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Characterizing refractive index and thickness of biological tissues using combined multiphoton microscopy and optical coherence tomography

机译:结合多光子显微镜和光学相干断层扫描表征生物组织的折射率和厚度

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摘要

We present a noninvasive method for characterizing the refractive index (RI) and thickness distribution in biological tissues using a combined multiphoton microscopy (MPM) and optical coherence tomography (OCT) system. Tissue layers are distinguished by the MPM and OCT images, and the RI and thickness of each layer are determined by analyzing the co-registered MPM and OCT images. The precision of this method is evaluated on four standard samples which are water, air, immersion oil and cover glass. Precision of within ~1% error compared to reference values is obtained. Biological tissue measurement is demonstrated on fish cornea. Three layers are detected, which are identified as the epithelium and stroma I and II of the cornea. The corresponding RI of each layer is measured to be ~1.446–1.448, 1.345–1.372, and 1.392–1.436, respectively. The difference of RI in the three layers correlates with the tissue compositions including cells in epithelium, large collagen fiber bundles in stroma I, and small collagen fibers in stroma II. The combined MPM/OCT technique is shown to be able to distinguish tissue layers through biochemically specific contrasts and measure RI and thickness of tissue layers at different depths.
机译:我们提出了一种非侵入性方法,用于结合多光子显微镜(MPM)和光学相干断层扫描(OCT)系统表征生物组织中的折射率(RI)和厚度分布。通过MPM和OCT图像区分组织层,并通过分析共同注册的MPM和OCT图像确定每层的RI和厚度。在四个标准样品(水,空气,浸油和盖玻片)上评估此方法的精度。与参考值相比,可获得约1%的误差。在鱼角膜上证明了生物组织测量。检测到三层,其被识别为角膜的上皮和基质I和II。每层的相应RI分别为〜1.446-1.448、1.345-1.372和1.392-1.436。三层中RI的差异与组织组成相关,包括上皮中的细胞,基质I中的大胶原纤维束和基质II中的小胶原纤维。 MPM / OCT组合技术显示出能够通过生化特异性对比来区分组织层,并能够测量不同深度的RI和组织层的厚度。

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