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Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe
A novel, facile sensor was further developed for microcystin-LR (MC-LR) determination by visible spectroscopy. Antibody-functionalized SiO(2)-coated magnetic nanoparticles (Fe(3)O(4)@SiO(2)) and aptamer-functionalized polydopamine nanospheres decorated with Cu nanoparticles (PDA/CuNPs) recognized sp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473965/ https://www.ncbi.nlm.nih.gov/pubmed/30832300 http://dx.doi.org/10.3390/nano9030332 |
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author | Tang, Xiaodi Yin, Zhengzhi Lei, Xiaoling Zeng, Yanbo Zhang, Zulei Lu, Yixia Zhou, Guobao Li, Lei Wu, Xiaohua |
author_facet | Tang, Xiaodi Yin, Zhengzhi Lei, Xiaoling Zeng, Yanbo Zhang, Zulei Lu, Yixia Zhou, Guobao Li, Lei Wu, Xiaohua |
author_sort | Tang, Xiaodi |
collection | PubMed |
description | A novel, facile sensor was further developed for microcystin-LR (MC-LR) determination by visible spectroscopy. Antibody-functionalized SiO(2)-coated magnetic nanoparticles (Fe(3)O(4)@SiO(2)) and aptamer-functionalized polydopamine nanospheres decorated with Cu nanoparticles (PDA/CuNPs) recognized specific sites in MC-LR and then the sandwich-type composites were separated magnetically. The Cu in the separated composites was converted to Cu(2+) ions in solution and turn-on visible absorption was achieved after reaction with bis(cyclohexanone)oxaldihydrazone (BCO) (λ(max) = 600 nm). There was a quantitative relationship between the spectral intensity and MC-LR concentration. In addition, under the optimum conditions, the sensor turns out to be a linear relationship from 0.05 to 25 nM, with a limit of detection of 0.05 nM (0.05 μg/L) (S/N = 3) for MC-LR. The sensitivity was dependent on the low background absorption from the off-to-on spectrum and label amplification by the polydopamine (PDA) surface. The sensor had high selectivity, which shows the importance of dual-site recognition by the aptamer and antibody and the highly specific color formed by BCO with Cu(2+). The bioassay was complete within 150 min, which enabled quick determination. The sensor was successfully used with real spiked samples. These results suggest it has potential applications in visible detection and could be used to detect other microcystin analogs. |
format | Online Article Text |
id | pubmed-6473965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64739652019-05-03 Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe Tang, Xiaodi Yin, Zhengzhi Lei, Xiaoling Zeng, Yanbo Zhang, Zulei Lu, Yixia Zhou, Guobao Li, Lei Wu, Xiaohua Nanomaterials (Basel) Article A novel, facile sensor was further developed for microcystin-LR (MC-LR) determination by visible spectroscopy. Antibody-functionalized SiO(2)-coated magnetic nanoparticles (Fe(3)O(4)@SiO(2)) and aptamer-functionalized polydopamine nanospheres decorated with Cu nanoparticles (PDA/CuNPs) recognized specific sites in MC-LR and then the sandwich-type composites were separated magnetically. The Cu in the separated composites was converted to Cu(2+) ions in solution and turn-on visible absorption was achieved after reaction with bis(cyclohexanone)oxaldihydrazone (BCO) (λ(max) = 600 nm). There was a quantitative relationship between the spectral intensity and MC-LR concentration. In addition, under the optimum conditions, the sensor turns out to be a linear relationship from 0.05 to 25 nM, with a limit of detection of 0.05 nM (0.05 μg/L) (S/N = 3) for MC-LR. The sensitivity was dependent on the low background absorption from the off-to-on spectrum and label amplification by the polydopamine (PDA) surface. The sensor had high selectivity, which shows the importance of dual-site recognition by the aptamer and antibody and the highly specific color formed by BCO with Cu(2+). The bioassay was complete within 150 min, which enabled quick determination. The sensor was successfully used with real spiked samples. These results suggest it has potential applications in visible detection and could be used to detect other microcystin analogs. MDPI 2019-03-02 /pmc/articles/PMC6473965/ /pubmed/30832300 http://dx.doi.org/10.3390/nano9030332 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tang, Xiaodi Yin, Zhengzhi Lei, Xiaoling Zeng, Yanbo Zhang, Zulei Lu, Yixia Zhou, Guobao Li, Lei Wu, Xiaohua Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title | Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title_full | Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title_fullStr | Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title_full_unstemmed | Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title_short | Colorimetric Method for Sensitive Detection of Microcystin-LR Using Surface Copper Nanoparticles of Polydopamine Nanosphere as Turn-On Probe |
title_sort | colorimetric method for sensitive detection of microcystin-lr using surface copper nanoparticles of polydopamine nanosphere as turn-on probe |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473965/ https://www.ncbi.nlm.nih.gov/pubmed/30832300 http://dx.doi.org/10.3390/nano9030332 |
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