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Protein-Localized Bright-Red Fluorescent Gold Nanoclusters as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes
[Image: see text] Herein, we describe a bright-red-emitting ovalbumin-protected gold nanoclusters (OVA–AuNCs) that were prepared and applied as a luminescent probe for a simple, rapid, and highly sensitive determination of cyanide ions (CN(–) ions) based on an emission quenching and colorimetric met...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644394/ https://www.ncbi.nlm.nih.gov/pubmed/31458104 http://dx.doi.org/10.1021/acsomega.8b02044 |
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author | Rajamanikandan, Ramar Ilanchelian, Malaichamy |
author_facet | Rajamanikandan, Ramar Ilanchelian, Malaichamy |
author_sort | Rajamanikandan, Ramar |
collection | PubMed |
description | [Image: see text] Herein, we describe a bright-red-emitting ovalbumin-protected gold nanoclusters (OVA–AuNCs) that were prepared and applied as a luminescent probe for a simple, rapid, and highly sensitive determination of cyanide ions (CN(–) ions) based on an emission quenching and colorimetric method. Initially, an intense red-emissive fluorescence of the OVA–AuNCs successfully disappeared upon the addition of CN(–) ions. The resultant emission-quenching process involved CN(–) ions etching the OVA–AuNC surface, which produced AuCN(2)(–) complexes in the presence of ambient oxygen. Under optimized experimental conditions, the relative emission intensity is inversely relative to CN(–) ion concentrations ranging from 5.00 × 10(–7) to 75.00 × 10(–7) mol/L with a linear correlation coefficient of 0.9932. Furthermore, OVA–AuNC-based optical detection systems on both colorimetric and fluorometric assays were tested, which expose highly sensitive and specific determination of CN(–) ions, and it is easily visualized by the naked eye (day light and UV light). Because of the distinct Elsner reaction between Au atoms of OVA–AuNCs and CN(–) ions, the recent nanoprobe offered ultrasensitivity and good selectivity with the lowest limit of detection value of 68.00 × 10(–9) mol/L. In addition, this fluorescence “turn-off” CN(–) ion detection method was executed in real water samples. The demonstrated route of OVA–AuNC preparation is extremely easy and quick, making the proposed selective and sensitive CN(–) ion sensing assay based on the fluorescence response of the OVA–AuNCs for numerous practical applications. |
format | Online Article Text |
id | pubmed-6644394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66443942019-08-27 Protein-Localized Bright-Red Fluorescent Gold Nanoclusters as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes Rajamanikandan, Ramar Ilanchelian, Malaichamy ACS Omega [Image: see text] Herein, we describe a bright-red-emitting ovalbumin-protected gold nanoclusters (OVA–AuNCs) that were prepared and applied as a luminescent probe for a simple, rapid, and highly sensitive determination of cyanide ions (CN(–) ions) based on an emission quenching and colorimetric method. Initially, an intense red-emissive fluorescence of the OVA–AuNCs successfully disappeared upon the addition of CN(–) ions. The resultant emission-quenching process involved CN(–) ions etching the OVA–AuNC surface, which produced AuCN(2)(–) complexes in the presence of ambient oxygen. Under optimized experimental conditions, the relative emission intensity is inversely relative to CN(–) ion concentrations ranging from 5.00 × 10(–7) to 75.00 × 10(–7) mol/L with a linear correlation coefficient of 0.9932. Furthermore, OVA–AuNC-based optical detection systems on both colorimetric and fluorometric assays were tested, which expose highly sensitive and specific determination of CN(–) ions, and it is easily visualized by the naked eye (day light and UV light). Because of the distinct Elsner reaction between Au atoms of OVA–AuNCs and CN(–) ions, the recent nanoprobe offered ultrasensitivity and good selectivity with the lowest limit of detection value of 68.00 × 10(–9) mol/L. In addition, this fluorescence “turn-off” CN(–) ion detection method was executed in real water samples. The demonstrated route of OVA–AuNC preparation is extremely easy and quick, making the proposed selective and sensitive CN(–) ion sensing assay based on the fluorescence response of the OVA–AuNCs for numerous practical applications. American Chemical Society 2018-10-25 /pmc/articles/PMC6644394/ /pubmed/31458104 http://dx.doi.org/10.1021/acsomega.8b02044 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Rajamanikandan, Ramar Ilanchelian, Malaichamy Protein-Localized Bright-Red Fluorescent Gold Nanoclusters as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title | Protein-Localized Bright-Red Fluorescent Gold Nanoclusters
as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title_full | Protein-Localized Bright-Red Fluorescent Gold Nanoclusters
as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title_fullStr | Protein-Localized Bright-Red Fluorescent Gold Nanoclusters
as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title_full_unstemmed | Protein-Localized Bright-Red Fluorescent Gold Nanoclusters
as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title_short | Protein-Localized Bright-Red Fluorescent Gold Nanoclusters
as Cyanide-Selective Colorimetric and Fluorometric Nanoprobes |
title_sort | protein-localized bright-red fluorescent gold nanoclusters
as cyanide-selective colorimetric and fluorometric nanoprobes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644394/ https://www.ncbi.nlm.nih.gov/pubmed/31458104 http://dx.doi.org/10.1021/acsomega.8b02044 |
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