Spatially multiplexed interferometric microscopy: principles and applications to biomedical imaging
Abstract Digital holographic microscopy (DHM) applied to quantitative phase imaging (QPI) has been successfully demonstrated as a powerful label-free method to analyse the optical properties of cells. Spatially multiplexed interferometric microscopy (SMIM) is a DHM technique that implements a common...
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Published in | JPhys photonics Vol. 3; no. 3; pp. 34005 - 34020 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Bristol
IOP Publishing
01.07.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract
Digital holographic microscopy (DHM) applied to quantitative phase imaging (QPI) has been successfully demonstrated as a powerful label-free method to analyse the optical properties of cells. Spatially multiplexed interferometric microscopy (SMIM) is a DHM technique that implements a common-path interferometric layout in the embodiment of a standard microscope to achieve QPI. More concretely, SMIM introduces three minimal modifications: (a) replaces the broadband illumination of the microscope by a coherent or partially coherent light source, (b) divides the input plane into two or three regions for transmission in parallel of both imaging and reference beams, and (c) includes a one-dimensional (1D) diffraction grating or a beam splitter cube for holographic recording. Hence, SMIM is a cost-effective, extremely simple, and highly stable manner of converting a standard bright field microscope into a holographic one. The goal of this contribution is to present the SMIM approaches implemented using a 1D diffraction grating, and highlight vast range of capabilities for biomedical imaging including super-resolved, reflective, transflective, noise-reduced and single-shot slightly off-axis amplitude and phase imaging. |
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Bibliography: | JPPHOTON-100340 |
ISSN: | 2515-7647 2515-7647 |
DOI: | 10.1088/2515-7647/abfc59 |