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Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration

Three different alkyne-terminated aggregation-induced emission molecules based on a para-substituted di-thioether were attached to the surface of ultrasmall gold nanoparticles (2 nm) by copper-catalyzed azide–alkyne cycloaddition (click chemistry). They showed a strong fluorescence and were well wat...

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Detalles Bibliográficos
Autores principales: Klein, Kai, Hayduk, Matthias, Kollenda, Sebastian, Schmiedtchen, Marco, Voskuhl, Jens, Epple, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949416/
https://www.ncbi.nlm.nih.gov/pubmed/35335152
http://dx.doi.org/10.3390/molecules27061788
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author Klein, Kai
Hayduk, Matthias
Kollenda, Sebastian
Schmiedtchen, Marco
Voskuhl, Jens
Epple, Matthias
author_facet Klein, Kai
Hayduk, Matthias
Kollenda, Sebastian
Schmiedtchen, Marco
Voskuhl, Jens
Epple, Matthias
author_sort Klein, Kai
collection PubMed
description Three different alkyne-terminated aggregation-induced emission molecules based on a para-substituted di-thioether were attached to the surface of ultrasmall gold nanoparticles (2 nm) by copper-catalyzed azide–alkyne cycloaddition (click chemistry). They showed a strong fluorescence and were well water-dispersible, in contrast to the dissolved AIE molecules. The AIE-loaded nanoparticles were not cytotoxic and easily penetrated the membrane of HeLa cells, paving the way for an intracellular application of AIE molecules, e.g., for imaging.
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spelling pubmed-89494162022-03-26 Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration Klein, Kai Hayduk, Matthias Kollenda, Sebastian Schmiedtchen, Marco Voskuhl, Jens Epple, Matthias Molecules Article Three different alkyne-terminated aggregation-induced emission molecules based on a para-substituted di-thioether were attached to the surface of ultrasmall gold nanoparticles (2 nm) by copper-catalyzed azide–alkyne cycloaddition (click chemistry). They showed a strong fluorescence and were well water-dispersible, in contrast to the dissolved AIE molecules. The AIE-loaded nanoparticles were not cytotoxic and easily penetrated the membrane of HeLa cells, paving the way for an intracellular application of AIE molecules, e.g., for imaging. MDPI 2022-03-09 /pmc/articles/PMC8949416/ /pubmed/35335152 http://dx.doi.org/10.3390/molecules27061788 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Klein, Kai
Hayduk, Matthias
Kollenda, Sebastian
Schmiedtchen, Marco
Voskuhl, Jens
Epple, Matthias
Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title_full Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title_fullStr Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title_full_unstemmed Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title_short Covalent Attachment of Aggregation-Induced Emission Molecules to the Surface of Ultrasmall Gold Nanoparticles to Enhance Cell Penetration
title_sort covalent attachment of aggregation-induced emission molecules to the surface of ultrasmall gold nanoparticles to enhance cell penetration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949416/
https://www.ncbi.nlm.nih.gov/pubmed/35335152
http://dx.doi.org/10.3390/molecules27061788
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