4.6 Article

Microscopic optical coherence tomography (mOCT) at 600 kHz for 4D volumetric imaging and dynamic contrast

期刊

BIOMEDICAL OPTICS EXPRESS
卷 12, 期 10, 页码 6024-6039

出版社

OPTICAL SOC AMER
DOI: 10.1364/BOE.425001

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资金

  1. German Science Foundation [EXC 2167, RA1771/4-1]
  2. Ministry of Research, Innovation and Science [13GW0228A]
  3. Helmholtz Center Munich of Health and Environment DZL-ARCN [82DZL001A2]
  4. European Union project within Interreg Deutschland-Denmark from the European Regional Development Fund (CELLTOM)

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High-speed 3D OCT imaging is achieved using a novel CMOS camera, enabling fast imaging of cellular structures and dynamic processes. This technology has the potential to play a significant role in clinical diagnosis and research applications in the future.
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 mu m axial and 1.1 mu m 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. (c) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

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