Sentence examples for quantitative phase microscopy from inspiring English sources

Compared to other traditional optical techniques such as phase contrast microscopy or differential interference contrast microscopy, quantitative phase microscopy (QPM) has been developed to visualize and quantitatively analyze the distribution of phase shift of transmitted light through a specimen with nanometer resolution [ 1– 3].

Non-stained cells are imaged either by quantitative phase microscopy (QPm) [IATIA, Box Hill North, Victoria, 3129, Australia [1]] or by Mirau interferometry.

We present a technical overview of a multimodal system combining Raman microspectroscopy and quantitative phase microscopy (QPM), which allows two independent and simultaneous measurements of both the local molecular content and dynamic sample morphology.

We presented the implementation of a multimodal microscope which combines Raman imaging, based on a parallel detection scheme through a line scanning configuration, and quantitative phase microscopy (QPM) based on off-axis digital holographic microscopy (DHM).

This second modality is based on quantitative phase microscopy (QPM), implemented as a digital holographic microscope (DHM), a wide-field imaging technique which enables the measurement of the quantitative phase shifts induced by the sample [11].

However, the majority of images obtained through quantitative phase microscopy is integrated along the illumination angle and cannot reflect additional information about the refractive map on a certain plane.

A further method, called dual-interference-channel quantitative-phase microscopy (DQPM), is based on a dual-channel interferometric setup that is able to simultaneously obtain two phase-shifted interferograms of the same sample [ 17, 18].

As a newly devised microscopy technique, this combination of full-field quantitative phase microcopy and interference reflection microscopy has demonstrated applications in the evaluation of cellular structure, height of cell, and adherent surface.

The candidates of label-free optical technique to determine the refractive index of hiPS cells would be the low-coherence quantitative phase microscope [ 8], the tomographic phase microscope [ 22] and the full-field optical coherence microscopy [ 23].

The transmitted light through cells was focused by the objective lens (UAPO20XW340/0.7, Olympus, Japan) and led to the quantitative phase imaging unit based on the diffraction phase microscopy described in reference [ 9].

The interferometric phase microscopy could provide the quantitative phase images associated with the optical path delays.