Detection of aflatoxin B1 by aptamer-based biosensor using PAMAM dendrimers as immobilization platform

被引:132
作者
Castillo, Gabriela [1 ]
Spinella, Katia [2 ,3 ]
Poturnayova, Alexandra [1 ,4 ]
Snejdarkova, Maja [4 ]
Mosiello, Lucia [3 ]
Hianik, Tibor [1 ]
机构
[1] Comenius Univ, Fac Math Phys & Informat, Bratislava 84248, Slovakia
[2] Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
[3] Ctr Ric Casaccia, Italian Natl Agcy New Technol Energy & Environm, ENEA, I-00123 Rome, Italy
[4] Slovak Acad Sci, Inst Anim Biochem & Genet, Ivanka Pri Dunaji 90028, Slovakia
关键词
Aflatoxin B-1; Aptamers; PAMAM dendrimers; Biosensor; Electrochemistry; Atomic force microscopy; Contaminated peanuts; ELECTROCHEMICAL IMMUNOSENSOR; DIFFERENT MYCOTOXINS; RAPID DETECTION; LABEL-FREE; APTASENSOR; RECOGNITION; ASSAY; CORN; ARRAY; REAGENTLESS;
D O I
10.1016/j.foodcont.2014.12.008
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
We report an aptamer-based biosensor for detection of aflatoxin B-1 (AFB(1)), a mycotoxin identified as contaminant in food. The sensor is assembled in a multilayer framework that utilizes cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) for acquiring the signal response by means of redox indicators: K[Fe(CN)(6)](-3/-4). Poly (amidoamine) dendrimers of fourth generation (PAMAM G4) immobilized on gold electrode covered by cystamine, were employed for attachment of single stranded amino-modified DNA aptamers specific to AFB(1). The cystamine-dendrimers (Cys-PAMAM) layers were compared with other immobilization platforms such as cystamine (Cys), 11-mercaptoundecanoic acid (MUA) and 11-mercaptoundecanoic acid-dendrimers (MUA-PAMAM), being the first approach the most appropriate for producing sensitive and reproducible signal in the range of concentrations 0.1-10 nM AFB(1). The sensor was validated in certified contaminated peanuts extract as well as in spiked samples of peanuts-corn snacks and the sensing response was evaluated and compared in terms of the matrix effect. The aptamer specificity was analyzed by testing the sensor in other mycotoxins such as aflatoxin By (AFB(2)) and ochratoxin A (OTA). The limit of detection achieved by this sensor was LOD = 0.40 +/- 0.03 nM, it was regenerable in 0.2 M glycine-HCI and it did not lose its stability up to 60 h storing at 4 degrees C. Atomic Force Microscopy (AFM) studies were also performed for illustrating individual steps of biosensor assembly. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9 / 18
页数:10
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