TY - GEN
T1 - Single-shot 4-phase shifting optical coherence microscopy
AU - Zurauskas, Mantas
AU - Iyer, Rishyashring R.
AU - Boppart, Stephen A.
N1 - Publisher Copyright:
© 2021 SPIE.
PY - 2021
Y1 - 2021
N2 - One limitation of phase shifting optical coherence microscopy (OCM) is that any changes in imaging conditions, caused by either system-level instability or movement of dynamic samples, will inevitably lead to reduction in image quality. Here we present a novel implementation of OCM which permits accurate measurements of phase and intensity, by simultaneously capturing four phase-shifted images on a single camera sensor. Uniquely, our approach enables probing the sample with unpolarized light, producing four phase-shifted interferograms, separated by Ïin two orthogonally polarized detection channel pairs. The proposed set-up is compatible with spatially incoherent illumination sources, enabling high resolution imaging due to its inherently reduced susceptibility to speckle noise. By simultaneously capturing the four phase-shifted images on a single CCD camera chip we demonstrate the capacity to acquire stable phase recordings with a phase sensitivity of 0.1 nm rms error at 500 Hz frame rates, a field-of-view of 250x250 μm, and 1μm lateral resolution. Instantaneous, coherence-gated, phase-sensitive imaging at high frame rates enables observations of the dynamics in cells and tissues, providing instant feedback on metabolic activity and tissue states. We present the novel design and methodology that enables ultrasensitive label-free coherence-gated measurements of intracellular dynamics in cells and cellular networks.
AB - One limitation of phase shifting optical coherence microscopy (OCM) is that any changes in imaging conditions, caused by either system-level instability or movement of dynamic samples, will inevitably lead to reduction in image quality. Here we present a novel implementation of OCM which permits accurate measurements of phase and intensity, by simultaneously capturing four phase-shifted images on a single camera sensor. Uniquely, our approach enables probing the sample with unpolarized light, producing four phase-shifted interferograms, separated by Ïin two orthogonally polarized detection channel pairs. The proposed set-up is compatible with spatially incoherent illumination sources, enabling high resolution imaging due to its inherently reduced susceptibility to speckle noise. By simultaneously capturing the four phase-shifted images on a single CCD camera chip we demonstrate the capacity to acquire stable phase recordings with a phase sensitivity of 0.1 nm rms error at 500 Hz frame rates, a field-of-view of 250x250 μm, and 1μm lateral resolution. Instantaneous, coherence-gated, phase-sensitive imaging at high frame rates enables observations of the dynamics in cells and tissues, providing instant feedback on metabolic activity and tissue states. We present the novel design and methodology that enables ultrasensitive label-free coherence-gated measurements of intracellular dynamics in cells and cellular networks.
KW - Coherence gated imaging
KW - Ocm
KW - Optical coherence microscopy
KW - Phase sensitive imaging
UR - http://www.scopus.com/inward/record.url?scp=85108699388&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85108699388&partnerID=8YFLogxK
U2 - 10.1117/12.2583583
DO - 10.1117/12.2583583
M3 - Conference contribution
AN - SCOPUS:85108699388
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Optical Coherence Tomography and Coherence Domain Optical Methods in Biomedicine XXV
A2 - Izatt, Joseph A.
A2 - Fujimoto, James G.
PB - SPIE
T2 - Optical Coherence Tomography and Coherence Domain Optical Methods in Biomedicine XXV 2021
Y2 - 6 March 2021 through 11 March 2021
ER -