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 Experiment Videos

High-resolution line-scanning optical coherence microscopy.

Yu Chen1, Shu-Wei Huang, Aaron D Aguirre

  • 1Department of Electrical Engineering and Computer Science and Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA. chen-yu@mit.edu

Optics Letters
|July 17, 2007
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Long noncoding RNA SALTe1, microvascular ageing, and cardiac dysfunction.

European heart journal·2026
Same author

Diagnostic accuracy of two-photon fluorescence microscopy in Mohs surgery of basal cell carcinomas.

Journal of the American Academy of Dermatology·2026
Same author

The Harvard-Emory ECG Database.

Scientific data·2026
Same author

Large Hypertransmission Defects Exhibit Choriocapillaris Flow Speed Impairment in Nonexudative Age-Related Macular Degeneration.

Ophthalmology science·2026
Same author

Rapid evaluation of muscularis propria in transurethral resection of bladder tumour specimens using non-linear microscopy (NLM).

Journal of clinical pathology·2025
Same author

Re-evaluating basophil count as a hematological indicator for bone density: a subgroup analysis from an East Asian population.

Frontiers in endocrinology·2025

This study introduces a novel optical coherence microscopy system for high-resolution imaging of biological tissues. The new line-scan method offers enhanced sensitivity and real-time cellular imaging capabilities.

Area of Science:

  • Biomedical optics
  • Microscopy
  • Optical imaging

Background:

  • Optical coherence microscopy (OCM) is a powerful technique for non-invasive imaging.
  • Traditional OCM systems can be limited by sensitivity to scattering and motion artifacts.
  • Advancements are needed for real-time, high-resolution imaging of biological samples.

Purpose of the Study:

  • To demonstrate a novel optical coherence microscopy system utilizing line illumination and detection.
  • To evaluate the system's resolution, sensitivity, and imaging speed.
  • To assess its suitability for real-time cellular-level imaging of biological tissues.

Main Methods:

  • Implementation of a Linnik-type interferometer.
  • Illumination with a broadband Ti:sapphire laser.

Related Experiment Videos

  • Detection using a high-speed, line-scan CCD camera.
  • Development of a line illumination and detection approach.
  • Main Results:

    • Achieved spatial resolutions of approximately 2 micrometers (transverse) x 3 micrometers (axial).
    • Demonstrated high sensitivity of 93 dB with averaging over 30 line scans.
    • Enabled en face, real-time, cellular-level imaging of biological tissues at approximately 2 frames/s.
    • Showed reduced sensitivity to incoherent scattering and sample motion compared to full-field imaging.

    Conclusions:

    • The developed line-scan optical coherence microscopy system provides high-resolution and sensitive imaging.
    • The system is capable of real-time, cellular-level visualization of biological tissues.
    • This approach offers advantages over traditional full-field imaging methods for dynamic biological samples.