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Tissue characterization with ballistic photons

机译:弹道光子对组织的表征

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We propose tissue characterization with ballistic photons, those whose direction or propagation speed is not affected by the presence of tissue. The most critical aspect of the tissue characterization problem is calibration of experimental measurements. The calibration method relates the fringe irradiance (power modulation in one interferometer arm) with the sample concentration under controlled conditions. During this step, the absorption and scattering indices β_a and β_(SC) are determined as a function of concentration for each material or tissue of interest, using a set of containers to vary travel distance D. It is assumed that linear scattering coefficient, k_(SC) (absorption coefficient, α_a), is proportional to the number of scattering particles per unit volume, or particle concentration, c, in [ml/1]. Attenuation is proportional to concentration of scattering (absorption) centers and the sample length. The sensitivity of method is estimated at 10"'9 with uncoated plate beam-splitters and intensified photon-counting detector.
机译:我们建议使用弹道光子来表征组织,这些光子的方向或传播速度不受组织的存在的影响。组织表征问题的最关键方面是实验测量值的校准。校准方法将条纹辐照度(一个干涉仪臂中的功率调制)与受控条件下的样品浓度相关联。在此步骤中,使用一组容器来改变行进距离D,将吸收和散射指数β_a和β_(SC)确定为每种目标材料或组织的浓度的函数。假设线性散射系数k_ (SC)(吸收系数,α_a)与单位体积的散射粒子数或粒子浓度c成正比,单位为[ml / 1]。衰减与散射(吸收)中心的浓度和样品长度成正比。使用未镀膜的平板分束器和增强的光子计数检测器,该方法的灵敏度估计为10“'9。

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