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Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs

The use of precision medicine for chemotherapy requires the individualization of the therapeutic regimen for each patient. This approach improves treatment efficacy and reduces the probability of administering ineffective drugs. To ensure accurate decision-making in a timely manner, anticancer drug...

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Autores principales: Moon, Hui-Sung, Yoo, Chang Eun, Kim, Sangmin, Lee, Jeong Eon, Park, Woong-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683738/
https://www.ncbi.nlm.nih.gov/pubmed/33230163
http://dx.doi.org/10.1038/s41598-020-77324-3
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author Moon, Hui-Sung
Yoo, Chang Eun
Kim, Sangmin
Lee, Jeong Eon
Park, Woong-Yang
author_facet Moon, Hui-Sung
Yoo, Chang Eun
Kim, Sangmin
Lee, Jeong Eon
Park, Woong-Yang
author_sort Moon, Hui-Sung
collection PubMed
description The use of precision medicine for chemotherapy requires the individualization of the therapeutic regimen for each patient. This approach improves treatment efficacy and reduces the probability of administering ineffective drugs. To ensure accurate decision-making in a timely manner, anticancer drug efficacy tests must be performed within a short timeframe using a small number of cancer cells. These requirements can be satisfied via microfluidics-based drug screening platforms, which are composed of complex fluidic channels and closed systems. Owing to their complexity, skilled manipulation is required. In this study, we developed a microfluidic platform, to accurately perform multiple drug efficacy tests using a small number of cells, which can be conducted via simple manipulation. As it is a small, open-chamber system, a minimal number of cells could be loaded through simple pipetting. Furthermore, the extracellular matrix gel inside the chamber provides an in vivo-like environment that enables the localized delivery of the drugs to spontaneously diffuse from the channels underneath the chamber without a pump, thereby efficiently and robustly testing the efficacy and resistance of multiple drugs. We demonstrated that this platform enabled the rapid and facile testing of multiple drugs using a small number of cells (~ 10,000) over a short period of time (~ 2 days). These results provide the possibility of using this powerful platform for selecting therapeutic medication, developing new drugs, and delivering personalized medicine to patients.
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spelling pubmed-76837382020-11-27 Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs Moon, Hui-Sung Yoo, Chang Eun Kim, Sangmin Lee, Jeong Eon Park, Woong-Yang Sci Rep Article The use of precision medicine for chemotherapy requires the individualization of the therapeutic regimen for each patient. This approach improves treatment efficacy and reduces the probability of administering ineffective drugs. To ensure accurate decision-making in a timely manner, anticancer drug efficacy tests must be performed within a short timeframe using a small number of cancer cells. These requirements can be satisfied via microfluidics-based drug screening platforms, which are composed of complex fluidic channels and closed systems. Owing to their complexity, skilled manipulation is required. In this study, we developed a microfluidic platform, to accurately perform multiple drug efficacy tests using a small number of cells, which can be conducted via simple manipulation. As it is a small, open-chamber system, a minimal number of cells could be loaded through simple pipetting. Furthermore, the extracellular matrix gel inside the chamber provides an in vivo-like environment that enables the localized delivery of the drugs to spontaneously diffuse from the channels underneath the chamber without a pump, thereby efficiently and robustly testing the efficacy and resistance of multiple drugs. We demonstrated that this platform enabled the rapid and facile testing of multiple drugs using a small number of cells (~ 10,000) over a short period of time (~ 2 days). These results provide the possibility of using this powerful platform for selecting therapeutic medication, developing new drugs, and delivering personalized medicine to patients. Nature Publishing Group UK 2020-11-23 /pmc/articles/PMC7683738/ /pubmed/33230163 http://dx.doi.org/10.1038/s41598-020-77324-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moon, Hui-Sung
Yoo, Chang Eun
Kim, Sangmin
Lee, Jeong Eon
Park, Woong-Yang
Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title_full Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title_fullStr Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title_full_unstemmed Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title_short Application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
title_sort application of an open-chamber multi-channel microfluidic device to test chemotherapy drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683738/
https://www.ncbi.nlm.nih.gov/pubmed/33230163
http://dx.doi.org/10.1038/s41598-020-77324-3
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