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Monte Carlo model to describe depth selective fluorescence spectra of epithelial tissue

机译:蒙特卡洛模型描述上皮组织的深度选择性荧光光谱

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摘要

We present a Monte Carlo model to predict fluorescence spectra of the oral mucosa obtained with a depth-selective fiber optic probe as a function of tissue optical properties. A model sensitivity analysis determines how variations in optical parameters associated with neoplastic development influence the intensity and shape of spectra, and elucidates the biological basis for differences in spectra from normal and premalignant oral sites. Predictions indicate that spectra of oral mucosa collected with a depth-selective probe are affected by variations in epithelial optical properties, and to a lesser extent, by changes in superficial stromal parameters, but not by changes in the optical properties of deeper stroma. The depth selective probe offers enhanced detection of epithelial fluorescence, with 90% of the detected signal originating from the epithelium and superficial stroma. Predicted depth-selective spectra are in good agreement with measured average spectra from normal and dysplastic oral sites. Changes in parameters associated with dysplastic progression lead to a decreased fluorescence intensity and a shift of the spectra to longer emission wavelengths. Decreased fluorescence is due to a drop in detected stromal photons, whereas the shift of spectral shape is attributed to an increased fraction of detected photons arising in the epithelium.
机译:我们提出了蒙特卡洛模型,以预测与深度选择性光纤探针获得的口腔黏膜的荧光光谱随组织光学特性的变化。模型敏感性分析确定与肿瘤形成相关的光学参数变化如何影响光谱的强度和形状,并阐明正常和恶变前口腔部位光谱差异的生物学基础。预测表明,用深度选择探针收集的口腔粘膜光谱受上皮光学特性变化的影响,而在较小程度上受表层基质参数的变化影响,但不受较深基质的光学特性变化的影响。深度选择探头可增强对上皮荧光的检测,检测信号的90%来自上皮和浅表基质。预测的深度选择性光谱与正常和发育异常的口腔部位的平均光谱测得的结​​果非常吻合。与发育不良的进展相关的参数变化会导致荧光强度降低以及光谱向更长的发射波长转移。荧光减少是由于检测到的基质光子下降所致,而光谱形状的变化归因于上皮细胞中检测到的光子分数的增加。

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