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A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection

Small molecule compounds are necessary to detect with high sensitivity since they may cause a strong effect on the human body even in small concentrations. But existing methods used to evaluate small molecules in blood are inconvenient, costly, time-consuming, and do not allow for portable usage. In...

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Autores principales: Yen, Yi-Kuang, Chiu, Chao-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031247/
https://www.ncbi.nlm.nih.gov/pubmed/32076079
http://dx.doi.org/10.1038/s41598-020-60057-8
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author Yen, Yi-Kuang
Chiu, Chao-Yuan
author_facet Yen, Yi-Kuang
Chiu, Chao-Yuan
author_sort Yen, Yi-Kuang
collection PubMed
description Small molecule compounds are necessary to detect with high sensitivity since they may cause a strong effect on the human body even in small concentrations. But existing methods used to evaluate small molecules in blood are inconvenient, costly, time-consuming, and do not allow for portable usage. In response to these shortcomings, we introduce a complementary metal-oxide-semiconductor bio-microelectromechanical system (CMOS BioMEMS) based piezoresistive membrane-bridge (MB) sensor for detecting small molecule (phenytoin) concentrations as the demonstration. Phenytoin is one of anticonvulsant drugs licensed for the management of seizures, which has a narrow therapeutic window hence a level of concentration monitoring was needed. The MB sensor was designed to enhance the structural stability and increase the sensitivity, which its signal response increased 2-fold higher than that of the microcantilever-based sensor. The MB sensor was used to detect phenytoin in different concentrations from 5 to 100  μg/mL. The limit of detection of the sensor was 4.06 ± 0.15  μg/mL and the linear detection range was 5–100  μg/mL, which was within the therapeutic range of phenytoin concentration (10–20  μg/mL). Furthermore, the MB sensor was integrated with an on-chip thermal effect eliminating modus and a reaction tank on a compact chip carrier for disposable utilization. The required amount of sample solution was only 10  μL and the response time of the sensor was about 25  minutes. The nano-mechanical MB sensing method with thermal effect compensation is specific, sensitive, robust, affordable and well reproducible; it is, therefore, an appropriate candidate for detecting small molecules.
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spelling pubmed-70312472020-02-26 A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection Yen, Yi-Kuang Chiu, Chao-Yuan Sci Rep Article Small molecule compounds are necessary to detect with high sensitivity since they may cause a strong effect on the human body even in small concentrations. But existing methods used to evaluate small molecules in blood are inconvenient, costly, time-consuming, and do not allow for portable usage. In response to these shortcomings, we introduce a complementary metal-oxide-semiconductor bio-microelectromechanical system (CMOS BioMEMS) based piezoresistive membrane-bridge (MB) sensor for detecting small molecule (phenytoin) concentrations as the demonstration. Phenytoin is one of anticonvulsant drugs licensed for the management of seizures, which has a narrow therapeutic window hence a level of concentration monitoring was needed. The MB sensor was designed to enhance the structural stability and increase the sensitivity, which its signal response increased 2-fold higher than that of the microcantilever-based sensor. The MB sensor was used to detect phenytoin in different concentrations from 5 to 100  μg/mL. The limit of detection of the sensor was 4.06 ± 0.15  μg/mL and the linear detection range was 5–100  μg/mL, which was within the therapeutic range of phenytoin concentration (10–20  μg/mL). Furthermore, the MB sensor was integrated with an on-chip thermal effect eliminating modus and a reaction tank on a compact chip carrier for disposable utilization. The required amount of sample solution was only 10  μL and the response time of the sensor was about 25  minutes. The nano-mechanical MB sensing method with thermal effect compensation is specific, sensitive, robust, affordable and well reproducible; it is, therefore, an appropriate candidate for detecting small molecules. Nature Publishing Group UK 2020-02-19 /pmc/articles/PMC7031247/ /pubmed/32076079 http://dx.doi.org/10.1038/s41598-020-60057-8 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yen, Yi-Kuang
Chiu, Chao-Yuan
A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title_full A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title_fullStr A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title_full_unstemmed A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title_short A CMOS MEMS-based Membrane-Bridge Nanomechanical Sensor for Small Molecule Detection
title_sort cmos mems-based membrane-bridge nanomechanical sensor for small molecule detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031247/
https://www.ncbi.nlm.nih.gov/pubmed/32076079
http://dx.doi.org/10.1038/s41598-020-60057-8
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