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One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging

In this work, we have developed one-pot aqueous synthesis of glutathione (GSH) binding CdTe quantum dots (QDs) for cell imaging. UV-Vis absorption spectrum, Fourier transform infrared spectrum, photoluminescence spectrum, and high-resolution transmission electron microscopy are applied to characteri...

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Detalles Bibliográficos
Autores principales: Chen, Xifeng, Guo, Zhenzhen, Miao, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968136/
https://www.ncbi.nlm.nih.gov/pubmed/29862341
http://dx.doi.org/10.1016/j.heliyon.2018.e00576
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author Chen, Xifeng
Guo, Zhenzhen
Miao, Peng
author_facet Chen, Xifeng
Guo, Zhenzhen
Miao, Peng
author_sort Chen, Xifeng
collection PubMed
description In this work, we have developed one-pot aqueous synthesis of glutathione (GSH) binding CdTe quantum dots (QDs) for cell imaging. UV-Vis absorption spectrum, Fourier transform infrared spectrum, photoluminescence spectrum, and high-resolution transmission electron microscopy are applied to characterize the physical and chemical properties of the nanocomposites. The bioimaging efficiency of the GSH-capped CdTe QDs is further evaluated on Hela cells. The groups on the surface of QDs are able to bind to basic proteins, which are abundant in cell nuclei, enabling the application of QDs for direct cell imaging. Experimental results also indicate the GSH layer on the surface of QDs is able to reduce the cytotoxicity significantly. In conclusion, the as-prepared GSH-capped QDs are highly promising fluorescent probes for cell imaging in the near future.
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spelling pubmed-59681362018-06-01 One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging Chen, Xifeng Guo, Zhenzhen Miao, Peng Heliyon Article In this work, we have developed one-pot aqueous synthesis of glutathione (GSH) binding CdTe quantum dots (QDs) for cell imaging. UV-Vis absorption spectrum, Fourier transform infrared spectrum, photoluminescence spectrum, and high-resolution transmission electron microscopy are applied to characterize the physical and chemical properties of the nanocomposites. The bioimaging efficiency of the GSH-capped CdTe QDs is further evaluated on Hela cells. The groups on the surface of QDs are able to bind to basic proteins, which are abundant in cell nuclei, enabling the application of QDs for direct cell imaging. Experimental results also indicate the GSH layer on the surface of QDs is able to reduce the cytotoxicity significantly. In conclusion, the as-prepared GSH-capped QDs are highly promising fluorescent probes for cell imaging in the near future. Elsevier 2018-03-14 /pmc/articles/PMC5968136/ /pubmed/29862341 http://dx.doi.org/10.1016/j.heliyon.2018.e00576 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Chen, Xifeng
Guo, Zhenzhen
Miao, Peng
One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title_full One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title_fullStr One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title_full_unstemmed One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title_short One-pot synthesis of GSH-Capped CdTe quantum dots with excellent biocompatibility for direct cell imaging
title_sort one-pot synthesis of gsh-capped cdte quantum dots with excellent biocompatibility for direct cell imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968136/
https://www.ncbi.nlm.nih.gov/pubmed/29862341
http://dx.doi.org/10.1016/j.heliyon.2018.e00576
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