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Dual-interference-channel quantitative-phase microscopy of live cell dynamics.

Publication ,  Journal Article
Shaked, NT; Rinehart, MT; Wax, A
Published in: Optics letters
March 2009

We introduce and experimentally demonstrate a fast and accurate method for quantitative imaging of the dynamics of live biological cells. Using a dual-channel interferometric setup, two phase-shifted interferograms of nearly transparent biological samples are acquired in a single digital camera exposure and digitally processed into the phase profile of the sample. Since two interferograms of the same sample are acquired simultaneously, most of the common phase noise is eliminated, enabling the visualization of millisecond-scale dynamic biological phenomena with subnanometer optical path length temporal stability.

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Published In

Optics letters

DOI

EISSN

1539-4794

ISSN

0146-9592

Publication Date

March 2009

Volume

34

Issue

6

Start / End Page

767 / 769

Related Subject Headings

  • Signal Processing, Computer-Assisted
  • Sensitivity and Specificity
  • Reproducibility of Results
  • Rats
  • Optics
  • Myocytes, Cardiac
  • Myocardial Contraction
  • Microscopy, Interference
  • Image Enhancement
  • Equipment Failure Analysis
 

Citation

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Shaked, N. T., Rinehart, M. T., & Wax, A. (2009). Dual-interference-channel quantitative-phase microscopy of live cell dynamics. Optics Letters, 34(6), 767–769. https://doi.org/10.1364/ol.34.000767
Shaked, Natan T., Matthew T. Rinehart, and Adam Wax. “Dual-interference-channel quantitative-phase microscopy of live cell dynamics.Optics Letters 34, no. 6 (March 2009): 767–69. https://doi.org/10.1364/ol.34.000767.
Shaked NT, Rinehart MT, Wax A. Dual-interference-channel quantitative-phase microscopy of live cell dynamics. Optics letters. 2009 Mar;34(6):767–9.
Shaked, Natan T., et al. “Dual-interference-channel quantitative-phase microscopy of live cell dynamics.Optics Letters, vol. 34, no. 6, Mar. 2009, pp. 767–69. Epmc, doi:10.1364/ol.34.000767.
Shaked NT, Rinehart MT, Wax A. Dual-interference-channel quantitative-phase microscopy of live cell dynamics. Optics letters. 2009 Mar;34(6):767–769.
Journal cover image

Published In

Optics letters

DOI

EISSN

1539-4794

ISSN

0146-9592

Publication Date

March 2009

Volume

34

Issue

6

Start / End Page

767 / 769

Related Subject Headings

  • Signal Processing, Computer-Assisted
  • Sensitivity and Specificity
  • Reproducibility of Results
  • Rats
  • Optics
  • Myocytes, Cardiac
  • Myocardial Contraction
  • Microscopy, Interference
  • Image Enhancement
  • Equipment Failure Analysis