Abstract

Aflatoxins are a group of extremely toxic and carcinogenic substances generated by the mold of the genus Aspergillus that contaminate agricultural products. When dairy cows ingest aflatoxin B1 (AFB1)−contaminated feeds, it is metabolized and transformed in the liver into a carcinogenic major form of aflatoxin M1 (AFM1), which is eliminated through the milk. The detection of AFM1 in milk is very important to be able to guarantee food safety and quality. In recent years, sensors have emerged as a quick, low–cost, and reliable platform for the detection of aflatoxins. Plasmonic sensors with molecularly imprinted polymers (MIPs) can be interesting alternatives for the determination of AFM1. In this work, we designed a molecularly–imprinted–based plasmonic sensor to directly detect lower amounts of AFM1 in raw milk samples. For this purpose, we prepared gold–nanoparticle–(AuNP)−integrated polymer nanofilm on a gold plasmonic sensor chip coated with allyl mercaptan. N−methacryloyl−l−phenylalanine (MAPA) was chosen as a functional monomer. The MIP nanofilm was prepared using the light–initiated polymerization of MAPA and ethylene glycol dimethacrylate in the presence of AFM1 as a template molecule. The developed method enabled the detection of AFM1 with a detection limit of 0.4 pg/mL and demonstrated good linearity (0.0003 ng/mL–20.0 ng/mL) under optimized experimental conditions. The AFM1 determination was performed in random dairy farmer milk samples. Using the analogous mycotoxins, it was also demonstrated that the plasmonic sensor platforms were specific to the detection of AFM1.

Highlights

  • Mycotoxins are secondary metabolites produced mainly by the filamentous fungi of the species Aspergillus, Penicillium, Claviceps, Fusarium, and Alternaria which may contaminate food and feed products [1,2,3]

  • It was demonstrated that the plasmonic sensor platforms were specific to the detection of aflatoxin M1 (AFM1)

  • Aflatoxin M1 (AFM1: C17 H12 O7 ; molecular weight = 328.27 g/mol) is the main hydroxylated form and a major metabolite of aflatoxin B1 (AFB1). It is produced during the biological processes of animals ingesting AFB1–contaminated feeds, and after the consumption of the contaminated feeds, it can be excreted in milk within 12 hours [8,14]. These highly toxic aflatoxins are categorized as group one human carcinogenic compounds according to the International Agency for Research on Cancer (IARC) of the World Health Organization (WHO) [15,16]

Read more

Summary

Introduction

Mycotoxins are secondary metabolites produced mainly by the filamentous fungi of the species Aspergillus, Penicillium, Claviceps, Fusarium, and Alternaria which may contaminate food and feed products [1,2,3]. Aflatoxin M1 (AFM1: C17 H12 O7 ; molecular weight = 328.27 g/mol) is the main hydroxylated form and a major metabolite of AFB1 It is produced during the biological processes of animals ingesting AFB1–contaminated feeds, and after the consumption of the contaminated feeds, it can be excreted in milk within 12 hours [8,14]. These highly toxic aflatoxins are categorized as group one human carcinogenic compounds according to the International Agency for Research on Cancer (IARC) of the World Health Organization (WHO) [15,16]. The polymer film coating characteristics, the real–time monitoring, and the reusability of the novel MIP−based plasmonic sensor for the detection of AFM1 in milk were evaluated

Chemicals and Apparatus
Development of Molecularly
The Removal of Template Molecule
Characterization of SPR Sensor
Detection of AFM1
Detection of AFM1 in Milk Samples
Discussion
Plasmonic
Experiments
Method
Kinetic Analysis and Adsorption Isotherm
Selectivity
Milk Sample
Reusability and Stability
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call