Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

22.0K
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,...
22.0K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

14.8K
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...
14.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Widefield pump-probe microscopy with coherent background subtraction by angle-compensated temporal shearing.

Optics express·2026
Same author

Subthreshold membrane depolarization powerfully engages intracellular calcium dynamics in the brain.

bioRxiv : the preprint server for biology·2026
Same author

Implications of temporal sampling in voltage imaging microscopy.

ArXiv·2026
Same author

Relative phase of membrane potential theta oscillations between individual hippocampal neurons code space.

bioRxiv : the preprint server for biology·2025
Same author

Superresolution imaging of live samples by centroid reassignment microscopy.

bioRxiv : the preprint server for biology·2025
Same author

Ultrasensitive in vivo infrared spectroscopic imaging via oblique photothermal microscopy.

Nature communications·2025
Same journal

Method of spatial scanning of modulated laser radiation for outline imaging of interphalangeal joints.

Journal of biomedical optics·2026
Same journal

Multimodal optical imaging for the assessment of the teratogenic effects of ethanol on zebrafish development.

Journal of biomedical optics·2026
Same journal

Fluorescence properties of collagen types I-V: a comprehensive study of spectral and lifetime characteristics.

Journal of biomedical optics·2026
Same journal

Spectral dependence of lipofuscin fluorescence lifetimes revealed by FLIM with a superconducting nanowire single-photon detector.

Journal of biomedical optics·2026
Same journal

Building the future of biophotonics through experiential education and seasonal schools.

Journal of biomedical optics·2026
Same journal

Time-of-flight fluorescence depth mapping using a spatiotemporal deep learning model.

Journal of biomedical optics·2026
See all related articles

Related Experiment Video

Updated: Mar 28, 2026

Multimodal Imaging and Spectroscopy Fiber-bundle Microendoscopy Platform for Non-invasive, In Vivo Tissue Analysis
10:35

Multimodal Imaging and Spectroscopy Fiber-bundle Microendoscopy Platform for Non-invasive, In Vivo Tissue Analysis

Published on: October 17, 2016

8.4K

Fast optically sectioned fluorescence HiLo endomicroscopy.

Tim N Ford1, Daryl Lim, Jerome Mertz

  • 1Boston University, Department of Biomedical Engineering, Boston, Massachusetts 02215, USA. timford@bu.edu

Journal of Biomedical Optics
|April 3, 2012
PubMed
Summary
This summary is machine-generated.

We developed a new fiber bundle endomicroscope using HiLo imaging for fast, optically sectioned fluorescence imaging. This technique offers high resolution and reduced motion artifacts, making it suitable for real-time clinical optical biopsies.

More Related Videos

Video-rate Scanning Confocal Microscopy and Microendoscopy
14:10

Video-rate Scanning Confocal Microscopy and Microendoscopy

Published on: October 20, 2011

28.7K
High-resolution Fiber-optic Microendoscopy for in situ Cellular Imaging
13:49

High-resolution Fiber-optic Microendoscopy for in situ Cellular Imaging

Published on: January 12, 2011

35.3K

Related Experiment Videos

Last Updated: Mar 28, 2026

Multimodal Imaging and Spectroscopy Fiber-bundle Microendoscopy Platform for Non-invasive, In Vivo Tissue Analysis
10:35

Multimodal Imaging and Spectroscopy Fiber-bundle Microendoscopy Platform for Non-invasive, In Vivo Tissue Analysis

Published on: October 17, 2016

8.4K
Video-rate Scanning Confocal Microscopy and Microendoscopy
14:10

Video-rate Scanning Confocal Microscopy and Microendoscopy

Published on: October 20, 2011

28.7K
High-resolution Fiber-optic Microendoscopy for in situ Cellular Imaging
13:49

High-resolution Fiber-optic Microendoscopy for in situ Cellular Imaging

Published on: January 12, 2011

35.3K

Area of Science:

  • Biomedical optics
  • Medical imaging technology
  • Microscopy

Background:

  • Flexible fiber bundle endomicroscopy enables in vivo imaging.
  • Optical sectioning is crucial for high-resolution microscopy.
  • Existing methods may suffer from motion artifacts and slow processing.

Purpose of the Study:

  • To present an improved nonscanning fiber bundle endomicroscope.
  • To achieve fast, optically sectioned fluorescence imaging with real-time processing.
  • To demonstrate the utility of HiLo imaging for endomicroscopy.

Main Methods:

  • Utilized HiLo imaging combining uniform and structured illumination.
  • Employed a graphics processing unit (GPU) for real-time image processing.
  • Incorporated a double-shutter camera to minimize motion artifacts.

Main Results:

  • Achieved lateral and axial resolutions of 2.6 μm and 17 μm, respectively.
  • Attained a net frame rate of 9.5 Hz through GPU processing.
  • Demonstrated successful imaging of fluorescently labeled chorioallantoic membrane (CAM) in G. gallus embryos.

Conclusions:

  • The improved HiLo endomicroscope provides fast, high-resolution optical sectioning.
  • The system effectively reduces motion artifacts for clearer imaging.
  • This technique is a promising candidate for low-cost, high-speed clinical optical biopsies.