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Speckle-based volume holographic microscopy for optically sectioned multi-plane fluorescent imaging.

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TLDR
The design, implementation, and experimental image data demonstrating the proposed speckle-based volume holographic microscopy system's ability to simultaneously obtain wide-field, optically sectioned, and multi-depth resolved images of fluorescently labeled microspheres and tissue structures are presented.
Abstract
Structured illumination microscopy has been widely used to reconstruct optically sectioned fluorescence images in wide-field fashion; however, it still requires axial scanning to obtain multiple depth information of a volumetric sample. In this paper, a new imaging scheme, called speckle-based volume holographic microscopy system, is presented. The proposed system incorporates volumetric speckle illumination and multiplexed volume holographic gratings to acquire multi-plane images with optical sectioning capability, without any axial scanning. We present the design, implementation, and experimental image data demonstrating the proposed system’s ability to simultaneously obtain wide-field, optically sectioned, and multi-depth resolved images of fluorescently labeled microspheres and tissue structures.

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Journal ArticleDOI

In vivo volumetric fluorescence sectioning microscopy with mechanical-scan-free hybrid illumination imaging.

TL;DR: The design, implementation, and experimentally demonstrate the proposed system's ability through 3D imaging of in vivo Canenorhabditis elegans' growth cones, with no mechanical moving parts.
Journal ArticleDOI

Volume holographic spatial-spectral imaging systems [Invited].

TL;DR: An overview of the recent developments in applications of volume holographic imaging techniques in microscopy is presented and simultaneous multiplane fluorescence microscopy for collecting spatial-spectral information is distinct and has great potential for hyperspectral imaging.
Journal ArticleDOI

Speckle illumination holographic non‐scanning fluorescence endoscopy

TL;DR: Wide-field, multiplane, optical sectioning endoscopic imaging, incorporating 3D active speckle-based illumination and multiplexed volume holographic gratings, to simultaneously obtain images of fluorescently labeled tissue structures from different depths, without the need of scanning.
Journal ArticleDOI

Multi-focus microscope with HiLo algorithm for fast 3-D fluorescent imaging

TL;DR: A new multi-focus microscope (MFM) system based on a phase mask and HiLo algorithm, achieving high-speed, high-resolution, low-noise 3-D fluorescent imaging, e.g., recording fast dynamic events at multiple depths in vivo.
Journal ArticleDOI

Talbot multi-focal holographic fluorescence endoscopy for optically sectioned imaging

TL;DR: The design, implementation, and experimental data demonstrating this endoscopic system's ability to obtain optically sectioned multi-plane fluorescent images of tissue samples in wide-field fashion without scanning in lateral and axial directions are described.
References
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Journal ArticleDOI

Coupled wave theory for thick hologram gratings

TL;DR: In this paper, a coupled wave analysis of the Bragg diffraction of light by thick hologram gratings is given, analogous to Phariseau's treatment of acoustic gratings and to the dynamical theory of X-ray diffraction.
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Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy.

TL;DR: This work developed digital scanned laser light sheet fluorescence microscopy and recorded nuclei localization and movement in entire wild-type and mutant zebrafish embryos over the first 24 hours of development to derive a model of germ layer formation and show that the mesendoderm forms from one-third of the embryo's cells in a single event.
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Fluorescence microscopy today.

TL;DR: The introduction of green fluorescent protein (GFP) and two-photon microscopy has allowed systematic imaging studies of protein localization in living cells and of the structure and function of living tissues.
Journal ArticleDOI

Optical sectioning microscopy.

TL;DR: The core concepts of confocal microscopes and important variables that adversely affect confocal images are described and computational optical sectioning techniques that can perform Optical sectioning without a confocal microscope are discussed.
Journal ArticleDOI

Fast, high-contrast imaging of animal development with scanned light sheet-based structured-illumination microscopy

TL;DR: This method discriminates the specimen-related scattered background from signal fluorescence, thereby removing out-of-focus light and optimizing the contrast of in-focus structures, and provides rapid control of the illumination pattern, exceptional imaging quality and high imaging speeds.
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