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Rapid Detection of Aspergillus flavus and Quantitative Determination of Aflatoxin B(1) in Grain Crops Using a Portable Raman Spectrometer Combined with Colloidal Au Nanoparticles

Aspergillus flavus and Aflatoxins in grain crops give rise to a serious threat to food security and cause huge economic losses. In particular, aflatoxin B(1) has been identified as a Class I carcinogen to humans by the International Agency for Research on Cancer (IARC). Compared with conventional me...

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Detalles Bibliográficos
Autores principales: Wang, Huiqin, Liu, Mengjia, Zhang, Yumiao, Zhao, Huimin, Lu, Wenjing, Lin, Taifeng, Zhang, Ping, Zheng, Dawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414248/
https://www.ncbi.nlm.nih.gov/pubmed/36014519
http://dx.doi.org/10.3390/molecules27165280
Descripción
Sumario:Aspergillus flavus and Aflatoxins in grain crops give rise to a serious threat to food security and cause huge economic losses. In particular, aflatoxin B(1) has been identified as a Class I carcinogen to humans by the International Agency for Research on Cancer (IARC). Compared with conventional methods, Surface-Enhanced Raman Scattering (SERS) has paved the way for the detection of Aspergillus flavus and Aflatoxins in grain crops as it is a rapid, nondestructive, and sensitive analytical method. In this work, the rapid detection of Aspergillus flavus and quantification of Aflatoxin B(1) in grain crops were performed by using a portable Raman spectrometer combined with colloidal Au nanoparticles (AuNPs). With the increase of the concentration of Aspergillus flavus spore suspension in the range of 10(2)–10(8) CFU/mL, the better the combination of Aspergillus flavus spores and AuNPs, the better the enhancement effect of AuNPs solution on the Aspergillus flavus. A series of different concentrations of aflatoxin B(1) methanol solution combined with AuNPs were determined based on SERS and their spectra were similar to that of solid powder. Moreover, the characteristic peak increased gradually with the increase of concentration in the range of 0.0005–0.01 mg/L and the determination limit was 0.0005 mg/L, which was verified by HPLC in ppM concentration. This rapid detection method can greatly shorten the detection time from several hours or even tens of hours to a few minutes, which can help to take effective measures to avoid causing large economic losses.