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Updated: May 4, 2026

Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules
Published on: August 8, 2019
Immersion Mirau interferometry for label-free live cell imaging in an epi-illumination geometry
Oleksandra V Lyulko1, Gerhard Randers-Pehrson1, David J Brenner1
1Center for Radiological Research, Columbia University, New York, NY 10533.
Insights
Immersion Mirau Interferometry (IMI) offers label-free imaging for living cells, avoiding UV-light damage. Simultaneous Immersion Mirau Interferometry (SIMI) overcomes vibration sensitivity, enabling high-quality cell imaging for experiments.
Area of Science:
- Cell biology
- Optical microscopy
- Biophysics
Background:
- Fluorescent stains and UV-light can damage cells during imaging.
- Label-free imaging techniques are crucial for studying live cells.
- Phase-shifting interferometry (PSI) is sensitive to environmental vibrations.
Purpose of the Study:
- To develop and validate Immersion Mirau Interferometry (IMI) for label-free imaging of living cells in medium.
- To introduce Simultaneous Immersion Mirau Interferometry (SIMI) to overcome vibration limitations of PSI.
- To enable high-quality cell imaging for subsequent targeted irradiation experiments.
Main Methods:
- Designed and built a custom immersion Mirau interferometric attachment for microscopy.
- Employed phase-shifting interferometry (PSI) principles.
- Developed SIMI using polarization optics for simultaneous interferogram acquisition, spatially separating two interferograms.
Main Results:
- IMI and SIMI successfully imaged live and fixed cells.
- The custom attachment ensured identical optical paths in test and reference arms.
- SIMI effectively eliminated vibration-induced artifacts, producing high-quality images.
Conclusions:
- IMI and SIMI are effective label-free imaging techniques for cell biology.
- The developed system provides sufficient image quality for targeted cellular irradiation.
- SIMI represents a significant advancement in interferometric microscopy for live-cell studies.
Abstract:
In cell biology studies it is often important to avoid the damaging effects caused by fluorescent stains or UV-light. Immersion Mirau Interferometry (IMI) is an epi-illumination label-free imaging technique developed at the Columbia University Radiological Research Accelerator Facility. It is based on the principles of phase-shifting interferometry (PSI) and represents a novel approach for interferometric imaging of living cells in medium. To accommodate the use of medium, a custom immersion Mirau interferometric attachment was designed and built in-house. The space between the reference mirror and the beam splitter is filled with liquid to ensure identical optical paths in the test and reference arms. The interferometer is mountable onto a microscope objective. The greatest limitation of standard PSI is the sensitivity to environmental vibrations, because it requires consecutive acquisition of several interferograms. We are developing Simultaneous Immersion Mirau Interferometry (SIMI), which facilitates simultaneous acquisition of all interferograms and eliminates the effects of vibration. Polarization optics, incorporated into the design, introduces a phase delay to one of the components of the test beam. This enables simultaneous creation and spatial separation of two interferograms, which are combined with the background image to reconstruct the intensity map of the specimen. Our results of imaging live and fixed cells with IMI and SIMI show that this system produces images of a quality that is sufficient to perform targeted cellular irradiation experiments.
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