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A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood

A rapid, ultrasensitive, and high-throughput fluorimetric microarray method has been developed using hydrophobic pattern as the microarray substrate and 3-aminopropyltriethoxysilane-coupled carboxylic acid calcium (APS-CCA) as the fluorescent probes for sensing Ca(2+) ions in blood. The hydrophobic...

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Autores principales: Ding, Yanjun, Ling, Jiang, Qiao, Yuchun, Li, Zhengjian, Sun, Zongzhao, Cai, Jifeng, Guo, Yadong, Wang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137002/
https://www.ncbi.nlm.nih.gov/pubmed/27917959
http://dx.doi.org/10.1038/srep38602
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author Ding, Yanjun
Ling, Jiang
Qiao, Yuchun
Li, Zhengjian
Sun, Zongzhao
Cai, Jifeng
Guo, Yadong
Wang, Hua
author_facet Ding, Yanjun
Ling, Jiang
Qiao, Yuchun
Li, Zhengjian
Sun, Zongzhao
Cai, Jifeng
Guo, Yadong
Wang, Hua
author_sort Ding, Yanjun
collection PubMed
description A rapid, ultrasensitive, and high-throughput fluorimetric microarray method has been developed using hydrophobic pattern as the microarray substrate and 3-aminopropyltriethoxysilane-coupled carboxylic acid calcium (APS-CCA) as the fluorescent probes for sensing Ca(2+) ions in blood. The hydrophobic pattern of the developed Ca(2+) analysis microarray could largely suppress the “coffee-ring” effects to facilitate the better distribution density of testing microspots toward the high-throughput detections, and especially prevent the cross-contamination of the multiple samples between adjacent microspots. Moreover, the use of APS matrix could endow the CCA probe the enhanced environmental stability and fluorescence intensity, which is about 2.3-fold higher than that of free CCA. The interactions between APS-CCA and Ca(2+) ions were systematically characterized by UV-vis and fluorescence measurements including microscopy imaging. It was demonstrated that the fluorimetric microarray could display the strong capacity of specifically sensing Ca(2+) ions with the minimal interferences from blood backgrounds. Such an APS-CCA-based fluorimetric microarray can allow for the analysis of Ca(2+) ions down to 0.0050 mM in blood, promising a highly sensitive and selective detection candidate for Ca(2+) ions to be applied in the clinical laboratory.
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spelling pubmed-51370022017-01-27 A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood Ding, Yanjun Ling, Jiang Qiao, Yuchun Li, Zhengjian Sun, Zongzhao Cai, Jifeng Guo, Yadong Wang, Hua Sci Rep Article A rapid, ultrasensitive, and high-throughput fluorimetric microarray method has been developed using hydrophobic pattern as the microarray substrate and 3-aminopropyltriethoxysilane-coupled carboxylic acid calcium (APS-CCA) as the fluorescent probes for sensing Ca(2+) ions in blood. The hydrophobic pattern of the developed Ca(2+) analysis microarray could largely suppress the “coffee-ring” effects to facilitate the better distribution density of testing microspots toward the high-throughput detections, and especially prevent the cross-contamination of the multiple samples between adjacent microspots. Moreover, the use of APS matrix could endow the CCA probe the enhanced environmental stability and fluorescence intensity, which is about 2.3-fold higher than that of free CCA. The interactions between APS-CCA and Ca(2+) ions were systematically characterized by UV-vis and fluorescence measurements including microscopy imaging. It was demonstrated that the fluorimetric microarray could display the strong capacity of specifically sensing Ca(2+) ions with the minimal interferences from blood backgrounds. Such an APS-CCA-based fluorimetric microarray can allow for the analysis of Ca(2+) ions down to 0.0050 mM in blood, promising a highly sensitive and selective detection candidate for Ca(2+) ions to be applied in the clinical laboratory. Nature Publishing Group 2016-12-05 /pmc/articles/PMC5137002/ /pubmed/27917959 http://dx.doi.org/10.1038/srep38602 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/
spellingShingle Article
Ding, Yanjun
Ling, Jiang
Qiao, Yuchun
Li, Zhengjian
Sun, Zongzhao
Cai, Jifeng
Guo, Yadong
Wang, Hua
A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title_full A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title_fullStr A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title_full_unstemmed A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title_short A high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
title_sort high-throughput fluorimetric microarray with enhanced fluorescence and suppressed “coffee-ring” effects for the detection of calcium ions in blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137002/
https://www.ncbi.nlm.nih.gov/pubmed/27917959
http://dx.doi.org/10.1038/srep38602
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