A Molecularly Imprinted Polymer Based on Fe3O4@Au Nanoparticles for Detection of Aflatoxin B1 in Food Samples

分子印迹聚合物 检出限 吸附 傅里叶变换红外光谱 扫描电子显微镜 黄曲霉毒素 材料科学 分子印迹 选择性 化学 分析化学(期刊) 核化学 色谱法 化学工程 有机化学 食品科学 催化作用 工程类 复合材料
作者
Maryam Pezeshkpur,Fariba Tadayon,Mahmoud Reza Sohrabi
出处
期刊:ChemistrySelect [Wiley]
卷期号:8 (15) 被引量:7
标识
DOI:10.1002/slct.202300112
摘要

Abstract Based on molecular imprinting and nanotechnology, a molecular imprinted polymer (MIP) coupled with Fe 3 O 4 −Au nanocomposite adsorbent has been successfully developed for rapid quantification of aflatoxin B1 in foodstuff. The characterization of the prepared Fe 3 O 4 −Au and Fe 3 O 4 −Au‐MIP was studied by scanning electron microscopy (SEM), energy dispersive X‐ray spectroscopy (EDX), transmission electron microscopy (TEM), Fourier‐transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), and vibrating sample magnetometer (VSM). The limit of detection (LOD) and limit of quantification (LOQ) were estimated to be 6.12 and 18.6 μg L −1 , respectively. The adsorption capacity was 8.975 mg g −1 which revealed that the synthesized magnetic MIP (MMIP) presented high selective recognition property to AFB1. The selectivity adsorption experiments indicated that compared with three different competetive Aflatoxins, MMIP showed excellent affinity to AFB1. It was found that the adsorption capacity of MMIP for AFB1 remained essentially the same after 6 adsorption‐desorption cycle which shows the acceptable repeatability and reusability of the MMIP. The proposed method was successfully applied to the estimation of AFB1 in non‐alcoholic beer and barley samples with good recoveries (94.47–97.31 %). Also, the relative standard deviation (RSD %) values were lower than 3.7 %. The selectivity, stability and reproducibility of the proposed method were acceptable. The results revealed that Fe 3 O 4 −Au@MIP could be used as an efficient and reusable adsorbent for AFB1 in food samples. This study provides a simple, inexpensive, fast, accurate and environmentally‐friendly technique instead of expensive and time‐consuming procedures for determining AFB1 in food matrices.
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