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Limited-angle tomographic phase microscopy utilizing confocal scanning fluorescence microscopy

机译:利用共聚焦扫描荧光显微镜的有限角度分层相显微镜显微镜

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摘要

We present a multimodal imaging technique, combining tomographic phase microscopy with limited angular projection range and number, and two-channel spinning-disk confocal scanning fluorescence microscopy. This technique allows high-accuracy 3D refractive index (RI) profiling of live cells in spite of the missing projections. The cellular outer shape and its interior organelles measured by the confocal fluorescence imaging not only specify the cell in molecular levels, but also provide the 3D distributions of the whole cell as well as its organelles. We take these additional 3D morphological details as constraints in Gerchberg-Papoulis-based optical diffraction tomography algorithm. We then obtain an accurate 3D RI tomogram, even with a sparse angular range having a small number of perspective projections, otherwise providing low-accuracy RI reconstruction. Then, we obtain both cellular molecular specificity and inner RI values of the cell and its organelles. We compare the reconstructed 3D RI profiles of various samples, demonstrating the superiority of the proposed technique.
机译:我们提出了一种多模式成像技术,将断层摄影阶段显微镜与有限的角度投影范围和数量组合,双通道纺丝盘共聚焦扫描荧光显微镜。尽管有缺失预测,这种技术允许活细胞的高精度3D折射率(RI)分析。通过共聚焦荧光成像测量的细胞外形及其内部细胞器不仅指定了分子水平的细胞,而且还提供了整个细胞的3D分布以及其细胞器。我们将这些额外的3D形态细节作为基于Gerchberg-Papoulis的光学衍射断层扫描算法的约束。然后,我们即使具有少量透视突起的稀疏角度范围,我们也可以获得精确的3D RI断层图像,否则提供低精度的RI重建。然后,我们获得细胞分子特异性和细胞的内部RI值及其细胞器。我们比较各种样本的重建的3D RI配置文件,展示了所提出的技术的优越性。

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