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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.
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.
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,...

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Related Experiment Video

Updated: May 29, 2026

Fluorescence-quenching of a Liposomal-encapsulated Near-infrared Fluorophore as a Tool for In Vivo Optical Imaging
10:55

Fluorescence-quenching of a Liposomal-encapsulated Near-infrared Fluorophore as a Tool for In Vivo Optical Imaging

Published on: January 5, 2015

Upconversion fluorescent nanoparticles as a potential tool for in-depth imaging.

Sounderya Nagarajan1, Yong Zhang

  • 1Division of Bioengineering, Faculty of Engineering, National University of Singapore, Singapore, Singapore. nsounderya@nus.edu.sg

Nanotechnology
|September 6, 2011
PubMed
Summary
This summary is machine-generated.

Upconversion nanoparticles (UCNs) enable deep tissue imaging. These UCNs allowed imaging cells up to 3 mm deep, showing potential for biological applications.

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Last Updated: May 29, 2026

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An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation
11:20

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation

Published on: August 30, 2017

Area of Science:

  • Nanotechnology
  • Biomedical Imaging
  • Materials Science

Background:

  • Upconversion nanoparticles (UCNs) absorb near-infrared (NIR) light and emit visible or NIR light.
  • Their ability to utilize NIR light, which penetrates tissues effectively, makes them promising for biological imaging.
  • This study investigates the imaging depth achievable with UCNs in biological tissues.

Purpose of the Study:

  • To determine the maximum depth at which cells can be imaged using upconversion nanoparticles.
  • To evaluate the performance of UCNs with different emission properties (visible vs. NIR).
  • To assess the impact of targeted UCNs on imaging depth in specific cellular structures.

Main Methods:

  • Synthesis of NaYF(4) nanocrystals doped with Yb(3+)/Er(3+) or Yb(3+)/Tm(3+).
  • Silica modification for aqueous dispersion and biomolecule conjugation.
  • Characterization via transmission electron microscopy and fluorescence spectroscopy.
  • Imaging experiments using tissue phantoms mimicking skin/muscle tissue.

Main Results:

  • Cells were successfully imaged up to a depth of 3 mm using NIR-emitting UCNs.
  • The study demonstrated the feasibility of deep-tissue cell imaging with UCNs.
  • Evaluation of imaging depth for UCNs targeted to cardiac cell gap junctions was performed.

Conclusions:

  • Upconversion nanoparticles, particularly those emitting in the NIR, are effective for deep-tissue biological imaging.
  • The developed UCNs can image cells at depths relevant for various biomedical applications.
  • Targeted UCNs show potential for high-resolution imaging of specific cellular components at depth.