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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2011
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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. |
format | Online Article Text |
id | pubmed-3114223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
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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