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Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance
Label-free detection of rare cells in biological samples is an important and highly demanded task for clinical applications and various fields of research, such as detection of circulating tumor cells for cancer therapy and stem cells studies. Surface Plasmon Resonance (SPR) as a label-free method i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384085/ https://www.ncbi.nlm.nih.gov/pubmed/25806834 http://dx.doi.org/10.3390/bios5010098 |
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author | Mousavi, Mansoureh Z. Chen, Huai-Yi Hou, Hsien-San Chang, Chou-Yuan-Yuan Roffler, Steve Wei, Pei-Kuen Cheng, Ji-Yen |
author_facet | Mousavi, Mansoureh Z. Chen, Huai-Yi Hou, Hsien-San Chang, Chou-Yuan-Yuan Roffler, Steve Wei, Pei-Kuen Cheng, Ji-Yen |
author_sort | Mousavi, Mansoureh Z. |
collection | PubMed |
description | Label-free detection of rare cells in biological samples is an important and highly demanded task for clinical applications and various fields of research, such as detection of circulating tumor cells for cancer therapy and stem cells studies. Surface Plasmon Resonance (SPR) as a label-free method is a promising technology for detection of rare cells for diagnosis or research applications. Short detection depth of SPR (400 nm) provides a sensitive method with minimum interference of non-targets in the biological samples. In this work, we developed a novel microfluidic chip integrated with gold nanoslit SPR platform for highly efficient immunomagnetic capturing and detection of rare cells in human blood. Our method offers simple yet efficient detection of target cells with high purity. The approach for detection consists of two steps. Target cells are firs captured on functionalized magnetic nanoparticles (MNPs) with specific antibody I. The suspension containing the captured cells (MNPs-cells) is then introduced into a microfluidic chip integrated with a gold nanoslit film. MNPs-cells bind with the second specific antibody immobilized on the surface of the gold nanoslit and are therefore captured on the sensor active area. The cell binding on the gold nanoslit was monitored by the wavelength shift of the SPR spectrum generated by the gold nanoslits. |
format | Online Article Text |
id | pubmed-4384085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43840852015-05-04 Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance Mousavi, Mansoureh Z. Chen, Huai-Yi Hou, Hsien-San Chang, Chou-Yuan-Yuan Roffler, Steve Wei, Pei-Kuen Cheng, Ji-Yen Biosensors (Basel) Article Label-free detection of rare cells in biological samples is an important and highly demanded task for clinical applications and various fields of research, such as detection of circulating tumor cells for cancer therapy and stem cells studies. Surface Plasmon Resonance (SPR) as a label-free method is a promising technology for detection of rare cells for diagnosis or research applications. Short detection depth of SPR (400 nm) provides a sensitive method with minimum interference of non-targets in the biological samples. In this work, we developed a novel microfluidic chip integrated with gold nanoslit SPR platform for highly efficient immunomagnetic capturing and detection of rare cells in human blood. Our method offers simple yet efficient detection of target cells with high purity. The approach for detection consists of two steps. Target cells are firs captured on functionalized magnetic nanoparticles (MNPs) with specific antibody I. The suspension containing the captured cells (MNPs-cells) is then introduced into a microfluidic chip integrated with a gold nanoslit film. MNPs-cells bind with the second specific antibody immobilized on the surface of the gold nanoslit and are therefore captured on the sensor active area. The cell binding on the gold nanoslit was monitored by the wavelength shift of the SPR spectrum generated by the gold nanoslits. MDPI 2015-03-23 /pmc/articles/PMC4384085/ /pubmed/25806834 http://dx.doi.org/10.3390/bios5010098 Text en © 2015 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/4.0/). |
spellingShingle | Article Mousavi, Mansoureh Z. Chen, Huai-Yi Hou, Hsien-San Chang, Chou-Yuan-Yuan Roffler, Steve Wei, Pei-Kuen Cheng, Ji-Yen Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title | Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title_full | Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title_fullStr | Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title_full_unstemmed | Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title_short | Label-Free Detection of Rare Cell in Human Blood Using Gold Nano Slit Surface Plasmon Resonance |
title_sort | label-free detection of rare cell in human blood using gold nano slit surface plasmon resonance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384085/ https://www.ncbi.nlm.nih.gov/pubmed/25806834 http://dx.doi.org/10.3390/bios5010098 |
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