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Optical Anisotropy Measurement in Normal and Cancerous Tissues: Backscattering Technique Publisher



Soltaninezhad M1 ; Bavali A1 ; Nazifinia Z1 ; Soleimani V2
Authors
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Authors Affiliations
  1. 1. Department of Energy Engineering and Physics, Amirkabir University of Technology (Tehran Polytechnic), Iran
  2. 2. Department of Cancer Institute, Imam Khomeini Medical Centre, Tehran, Iran

Source: Biomedical Optics Express Published:2020


Abstract

Investigating the deformation of tissue architecture is one of the most important clinical methods for cancer diagnosis. Optical methods are now widely developed for rapid, precise, and real-time assessment of these alterations at the microscopic scale. One of the proposed methods is enhanced backscattering (EBS) technique that allows in-vivo measurement of the optical scattering characteristics. Here, EBS technique is employed to evaluate the optical anisotropy of human epithelial tissues as a measure to distinguish between normal and cancerous one. Orientation dependence of the mean scattering length is assessed in healthy and cancerous tissues of five different human organs i. e. uterus, bladder, colon, kidney, and liver. Helicity preserving channel and rotating ground glass diffuser are utilized to eliminate the polarization induced anisotropy and the background speckle noises respectively. Analysis of the backscattering cones recorded by a high-resolution CCD camera reveals the modification of the strength and degree of optical anisotropy in different tissues during cancer progression. Pathology data affirm the correlation between the experimental results and the morphological alteration of the epithelial cells in each carcinoma type. In general, tissues with fibrous constructional cells are subject to a decrease in anisotropy due to cancer, whereas those with cuboidal cells experience an increase in anisotropy. This complementary information enhances the potency of the EBS technique as a fast, non-destructive, and easily accessible tool for real-time tissue diagnosis. © 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.