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Developing Gold Nanoparticles-Conjugated Aflatoxin B1 Antifungal Strips

Authors :
Hugh J. Byrne
Furong Tian
Daxiang Cui
Kan Wang
Kangze Liu
James F. Curtin
Tobiloba Sojinrin
Source :
Articles, International Journal of Molecular Sciences, Volume 20, Issue 24
Publication Year :
2019
Publisher :
Technological University Dublin, 2019.

Abstract

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&ndash<br />16 ng/mL) were tested with AFB1 antibody&ndash<br />BSA&ndash<br />AuNPs (conjugated AuNPs) and then analysed by scanning electron microscopy, ultraviolet&ndash<br />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.

Details

Database :
OpenAIRE
Journal :
Articles, International Journal of Molecular Sciences, Volume 20, Issue 24
Accession number :
edsair.doi.dedup.....cf22f42721eae7f12d0be9152e35af14