Abstract

The study of cell proliferation is of great importance for medical and biological research, as well as for industrial applications. To render the proliferation process accurately over time, real-time cell proliferation assay methods are required. This work presents a novel real-time and label-free approach for monitoring cell proliferation by continuously measuring changes in thermal properties that occur at the sensor interface during the process. The sensor consists of a single planar resistive structure deposited on a thin foil substrate, integrated at the bottom of a cell culture reservoir. During measurement, the structure is excited with square wave current pulses. Meanwhile, the temperature-induced voltage change measured over the structure is used to derive variations in the number of cells at the interface. This principle is demonstrated first by performing cell sedimentation measurements to quantify the presence of cells at the sensor interface in the absence of cell growth. Later, cell proliferation experiments were performed, whereby parameters such as the available nutrient content and the cell starting concentration were modified. Results from these experiments show that the thermal-based sensor is able to accurately measure variations in the number of cells at the interface. Moreover, the influence of the modified parameters could be observed in the obtained proliferation curves. These findings highlight the potential for the presented thermal method to be incorporated in a standardized well plate format for high-throughput monitoring of cell proliferation.

Highlights

  • The study of cell proliferation plays an important role in many medical and biological research fields

  • Investigating the influence of certain compounds on the cell proliferation process is crucial to drug discovery research [4,5,6]

  • In order to study the ability of the sensor to monitor the presence of cells, in the absence of cell growth, yeast cells were allowed to sediment on the sensor surface in the absence of nutrients

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Summary

Introduction

The study of cell proliferation plays an important role in many medical and biological research fields. Proliferation experiments contribute greatly to advances in the emerging field of regenerative medicine, such as tissue engineering [7,8]. These many useful applications generate a great demand for reliable high-throughput methods for monitoring cell proliferation. The most common way of assesing the growth in cell cultures is by visual examination using a microscope or spectrophotometry [9,10,11,12]. These methods require sampling a fixed volume from the cell suspension, which can be time-consuming. A drawback of this technique is that it is an endpoint method, and only provides information on the proliferation process at a specific moment [13]

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