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Fluorescence Spectroscopy of Oral Tissue: Monte Carlo Modeling with Site-Specific Tissue Properties

机译:口腔组织的荧光光谱:具有特定部位组织特性的蒙特卡洛建模

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摘要

A Monte Carlo model with site-specific input was used to predict depth-resolved fluorescence spectra from individual normal, inflammatory, and neoplastic oral sites. Our goal in developing this model was to provide a computational tool to study how the morphological characteristics of the tissue affect clinically measured spectra. Tissue samples from the measured sites were imaged using fluorescence confocal microscopy; autofluorescence patterns were measured as a function of depth and tissue sublayer for each individual site. These fluorescence distributions were used as input to the Monte Carlo model to generate predictions of fluorescence spectra, which were compared to clinically measured spectra on a site-by-site basis. A lower fluorescence intensity and longer peak emission wavelength observed in clinical spectra from dysplastic and cancerous sites were found to be associated with a decrease in measured fluorescence originating from the stroma or deeper fibrous regions, and an increase in the measured fraction of photons originating from the epithelium or superficial tissue layers. The simulation approach described here can be used to suggest an optical probe design that samples fluorescence at a depth that gives optimal separation in the spectral signal measured for benign, dysplastic and cancerous oral mucosa.
机译:使用具有特定位置输入的蒙特卡洛模型来预测来自各个正常,炎性和赘生性口腔部位的深度分辨荧光光谱。我们开发此模型的目的是提供一种计算工具,以研究组织的形态特征如何影响临床测量的光谱。使用荧光共聚焦显微镜对来自测量部位的组织样品进行成像;根据每个单独部位的深度和组织亚层来测量自身荧光模式。这些荧光分布被用作蒙特卡洛模型的输入,以生成荧光光谱的预测,并将其与逐个站点的临床测量光谱进行比较。在临床光谱中,从发育异常和癌变部位观察到的较低的荧光强度和较长的峰值发射波长被发现与源自基质或较深纤维区域的测得的荧光减少以及源自于基质或较深纤维区域的光子的测得分数增加有关。上皮或浅表组织层。此处描述的模拟方法可用于建议一种光学探针设计,该探针在一定深度处对荧光进行采样,该深度可为所测得的口腔粘膜,良性增生和癌性光谱信号提供最佳分离。

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