Abstract

.Significance: High temporal stability, wavelength independency, and scalable field of view (FOV) are the primary requirements of a quantitative phase microscopy (QPM) system. The high temporal stability of the system provides accurate measurement of minute membrane fluctuations of the biological cells that can be an indicator of disease diagnosis.Aim: The main aim of this work is to develop a high temporal stable technique that can accurately quantify the cell’s dynamics such as membrane fluctuations of human erythrocytes. Further, the technique should be capable of acquiring scalable FOV and resolution at multiple wavelengths to make it viable for various biological applications.Approach: We developed a single-element nearly common path, wavelength-independent, and scalable resolution/FOV QPM system to obtain temporally stable holograms/interferograms of the biological specimens.Results: With the proposed system, the temporal stability is obtained without using any vibration isolation table. The capability of the proposed system is first demonstrated on USAF resolution chart and polystyrene spheres ( diameter). Further, the system is implemented for single shot, wavelength-independent quantitative phase imaging of human red blood cells (RBCs) with scalable resolution using color CCD camera. The membrane fluctuation of healthy human RBCs is also measured and was found to be around 47 nm.Conclusions: Contrary to its optical counterparts, the present system offers an energy efficient, cost effective, and simple way of generating object and reference beam for the development of common-path QPM. The present system provides the flexibility to the user to acquire multi-wavelength quantitative phase images at scalable FOV and resolution.

Highlights

  • The present system provides the flexibility to the user to acquire multiwavelength quantitative phase images at scalable field of view (FOV) and resolution

  • Quantitative phase microscopy (QPM) is a powerful technique, which works on the principle of interferometry.[1]

  • Are generally employed to produce two coherent beams, one from the reference arm and other from the object arm. These optical configurations for QPM, being non-common path in nature, suffer from several serious problems: time-varying phase noise due to vibration, temperature gradient, and air flow, which deteriorate the stability of QPM.[3,14]. These issues limit the application of QPM systems for the study of live cells dynamics, i.e., measurement of membrane fluctuations, which is a good indicator for the detection of several diseases.[14]

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Summary

Introduction

Quantitative phase microscopy (QPM) is a powerful technique, which works on the principle of interferometry.[1]. Are generally employed to produce two coherent beams, one from the reference arm and other from the object arm. These optical configurations for QPM, being non-common path in nature, suffer from several serious problems: time-varying phase noise due to vibration, temperature gradient, and air flow, which deteriorate the stability of QPM.[3,14] These issues limit the application of QPM systems for the study of live cells dynamics, i.e., measurement of membrane fluctuations, which is a good indicator for the detection of several diseases.[14]

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