGM model achieves an improved performance in providing accurate spatial localization while preserving morphological details.Significance.Our findings suggest that the SLHGM model has the potential to advance the application of FMT in biological research, not only in simulation but also inin vivostudies.
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