Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Mar 15;45(6):1487-1490.
doi: 10.1364/OL.379732.

Harmonically decoupled gradient light interference microscopy (HD-GLIM)

Harmonically decoupled gradient light interference microscopy (HD-GLIM)

Yi Wang et al. Opt Lett. .

Abstract

Differential phase sensitive methods, such as Nomarski microscopy, play an important role in quantitative phase imaging due to their compatibility with partially coherent illumination and excellent optical sectioning ability. In this Letter, we propose a new system, to the best of our knowledge, to retrieve differential phase information from transparent samples. It is based on a 4f optical system with an amplitude-type spatial light modulator (SLM), which removes the need for traditional differential interference contrast (DIC) optics and specialized phase-only SLMs. We demonstrate the principle of harmonically decoupled gradient light interference microscopy using standard samples, as well as static and dynamic biospecimens.

PubMed Disclaimer

Conflict of interest statement

Disclosures. The authors declare no conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Schematic demonstration of HD-GLIM system. Four phase-shifted patterns with Δδ = π/2 are added on the SLM.
Fig. 2.
Fig. 2.
(a) Phase distribution of 4.5 μm polymetric microbeads. (b) Simulation and measurement data.
Fig. 3.
Fig. 3.
(a) and (b) Spatiotemporal noise distribution with log operation at kx = 0 and kx = π. (c) Spatial noise distribution. (d) Temporal phase fluctuation of the point marked in (c). Color bar in (a) and (b) is rad2/[rad/ μm]2 [rad/s].
Fig. 4.
Fig. 4.
(a)-(d) Four differential interference data used for phase demodulation. (e)-(f) Phase of CW620 cells and its corresponding details.
Fig. 5.
Fig. 5.
(a)-(d) Four differential interference data used for phase demodulation. (e)-(g) Phase of pancreas tissue and its different details.
Fig. 6.
Fig. 6.
(a) and (b) Phase results under NAc = 0.09. (c) and (d) are the phase results under NAc = 0.55.

References

    1. Popescu G, Quantitative Phase Imaging of Cells and Tissues (McGraw-Hill, 2011).
    1. Marquet P, Rappaz B, Magistretti PJ, Cuche E, Emery Y, Colomb T, and Depeursinge C, Opt. Lett 30,468 (2005). - PubMed
    1. Arnison MR, Larkin KG, Sheppard CJ, Smith NI, and Cogswell CJ, J. Microsc 214, 7 (2004). - PubMed
    1. Ding H, Wang Z, Nguyen F, Boppart SA, and Popescu G, Phys. Rev. Lett 101, 238102 (2008). - PMC - PubMed
    1. Merola F, Memmolo P, Miccio L, Savoia R, Mugnano M, Fontana A, D’Ippolito G, Sardo A, Iolascon A, and Gambale A, Light Sci. Appl 6, e16241 (2017). - PMC - PubMed