4.6 Article

A novel colorimetric biosensor for sensitive detection of aflatoxin mediated by bacterial enzymatic reaction in saffron samples

期刊

NANOTECHNOLOGY
卷 32, 期 50, 页码 -

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IOP PUBLISHING LTD
DOI: 10.1088/1361-6528/ac23f7

关键词

AFB1; gold nanoparticle; gelatin; biosensor; saffron

资金

  1. Saffron Institute, University of Torbat Heydarieh [P/123747]

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A colorimetric competitive assay for detecting AFB1 in foods was developed based on the interaction of AuNPs@gelatin. The method showed a linear detection range of 10 to 140 pg ml(-1), with a detection limit of 4 pg ml(-1) and recoveries percentage of 92.4%-95.3% in real saffron samples. This approach offers a simple, cost effective, and specific method for AFB1 toxin detection in food samples.
Aflatoxin is regarded as the potent carcinogenic agent which is secreted from fungi and present in some food products. So far, many detection methods have been developed to determine the trace amounts of aflatoxin in foods. In the present study a colorimetric competitive assay for detection of aflatoxin B1 (AFB1) has been developed based on interaction of gelatin functionalized gold nanoparticles (AuNPs@gelatin) in specific enzymatic reaction. Bacterial supernatant containing gelatinase enzyme were used as the substrate that could digest the coated gelatin on the surface of AuNPs and following in the presence of NaCl medium ingredient resulted to color change of AuNPs colloidal solution from red to purple. It was observed that with addition of aflatoxin to the bacterial supernatant, aflatoxin could interfere in aggregation of AuNPs and inhibited the process which subsequently prevent the expected color change induced by AuNPs aggregation. The supernatant containing AuNPs were investigated to analyze their induced surface plasmon resonance spectra through UV-visible spectroscopy. The absorption values were directly proportional with the applied AFB1 concentration. The experiment conditions including incubation time, AuNPs concentration and pH were investigated. The obtained results showed that through this approach we could detect the AFB1 in a linear range from 10 to 140 pg ml(-1), with detection limit of 4 pg ml(-1). Real sample assay in saffron samples showed recoveries percentage of 92.4%-95.3%. The applied approach proposed simple, cost effective and specific method for detection of AFB1 toxin in food samples.

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