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Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network
Directed transport of biological species across the surface of a substrate is essential for realizing lab-on-chip technologies. Approaches that utilize localized magnetic fields to manipulate magnetic particles carrying biological entities are attractive owing to their sensitivity, selectivity, and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579241/ https://www.ncbi.nlm.nih.gov/pubmed/28860460 http://dx.doi.org/10.1038/s41598-017-10149-9 |
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author | Rapoport, Elizabeth Beach, Geoffrey S. D. |
author_facet | Rapoport, Elizabeth Beach, Geoffrey S. D. |
author_sort | Rapoport, Elizabeth |
collection | PubMed |
description | Directed transport of biological species across the surface of a substrate is essential for realizing lab-on-chip technologies. Approaches that utilize localized magnetic fields to manipulate magnetic particles carrying biological entities are attractive owing to their sensitivity, selectivity, and minimally disruptive impact on biomaterials. Magnetic domain walls in magnetic tracks produce strong localized fields and can be used to capture, transport, and detect individual superparamagnetic microbeads. The dynamics of magnetic microbead transport by domain walls has been well studied. However, demonstration of more complex functions such as selective motion and sorting using continuously driven domain walls in contiguous magnetic tracks is lacking. Here, a junction architecture is introduced that allows for branching networks in which superparamagnetic microbeads can be routed along dynamically-selected paths by a combination of rotating in-plane field for translation, and a pulsed out-of-plane field for path selection. Moreover, experiments and modeling show that the select-field amplitude is bead-size dependent, which allows for digital sorting of multiple bead populations using automated field sequences. This work provides a simple means to implement complex routing networks and selective transport functionalities in chip-based devices using magnetic domain wall conduits. |
format | Online Article Text |
id | pubmed-5579241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55792412017-09-06 Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network Rapoport, Elizabeth Beach, Geoffrey S. D. Sci Rep Article Directed transport of biological species across the surface of a substrate is essential for realizing lab-on-chip technologies. Approaches that utilize localized magnetic fields to manipulate magnetic particles carrying biological entities are attractive owing to their sensitivity, selectivity, and minimally disruptive impact on biomaterials. Magnetic domain walls in magnetic tracks produce strong localized fields and can be used to capture, transport, and detect individual superparamagnetic microbeads. The dynamics of magnetic microbead transport by domain walls has been well studied. However, demonstration of more complex functions such as selective motion and sorting using continuously driven domain walls in contiguous magnetic tracks is lacking. Here, a junction architecture is introduced that allows for branching networks in which superparamagnetic microbeads can be routed along dynamically-selected paths by a combination of rotating in-plane field for translation, and a pulsed out-of-plane field for path selection. Moreover, experiments and modeling show that the select-field amplitude is bead-size dependent, which allows for digital sorting of multiple bead populations using automated field sequences. This work provides a simple means to implement complex routing networks and selective transport functionalities in chip-based devices using magnetic domain wall conduits. Nature Publishing Group UK 2017-08-31 /pmc/articles/PMC5579241/ /pubmed/28860460 http://dx.doi.org/10.1038/s41598-017-10149-9 Text en © The Author(s) 2017 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 Rapoport, Elizabeth Beach, Geoffrey S. D. Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title | Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title_full | Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title_fullStr | Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title_full_unstemmed | Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title_short | Architecture for Directed Transport of Superparamagnetic Microbeads in a Magnetic Domain Wall Routing Network |
title_sort | architecture for directed transport of superparamagnetic microbeads in a magnetic domain wall routing network |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579241/ https://www.ncbi.nlm.nih.gov/pubmed/28860460 http://dx.doi.org/10.1038/s41598-017-10149-9 |
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