Related Experiment Video
Updated: Jul 11, 2025

09:04
Lens-free Video Microscopy for the Dynamic and Quantitative Analysis of Adherent Cell Culture
Published on: February 23, 2018
9.5K
E2E-BPF microscope: extended depth-of-field microscopy using learning-based implementation of binary phase filter and
Baekcheon Seong1, Woovin Kim1, Younghun Kim1
1Department of Mechanical Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Light, Science & Applications
|November 12, 2023
Summary
This study introduces the E2E-BPF microscope, a novel computational imaging platform. It achieves high-resolution, large-area imaging without refocusing, significantly extending the depth-of-field for biomedical applications.
Area of Science:
- Biomedical imaging
- Optical microscopy
- Computational imaging
Background:
- High-resolution imaging is crucial for biomedical diagnoses.
- Conventional microscopes face a trade-off between depth-of-field and spatial resolution, necessitating time-consuming refocusing.
- Large-scale imaging requires extended depth-of-field capabilities.
Purpose of the Study:
- To develop a computational imaging platform for large-area, high-resolution imaging without serial refocusing.
- To overcome the depth-of-field limitation in conventional microscopy.
- To enable rapid, image-based biomedical diagnoses.
Main Methods:
- Developed a physics-incorporated, deep-learned binary phase filter (BPF).
- Employed a jointly optimized deconvolution neural network.
- Integrated BPF design with deconvolution for extended depth-of-field imaging.
Main Results:
- Achieved high-resolution, high-contrast imaging over extended depth ranges.
- Demonstrated a 15.5-fold larger depth-of-field compared to conventional microscopes.
- Validated through numerical simulations and experiments with fluorescent beads, cells, and tissue sections.
Conclusions:
- The E2E-BPF microscope offers a scalable strategy for depth-of-field-extended optical imaging.
- This method enables large-area, high-resolution imaging without the need for refocusing.
- Potential applications include rapid diagnosis, optical vision, and metrology.
Related Concept Videos
Super-resolution Fluorescence Microscopy
7.0K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.0K
Confocal Fluorescence Microscopy
13.3K
Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
13.3K
Phase Contrast and Differential Interference Contrast Microscopy
8.1K
Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
8.1K

