TY - JOUR
T1 - Microscopic optical coherence tomography (mOCT) at 600 kHz for 4D volumetric imaging and dynamic contrast
AU - MUNTER, MICHAEL
AU - PIEPER, MARIO
AU - KOHLFAERBER, TABEA
AU - BODENSTORFER, ERNST
AU - AHRENS, MARTIN
AU - WINTER, CHRISTIAN
AU - HUBER, ROBERT
AU - KONIG, PETER
AU - HUTTMANN, GEREON
AU - SCHULZ-HILDEBRANDT, HINNERK
N1 - Publisher Copyright:
© 2021 Optical Society of America.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Volumetric imaging of dynamic processes with microscopic resolution holds a huge potential in biomedical research and clinical diagnosis. Using supercontinuum light sources and high numerical aperture (NA) objectives, optical coherence tomography (OCT) achieves microscopic resolution and is well suited for imaging cellular and subcellular structures of biological tissues. Currently, the imaging speed of microscopic OCT (mOCT) is limited by the line-scan rate of the spectrometer camera and ranges from 30 to 250 kHz. This is not fast enough for volumetric imaging of dynamic processes in vivo and limits endoscopic application. Using a novel CMOS camera, we demonstrate fast 3-dimensional OCT imaging with 600,000 A-scans/s at 1.8 μm axial and 1.1 μm lateral resolution. The improved speed is used for imaging of ciliary motion and particle transport in ex vivo mouse trachea. Furthermore, we demonstrate dynamic contrast OCT by evaluating the recorded volumes rather than en face planes or B-scans. High-speed volumetric mOCT will enable the correction of global tissue motion and is a prerequisite for applying dynamic contrast mOCT in vivo. With further increase in imaging speed and integration in flexible endoscopes, volumetric mOCT may be used to complement or partly replace biopsies.
AB - Volumetric imaging of dynamic processes with microscopic resolution holds a huge potential in biomedical research and clinical diagnosis. Using supercontinuum light sources and high numerical aperture (NA) objectives, optical coherence tomography (OCT) achieves microscopic resolution and is well suited for imaging cellular and subcellular structures of biological tissues. Currently, the imaging speed of microscopic OCT (mOCT) is limited by the line-scan rate of the spectrometer camera and ranges from 30 to 250 kHz. This is not fast enough for volumetric imaging of dynamic processes in vivo and limits endoscopic application. Using a novel CMOS camera, we demonstrate fast 3-dimensional OCT imaging with 600,000 A-scans/s at 1.8 μm axial and 1.1 μm lateral resolution. The improved speed is used for imaging of ciliary motion and particle transport in ex vivo mouse trachea. Furthermore, we demonstrate dynamic contrast OCT by evaluating the recorded volumes rather than en face planes or B-scans. High-speed volumetric mOCT will enable the correction of global tissue motion and is a prerequisite for applying dynamic contrast mOCT in vivo. With further increase in imaging speed and integration in flexible endoscopes, volumetric mOCT may be used to complement or partly replace biopsies.
UR - http://www.scopus.com/inward/record.url?scp=85114674967&partnerID=8YFLogxK
U2 - 10.1364/BOE.425001
DO - 10.1364/BOE.425001
M3 - Journal articles
AN - SCOPUS:85114674967
SN - 2156-7085
VL - 12
SP - 6024
EP - 6039
JO - Biomedical Optics Express
JF - Biomedical Optics Express
IS - 10
ER -