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Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling
Giant magnetoresistive (GMR) sensors have been shown to be among the most sensitive biosensors reported. While high-density and scalable sensor arrays are desirable for achieving multiplex detection, scalability remains challenging because of long data acquisition time using conventional readout met...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220270/ https://www.ncbi.nlm.nih.gov/pubmed/30405155 http://dx.doi.org/10.1038/s41598-018-34720-0 |
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author | Kim, Kyunglok Hall, Drew A. Yao, Chengyang Lee, Jung-Rok Ooi, Chin C. Bechstein, Daniel J. B. Guo, Yue Wang, Shan X. |
author_facet | Kim, Kyunglok Hall, Drew A. Yao, Chengyang Lee, Jung-Rok Ooi, Chin C. Bechstein, Daniel J. B. Guo, Yue Wang, Shan X. |
author_sort | Kim, Kyunglok |
collection | PubMed |
description | Giant magnetoresistive (GMR) sensors have been shown to be among the most sensitive biosensors reported. While high-density and scalable sensor arrays are desirable for achieving multiplex detection, scalability remains challenging because of long data acquisition time using conventional readout methods. In this paper, we present a scalable magnetoresistive biosensor array with an on-chip magnetic field generator and a high-speed data acquisition method. The on-chip field generators enable magnetic correlated double sampling (MCDS) and global chopper stabilization to suppress 1/f noise and offset. A measurement with the proposed system takes only 20 ms, approximately 50× faster than conventional frequency domain analysis. A corresponding time domain temperature correction technique is also presented and shown to be able to remove temperature dependence from the measured signal without extra measurements or reference sensors. Measurements demonstrate detection of magnetic nanoparticles (MNPs) at a signal level as low as 6.92 ppm. The small form factor enables the proposed platform to be portable as well as having high sensitivity and rapid readout, desirable features for next generation diagnostic systems, especially in point-of-care (POC) settings. |
format | Online Article Text |
id | pubmed-6220270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62202702018-11-08 Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling Kim, Kyunglok Hall, Drew A. Yao, Chengyang Lee, Jung-Rok Ooi, Chin C. Bechstein, Daniel J. B. Guo, Yue Wang, Shan X. Sci Rep Article Giant magnetoresistive (GMR) sensors have been shown to be among the most sensitive biosensors reported. While high-density and scalable sensor arrays are desirable for achieving multiplex detection, scalability remains challenging because of long data acquisition time using conventional readout methods. In this paper, we present a scalable magnetoresistive biosensor array with an on-chip magnetic field generator and a high-speed data acquisition method. The on-chip field generators enable magnetic correlated double sampling (MCDS) and global chopper stabilization to suppress 1/f noise and offset. A measurement with the proposed system takes only 20 ms, approximately 50× faster than conventional frequency domain analysis. A corresponding time domain temperature correction technique is also presented and shown to be able to remove temperature dependence from the measured signal without extra measurements or reference sensors. Measurements demonstrate detection of magnetic nanoparticles (MNPs) at a signal level as low as 6.92 ppm. The small form factor enables the proposed platform to be portable as well as having high sensitivity and rapid readout, desirable features for next generation diagnostic systems, especially in point-of-care (POC) settings. Nature Publishing Group UK 2018-11-07 /pmc/articles/PMC6220270/ /pubmed/30405155 http://dx.doi.org/10.1038/s41598-018-34720-0 Text en © The Author(s) 2018 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 Kim, Kyunglok Hall, Drew A. Yao, Chengyang Lee, Jung-Rok Ooi, Chin C. Bechstein, Daniel J. B. Guo, Yue Wang, Shan X. Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title | Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title_full | Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title_fullStr | Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title_full_unstemmed | Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title_short | Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
title_sort | magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220270/ https://www.ncbi.nlm.nih.gov/pubmed/30405155 http://dx.doi.org/10.1038/s41598-018-34720-0 |
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