Quantitative reflection phase mesoscopy by remote coherence tuning of phase-shift interference patterns.

Sci Rep

1] Biomedical Engineering Department, Ben-Gurion University of the Negev, 1 Ben Gurion Blvd, Be'er-Sheva 8410501, Israel [2] Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev, 1 Ben Gurion Blvd, Be'er-Sheva 8410501, Israel.

Published: July 2015

AI Article Synopsis

  • Conventional low-magnification phase-contrast microscopy is traditionally a qualitative tool for studying clear objects on a larger scale, particularly in physical and biological environments.
  • By incorporating a phase-shifting Michelson interferometer into a standard microscope, researchers developed a new phase mesoscope that captures detailed and quantitative phase information from thin, transparent samples with high precision.
  • This advanced system demonstrates its effectiveness by mapping the uniformity of nanometer-thick glass and quantitatively analyzing human cancer cells, while also proving its potential for monitoring fluid dynamics over large areas.

Article Abstract

Conventional low-magnification phase-contrast microscopy is an invaluable, yet a qualitative, imaging tool for the interrogation of transparent objects over a mesoscopic millimeter-scale field-of-view in physical and biological settings. Here, we demonstrate that introducing a compact, unbalanced phase-shifting Michelson interferometer into a standard reflected brightfield microscope equipped with low-power infinity-corrected objectives and white light illumination forms a phase mesoscope that retrieves remotely and quantitatively the reflection phase distribution of thin, transparent, and weakly scattering samples with high temporal (1.38 nm) and spatial (0.87 nm) axial-displacement sensitivity and micrometer lateral resolution (2.3 μm) across a mesoscopic field-of-view (2.25 × 1.19 mm(2)). Using the system, we evaluate the etch-depth uniformity of a large-area nanometer-thick glass grating and show quantitative mesoscopic maps of the optical thickness of human cancer cells without any area scanning. Furthermore, we provide proof-of-principle of the utility of the system for the quantitative monitoring of fluid dynamics within a wide region.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517165PMC
http://dx.doi.org/10.1038/srep12560DOI Listing

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