Related Experiment Video
Updated: Jan 17, 2026

12:44
Super-resolution Imaging of the Cytokinetic Z Ring in Live Bacteria Using Fast 3D-Structured Illumination Microscopy f3D-SIM
Published on: September 29, 2014
20.4K
Deep imaging by NIR-II multifocal structured illumination microscopy with enhanced super-resolution radial
Optics Letters
|January 15, 2026
Summary
New NIR-II MSIM-eSRRF microscopy combines techniques to overcome scattering and motion artifacts. This advanced deep imaging platform enhances resolution and contrast for studying live tissues, improving intravital microscopy.
Area of Science:
- Biomedical Imaging
- Optical Microscopy
- Super-resolution Microscopy
Background:
- Second near-infrared (NIR-II) multifocal structured illumination microscopy (MSIM) offers improved resolution and depth for turbid specimens.
- However, scattering-induced noise and motion artifacts limit its application in live-tissue imaging.
Purpose of the Study:
- To develop a novel microscopy technique that enhances deep imaging capabilities in scattering biological tissues.
- To overcome limitations of background noise and motion artifacts in NIR-II MSIM.
Main Methods:
- Integration of enhanced super-resolution radial fluctuation (eSRRF) with NIR-II MSIM.
- Testing the hybrid NIR-II MSIM-eSRRF platform on Intralipid phantoms, ex-vivo pork tissue, and live mice.
Main Results:
- NIR-II MSIM-eSRRF demonstrated improved spatial resolution and contrast in turbid specimens.
- The technique effectively suppressed motion artifacts, enabling artifact-free visualization of cerebral vasculature in live mice.
- Achieved enhanced deep imaging performance in challenging scattering environments.
Conclusions:
- NIR-II MSIM-eSRRF is a powerful tool for deep imaging in highly scattering environments.
- This platform advances intravital fluorescence microscopy for studying physiological processes.
- The technique holds promise for accelerating discoveries in live-tissue imaging research.
Related Concept Videos
Super-resolution Fluorescence Microscopy
12.2K
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...
12.2K
Three-Dimensional Microscopy in Microbiology
772
Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
772
Total Internal Reflection Fluorescence Microscopy
11.0K
Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
11.0K
Confocal Fluorescence Microscopy
20.0K
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,...
20.0K

