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Optical methodologies for the detection of field carcinogenesis: Investigation of low-coherence enhanced backscattering spectroscopy, polarization gating spectroscopy, and partial coherence speckle.

机译:用于检测场致癌物的光学方法:低相干增强背向散射光谱,偏振门控光谱和部分相干斑点的研究。

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摘要

It is now widely accepted that light scattering is a highly sensitive tool that has the potential to be used for cancer detection and many groups have applied light scattering for the detection and diagnosis of disease. Our group has shown that the backscattering signal is sensitive to the architectural changes of cancer at stages that occur earlier than any available biomarker (Kim, et al., 2005b, Roy, et al., 2006b, Roy, et al., 2005b, Roy, et al., 2004c, Roy, et al., 2004d, Wali, et al., 2005b). We have demonstrated that the backscattering signal has the potential to sense subtle changes in tissue architecture with the potential for detecting colorectal or pancreatic cancer by observing tissue away from the site of the tumor. In this thesis, several techniques are presented which can quantify the properties of biological media by observing the backscattering signal. The techniques are shown to be able to distinguish between healthy patients and patients with pre-cancer or cancer by evaluating a small amount of tissue at an uninvolved location. Probe designs as well as in vivo data are also presented to demonstrate the potential of these techniques for impacting clinical practice. Finally, a correspondence between the measured parameters and the optical properties of the scattering medium is established with experiments on polystyrene microsphere suspensions and light Monte Carlo simulations. The techniques discussed, include low coherence enhanced backscattering spectroscopy (LEBS), polarization gating spectroscopy, and partial coherence speckle. Each of them utilizes an independent physical principle to obtain a depth-selective signal from tissue scattering. We demonstrate how using these methods can aid in diagnosing colon cancer and pancreatic cancer by quantifying the microscopically unapparent changes that accompany field carcinogenesis.
机译:现在,人们普遍认为光散射是一种高度敏感的工具,具有用于癌症检测的潜力,许多组织已将光散射应用于疾病的检测和诊断。我们的研究小组表明,在比任何可用生物标志物更早发生的阶段,反向散射信号对癌症的结构变化均敏感(Kim等人,2005b; Roy等人,2006b; Roy等人,2005b; Roy等,2004c,Roy等,2004d,Wali等,2005b)。我们已经证明,背向散射信号具有感知组织结构中细微变化的潜力,并且具有通过观察远离肿瘤部位的组织来检测结直肠癌或胰腺癌的潜力。本文提出了几种可以通过观察反向散射信号来量化生物介质特性的技术。通过评估未受累部位的少量组织,显示出该技术能够区分健康患者和癌前期或癌症患者。还介绍了探针设计以及体内数据,以证明这些技术对影响临床实践的潜力。最后,通过在聚苯乙烯微球悬浮液上的实验和光蒙特卡洛模拟,建立了测得的参数与散射介质的光学特性之间的对应关系。讨论的技术包括低相干增强背向散射光谱(LEBS),偏振门控光谱和部分相干散斑。它们中的每一个都利用独立的物理原理来从组织散射中获得深度选择信号。我们演示了如何使用这些方法通过量化伴随现场致癌作用的微观上不明显的变化来帮助诊断结肠癌和胰腺癌。

著录项

  • 作者

    Turzhitsky, Vladimir.;

  • 作者单位

    Northwestern University.;

  • 授予单位 Northwestern University.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 219 p.
  • 总页数 219
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:38:30

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