Unknown

Dataset Information

0

Speckle illumination holographic non-scanning fluorescence endoscopy.


ABSTRACT: Optical sectioning endoscopy such as confocal endoscopy offers capabilities to obtain three-dimensional (3D) information from various biological samples by discriminating between the desired in-focus signals and out-of-focus background. However, in general confocal images are formed through point-by-point scanning and the scanning time is proportional to the 3D space-bandwidth product. Recently, structured illumination endoscopy has been utilized for optically sectioned wide-field imaging, but it still needs axial scanning to acquire images from different depths of focal plane. Here, we report 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. We present the design, and implementation, as well as experimental data, demonstrating this endoscopic system's ability to obtain optically sectioned multiplane fluorescent images of tissue samples, with cellular level resolution in wide-field fashion, and no need for mechanical or optical axial scanning.(A) Schematic drawing of the SIHN endoscopy to simultaneously acquire multiplane images from different depths. (B) Uniform, and (C) SIHN illuminated images of standard fluorescence beads (25??m in diameter) for the two axial planes. (D) Intensity profile on fluorescently labeled signal (ie, in-focus) and background (ie, out-of-focus) of microspheres.

SUBMITTER: Lin WT 

PROVIDER: S-EPMC6466634 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Speckle illumination holographic non-scanning fluorescence endoscopy.

Lin Wei-Tang WT   Lin Chen-Yen CY   Singh Vijay Raj VR   Luo Yuan Y  

Journal of biophotonics 20180709 11


Optical sectioning endoscopy such as confocal endoscopy offers capabilities to obtain three-dimensional (3D) information from various biological samples by discriminating between the desired in-focus signals and out-of-focus background. However, in general confocal images are formed through point-by-point scanning and the scanning time is proportional to the 3D space-bandwidth product. Recently, structured illumination endoscopy has been utilized for optically sectioned wide-field imaging, but i  ...[more]

Similar Datasets

| S-EPMC4321697 | biostudies-literature
| S-EPMC4648106 | biostudies-literature
| S-EPMC8285059 | biostudies-literature
| S-EPMC7244762 | biostudies-literature
| S-EPMC6672017 | biostudies-literature
| S-EPMC6059898 | biostudies-other
| S-EPMC8270910 | biostudies-literature
| S-EPMC6279961 | biostudies-literature
| S-EPMC8443636 | biostudies-literature
| S-EPMC3691569 | biostudies-literature