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Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging
Directed self-assemblies in water are known as the most efficient means of forming complex higher ordered structures in nature. Here we show a straightforward and robust method for particle assembly which utilises the amphiphilic tri-block co-polymer poloxamer-188 and a hydrophobic fluorophore as th...
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/PMC5709404/ https://www.ncbi.nlm.nih.gov/pubmed/29192150 http://dx.doi.org/10.1038/s41467-017-02060-8 |
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author | Cheung, Shane O’Shea, Donal F. |
author_facet | Cheung, Shane O’Shea, Donal F. |
author_sort | Cheung, Shane |
collection | PubMed |
description | Directed self-assemblies in water are known as the most efficient means of forming complex higher ordered structures in nature. Here we show a straightforward and robust method for particle assembly which utilises the amphiphilic tri-block co-polymer poloxamer-188 and a hydrophobic fluorophore as the two designer components, which have a built-in ability to convey spatial and temporal information about their surroundings to an observer. Templating of particle self-assembly is attributed to interactions between the fluorophore and hydrophobic segment of the poloxamer. Particle fluorescence in water is quenched but can be induced to selectively switch on in response to temperature, surface adsorption and cellular uptake. The ability of the particles to dynamically modulate emission intensity can be exploited for selective labelling and real-time imaging of drug crystal surfaces, natural fibres and insulin fibrils, and cellular delivery. As particle solutions are easily prepared, further applications for this water-based NIR-fluorescent paint are anticipated. |
format | Online Article Text |
id | pubmed-5709404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57094042017-12-04 Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging Cheung, Shane O’Shea, Donal F. Nat Commun Article Directed self-assemblies in water are known as the most efficient means of forming complex higher ordered structures in nature. Here we show a straightforward and robust method for particle assembly which utilises the amphiphilic tri-block co-polymer poloxamer-188 and a hydrophobic fluorophore as the two designer components, which have a built-in ability to convey spatial and temporal information about their surroundings to an observer. Templating of particle self-assembly is attributed to interactions between the fluorophore and hydrophobic segment of the poloxamer. Particle fluorescence in water is quenched but can be induced to selectively switch on in response to temperature, surface adsorption and cellular uptake. The ability of the particles to dynamically modulate emission intensity can be exploited for selective labelling and real-time imaging of drug crystal surfaces, natural fibres and insulin fibrils, and cellular delivery. As particle solutions are easily prepared, further applications for this water-based NIR-fluorescent paint are anticipated. Nature Publishing Group UK 2017-12-01 /pmc/articles/PMC5709404/ /pubmed/29192150 http://dx.doi.org/10.1038/s41467-017-02060-8 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 Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative 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 Cheung, Shane O’Shea, Donal F. Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title | Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title_full | Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title_fullStr | Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title_full_unstemmed | Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title_short | Directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
title_sort | directed self-assembly of fluorescence responsive nanoparticles and their use for real-time surface and cellular imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709404/ https://www.ncbi.nlm.nih.gov/pubmed/29192150 http://dx.doi.org/10.1038/s41467-017-02060-8 |
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