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A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe

Hydrogen sulfide (H(2)S) is a highly toxic gas as a cause of inhalational death. Accurate detection of H(2)S poisoning concentration is valuable and vital for forensic workers to estimate the cause of death. But so far, it is no uniform and reliable standard method to measure sulfide concentrations...

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Autores principales: Ding, Yanjun, Li, Xingmei, Chen, Ceng, Ling, Jiang, Li, Weichen, Guo, Yadong, Yan, Jie, Zha, Lagabaiyla, Cai, Jifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575022/
https://www.ncbi.nlm.nih.gov/pubmed/28852006
http://dx.doi.org/10.1038/s41598-017-09960-1
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author Ding, Yanjun
Li, Xingmei
Chen, Ceng
Ling, Jiang
Li, Weichen
Guo, Yadong
Yan, Jie
Zha, Lagabaiyla
Cai, Jifeng
author_facet Ding, Yanjun
Li, Xingmei
Chen, Ceng
Ling, Jiang
Li, Weichen
Guo, Yadong
Yan, Jie
Zha, Lagabaiyla
Cai, Jifeng
author_sort Ding, Yanjun
collection PubMed
description Hydrogen sulfide (H(2)S) is a highly toxic gas as a cause of inhalational death. Accurate detection of H(2)S poisoning concentration is valuable and vital for forensic workers to estimate the cause of death. But so far, it is no uniform and reliable standard method to measure sulfide concentrations in H(2)S poisoning blood for forensic identification. This study introduces a fluorescence sensing technique into forensic research, in which a DNA-templated copper/silver nanocluster (DNA-Cu/AgNCs) fluorescence probe has been proposed to selective detection of S(2−). Under an optimized condition, the proposed method can allow for determination of S(2−) in the concentration range of 10 pM to 1 mM with a linear equation: y = −0.432 lg[S(2−)] + 0.675 (R(2) = 0.9844), with the limit of detection of 3.75 pM. Moreover, acute H(2)S poisoning mouse models were established by intraperitoneally injected different doses of Na(2)S, and the practical feasibility of the proposed fluorescence sensor has been demonstrated by 35 poisoning blood samples. This proposed method is proved to be quite simple and straightforward for the detection of H(2)S poisoning blood. Also it may provide a basis for sulfide metabolizing study in body, and it would be meaningful to further push forensic toxicology identification and clinical laboratory research.
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spelling pubmed-55750222017-09-01 A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe Ding, Yanjun Li, Xingmei Chen, Ceng Ling, Jiang Li, Weichen Guo, Yadong Yan, Jie Zha, Lagabaiyla Cai, Jifeng Sci Rep Article Hydrogen sulfide (H(2)S) is a highly toxic gas as a cause of inhalational death. Accurate detection of H(2)S poisoning concentration is valuable and vital for forensic workers to estimate the cause of death. But so far, it is no uniform and reliable standard method to measure sulfide concentrations in H(2)S poisoning blood for forensic identification. This study introduces a fluorescence sensing technique into forensic research, in which a DNA-templated copper/silver nanocluster (DNA-Cu/AgNCs) fluorescence probe has been proposed to selective detection of S(2−). Under an optimized condition, the proposed method can allow for determination of S(2−) in the concentration range of 10 pM to 1 mM with a linear equation: y = −0.432 lg[S(2−)] + 0.675 (R(2) = 0.9844), with the limit of detection of 3.75 pM. Moreover, acute H(2)S poisoning mouse models were established by intraperitoneally injected different doses of Na(2)S, and the practical feasibility of the proposed fluorescence sensor has been demonstrated by 35 poisoning blood samples. This proposed method is proved to be quite simple and straightforward for the detection of H(2)S poisoning blood. Also it may provide a basis for sulfide metabolizing study in body, and it would be meaningful to further push forensic toxicology identification and clinical laboratory research. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575022/ /pubmed/28852006 http://dx.doi.org/10.1038/s41598-017-09960-1 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 Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative 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
Ding, Yanjun
Li, Xingmei
Chen, Ceng
Ling, Jiang
Li, Weichen
Guo, Yadong
Yan, Jie
Zha, Lagabaiyla
Cai, Jifeng
A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title_full A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title_fullStr A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title_full_unstemmed A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title_short A rapid evaluation of acute hydrogen sulfide poisoning in blood based on DNA-Cu/Ag nanocluster fluorescence probe
title_sort rapid evaluation of acute hydrogen sulfide poisoning in blood based on dna-cu/ag nanocluster fluorescence probe
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575022/
https://www.ncbi.nlm.nih.gov/pubmed/28852006
http://dx.doi.org/10.1038/s41598-017-09960-1
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