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Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection

An efficient and low cost optical method for directly measuring the concentration of homogenous biological solutes is proposed and demonstrated. The proposed system operates by Fresnel reflection, with a flat-cleaved single-mode fiber serving as the sensor probe. A laser provides a 12.9 dBm sensor s...

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Autores principales: Ahmad, Harith, Thambiratnam, Kavintheran, Zulkifli, Ahmad Z., Lawrence, Anthony, Jasim, Ali A., Kunasekaran, Wijenthiran, Musa, Sabri, Gnanasegaran, Nareshwaran, Vasanthan, Punitha, Jayaraman, Pukana, Kasim, Noor H. A., Govindasamy, Vijayendran, Shahrir, Mohammad S., Harun, Sulaiman W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859063/
https://www.ncbi.nlm.nih.gov/pubmed/24084118
http://dx.doi.org/10.3390/s131013276
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author Ahmad, Harith
Thambiratnam, Kavintheran
Zulkifli, Ahmad Z.
Lawrence, Anthony
Jasim, Ali A.
Kunasekaran, Wijenthiran
Musa, Sabri
Gnanasegaran, Nareshwaran
Vasanthan, Punitha
Jayaraman, Pukana
Kasim, Noor H. A.
Govindasamy, Vijayendran
Shahrir, Mohammad S.
Harun, Sulaiman W.
author_facet Ahmad, Harith
Thambiratnam, Kavintheran
Zulkifli, Ahmad Z.
Lawrence, Anthony
Jasim, Ali A.
Kunasekaran, Wijenthiran
Musa, Sabri
Gnanasegaran, Nareshwaran
Vasanthan, Punitha
Jayaraman, Pukana
Kasim, Noor H. A.
Govindasamy, Vijayendran
Shahrir, Mohammad S.
Harun, Sulaiman W.
author_sort Ahmad, Harith
collection PubMed
description An efficient and low cost optical method for directly measuring the concentration of homogenous biological solutes is proposed and demonstrated. The proposed system operates by Fresnel reflection, with a flat-cleaved single-mode fiber serving as the sensor probe. A laser provides a 12.9 dBm sensor signal at 1,550 nm, while a computer-controlled optical power meter measures the power of the signal returned by the probe. Three different mesenchymal stem cell (MSC) lines were obtained, sub-cultured and trypsinized daily over 9 days. Counts were measured using a haemocytometer and the conditioned media (CM) was collected daily and stored at −80 °C. MSCs release excretory biomolecules proportional to their growth rate into the CM, which changes the refractive index of the latter. The sensor is capable of detecting changes in the number of stem cells via correlation to the change in the refractive index of the CM, with the measured power loss decreasing approximately 0.4 dB in the CM sample per average 1,000 cells in the MSC subculture. The proposed system is highly cost-effective, simple to deploy, operate, and maintain, is non-destructive, and allows reliable real-time measurement of various stem cell proliferation parameters.
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spelling pubmed-38590632013-12-11 Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection Ahmad, Harith Thambiratnam, Kavintheran Zulkifli, Ahmad Z. Lawrence, Anthony Jasim, Ali A. Kunasekaran, Wijenthiran Musa, Sabri Gnanasegaran, Nareshwaran Vasanthan, Punitha Jayaraman, Pukana Kasim, Noor H. A. Govindasamy, Vijayendran Shahrir, Mohammad S. Harun, Sulaiman W. Sensors (Basel) Article An efficient and low cost optical method for directly measuring the concentration of homogenous biological solutes is proposed and demonstrated. The proposed system operates by Fresnel reflection, with a flat-cleaved single-mode fiber serving as the sensor probe. A laser provides a 12.9 dBm sensor signal at 1,550 nm, while a computer-controlled optical power meter measures the power of the signal returned by the probe. Three different mesenchymal stem cell (MSC) lines were obtained, sub-cultured and trypsinized daily over 9 days. Counts were measured using a haemocytometer and the conditioned media (CM) was collected daily and stored at −80 °C. MSCs release excretory biomolecules proportional to their growth rate into the CM, which changes the refractive index of the latter. The sensor is capable of detecting changes in the number of stem cells via correlation to the change in the refractive index of the CM, with the measured power loss decreasing approximately 0.4 dB in the CM sample per average 1,000 cells in the MSC subculture. The proposed system is highly cost-effective, simple to deploy, operate, and maintain, is non-destructive, and allows reliable real-time measurement of various stem cell proliferation parameters. Molecular Diversity Preservation International (MDPI) 2013-09-30 /pmc/articles/PMC3859063/ /pubmed/24084118 http://dx.doi.org/10.3390/s131013276 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Ahmad, Harith
Thambiratnam, Kavintheran
Zulkifli, Ahmad Z.
Lawrence, Anthony
Jasim, Ali A.
Kunasekaran, Wijenthiran
Musa, Sabri
Gnanasegaran, Nareshwaran
Vasanthan, Punitha
Jayaraman, Pukana
Kasim, Noor H. A.
Govindasamy, Vijayendran
Shahrir, Mohammad S.
Harun, Sulaiman W.
Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title_full Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title_fullStr Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title_full_unstemmed Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title_short Quantification of Mesenchymal Stem Cell Growth Rates through Secretory and Excretory Biomolecules in Conditioned Media via Fresnel Reflection
title_sort quantification of mesenchymal stem cell growth rates through secretory and excretory biomolecules in conditioned media via fresnel reflection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859063/
https://www.ncbi.nlm.nih.gov/pubmed/24084118
http://dx.doi.org/10.3390/s131013276
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