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Depth-resolved Mueller matrix polarimetry microscopy of the rat cornea

机译:深度分辨的穆勒·矩阵偏振矩阵偏振物鼠角膜的显微镜

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摘要

Mueller matrix polarimetry (MMP) is a promising linear imaging modality that can enable visualization and measurement of the polarization properties of the cornea. Although the distribution of corneal birefringence has been reported, depth resolved MMP imaging of the cornea has not been archived and remains challenging. In this work, we perform depth-resolved imaging of the cornea using an improved system that combines Mueller matrix reflectance and transmission microscopy together with nonlinear microscopy utilizing second harmonic generation (SHG) and two photon excitation fluorescence (TPEF). We show that TPEF can reveal corneal epithelial cellular network while SHG can highlight the presence of corneal stromal lamellae. We then demonstrate that, in confocal reflectance measurement, as depth increases from 0 to 80 μm both corneal depolarization and retardation increase. Furthermore, it is shown that the spatial distribution of corneal depolarization and retardation displays similar complexity in both reflectance (confocal and non-confocal) and transmission measurement, likely due to the strong degree of heterogeneity in the stromal lamellae.
机译:Mueller Matrix偏振物(MMP)是一种有前途的线性成像模态,可以实现角膜的偏振特性的可视化和测量。虽然已经报道了角膜双折射的分布,但是尚未存档角膜的深度已解决的MMP成像并仍然具有挑战性。在这项工作中,我们使用一种改进的系统对角膜进行深度分辨的成像,该改进的系统将穆勒矩阵反射率和透射显微镜与非线性显微镜一起使用第二谐波产生(SHG)和两个光子激发荧光(TPEF)。我们表明TPEF可以揭示角膜上皮细胞网络,而SHG可以突出角膜基质薄片的存在。然后,我们证明,在共聚焦反射率测量中,随着深度从0到80μm的深度增加,两个角膜去极化和延迟增加。此外,表明角膜去极化和延迟的空间分布在反射率(共焦和非共焦)和透射测量中显示出类似的复杂性,这可能由于基质薄片中的异质性强烈程度。

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