TY - JOUR
T1 - High-contrast multifocus microscopy with a single camera and z-splitter prism
AU - Xiao, Sheng
AU - Gritton, Howard
AU - Tseng, Hua An
AU - Zemel, Dana
AU - Han, Xue
AU - Mertz, Jerome
N1 - Funding Information:
National Institutes of Health (R01EB029171, R21GM128020).
Publisher Copyright:
© 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
PY - 2020/10/22
Y1 - 2020/10/22
N2 - Optical microscopy has been an indispensable tool for studying complex biological systems, but is often hampered by problems of speed and complexity when performing 3D volumetric imaging. Here, we present a multifocus imaging strategy based on the use of a simple z-splitter prism that can be assembled from off-the-shelf components. Our technique enables a widefield image stack to be distributed onto a single camera and recorded simultaneously. We exploit the volumetric nature of our image acquisition by further introducing a novel extended-volume 3D deconvolution strategy to suppress far-out-of-focus fluorescence background to significantly improve the contrast of our recorded images, conferring to our system a capacity for quasi-optical sectioning. By swapping in different z-splitter configurations, we can prioritize high speed or large 3D field-of-view imaging depending on the application of interest. Moreover, our system can be readily applied to a variety of imaging modalities in addition to fluorescence, such as phase-contrast and darkfield imaging. Because of its simplicity, versatility, and performance, we believe our system will be a useful tool for general biological or biomedical imaging applications.
AB - Optical microscopy has been an indispensable tool for studying complex biological systems, but is often hampered by problems of speed and complexity when performing 3D volumetric imaging. Here, we present a multifocus imaging strategy based on the use of a simple z-splitter prism that can be assembled from off-the-shelf components. Our technique enables a widefield image stack to be distributed onto a single camera and recorded simultaneously. We exploit the volumetric nature of our image acquisition by further introducing a novel extended-volume 3D deconvolution strategy to suppress far-out-of-focus fluorescence background to significantly improve the contrast of our recorded images, conferring to our system a capacity for quasi-optical sectioning. By swapping in different z-splitter configurations, we can prioritize high speed or large 3D field-of-view imaging depending on the application of interest. Moreover, our system can be readily applied to a variety of imaging modalities in addition to fluorescence, such as phase-contrast and darkfield imaging. Because of its simplicity, versatility, and performance, we believe our system will be a useful tool for general biological or biomedical imaging applications.
UR - http://www.scopus.com/inward/record.url?scp=85095416625&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85095416625&partnerID=8YFLogxK
U2 - 10.1364/OPTICA.404678
DO - 10.1364/OPTICA.404678
M3 - Article
AN - SCOPUS:85095416625
SN - 2334-2536
VL - 7
SP - 1477
EP - 1486
JO - Optica
JF - Optica
IS - 11
ER -