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Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads

[Image: see text] Highly luminescent quantum dot beads (QBs) were synthesized by encapsulating CdSe/ZnS and used for the first time as immunochromatographic assay (ICA) signal amplification probe for ultrasensitive detection of aflatoxin B(1) (AFB(1)) in maize. The challenges to using high brightnes...

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Autores principales: Ren, Meiling, Xu, Hengyi, Huang, Xiaolin, Kuang, Min, Xiong, Yonghua, Xu, Hong, Xu, Yang, Chen, Hongyu, Wang, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149326/
https://www.ncbi.nlm.nih.gov/pubmed/25109633
http://dx.doi.org/10.1021/am503517s
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author Ren, Meiling
Xu, Hengyi
Huang, Xiaolin
Kuang, Min
Xiong, Yonghua
Xu, Hong
Xu, Yang
Chen, Hongyu
Wang, Andrew
author_facet Ren, Meiling
Xu, Hengyi
Huang, Xiaolin
Kuang, Min
Xiong, Yonghua
Xu, Hong
Xu, Yang
Chen, Hongyu
Wang, Andrew
author_sort Ren, Meiling
collection PubMed
description [Image: see text] Highly luminescent quantum dot beads (QBs) were synthesized by encapsulating CdSe/ZnS and used for the first time as immunochromatographic assay (ICA) signal amplification probe for ultrasensitive detection of aflatoxin B(1) (AFB(1)) in maize. The challenges to using high brightness QBs as probes for ICA are smooth flow of QBs and nonspecific binding on nitrocellulose (NC) membrane, which are overcome by unique polymer encapsulation of quantum dots (QDs) and surface blocking method. Under optimal conditions, the QB-based ICA (QB-ICA) sensor exhibited dynamic linear detection of AFB(1) in maize extract from 5 to 60 pg mL(–1), with a median inhibitory concentration (IC(50)) of 13.87 ± 0.16 pg mL(–1), that is significantly (39-fold) lower than those of the QD as a signal probe (IC(50) = 0.54 ± 0.06 ng mL(–1)). The limit of detection (LOD) for AFB(1) using QB-ICA sensor was 0.42 pg mL(–1) in maize extract, which is approximately 2 orders of magnitude better than those of previously reported gold nanoparticle based immunochromatographic assay (AuNP-ICA) and is even comparable with or better than the conventional enzyme-linked immunosorbent assay (ELISA) method. The performance and practicability of our QB-ICA sensor were validated with a commercial ELISA kit and further confirmed with liquid chromatography tandem mass spectrometry (LC–MS/MS). Given its efficient signal amplification performance, the proposed QB-ICA offers great potential for rapid, sensitive, and cost-effective quantitative detection of analytes in food safety monitoring.
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spelling pubmed-41493262015-08-09 Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads Ren, Meiling Xu, Hengyi Huang, Xiaolin Kuang, Min Xiong, Yonghua Xu, Hong Xu, Yang Chen, Hongyu Wang, Andrew ACS Appl Mater Interfaces [Image: see text] Highly luminescent quantum dot beads (QBs) were synthesized by encapsulating CdSe/ZnS and used for the first time as immunochromatographic assay (ICA) signal amplification probe for ultrasensitive detection of aflatoxin B(1) (AFB(1)) in maize. The challenges to using high brightness QBs as probes for ICA are smooth flow of QBs and nonspecific binding on nitrocellulose (NC) membrane, which are overcome by unique polymer encapsulation of quantum dots (QDs) and surface blocking method. Under optimal conditions, the QB-based ICA (QB-ICA) sensor exhibited dynamic linear detection of AFB(1) in maize extract from 5 to 60 pg mL(–1), with a median inhibitory concentration (IC(50)) of 13.87 ± 0.16 pg mL(–1), that is significantly (39-fold) lower than those of the QD as a signal probe (IC(50) = 0.54 ± 0.06 ng mL(–1)). The limit of detection (LOD) for AFB(1) using QB-ICA sensor was 0.42 pg mL(–1) in maize extract, which is approximately 2 orders of magnitude better than those of previously reported gold nanoparticle based immunochromatographic assay (AuNP-ICA) and is even comparable with or better than the conventional enzyme-linked immunosorbent assay (ELISA) method. The performance and practicability of our QB-ICA sensor were validated with a commercial ELISA kit and further confirmed with liquid chromatography tandem mass spectrometry (LC–MS/MS). Given its efficient signal amplification performance, the proposed QB-ICA offers great potential for rapid, sensitive, and cost-effective quantitative detection of analytes in food safety monitoring. American Chemical Society 2014-08-09 2014-08-27 /pmc/articles/PMC4149326/ /pubmed/25109633 http://dx.doi.org/10.1021/am503517s Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Ren, Meiling
Xu, Hengyi
Huang, Xiaolin
Kuang, Min
Xiong, Yonghua
Xu, Hong
Xu, Yang
Chen, Hongyu
Wang, Andrew
Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title_full Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title_fullStr Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title_full_unstemmed Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title_short Immunochromatographic Assay for Ultrasensitive Detection of Aflatoxin B(1) in Maize by Highly Luminescent Quantum Dot Beads
title_sort immunochromatographic assay for ultrasensitive detection of aflatoxin b(1) in maize by highly luminescent quantum dot beads
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149326/
https://www.ncbi.nlm.nih.gov/pubmed/25109633
http://dx.doi.org/10.1021/am503517s
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