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用于癌症诊断的人体结肠组织穆勒矩阵成像:蒙特卡罗建模如何助力实验数据解读

Mueller matrix imaging of human colon tissue for cancer diagnostics: how Monte Carlo modeling can help in the interpretation of experimental data.

作者信息

Antonelli Maria-Rosaria, Pierangelo Angelo, Novikova Tatiana, Validire Pierre, Benali Abdelali, Gayet Brice, De Martino Antonello

机构信息

LPICM, Ecole polytechnique, CNRS, Palaiseau 91128, France.

出版信息

Opt Express. 2010 May 10;18(10):10200-8. doi: 10.1364/OE.18.010200.

Abstract

Colon samples with both healthy and cancerous regions have been imaged in diffuse light and backscattering geometry by using a Mueller imaging polarimeter. The tumoral parts at the early stage of cancer are found to be less depolarizing than the healthy ones. This trend clearly shows that polarimetric imaging may provide useful contrasts for optical biopsy. Moreover, both types of tissues are less depolarizing when the incident polarization is linear rather than circular. However, to really optimize an optical biopsy technique based on polarimetric imaging a realistic model is needed for polarized light scattering by tissues. Our approach to this goal is based on numerical Monte-Carlo simulations of polarized light propagation in biological tissues modeled as suspensions of monodisperse spherical scatterers representing the cell nuclei. The numerical simulations were validated by comparison with measurements on aqueous polystyrene sphere suspensions, which are commonly used as tissue phantoms. Such systems exhibit lower depolarization for incident linear polarization in the Rayleigh scattering regime, i.e. when the sphere diameters are smaller than the wavelength, which is obviously not the case for cell nuclei. In contrast, our results show that this behaviour can also be seen for "large" scatterers provided the optical index contrast between the spheres and the surrounding medium is small enough, as it is likely to be the case in biological tissues.

摘要

利用穆勒成像偏振仪,在漫射光和后向散射几何条件下对含有健康区域和癌性区域的结肠样本进行了成像。研究发现,癌症早期的肿瘤部分比健康部分的去极化程度更低。这一趋势清楚地表明,偏振成像可为光学活检提供有用的对比度。此外,当入射偏振为线性而非圆偏振时,两种类型的组织去极化程度都更低。然而,要真正优化基于偏振成像的光学活检技术,需要一个关于组织偏振光散射的现实模型。我们实现这一目标的方法是基于对偏振光在生物组织中传播的数值蒙特卡罗模拟,该生物组织被建模为代表细胞核的单分散球形散射体的悬浮液。通过与通常用作组织模型的聚苯乙烯水溶液悬浮液的测量结果进行比较,对数值模拟进行了验证。在瑞利散射 regime 中,即当球体直径小于波长时,此类系统对入射线性偏振表现出较低的去极化,而细胞核显然并非如此。相比之下,我们的结果表明,只要球体与周围介质之间的光学折射率对比度足够小,对于“大”散射体也能观察到这种行为,生物组织中可能就是这种情况。

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