Correction of Eq. (20) in our published article [Opt. Express18, 22527 (2010)10.1364/OE.18.022527].
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http://dx.doi.org/10.1364/OE.421444 | DOI Listing |
J Biophotonics
July 2022
College of Information Science and Engineering, Fujian Key Laboratory of Light Propagation and Transformation, Huaqiao University, Xiamen, Fujian, China.
Quantitative phase microscopy (QPM) has been emerged as an indispensable diagnostic and characterization tool in biomedical imaging with its characteristic nature of label-free, noninvasive, and real time imaging modality. The integration of holography to the conventional microscopy opens new advancements in QPM featuring high-resolution and quantitative three-dimensional image reconstruction. However, the holography schemes suffer in space-bandwidth and time-bandwidth issues in the off-axis and phase-shifting configuration, respectively.
View Article and Find Full Text PDFA volume holographic (VHG) grating-based multi-plane differential confocal microscopy (DCM) is proposed for axial scan-free imaging. Also, we briefly reviewed our previous works on volume holographic-based confocal imaging. We show that without degrading imaging performance, it is possible to simultaneously obtain two depth-resolved optically sectioned images with improved axial resolution using multi-plane DCM.
View Article and Find Full Text PDFCorrection of Eq. (20) in our published article [Opt. Express18, 22527 (2010)10.
View Article and Find Full Text PDFJ Biomed Opt
November 2020
National Taiwan University, Institute of Medical Device and Imaging, Taipei, Taiwan.
Significance: Two-photon (2P) fluorescence imaging can provide background-free high-contrast images from the scattering tissues. However, obtaining a multiplane image is not straightforward. We present a two-photon volume holographic imaging (2P-VHI) system for multiplane imaging.
View Article and Find Full Text PDFA contemporary challenge across the natural sciences is the simultaneous optical imaging or stimulation of small numbers of cells or colloidal particles organized into arbitrary geometries. We demonstrate the use of temporal focusing with holographic optical tweezers in order to achieve depth-resolved two-photon imaging of trapped objects arranged in arbitrary three-dimensional (3D) geometries using a single objective. Trapping allows for the independent position control of multiple objects by holographic beam shaping.
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