GO-amplified fluorescence polarization assay for high-sensitivity detection of aflatoxin B1 with low dosage aptamer probe

被引:0
作者
Hua Ye
Qianqian Lu
Nuo Duan
Zhouping Wang
机构
[1] Jiangnan University,State Key Laboratory of Food Science and Technology, School of Food Science and Technology
[2] Anhui Science and Technology University,College of Food Engineering
[3] Dalian Polytechnic University,National Engineering Research Center of Seafood, School of Food Science and Technology
[4] Jiangnan University,International Joint Laboratory on Food Safety
[5] Collaborative Innovation Center of Food Safety and Quality Control of Jiangsu Province,undefined
来源
Analytical and Bioanalytical Chemistry | 2019年 / 411卷
关键词
Aptamer; Fluorescence polarization; Graphene oxide; Signal amplifier; Aflatoxin B;
D O I
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中图分类号
学科分类号
摘要
Aflatoxin B1 (AFB1) is the most toxic mycotoxin of the aflatoxins (AFs) and shows carcinogenic, teratogenic and mutagenic effects in humans and animals. AFB1 is widely seen in cereal products such as rice and wheat. This research proposed a low-cost, high-sensitivity fluorescence polarization (FP) assay for detection of AFB1 using aptamer biosensors based on graphene oxide (GO). The aptamers labelled with fluorescein amidite (FAM) were adsorbed on the surface of GO through π–π stacking and electrostatic interaction, thus forming aptamer/GO macromolecular complexes. Under these conditions, the local rotation of fluorophores was limited and the system had a high FP value. When there was AFB1 in the system, aptamers were dissociated from the GO surface and combined with AFB1 owing to their specificity to form aptamer/AFB1 complexes. As a result, large changes were observed in the molecular weights of aptamers before, and after, the combination, therefore leading to the apparent changes in FP value. The results showed that when only 10 nM of aptamer was used, the changes in FP and the AFB1 concentration had a favourable linear relationship within 0.05 to 5 nM of AFB1, and the lowest detection limit (LOD) was 0.05 nM. In addition, the recoveries of rice sample extract ranged from 89.2% to 112%. The method is simple, highly sensitive, cost-efficient and shows potential application prospects.
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页码:1107 / 1115
页数:8
相关论文
共 191 条
[21]  
Ashley DL(2018)Magnetically controlled fluorescence aptasensor for simultaneous determination of ochratoxin A and aflatoxin B1 Anal Chim Acta 1019 119-30
[22]  
Hill RH(2018)Competitive horseradish peroxidase-linked aptamer assay for sensitive detection of aflatoxin B1 Talanta 179 344-257
[23]  
Zdena Ďuračková VB(2018)A direct determination of AFBs in vinegar by aptamer-based surface plasmon resonance biosensor Toxicon 146 24-4034
[24]  
Nemec P(2018)Dual-competitive lateral flow aptasensor for detection of aflatoxin B1 in food and feedstuffs J Hazard Mater 344 249-32
[25]  
Alizadeh N(2016)Size-dependent modulation of graphene oxide-aptamer interactions for an amplified fluorescence-based detection of aflatoxin B1 with a tunable dynamic range Analyst 141 4029-1507
[26]  
Memar MY(2017)Development of aflatoxin B1 aptasensor based on wide-range fluorescence detection using graphene oxide quencher Colloids Surf B Biointerfaces 154 27-3121
[27]  
Mehramuz B(2008)Fluorescence polarization immunoassays and related methods for simple, high-throughput screening of small molecules Anal Bioanal Chem 391 1499-129
[28]  
Abibiglou SS(2002)Development of a fluorescence polarization assay for the determination of aflatoxins in grains J Agric Food Chem 50 3116-175
[29]  
Hemmati F(2014)The development of a fluorescence polarization immunoassay for aflatoxin detection Biomed Environ Sci 27 126-86050
[30]  
Samadi Kafil H(2015)Rapid screening of aflatoxin B1 in beer by fluorescence polarization immunoassay Talanta 142 170-450