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Translational label-free nonlinear imaging biomarkers to classify the human corneal microstructure

机译:无需平移标记的非线性成像生物标记物可对人类角膜微结构进行分类

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Diseases that affect the cornea can lead to severe vision loss and have tremendous social impact. These diseases are associated to deviations from normal structural order and orientation of collagen fibril bundles. Unfortunately, resolving non-invasively the corneal collagen structure is not possible to date. In this work, polarization sensitive second harmonic generation (pSHG) microscopy is used to obtain information with molecular specificity on microstructure of human corneas. This information is used to develop a set of label-free imaging biomarkers that were generated by means of a novel methodology based on mathematical tensorial calculus. The method is proven to be highly sensitive and robust. The use of these biomarkers permits accurate characterization of the anisotropic, depth-dependent, structural organization of corneal collagen fibril bundles without any a priori information. The method can be valuable to improve understanding of microstructural pathophysiological changes of the human cornea close to in vivo conditions.
机译:影响角膜的疾病可能导致严重的视力丧失,并产生巨大的社会影响。这些疾病与胶原原纤维束正常结构顺序和方向的偏离有关。不幸的是,迄今为止不可能无创地解决角膜胶原结构。在这项工作中,偏振敏感的二次谐波产生(pSHG)显微镜用于获得有关人类角膜微观结构的分子特异性信息。此信息用于开发一组无标记的成像生物标记,这些标记是通过基于数学张量演算的新方法生成的。该方法被证明是高度灵敏且稳健的。这些生物标记物的使用允许角膜胶原原纤维束的各向异性,深度依赖性的结构组织的准确表征,而无需任何先验信息。该方法对于增进对接近体内条件的人角膜的微结构病理生理变化的理解可能是有价值的。

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