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Quantitative phase imaging through scattering media by means of coherence-controlled holographic microscope. | LitMetric

Quantitative phase imaging through scattering media by means of coherence-controlled holographic microscope.

J Biomed Opt

Brno University of Technology, CEITEC-Central European Institute of Technology, Technicka 3058/10, Brno 616 00, Czech RepublicbBrno University of Technology, Institute of Physical Engineering, Faculty of Mechanical Engineering, Technicka 2896/2, Brno 616.

Published: June 2016

AI Article Synopsis

  • CCHM allows for advanced phase imaging even through scattering materials, utilizing both coherent and incoherent light sources.
  • The study focuses on how varying the spatial coherence of light affects the quality of imaging through different levels of scattering.
  • Experimental results from imaging a model phase object and live carcinoma cells support the theoretical and simulation findings, showing that phase information can still be captured despite strong scattering.

Article Abstract

A coherence-controlled holographic microscope (CCHM) enables quantitative phase imaging with coherent as well as incoherent illumination. The low spatially coherent light induces a coherence gating effect, which makes observation of samples possible also through scattering media. The paper describes theoretically and simulates numerically imaging of a two-dimensional object through a static scattering layer by means of CCHM, with the main focus on the quantitative phase imaging quality. The authors have investigated both strongly and weakly scattering media characterized by different amounts of ballistic and diffuse light. It is demonstrated that the phase information can be revealed also for the case of the static, strongly scattering layer. The dependence of the quality of imaging process on the spatial light coherence is demonstrated. The theoretical calculations and numerical simulations are supported by experimental data gained with a model phase object, as well as living carcinoma cells treated in an optically turbid emulsion.

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Source
http://dx.doi.org/10.1117/1.JBO.20.11.111206DOI Listing

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