Department of Electrical and Computer Engineering, Duke University, 101 Science Drive, Durham NC 27708, United States of America.
Phys Med Biol. 2018 Jan 9;63(2):025007. doi: 10.1088/1361-6560/aa9cfe.
In situ measurements of diffusive particle transport provide insight into tissue architecture, drug delivery, and cellular function. Analogous to diffusion-tensor magnetic resonance imaging (DT-MRI), where the anisotropic diffusion of water molecules is mapped on the millimeter scale to elucidate the fibrous structure of tissue, here we propose diffusion-tensor optical coherence tomography (DT-OCT) for measuring directional diffusivity and flow of optically scattering particles within tissue. Because DT-OCT is sensitive to the sub-resolution motion of Brownian particles as they are constrained by tissue macromolecules, it has the potential to quantify nanoporous anisotropic tissue structure at micrometer resolution as relevant to extracellular matrices, neurons, and capillaries. Here we derive the principles of DT-OCT, relating the detected optical signal from a minimum of six probe beams with the six unique diffusion tensor and three flow vector components. The optimal geometry of the probe beams is determined given a finite numerical aperture, and a high-speed hardware implementation is proposed. Finally, Monte Carlo simulations are employed to assess the ability of the proposed DT-OCT system to quantify anisotropic diffusion of nanoparticles in a collagen matrix, an extracellular constituent that is known to become highly aligned during tumor development.
原位测量扩散粒子输运可深入了解组织架构、药物输送和细胞功能。类似于扩散张量磁共振成像(DT-MRI),后者可在毫米尺度上绘制水分子的各向异性扩散,以阐明组织的纤维结构,在此我们提出扩散张量光相干断层扫描(DT-OCT),用于测量组织内光散射粒子的方向扩散率和流动。由于 DT-OCT 对受组织大分子约束的布朗粒子的亚分辨率运动敏感,因此它有可能以与细胞外基质、神经元和毛细血管相关的微米分辨率定量纳米多孔各向异性组织结构。在这里,我们推导了 DT-OCT 的原理,将来自至少六个探测光束的检测光信号与六个独特的扩散张量和三个流动矢量分量相关联。给定有限的数值孔径,确定了探测光束的最佳几何形状,并提出了高速硬件实现。最后,采用蒙特卡罗模拟评估所提出的 DT-OCT 系统定量胶原基质中纳米粒子各向异性扩散的能力,胶原基质是一种已知在肿瘤发展过程中变得高度有序的细胞外成分。