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Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips

Lateral flow immunochromatographic assays are a powerful diagnostic tool for point-of-care tests, based on their simplicity, specificity, and sensitivity. In this study, a rapid and sensitive gold nanoparticle (AuNP) immunochromatographic strip is produced for detecting aflatoxin B1 (AFB1) in suspic...

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Detalles Bibliográficos
Autores principales: Sojinrin, Tobiloba, Liu, Kangze, Wang, Kan, Cui, Daxiang, J. Byrne, Hugh, Curtin, James F., Tian, Furong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941036/
https://www.ncbi.nlm.nih.gov/pubmed/31842251
http://dx.doi.org/10.3390/ijms20246260
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author Sojinrin, Tobiloba
Liu, Kangze
Wang, Kan
Cui, Daxiang
J. Byrne, Hugh
Curtin, James F.
Tian, Furong
author_facet Sojinrin, Tobiloba
Liu, Kangze
Wang, Kan
Cui, Daxiang
J. Byrne, Hugh
Curtin, James F.
Tian, Furong
author_sort Sojinrin, Tobiloba
collection PubMed
description Lateral flow immunochromatographic assays are a powerful diagnostic tool for point-of-care tests, based on their simplicity, specificity, and sensitivity. In this study, a rapid and sensitive gold nanoparticle (AuNP) immunochromatographic strip is produced for detecting aflatoxin B1 (AFB1) in suspicious fungi-contaminated food samples. The 10 nm AuNPs were encompassed by bovine serum albumin (BSA) and AFB1 antibody. Thin-layer chromatography, gel electrophoresis and nuclear magnetic resonance spectroscopy were employed for analysing the chemical complexes. Various concentrations of AFB1 antigen (0–16 ng/mL) were tested with AFB1 antibody–BSA–AuNPs (conjugated AuNPs) and then analysed by scanning electron microscopy, ultraviolet–visible spectroscopy, and Zetasizer. The results showed that the AFB1 antibody was coupled to BSA by the N-hydroxysuccinimide ester method. The AuNPs application has the potential to contribute to AFB1 detection by monitoring a visible colour change from red to purple-blue, with a detection limit of 2 ng/mL in a 96-well plate. The lateral flow immunochromatographic strip tests are rapid, taking less than 10 min., and they have a detection capacity of 10 ng/g. The smartphone analysis of strips provided the results in 3 s, with a detection limit of 0.3 ng/g for AFB1 when the concentration was below 10 ng/g. Excellent agreement was found with AFB1 determination by high-performance liquid chromatography in the determination of AFB1 among 20 samples of peanuts, corn, rice, and bread.
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spelling pubmed-69410362020-01-09 Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips Sojinrin, Tobiloba Liu, Kangze Wang, Kan Cui, Daxiang J. Byrne, Hugh Curtin, James F. Tian, Furong Int J Mol Sci Article Lateral flow immunochromatographic assays are a powerful diagnostic tool for point-of-care tests, based on their simplicity, specificity, and sensitivity. In this study, a rapid and sensitive gold nanoparticle (AuNP) immunochromatographic strip is produced for detecting aflatoxin B1 (AFB1) in suspicious fungi-contaminated food samples. The 10 nm AuNPs were encompassed by bovine serum albumin (BSA) and AFB1 antibody. Thin-layer chromatography, gel electrophoresis and nuclear magnetic resonance spectroscopy were employed for analysing the chemical complexes. Various concentrations of AFB1 antigen (0–16 ng/mL) were tested with AFB1 antibody–BSA–AuNPs (conjugated AuNPs) and then analysed by scanning electron microscopy, ultraviolet–visible spectroscopy, and Zetasizer. The results showed that the AFB1 antibody was coupled to BSA by the N-hydroxysuccinimide ester method. The AuNPs application has the potential to contribute to AFB1 detection by monitoring a visible colour change from red to purple-blue, with a detection limit of 2 ng/mL in a 96-well plate. The lateral flow immunochromatographic strip tests are rapid, taking less than 10 min., and they have a detection capacity of 10 ng/g. The smartphone analysis of strips provided the results in 3 s, with a detection limit of 0.3 ng/g for AFB1 when the concentration was below 10 ng/g. Excellent agreement was found with AFB1 determination by high-performance liquid chromatography in the determination of AFB1 among 20 samples of peanuts, corn, rice, and bread. MDPI 2019-12-12 /pmc/articles/PMC6941036/ /pubmed/31842251 http://dx.doi.org/10.3390/ijms20246260 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
Sojinrin, Tobiloba
Liu, Kangze
Wang, Kan
Cui, Daxiang
J. Byrne, Hugh
Curtin, James F.
Tian, Furong
Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title_full Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title_fullStr Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title_full_unstemmed Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title_short Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips
title_sort developing gold nanoparticles-conjugated aflatoxin b1 antifungal strips
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941036/
https://www.ncbi.nlm.nih.gov/pubmed/31842251
http://dx.doi.org/10.3390/ijms20246260
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