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Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference

Gold nanoclusters (Au NCs) are promising luminescent nanomaterials due to their outstanding optical properties. However, their relatively low quantum yields and environment-dependent photoluminescence properties have limited their biological applications. To address these problems, we developed a no...

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Autores principales: Yu, Qi, Gao, Pengli, Zhang, Kenneth Yin, Tong, Xiao, Yang, Huiran, Liu, Shujuan, Du, Jing, Zhao, Qiang, Huang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062025/
https://www.ncbi.nlm.nih.gov/pubmed/30167221
http://dx.doi.org/10.1038/lsa.2017.107
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author Yu, Qi
Gao, Pengli
Zhang, Kenneth Yin
Tong, Xiao
Yang, Huiran
Liu, Shujuan
Du, Jing
Zhao, Qiang
Huang, Wei
author_facet Yu, Qi
Gao, Pengli
Zhang, Kenneth Yin
Tong, Xiao
Yang, Huiran
Liu, Shujuan
Du, Jing
Zhao, Qiang
Huang, Wei
author_sort Yu, Qi
collection PubMed
description Gold nanoclusters (Au NCs) are promising luminescent nanomaterials due to their outstanding optical properties. However, their relatively low quantum yields and environment-dependent photoluminescence properties have limited their biological applications. To address these problems, we developed a novel strategy to prepare chitosan oligosaccharide lactate (Chi)-functionalized Au NCs (Au NCs@Chi), which exhibited emission with enhanced quantum yield and elongated emission lifetime as compared to the Au NCs, as well as exhibited environment-independent photoluminescence properties. In addition, utilizing the free amino groups of Chi onto Au NCs@Chi, we designed a FRET-based sensing platform for the detection of hydrogen sulfide (H(2)S). The Au NCs and the specific H(2)S-sensitive merocyanine compound were respectively employed as an energy donor and acceptor in the platform. The addition of H(2)S induced changes in the emission profile and luminescence lifetime of the platform with high sensitivity and selectivity. Utilization of the platform was demonstrated to detect exogenous and endogenous H(2)S in vitro and in vivo through wavelength-ratiometric and time-resolved luminescence imaging (TLI). Compared to previously reported luminescent molecules, the platform was less affected by experimental conditions and showed minimized autofluorescence interference and improved accuracy of detection.
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spelling pubmed-60620252018-08-30 Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference Yu, Qi Gao, Pengli Zhang, Kenneth Yin Tong, Xiao Yang, Huiran Liu, Shujuan Du, Jing Zhao, Qiang Huang, Wei Light Sci Appl Original Article Gold nanoclusters (Au NCs) are promising luminescent nanomaterials due to their outstanding optical properties. However, their relatively low quantum yields and environment-dependent photoluminescence properties have limited their biological applications. To address these problems, we developed a novel strategy to prepare chitosan oligosaccharide lactate (Chi)-functionalized Au NCs (Au NCs@Chi), which exhibited emission with enhanced quantum yield and elongated emission lifetime as compared to the Au NCs, as well as exhibited environment-independent photoluminescence properties. In addition, utilizing the free amino groups of Chi onto Au NCs@Chi, we designed a FRET-based sensing platform for the detection of hydrogen sulfide (H(2)S). The Au NCs and the specific H(2)S-sensitive merocyanine compound were respectively employed as an energy donor and acceptor in the platform. The addition of H(2)S induced changes in the emission profile and luminescence lifetime of the platform with high sensitivity and selectivity. Utilization of the platform was demonstrated to detect exogenous and endogenous H(2)S in vitro and in vivo through wavelength-ratiometric and time-resolved luminescence imaging (TLI). Compared to previously reported luminescent molecules, the platform was less affected by experimental conditions and showed minimized autofluorescence interference and improved accuracy of detection. Nature Publishing Group 2017-12-01 /pmc/articles/PMC6062025/ /pubmed/30167221 http://dx.doi.org/10.1038/lsa.2017.107 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Yu, Qi
Gao, Pengli
Zhang, Kenneth Yin
Tong, Xiao
Yang, Huiran
Liu, Shujuan
Du, Jing
Zhao, Qiang
Huang, Wei
Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title_full Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title_fullStr Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title_full_unstemmed Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title_short Luminescent gold nanocluster-based sensing platform for accurate H(2)S detection in vitro and in vivo with improved anti-interference
title_sort luminescent gold nanocluster-based sensing platform for accurate h(2)s detection in vitro and in vivo with improved anti-interference
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062025/
https://www.ncbi.nlm.nih.gov/pubmed/30167221
http://dx.doi.org/10.1038/lsa.2017.107
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