Open Access Presentation + Paper
1 March 2019 In vivo label-free confocal imaging of adult mouse brain up to 1.3-mm depth with NIR-II illumination
Author Affiliations +
Proceedings Volume 10865, Neural Imaging and Sensing 2019; 1086504 (2019) https://doi.org/10.1117/12.2509132
Event: SPIE BiOS, 2019, San Francisco, California, United States
Abstract
We combined NIR-II illumination at ~1.7 μm with reflectance confocal microscopy and achieved an imaging depth of ~1.3 mm with high spatial resolution in adult mouse brain in vivo, which is 3-4 times deeper than that of conventional confocal microscopy using visible wavelength. We showed that the method can be added as an additional channel to any laser-scanning microscope with low-cost sources and detectors, such as continuous-wave (CW) diode lasers and InGaAs photodiodes. The technique is label-free, simple and requires low illumination power, potentially creating new opportunities for deep tissue imaging in various biological and clinical applications.
Conference Presentation
© (2019) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Fei Xia, Chunyan Wu, David Sinefeld, Bo Li, Yifan Qin, and Chris Xu "In vivo label-free confocal imaging of adult mouse brain up to 1.3-mm depth with NIR-II illumination", Proc. SPIE 10865, Neural Imaging and Sensing 2019, 1086504 (1 March 2019); https://doi.org/10.1117/12.2509132
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KEYWORDS
Confocal microscopy

Brain

Neuroimaging

Reflectivity

In vivo imaging

Continuous wave operation

Sensors

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