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Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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 developed.
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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,...
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

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.

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Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
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Published on: April 9, 2014

Upconversion Nanoparticle-Guided Virtual Deformable Mirror for Computational Adaptive Optics in Scattering

Weilong Kong1, Yu Huang2, Congyi Feng1

  • 1School of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu, China.

Nano Letters
|June 23, 2026
PubMed
Summary
This summary is machine-generated.

We developed virtual deformable mirror adaptive optics (VDM-AO), a digital method for correcting deep-tissue optical aberrations. This technique uses upconversion nanoparticles as guide stars, enabling high-resolution imaging without complex hardware.

Keywords:
aberration correctionadaptive opticsdeep learningupconversion nanoparticles

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Area of Science:

  • Biomedical Optics
  • Microscopy
  • Computational Imaging

Background:

  • Deep-tissue fluorescence microscopy suffers from optical aberrations, reducing image quality and resolution.
  • Conventional adaptive optics (AO) systems are complex, hardware-intensive, and limited in speed for photon-scarce deep-tissue imaging.

Purpose of the Study:

  • To introduce a novel computational adaptive optics framework, virtual deformable mirror AO (VDM-AO), for digital aberration correction.
  • To enable high-resolution deep-tissue imaging without physical wavefront modulators.

Main Methods:

  • Developed a deep-learning framework (VDM-AO) integrating Zernike aberration modeling and a residual channel attention network.
  • Utilized dual-near-infrared lanthanide-doped upconversion nanoparticles (UCNPs) as embedded guide stars for aberration sensing in scattering tissue.
  • Digitally reconstructed aberration-corrected images from distorted inputs.

Main Results:

  • VDM-AO successfully corrected severe optical aberrations in scattering tissue.
  • Achieved high-resolution fluorescence imaging at depths up to 360 μm.
  • Demonstrated accurate recovery of distorted images.

Conclusions:

  • VDM-AO offers a hardware-free, digital solution for aberration correction in deep-tissue microscopy.
  • The integration of UCNP guide stars with computational AO provides a low-cost, high-throughput method for reliable deep-tissue imaging.