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Laser speckle imaging in the spatial frequency domain

Laser Speckle Imaging (LSI) images interference patterns produced by coherent addition of scattered laser light to map subsurface tissue perfusion. However, the effect of longer path length photons is typically unknown and poses a limitation towards absolute quantification. In this work, LSI is inte...

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Autores principales: Mazhar, Amaan, Cuccia, David J., Rice, Tyler B., Carp, Stefan A., Durkin, Anthony J., Boas, David A., Choi, Bernard, Tromberg, Bruce J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114223/
https://www.ncbi.nlm.nih.gov/pubmed/21698018
http://dx.doi.org/10.1364/BOE.2.001553
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author Mazhar, Amaan
Cuccia, David J.
Rice, Tyler B.
Carp, Stefan A.
Durkin, Anthony J.
Boas, David A.
Choi, Bernard
Tromberg, Bruce J.
author_facet Mazhar, Amaan
Cuccia, David J.
Rice, Tyler B.
Carp, Stefan A.
Durkin, Anthony J.
Boas, David A.
Choi, Bernard
Tromberg, Bruce J.
author_sort Mazhar, Amaan
collection PubMed
description Laser Speckle Imaging (LSI) images interference patterns produced by coherent addition of scattered laser light to map subsurface tissue perfusion. However, the effect of longer path length photons is typically unknown and poses a limitation towards absolute quantification. In this work, LSI is integrated with spatial frequency domain imaging (SFDI) to suppress multiple scattering and absorption effects. First, depth sensitive speckle contrast is shown in phantoms by separating a deep source (4 mm) from a shallow source (2 mm) of speckle contrast by using a high spatial frequency of illumination (0.24 mm(−1)). We develop an SFD adapted correlation diffusion model and show that with high frequency (0.24 mm(−1)) illumination, doubling of absorption contrast results in only a 1% change in speckle contrast versus 25% change using a planar unmodulated (0 mm(−1)) illumination. Similar absorption change is mimicked in vivo imaging a finger occlusion and the relative speckle contrast change from baseline is 10% at 0.26 mm(−1) versus 60% at 0 mm(−1) during a finger occlusion. These results underscore the importance of path length and optical properties in determining speckle contrast. They provide an integrated approach for simultaneous mapping of blood flow (speckle contrast) and oxygenation (optical properties) which can be used to inform tissue metabolism.
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spelling pubmed-31142232011-06-22 Laser speckle imaging in the spatial frequency domain Mazhar, Amaan Cuccia, David J. Rice, Tyler B. Carp, Stefan A. Durkin, Anthony J. Boas, David A. Choi, Bernard Tromberg, Bruce J. Biomed Opt Express Optics of Tissue and Turbid Media Laser Speckle Imaging (LSI) images interference patterns produced by coherent addition of scattered laser light to map subsurface tissue perfusion. However, the effect of longer path length photons is typically unknown and poses a limitation towards absolute quantification. In this work, LSI is integrated with spatial frequency domain imaging (SFDI) to suppress multiple scattering and absorption effects. First, depth sensitive speckle contrast is shown in phantoms by separating a deep source (4 mm) from a shallow source (2 mm) of speckle contrast by using a high spatial frequency of illumination (0.24 mm(−1)). We develop an SFD adapted correlation diffusion model and show that with high frequency (0.24 mm(−1)) illumination, doubling of absorption contrast results in only a 1% change in speckle contrast versus 25% change using a planar unmodulated (0 mm(−1)) illumination. Similar absorption change is mimicked in vivo imaging a finger occlusion and the relative speckle contrast change from baseline is 10% at 0.26 mm(−1) versus 60% at 0 mm(−1) during a finger occlusion. These results underscore the importance of path length and optical properties in determining speckle contrast. They provide an integrated approach for simultaneous mapping of blood flow (speckle contrast) and oxygenation (optical properties) which can be used to inform tissue metabolism. Optical Society of America 2011-05-13 /pmc/articles/PMC3114223/ /pubmed/21698018 http://dx.doi.org/10.1364/BOE.2.001553 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Optics of Tissue and Turbid Media
Mazhar, Amaan
Cuccia, David J.
Rice, Tyler B.
Carp, Stefan A.
Durkin, Anthony J.
Boas, David A.
Choi, Bernard
Tromberg, Bruce J.
Laser speckle imaging in the spatial frequency domain
title Laser speckle imaging in the spatial frequency domain
title_full Laser speckle imaging in the spatial frequency domain
title_fullStr Laser speckle imaging in the spatial frequency domain
title_full_unstemmed Laser speckle imaging in the spatial frequency domain
title_short Laser speckle imaging in the spatial frequency domain
title_sort laser speckle imaging in the spatial frequency domain
topic Optics of Tissue and Turbid Media
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114223/
https://www.ncbi.nlm.nih.gov/pubmed/21698018
http://dx.doi.org/10.1364/BOE.2.001553
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