Related Experiment Video
Updated: Feb 16, 2026

10:07
Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
Published on: April 9, 2014
10.6K
High-resolution adaptive optical imaging within thick scattering media using closed-loop accumulation of single
Sungsam Kang1,2, Pilsung Kang1,2, Seungwon Jeong1,2
1Center for Molecular Spectroscopy and Dynamics, Institute for Basic Science (IBS), Seoul, 02841, Korea.
Nature Communications
|December 20, 2017
Summary
This study introduces a novel optical coherence imaging method to overcome light scattering and aberrations in thick biological tissues. This technique significantly improves deep-tissue imaging resolution and depth, advancing microscopy capabilities.
Area of Science:
- Biomedical Optics
- Optical Imaging
- Microscopy
Background:
- Thick biological tissues cause light scattering and wave aberrations, limiting imaging depth and resolution in conventional optical microscopy.
- Existing methods struggle to address both multiple scattering and aberrations simultaneously, restricting sub-micron resolution to shallow depths.
Purpose of the Study:
- To develop an optical coherence imaging method capable of identifying and eliminating wave aberrations independently of multiple light scattering.
- To enhance deep-tissue imaging resolution and penetration depth in biological samples.
Main Methods:
- The proposed method utilizes time-gated complex-field maps of backscattered waves across multiple illumination channels.
- It employs a closed-loop optimization process for signal waves, incorporating both forward and phase-conjugation techniques.
- Aberrations of incident and reflected waves are identified and corrected separately.
Main Results:
- Demonstrated a Strehl ratio enhancement exceeding 500 times, significantly outperforming conventional adaptive optics.
- Achieved a spatial resolution of 600 nm.
- Enabled imaging at depths up to seven scattering mean free paths within biological tissues.
Conclusions:
- The developed optical coherence imaging method effectively overcomes the limitations of light scattering and aberrations in thick tissues.
- This advancement offers a substantial improvement in deep-tissue imaging resolution and penetration, paving the way for new biological investigations.
Related Concept Videos
Confocal Fluorescence Microscopy
21.3K
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,...
21.3K
Super-resolution Fluorescence Microscopy
14.6K
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...
14.6K

