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

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

6.7K
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...
6.7K
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

12.8K
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,...
12.8K
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

5.6K
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.
5.6K

You might also read

Related Articles

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

Sort by
Same author

Reconstruction from multi-planar MRI with foundation models for uterine fibroid analysis.

NPJ digital medicine·2026
Same author

Electrostatic asymmetry-assisted polarization enables tertiary amine anchoring in single-molecule junctions.

Chemical communications (Cambridge, England)·2026
Same author

Mendelian randomization evidence for a causal link between Epstein-Barr virus antibody levels and head and neck cancer risk.

Medicine·2026
Same author

Charge-Competition AIEgens Induce Mitochondrial Dysfunction for Selective Eradication of <i>Candida albicans</i> while Restoring Vaginal Microbiota.

Journal of microbiology and biotechnology·2026
Same author

Correction: Genetic Evidence Supports a Potential Role of WTAP-related m6A Regulation in Vascular Dementia: Insights from Mendelian Randomization and Multi-omics Analyses.

Journal of molecular neuroscience : MN·2026
Same author

Socioeconomic differences in help-seeking intention for stress urinary incontinence: evidence from an information-motivation-behavioral skills model framework.

Frontiers in public health·2026
Same journal

Correction to "Characterization of Cerebrovascular Changes in Mice Treated With Alcohol by Photoacoustic Imaging".

Journal of biophotonics·2026
Same journal

Defining Safe Light Intensity Limits of Near-Infrared Illumination Avoiding Skin Heating in Medical Optical Diagnostic Methods.

Journal of biophotonics·2026
Same journal

Review of the SWIR Windows to Study Osteoarthritis.

Journal of biophotonics·2026
Same journal

FTIR-ATR Spectroscopy as a Tool to Differentiate Listeria monocytogenes by Geno-Serogroups, Growth Conditions and Persistence Status.

Journal of biophotonics·2026
Same journal

Utilizing Serum Fluorescence Spectra and Machine Learning Algorithms for Efficient Diagnosis of Sheep Brucellosis.

Journal of biophotonics·2026
Same journal

Fluorescence Profiling of Water-Based Breast Tissue Homogenates Combined With Chemometric Analyses for Discrimination of Benign and Malignant Lesions.

Journal of biophotonics·2026
See all related articles

Related Experiment Video

Updated: May 10, 2025

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

8.9K

High-Resolution Lensless Microscopy Imaging Based on Fluorescence Intermittency.

Zhiping Zeng1, Xinyi Chen1, Biqing Xu1

  • 1College of Physics and Information Engineering, Fuzhou University, Fuzhou, China.

Journal of Biophotonics
|April 21, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces a lensless imaging microscopy technique that enhances spatial resolution by combining a phase mask, CMOS sensor, and fluorescence fluctuation super-resolution microscopy (FF-SRM) algorithms. The method achieves high-resolution imaging of subcellular organelles with improved simplicity and affordability.

Keywords:
fluorescence intermittencylensless imagingmulti‐algorithm synergysuper‐resolution reconstruction

More Related Videos

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip
14:09

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip

Published on: November 16, 2019

6.8K
Lensless Fluorescent Microscopy on a Chip
11:23

Lensless Fluorescent Microscopy on a Chip

Published on: August 17, 2011

17.6K

Related Experiment Videos

Last Updated: May 10, 2025

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

8.9K
High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip
14:09

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip

Published on: November 16, 2019

6.8K
Lensless Fluorescent Microscopy on a Chip
11:23

Lensless Fluorescent Microscopy on a Chip

Published on: August 17, 2011

17.6K

Area of Science:

  • Biophysics
  • Microscopy
  • Optical Engineering

Background:

  • Lensless imaging microscopy offers system compactness and cost-efficiency but typically has lower spatial resolution than lens-based systems.
  • Enhancing the spatial resolution of lensless microscopy is crucial for detailed biological imaging.

Purpose of the Study:

  • To develop a lensless imaging system with enhanced spatial resolution for visualizing subcellular structures.
  • To leverage fluorescence intermittency (FI) and super-resolution algorithms for improved lensless imaging.

Main Methods:

  • Integrated a phase mask and CMOS image sensor into a lensless imaging system.
  • Employed fluorescence fluctuation super-resolution microscopy (FF-SRM) algorithms to analyze fluorescence intermittency (FI).
  • Utilized Wiener deconvolution for image sequence processing and combined with expansion microscopy (ExM) and multi-algorithm synergy.

Main Results:

  • Lensless image sequences processed with Wiener deconvolution effectively retained FI information for FF-SRM reconstruction.
  • Achieved significant improvements in spatial resolution and image quality for lensless imaging.
  • Enabled clear visualization of biological subcellular organelles.

Conclusions:

  • The developed lensless imaging scheme significantly enhances spatial resolution through FF-SRM and FI analysis.
  • Combining ExM and multi-algorithm synergy further boosts resolution and image quality.
  • This approach provides a simple, affordable, and effective pathway for high-resolution lensless imaging.