Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods

© The Author(s) 2016. In recent years, it has been shown that inflammatory biomarkers can be used as an effective signal for disease diagnoses. The early detection of these signals provides useful information that could prevent the occurrence of severe diseases. Here, we employed surface-enhanced Ra...

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Main Authors: Dakrong Pissuwan, Yusuke Hattori
Other Authors: Osaka University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/42629
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spelling th-mahidol.426292019-03-14T15:03:39Z Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods Dakrong Pissuwan Yusuke Hattori Osaka University Mahidol University Musashino University Engineering © The Author(s) 2016. In recent years, it has been shown that inflammatory biomarkers can be used as an effective signal for disease diagnoses. The early detection of these signals provides useful information that could prevent the occurrence of severe diseases. Here, we employed surface-enhanced Raman scattering (SERS) probe gold nanorods (GNRs) as a tool for the early detection of inflammatory molecules in inflamed cells. A murine macrophage cell line (Raw264.7) stimulated with lipopolysaccharide (LPS) was used as a model in this study. The prepared SERS probe GNRs containing 4-mercaptobenzoic acid as a Raman reporter to generate SERS signals were used for detection of intracellular adhesion molecule-1 (ICAM-1) in macrophages after treatment with LPS for varying lengths of time. Our results show that SERS probe GNRs could detect significant differences in the expression of ICAM-1 molecules in LPS-treated macrophages compared to those in untreated macrophages after only 1 h of LPS treatment. In contrast, when using fluorescent labeling or enzyme-linked immunosorbent assays (ELISA) to detect ICAM-1, significant differences between inflamed and un-inflamed macrophages were not seen until the cells had been treated with LPS for 5 h. These results indicate that our SERS probe GNRs provide a higher sensitivity for detecting biomarker molecules in inflamed macrophages than the conventional fluorescence and ELISA techniques, and could therefore be useful as a potential diagnostic tool for managing disease risk. 2018-12-21T07:42:39Z 2019-03-14T08:03:39Z 2018-12-21T07:42:39Z 2019-03-14T08:03:39Z 2017-01-01 Article Nano-Micro Letters. Vol.9, No.1 (2017) 10.1007/s40820-016-0111-7 21505551 23116706 2-s2.0-85015341097 https://repository.li.mahidol.ac.th/handle/123456789/42629 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85015341097&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Engineering
spellingShingle Engineering
Dakrong Pissuwan
Yusuke Hattori
Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
description © The Author(s) 2016. In recent years, it has been shown that inflammatory biomarkers can be used as an effective signal for disease diagnoses. The early detection of these signals provides useful information that could prevent the occurrence of severe diseases. Here, we employed surface-enhanced Raman scattering (SERS) probe gold nanorods (GNRs) as a tool for the early detection of inflammatory molecules in inflamed cells. A murine macrophage cell line (Raw264.7) stimulated with lipopolysaccharide (LPS) was used as a model in this study. The prepared SERS probe GNRs containing 4-mercaptobenzoic acid as a Raman reporter to generate SERS signals were used for detection of intracellular adhesion molecule-1 (ICAM-1) in macrophages after treatment with LPS for varying lengths of time. Our results show that SERS probe GNRs could detect significant differences in the expression of ICAM-1 molecules in LPS-treated macrophages compared to those in untreated macrophages after only 1 h of LPS treatment. In contrast, when using fluorescent labeling or enzyme-linked immunosorbent assays (ELISA) to detect ICAM-1, significant differences between inflamed and un-inflamed macrophages were not seen until the cells had been treated with LPS for 5 h. These results indicate that our SERS probe GNRs provide a higher sensitivity for detecting biomarker molecules in inflamed macrophages than the conventional fluorescence and ELISA techniques, and could therefore be useful as a potential diagnostic tool for managing disease risk.
author2 Osaka University
author_facet Osaka University
Dakrong Pissuwan
Yusuke Hattori
format Article
author Dakrong Pissuwan
Yusuke Hattori
author_sort Dakrong Pissuwan
title Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
title_short Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
title_full Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
title_fullStr Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
title_full_unstemmed Detection of adhesion molecules on inflamed macrophages at early-stage using SERS probe gold nanorods
title_sort detection of adhesion molecules on inflamed macrophages at early-stage using sers probe gold nanorods
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/42629
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