4.6 Article

Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time

期刊

SENSORS
卷 21, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/s21072440

关键词

biofilm; cell proliferation; Saccharomyces cerevisiae; pulsed thermal method

资金

  1. Research Foundation Flanders FWO [G.0791.16]
  2. BIOMAT project
  3. European Union
  4. European Regional Development Fund
  5. province of Limburg-Belgium

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The study introduces a novel approach for monitoring cell proliferation by continuously measuring changes in thermal properties at the sensor interface. The method accurately measures variations in the number of cells and shows potential for high-throughput monitoring of cell proliferation.
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.

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