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Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces
It has recently been shown that surface plasmon microscopy (SPM) allows single nanoparticles (NPs) on sensor surfaces to be detected and analyzed. The authors have applied this technique to study the adsorption of single metallic and plastic NPs. Binding of gold NPs (40, 60 and 100 nm in size) and o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061841/ https://www.ncbi.nlm.nih.gov/pubmed/27795582 http://dx.doi.org/10.1007/s00604-016-1956-7 |
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author | Scherbahn, Vitali Nizamov, Shavkat Mirsky, Vladimir M. |
author_facet | Scherbahn, Vitali Nizamov, Shavkat Mirsky, Vladimir M. |
author_sort | Scherbahn, Vitali |
collection | PubMed |
description | It has recently been shown that surface plasmon microscopy (SPM) allows single nanoparticles (NPs) on sensor surfaces to be detected and analyzed. The authors have applied this technique to study the adsorption of single metallic and plastic NPs. Binding of gold NPs (40, 60 and 100 nm in size) and of 100 nm polystyrene NPs to gold surfaces modified by differently ω-functionalized alkyl thiols was studied first. Self-assembled monolayers (SAM) with varying terminal functions including amino, carboxy, oligo(ethylene glycol), methyl, or trimethylammonium groups were deposited on gold films to form surfaces possessing different charge and hydrophobicity. The affinity of NPs to these surfaces depends strongly on the type of coating. SAMs terminated with trimethylammonium groups and carboxy group display highly different affinity and therefore were preferred when creating patterned charged surfaces. Citrate-stabilized gold NPs and sulfate-terminated polystyrene NPs were used as negatively charged NPs, while branched polyethylenimine-coated silver NPs were used as positively charged NPs. It is shown that the charged patterned areas on the gold films are capable of selectively adsorbing oppositely charged NPs that can be detected and analyzed with an ~1 ng⋅mL(−1) detection limit. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00604-016-1956-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5061841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-50618412016-10-26 Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces Scherbahn, Vitali Nizamov, Shavkat Mirsky, Vladimir M. Mikrochim Acta Original Paper It has recently been shown that surface plasmon microscopy (SPM) allows single nanoparticles (NPs) on sensor surfaces to be detected and analyzed. The authors have applied this technique to study the adsorption of single metallic and plastic NPs. Binding of gold NPs (40, 60 and 100 nm in size) and of 100 nm polystyrene NPs to gold surfaces modified by differently ω-functionalized alkyl thiols was studied first. Self-assembled monolayers (SAM) with varying terminal functions including amino, carboxy, oligo(ethylene glycol), methyl, or trimethylammonium groups were deposited on gold films to form surfaces possessing different charge and hydrophobicity. The affinity of NPs to these surfaces depends strongly on the type of coating. SAMs terminated with trimethylammonium groups and carboxy group display highly different affinity and therefore were preferred when creating patterned charged surfaces. Citrate-stabilized gold NPs and sulfate-terminated polystyrene NPs were used as negatively charged NPs, while branched polyethylenimine-coated silver NPs were used as positively charged NPs. It is shown that the charged patterned areas on the gold films are capable of selectively adsorbing oppositely charged NPs that can be detected and analyzed with an ~1 ng⋅mL(−1) detection limit. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00604-016-1956-7) contains supplementary material, which is available to authorized users. Springer Vienna 2016-10-04 2016 /pmc/articles/PMC5061841/ /pubmed/27795582 http://dx.doi.org/10.1007/s00604-016-1956-7 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Paper Scherbahn, Vitali Nizamov, Shavkat Mirsky, Vladimir M. Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title | Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title_full | Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title_fullStr | Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title_full_unstemmed | Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title_short | Plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
title_sort | plasmonic detection and visualization of directed adsorption of charged single nanoparticles to patterned surfaces |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061841/ https://www.ncbi.nlm.nih.gov/pubmed/27795582 http://dx.doi.org/10.1007/s00604-016-1956-7 |
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