Abstract

Cells mechanical property assessment has been a promising label-free method for cell differentiation. Several methods have been proposed for single-cell mechanical properties analysis. Dielectrophoresis (DEP) is one method used for single-cell mechanical property assessment, cell separation, and sorting. DEP method has overcome weaknesses of other techniques, including compatibility with microfluidics, high throughput assessment, and high accuracy. However, due to the lack of a general and explicit model for this method, it has not been known as an ideal cell mechanical property evaluation method. Here we present an explicit model using the most general electromagnetic equation (Maxwell Stress Tensor) for single-cell mechanical evaluation based on the DEP method. For proof of concept, we used the proposed model for differentiation between three different types of cells, namely erythrocytes, peripheral blood mononuclear cells (PBMC), and an epithelial breast cancer cells line (T-47D). The results show that, by a lumped parameter that depends on cells' mechanical and electrical properties, the proposed model can successfully distinguish between the mentioned cell types that can be in a single blood sample. The proposed model would open up the chance to use a mechanical assessment method for cell searching in parallel with other methods.

Highlights

  • Cells mechanical property assessment has been a promising label-free method for cell differentiation

  • It is worth to be mentioned that epithelial-mesenchymal transitions (EMTs) has been considered as a decisive factor for the CellSearch s­ ystem[6], which is the only FDA-approved system for the detection of the circulating tumor cells (CTCs)[7]

  • The Atomic Force Microscopic (AFM) method is only applicable to adherent cells, while the micropipette aspiration method is only applicable to the nonadherent cells

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Summary

Introduction

Cells mechanical property assessment has been a promising label-free method for cell differentiation. The proposed model would open up the chance to use a mechanical assessment method for cell searching in parallel with other methods. Subcellular components such as the cytoskeleton, lipid bilayer membrane, cytoplasm, focal adhesion proteins, and extracellular matrix (ECM) are integral components of the cell structure and mechanics in health and disease ­cells[1]. Assessing single-cell mechanical property can be a label-free method for pathology studies, including cancer detection. We can conclude that further research in this field is required to propose an ideal lab-on-a-Chip method for high throughput cell mechanical properties assessment at a single-level

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