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Related Concept Videos

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,...
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.

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Multiplexing Focused Ultrasound Stimulation with Fluorescence Microscopy
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Pulsed-light imaging for fluorescence guided surgery under normal room lighting.

Kristian Sexton1, Scott C Davis, David McClatchy

  • 1Thayer School of Engineering at Dartmouth College, Hanover, New Hampshire 03755, USA. kristian.j.sexton.th@dartmouth.edu

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This study introduces a novel fluorescence-guided surgery (FGS) system that works in normal room light. This innovation improves surgical workflow by eliminating the need for dim lighting, enhancing visualization of fluorescent markers.

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Area of Science:

  • Medical technology
  • Surgical imaging
  • Biophotonics

Background:

  • Fluorescence-guided surgery (FGS) enhances surgical outcomes but requires dim lighting, disrupting workflow.
  • Current FGS systems necessitate dark environments, posing practical challenges in operating rooms.

Purpose of the Study:

  • To develop a novel FGS system capable of imaging fluorescence under normal room lighting conditions.
  • To overcome the workflow disruptions associated with traditional dim-light FGS systems.

Main Methods:

  • A new FGS system utilizing pulsed excitation and gated acquisition was designed.
  • Performance was evaluated using tissue-simulating phantoms and in vivo orthotopic brain tumor models in mice.

Main Results:

  • The system achieved visual detection of protoporphyrin IX down to 0.25 μM under 125 μW/cm2 ambient light.
  • Sensitivity was demonstrated to be over an order of magnitude greater than a commercial FGS system (Zeiss Pentero) operating in the dark.
  • In vivo studies showed superior sensitivity for detecting orthotopic brain tumors.

Conclusions:

  • The novel pulsed-light FGS system enables fluorescence imaging under normal room light, significantly improving upon existing technologies.
  • This advancement offers enhanced sensitivity and overcomes workflow limitations, paving the way for broader adoption of FGS.