Abstract

Diffuse correlation spectroscopy (DCS) has widely been used as a non-invasive optical technique to measure tissue perfusion in vivo. DCS measurements are quantified to yield information about moving scatterers using photon diffusion theory and are therefore obtained at long source-detector separations (SDS). However, short SDS DCS could be used for measuring perfusion in small animal models or endoscopically in clinical studies. Here, we investigate the errors in analytically retrieved flow coefficients from simulated and experimental data acquired at short SDS. Monte Carlo (MC) simulations of photon correlation transport was programmed to simulate DCS measurements and used to (a) examine the accuracy and validity of theoretical analyses, and (b) model experimental measurements made on phantoms at short SDS. Experiments consisted of measurements from a series of optical phantoms containing an embedded flow channel. Both the fluid flow rate and depth of the flow channel from the liquid surface were varied. Inputs to MC simulations required to model experiments were obtained from corrected theoretical analyses. Results show that the widely used theoretical DCS model is robust for quantifying relative changes in flow. We also show that retrieved flow coefficients at short SDS can be scaled to retrieve absolute values via MC simulations.

Highlights

  • Diffuse correlation spectroscopy (DCS) is a well-established optical technique capable of sensing blood flow in biological tissue using multiply scattered light and has widely been applied to quantify tissue perfusion in vivo [1,2,3,4,5,6,7,8,9,10,11,12,13]

  • We show that retrieved flow coefficients at short source-detector separations (SDS) can be scaled to retrieve absolute values via Monte Carlo (MC) simulations

  • The light source used in DCS is a long coherence length laser, which is delivered to a medium of interest through a large-core optical fiber while the back-scattered intensity is collected using a small-core fiber, placed at a fixed distance from the center of the source fiber

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Summary

Introduction

Diffuse correlation spectroscopy (DCS) is a well-established optical technique capable of sensing blood flow in biological tissue using multiply scattered light and has widely been applied to quantify tissue perfusion in vivo [1,2,3,4,5,6,7,8,9,10,11,12,13]. Experimental DCS measurements yield the normalized intensity autocorrelation function, g2 (τ) measured for a given fiber geometry, which in turn is quantified by fitting via an analytical expression to extract flow-dependent coefficients that characterize the dynamically scattered photon transport [15,16,17].

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