TY - JOUR
T1 - Bichromatic tetraphasic full-field optical coherence microscopy
AU - Iyer, Rishyashring R.
AU - Žurauskas, Mantas
AU - Rao, Yug
AU - Chaney, Eric J.
AU - Boppart, Stephen A.
N1 - This research was supported in part by grants from the National Institutes of Health (R01EY029397, R01EB028615, R01CA241618, P41EB031772) and the Air Force Office of Scientific Research (FA9550-17-1-0387). RRI was supported by the Tissue Microenvironment Training Program funded by National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health under Award Number T32EB019944. The authors would like to thank Janet E. Sorrells, Lingxiao Yang, Kevin K. D. Tan, and Carlos A. Renteria for assisting with the cells and for their valuable discussions to this study. The authors would also like to thank Marina Marjanovic and Darold R. Spillman Jr. for their assistance in coordinating and executing this study.
PY - 2024/6/15
Y1 - 2024/6/15
N2 - Significance: Full-field optical coherence microscopy (FF-OCM) is a prevalent technique for backscattering and phase imaging with epi-detection. Traditional methods have two limitations: suboptimal utilization of functional information about the sample and complicated optical design with several moving parts for phase contrast. Aim: We report an OCM setup capable of generating dynamic intensity, phase, and pseudo-spectroscopic contrast with single-shot full-field video-rate imaging called bichromatic tetraphasic (BiTe) full-field OCM with no moving parts. Approach: BiTe OCM resourcefully uses the phase-shifting properties of antireflection (AR) coatings outside the rated bandwidths to create four unique phase shifts, which are detected with two emission filters for spectroscopic contrast. Results: BiTe OCM overcomes the disadvantages of previous FF-OCM setup techniques by capturing both the intensity and phase profiles without any artifacts or speckle noise for imaging scattering samples in three-dimensional (3D). BiTe OCM also utilizes the raw data effectively to generate three complementary contrasts: intensity, phase, and color. We demonstrate BiTe OCM to observe cellular dynamics, image live, and moving micro-animals in 3D, capture the spectroscopic hemodynamics of scattering tissues along with dynamic intensity and phase profiles, and image the microstructure of fall foliage with two different colors. Conclusions: BiTe OCM can maximize the information efficiency of FF-OCM while maintaining overall simplicity in design for quantitative, dynamic, and spectroscopic characterization of biological samples.
AB - Significance: Full-field optical coherence microscopy (FF-OCM) is a prevalent technique for backscattering and phase imaging with epi-detection. Traditional methods have two limitations: suboptimal utilization of functional information about the sample and complicated optical design with several moving parts for phase contrast. Aim: We report an OCM setup capable of generating dynamic intensity, phase, and pseudo-spectroscopic contrast with single-shot full-field video-rate imaging called bichromatic tetraphasic (BiTe) full-field OCM with no moving parts. Approach: BiTe OCM resourcefully uses the phase-shifting properties of antireflection (AR) coatings outside the rated bandwidths to create four unique phase shifts, which are detected with two emission filters for spectroscopic contrast. Results: BiTe OCM overcomes the disadvantages of previous FF-OCM setup techniques by capturing both the intensity and phase profiles without any artifacts or speckle noise for imaging scattering samples in three-dimensional (3D). BiTe OCM also utilizes the raw data effectively to generate three complementary contrasts: intensity, phase, and color. We demonstrate BiTe OCM to observe cellular dynamics, image live, and moving micro-animals in 3D, capture the spectroscopic hemodynamics of scattering tissues along with dynamic intensity and phase profiles, and image the microstructure of fall foliage with two different colors. Conclusions: BiTe OCM can maximize the information efficiency of FF-OCM while maintaining overall simplicity in design for quantitative, dynamic, and spectroscopic characterization of biological samples.
KW - biological dynamics
KW - optical coherence microscopy
KW - phase imaging
KW - spectroscopic imaging
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U2 - 10.1117/1.JBO.29.S2.S22704
DO - 10.1117/1.JBO.29.S2.S22704
M3 - Article
C2 - 38584966
AN - SCOPUS:85190398049
SN - 1083-3668
VL - 29
JO - Journal of biomedical optics
JF - Journal of biomedical optics
M1 - S22704
ER -