| Literature DB >> 24392197 |
Oleksandra V Lyulko1, Gerhard Randers-Pehrson1, David J Brenner1.
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.Entities:
Keywords: Interferometry; dynamic imaging; label-free imaging; live cell imaging.; no-stain imaging; phase shifting; polarization; simultaneous interferometric imaging; vibration
Year: 2010 PMID: 24392197 PMCID: PMC3877336 DOI: 10.1117/12.855651
Source DB: PubMed Journal: Proc SPIE Int Soc Opt Eng ISSN: 0277-786X