Quantitative phase imaging of erythrocytes under microfluidic constriction in a high refractive index medium reveals water content changes.

Abstract

Changes in the deformability of red blood cells can reveal a range of pathologies. For example, cells which have been stored for transfusion are known to exhibit progressively impaired deformability. Thus, this aspect of red blood cells has been characterized previously using a range of techniques. In this paper, we show a novel approach for examining the biophysical response of the cells with quantitative phase imaging. Specifically, optical volume changes are observed as the cells transit restrictive channels of a microfluidic chip in a high refractive index medium. The optical volume changes indicate an increase of cell's internal density, ostensibly due to water displacement. Here, we characterize these changes over time for red blood cells from two subjects. By storage day 29, a significant decrease in the magnitude of optical volume change in response to mechanical stress was witnessed. The exchange of water with the environment due to mechanical stress is seen to modulate with storage time, suggesting a potential means for studying cell storage.

Department

Description

Provenance

Subjects

Engineering, Other photonics

Citation

Published Version (Please cite this version)

10.1038/s41378-019-0113-y

Publication Info

Park, Han Sang, Will J Eldridge, Wen-Hsuan Yang, Michael Crose, Silvia Ceballos, John D Roback, Jen-Tsan Ashley Chi, Adam Wax, et al. (2019). Quantitative phase imaging of erythrocytes under microfluidic constriction in a high refractive index medium reveals water content changes. Microsystems & nanoengineering, 5(1). p. 63. 10.1038/s41378-019-0113-y Retrieved from https://hdl.handle.net/10161/19666.

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Scholars@Duke

Wax

Adam P. Wax

Professor of Biomedical Engineering

Dr. Wax's research interests include optical spectroscopy for early cancer detection, novel microscopy and interferometry techniques.

The study of intact, living cells with optical spectroscopy offers the opportunity to observe cellular structure, organization and dynamics in a way that is not possible with traditional methods. We have developed a set of novel spectroscopic techniques for measuring spatial, temporal and refractive structure on sub-hertz and sub-wavelength scales based on using low-coherence interferometry (LCI) to detect scattered light. We have applied these techniques in different types of cell biology experiments. In one experiment, LCI measurements of the angular pattern of backscattered light are used to determine non-invasively the structure of sub-cellular organelles in cell monolayers, and the components of epithelial tissue from freshly excised rat esophagus. This work has potential as a diagnostic method for early cancer detection. In another experiment, LCI phase measurements are used to examine volume changes of epithelial cells in a monolayer in response to environmental osmolarity changes. Although cell volume changes have been measured previously, this work demonstrates for the first time the volume of just a few cells (2 or 3) tracked continuously and in situ.


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