Designing and Building a Deep Imaging Multi-Parametric Optical Coherence Tomography System for Disease Assessment

Bruce Vagt, Matthew Foster, Richard L. Blackmon
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Abstract

Early cancer detection remains an important problem in healthcare today. Since the mid-1990s, Optical Coherence Tomography (OCT) has been explored as a cancer detection instrument. Previous studies have shown connections between tissue porosity, cell behavior, cell topology, and their relation to cancer and disease progression. Previous researchers have found that in a healthy cell, the pore size of the surrounding extracellular matrix (ECM) is homogenous. However, in a cancerous cell, heterogeneous pores appear. Additionally, as cancer progresses, pore size decreases. Herein, we propose a new method of improving cancer detection using OCT. In a study utilizing an artificial ECM, a connection between pore size and gold nanorod (GNR) diffusion was established such that smaller pores lead to less diffusion, and vice versa. Cell behavior is measured by cell motility, which refers to the rapid, in-place motions of intracellular parts that can be used to assess cell response to therapy, their surrounding environment, and potentially reveal premalignant behavior. Previous investigators have defined two metrics of cell movement, alpha, and motility, which correspond to signal auto-decorrelation and signal amplitude, respectively. Cell topology refers to the 3D structure and shape of cells and cell clusters, which has been shown to mutate in diseases such as cancer. By quantifying cell topology, cellular health can be examined. Techniques using OCT have also been used to monitor the response of diseased tissue to treatment. These studies have been largely independent of each other, and the need for a more holistic measuring system has been called for. This research aims to create a custom OCT system capable of obtaining these metrics simultaneously and with improved imaging depth and comparable resolution. Through an integration of a near-infrared (NIR) laser, interferometer, and LabVIEW control of the system, a new Deep-Imaging, Multi-Parameter OCT (DIMP-OCT) is being created. The system bodes a 4.6µm resolution and 5.4mm imaging depth. This is made possible by a 50-50 fiber optic beam splitter using a 1300nm wavelength laser with 160nm bandwidth, and 2048-pixel spectrometer with a 140kHz linerate. Here, we report the design of the system being built, the techniques used to build and test the hardware, and the approach to developing the graphical user interface. We also will report results from tests to assess DIMP-OCT subsystems.
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用于疾病评估的深度成像多参数光学相干层析成像系统的设计与构建
早期癌症检测仍然是当今医疗保健中的一个重要问题。自20世纪90年代中期以来,光学相干断层扫描(OCT)作为一种癌症检测仪器被探索。先前的研究已经显示了组织孔隙度、细胞行为、细胞拓扑结构及其与癌症和疾病进展的关系之间的联系。先前的研究人员发现,在健康细胞中,周围细胞外基质(ECM)的孔径是均匀的。然而,在癌细胞中,出现了不均匀的毛孔。此外,随着癌症的发展,孔隙大小会减小。在此,我们提出了一种利用oct改进癌症检测的新方法。在一项利用人工ECM的研究中,我们建立了孔径与金纳米棒(GNR)扩散之间的联系,即孔径越小,扩散越少,反之亦然。细胞行为是通过细胞运动来测量的,细胞运动是指细胞内部分的快速、原位运动,可用于评估细胞对治疗的反应、周围环境,并可能揭示癌前行为。先前的研究者已经定义了细胞运动的两个指标,α和运动性,分别对应于信号的自相关和信号幅度。细胞拓扑是指细胞和细胞簇的三维结构和形状,已被证明在癌症等疾病中会发生突变。通过量化细胞拓扑结构,可以检查细胞健康状况。OCT技术也被用于监测病变组织对治疗的反应。这些研究在很大程度上是相互独立的,因此需要一个更全面的测量系统。本研究旨在创建一个定制的OCT系统,能够同时获得这些指标,并具有改进的成像深度和可比较的分辨率。通过集成近红外(NIR)激光器、干涉仪和系统的LabVIEW控制,一种新的深度成像、多参数OCT (dip -OCT)正在创建中。该系统的分辨率为4.6 μ m,成像深度为5.4mm。这是通过一个50-50光纤分束器实现的,该分束器使用1300nm波长的激光器,带宽为160nm, 2048像素光谱仪,带宽为140kHz。在这里,我们报告了正在构建的系统的设计,用于构建和测试硬件的技术,以及开发图形用户界面的方法。我们还将报告评估DIMP-OCT子系统的测试结果。
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