Rice Tyler B, Kwan Elliott, Hayakawa Carole K, Durkin Anthony J, Choi Bernard, Tromberg Bruce J
Department of Physics, 4129 Frederick Reines Hall, University of California Irvine, Irvine, CA 92697 USA ; Laser Microbeam and Medical Program (LAMMP), Beckman Laser Institute, 1002 Health Sciences Road, Irvine, CA 92612, USA.
Laser Microbeam and Medical Program (LAMMP), Beckman Laser Institute, 1002 Health Sciences Road, Irvine, CA 92612, USA.
Biomed Opt Express. 2013 Nov 19;4(12):2880-92. doi: 10.1364/BOE.4.002880. eCollection 2013.
Laser Speckle Imaging (LSI) is a simple, noninvasive technique for rapid imaging of particle motion in scattering media such as biological tissue. LSI is generally used to derive a qualitative index of relative blood flow due to unknown impact from several variables that affect speckle contrast. These variables may include optical absorption and scattering coefficients, multi-layer dynamics including static, non-ergodic regions, and systematic effects such as laser coherence length. In order to account for these effects and move toward quantitative, depth-resolved LSI, we have developed a method that combines Monte Carlo modeling, multi-exposure speckle imaging (MESI), spatial frequency domain imaging (SFDI), and careful instrument calibration. Monte Carlo models were used to generate total and layer-specific fractional momentum transfer distributions. This information was used to predict speckle contrast as a function of exposure time, spatial frequency, layer thickness, and layer dynamics. To verify with experimental data, controlled phantom experiments with characteristic tissue optical properties were performed using a structured light speckle imaging system. Three main geometries were explored: 1) diffusive dynamic layer beneath a static layer, 2) static layer beneath a diffuse dynamic layer, and 3) directed flow (tube) submerged in a dynamic scattering layer. Data fits were performed using the Monte Carlo model, which accurately reconstructed the type of particle flow (diffusive or directed) in each layer, the layer thickness, and absolute flow speeds to within 15% or better.
激光散斑成像(LSI)是一种简单的非侵入性技术,用于对生物组织等散射介质中的粒子运动进行快速成像。由于影响散斑对比度的几个变量存在未知影响,LSI通常用于得出相对血流的定性指标。这些变量可能包括光吸收和散射系数、包括静态、非遍历区域的多层动力学以及激光相干长度等系统效应。为了考虑这些效应并朝着定量的、深度分辨的LSI发展,我们开发了一种方法,该方法结合了蒙特卡罗建模、多曝光散斑成像(MESI)、空间频域成像(SFDI)和仔细的仪器校准。蒙特卡罗模型用于生成总动量传递分布和特定层的分数动量传递分布。该信息用于预测散斑对比度作为曝光时间、空间频率、层厚度和层动力学的函数。为了用实验数据进行验证,使用结构化光散斑成像系统进行了具有特征性组织光学特性的受控体模实验。探索了三种主要几何结构:1)静态层下方的扩散动态层,2)扩散动态层下方的静态层,3)浸没在动态散射层中的定向流(管)。使用蒙特卡罗模型进行数据拟合,该模型能够准确地重建每层中的粒子流类型(扩散或定向)、层厚度以及绝对流速,误差在15%以内或更小。