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

Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

6.8K
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
6.8K
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

15.4K
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,...
15.4K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

8.5K
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...
8.5K

You might also read

Related Articles

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

Sort by
Same author

Canine Halitosis Improved With a Postbiotic: A Validation Study.

Journal of veterinary dentistry·2026
Same author

Electrically switchable continuous phase liquid crystal Fresnel zone plate.

Light, science & applications·2026
Same author

A Postbiotic Positively Shifts the Canine Oral Microbiome.

Journal of veterinary dentistry·2026
Same author

Raman Microspectroscopy for Structural Indication in Ultrafast Laser Writing.

Small methods·2026
Same author

Wavefront estimation through structured detection in laser scanning microscopy.

Biomedical optics express·2026
Same author

Inaugural message from the new Co-Editor-in-Chief.

Light, science & applications·2026
Same journal

Generalizable framework for multi-site bone density prediction using non-dominant wrist optical biomarkers.

Biomedical optics express·2026
Same journal

Erratum: Review of dynamic optical coherence tomography for intracellular motility [Invited]: errata.

Biomedical optics express·2026
Same journal

Digital-micromirror-device-based illumination strategies for background suppression in single-molecule localization microscopy.

Biomedical optics express·2026
Same journal

Synergistic combination of convective self-assembly and hollow core fiber for sensitive SERS detection of glucose molecules.

Biomedical optics express·2026
Same journal

Multimodal diagnostic network integrating infrared and mass spectra for lung cancer.

Biomedical optics express·2026
Same journal

Multimodal Optical Biosensing for Precision Medicine and Healthcare: Introduction to the feature issue.

Biomedical optics express·2026
See all related articles

Related Experiment Video

Updated: Sep 30, 2025

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy oSLO and Optical Coherence Tomography OCT
12:22

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy oSLO and Optical Coherence Tomography OCT

Published on: August 4, 2018

8.6K

Repeated imaging through a multimode optical fiber using adaptive optics.

Carla C Schmidt1,2, Raphaël Turcotte3,2, Martin J Booth4

  • 1Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, United Kingdom.

Biomedical Optics Express
|March 14, 2022
PubMed
Summary
This summary is machine-generated.

This study presents a novel method for high-quality fluorescence imaging in deep brain regions using multimode optical fibers (MMF). A custom headplate and adaptive optics enable precise MMF repositioning for repeated, reliable imaging.

More Related Videos

Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping
09:43

Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping

Published on: March 20, 2017

10.0K
Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

10.2K

Related Experiment Videos

Last Updated: Sep 30, 2025

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy oSLO and Optical Coherence Tomography OCT
12:22

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy oSLO and Optical Coherence Tomography OCT

Published on: August 4, 2018

8.6K
Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping
09:43

Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping

Published on: March 20, 2017

10.0K
Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

10.2K

Area of Science:

  • Neuroscience
  • Optical Engineering
  • Biomedical Imaging

Background:

  • Multimode optical fibers (MMF) offer potential for minimally invasive deep brain fluorescence imaging.
  • Repeated imaging is crucial for studying synaptic roles in neurological function and disease.
  • Current MMF imaging requires calibration, which is invalidated by manual repositioning for repeated measurements.

Purpose of the Study:

  • To develop a robust method for high-quality fluorescence imaging using MMF that overcomes calibration issues associated with repeated repositioning.
  • To enable long-term, repeated imaging in the same brain region for neuroscience research.

Main Methods:

  • A two-step solution was implemented: a custom headplate for precise MMF implant reinsertion and sensorless adaptive optics to correct positional shifts.
  • The headplate ensures low-quality focusing upon reinsertion.
  • Adaptive optics corrects translational shifts to achieve high-quality imaging foci.

Main Results:

  • The combined approach successfully enabled fluorescence imaging after repeated removal and reinsertion of the MMF.
  • High-quality imaging foci were generated despite manual repositioning challenges.
  • The method addresses the calibration invalidation problem for longitudinal MMF imaging.

Conclusions:

  • This technique provides a reliable solution for repeated, high-quality fluorescence imaging of deep brain regions using MMF.
  • It facilitates long-term studies of brain function and disease by enabling consistent MMF placement.
  • The developed system enhances the utility of MMF for advanced neuroscience research.