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Snapshot Imaging of Stokes Vector Polarization Speckle in Turbid Optical Phantoms and In Vivo Tissues Louie, Daniel C.; Kulcsar, Carla; Contreras-Sánchez, Héctor A.; Zabel, W. Jeffrey; Lee, Tim K.
Abstract
Significance: We present a system to measure and analyze the complete polarization state distribution of speckle patterns generated from in vivo tissue. Accurate measurement of polarization speckle requires both precise spatial registration and rapid polarization state acquisition. A unique measurement system must be designed to achieve accurate images of polarization speckle patterns for detailed investigation of the scattering properties of biological tissues in vivo. Aim and approach: This system features a polarization state analyzer with no moving parts. Two pixel-polarizer cameras allow for the instantaneous acquisition of the spatial Stokes vector distribution of polarization speckle patterns. System design and calibration methods are presented, and representative images from measurements on liquid phantoms (microsphere suspensions) and in vivo healthy and tumor murine models are demonstrated and discussed. Results and Conclusions: Quantitative measurements of polarization speckle from microsphere suspensions with controlled scattering coefficients demonstrate differences in speckle contrast, speckle size, and the degree of polarization. Measurements on in vivo murine skin and xenograft tumor tissue demonstrate the ability of the system to acquire snapshot polarization speckle images in living systems. The developed system can thus rapidly and accurately acquire polarization speckle images from different media in dynamic conditions such as in vivo tissue. This capability opens the potential for future detailed investigation of polarization speckle for in vivo biomedical applications.
Item Metadata
Title |
Snapshot Imaging of Stokes Vector Polarization Speckle in Turbid Optical Phantoms and In Vivo Tissues
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Creator | |
Contributor | |
Publisher |
Multidisciplinary Digital Publishing Institute
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Date Issued |
2025-01-11
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Description |
Significance: We present a system to measure and analyze the complete polarization state distribution of speckle patterns generated from in vivo tissue. Accurate measurement of polarization speckle requires both precise spatial registration and rapid polarization state acquisition. A unique measurement system must be designed to achieve accurate images of polarization speckle patterns for detailed investigation of the scattering properties of biological tissues in vivo. Aim and approach: This system features a polarization state analyzer with no moving parts. Two pixel-polarizer cameras allow for the instantaneous acquisition of the spatial Stokes vector distribution of polarization speckle patterns. System design and calibration methods are presented, and representative images from measurements on liquid phantoms (microsphere suspensions) and in vivo healthy and tumor murine models are demonstrated and discussed. Results and Conclusions: Quantitative measurements of polarization speckle from microsphere suspensions with controlled scattering coefficients demonstrate differences in speckle contrast, speckle size, and the degree of polarization. Measurements on in vivo murine skin and xenograft tumor tissue demonstrate the ability of the system to acquire snapshot polarization speckle images in living systems. The developed system can thus rapidly and accurately acquire polarization speckle images from different media in dynamic conditions such as in vivo tissue. This capability opens the potential for future detailed investigation of polarization speckle for in vivo biomedical applications.
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Subject | |
Genre | |
Type | |
Language |
eng
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Date Available |
2025-02-04
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Provider |
Vancouver : University of British Columbia Library
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Rights |
CC BY 4.0
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DOI |
10.14288/1.0447970
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URI | |
Affiliation | |
Citation |
Photonics 12 (1): 59 (2025)
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Publisher DOI |
10.3390/photonics12010059
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty; Researcher
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
CC BY 4.0