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Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time

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 a...

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Autores principales: Bormans, Seppe, Oudebrouckx, Gilles, Vandormael, Patrick, Vandenryt, Thijs, Wagner, Patrick, Somers, Veerle, Thoelen, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036761/
https://www.ncbi.nlm.nih.gov/pubmed/33916287
http://dx.doi.org/10.3390/s21072440
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author Bormans, Seppe
Oudebrouckx, Gilles
Vandormael, Patrick
Vandenryt, Thijs
Wagner, Patrick
Somers, Veerle
Thoelen, Ronald
author_facet Bormans, Seppe
Oudebrouckx, Gilles
Vandormael, Patrick
Vandenryt, Thijs
Wagner, Patrick
Somers, Veerle
Thoelen, Ronald
author_sort Bormans, Seppe
collection PubMed
description 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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spelling pubmed-80367612021-04-12 Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time Bormans, Seppe Oudebrouckx, Gilles Vandormael, Patrick Vandenryt, Thijs Wagner, Patrick Somers, Veerle Thoelen, Ronald Sensors (Basel) Article 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. MDPI 2021-04-01 /pmc/articles/PMC8036761/ /pubmed/33916287 http://dx.doi.org/10.3390/s21072440 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bormans, Seppe
Oudebrouckx, Gilles
Vandormael, Patrick
Vandenryt, Thijs
Wagner, Patrick
Somers, Veerle
Thoelen, Ronald
Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title_full Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title_fullStr Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title_full_unstemmed Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title_short Pulsed Thermal Method for Monitoring Cell Proliferation in Real-Time
title_sort pulsed thermal method for monitoring cell proliferation in real-time
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036761/
https://www.ncbi.nlm.nih.gov/pubmed/33916287
http://dx.doi.org/10.3390/s21072440
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