Development of an electrochemical immunosensor to determine zearalenone in maize using carbon screen printed electrodes modified with multi-walled carbon nanotubes/polyethyleneimine dispersions

被引:73
作者
Ivan Riberi, Walter [1 ]
Viviana Tarditto, Lorena [1 ]
Alicia Zon, Maria [1 ]
Javier Arevalo, Fernando [1 ]
Fernandez, Hector [1 ]
机构
[1] Univ Nacl Rio Cuarto, Fac Ciencias Exactas Fis Quim & Nat, Dept Quim, Grp Electroanalit GEANA, Agencia Postal 3, RA-5800 Rio Cuarto, Argentina
关键词
Zearale none; Electrochemical immunosensor; Amperometry; Multi-walled carbon; nanotubes/polyethyleneimine dispersions; Maize samples; PERFORMANCE LIQUID-CHROMATOGRAPHY; IMMUNOAFFINITY COLUMN CLEANUP; ALPHA-ZEARALENOL; LC-MS/MS; VALIDATION; CORN; DEOXYNIVALENOL; IMMUNOASSAY; METABOLITES; OCHRATOXIN;
D O I
10.1016/j.snb.2017.07.113
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An electrochemical immunosensor is developed to determine zearalenone (ZEA) mycotoxin in maize samples. It is based on the use of a composite, which was prepared from anti-ZEA poly-clonal antibody bonded to gold nanoparticles immobilized on multi-walled carbon nanotubes/polyethyleneimine dispersions. Carbon screen printed-electrodes (CSPE) were used in the electrochemical transduction stage. The immunoassay is based on a direct competitive assay between ZEA in maize samples and ZEA labeled with horseradish peroxidase enzyme (ZEA-HRP). ZEA determination was performed by amperometry, using an applied potential of -0.3 V. The H2O2, which was not consumed by HRP, was reduced at the electrochemical immunosensor surface. Thus, the reduction current was proportional to the amount of ZEA present in samples. All experimental variables involved in the construction of the electrochemical immunosensor were optimized. The linear concentration range is from 1 x 10(-4) to 1 x 10(-1) ng mL(-1). The limit of detection and SC50 were 0.15 pg mL(-1) and 2 pg mL(-1), respectively. In addition, an acceptable accuracy, with a percentual coefficient of variation (%CV) less than 20%, and recovery percentages close to 105% were found. The electrochemical immunosensor has great advantages such as no pre-treatment of the sample is required, the sample volume is of 20 mu L, the experiments require short times and a very low limit of detection is obtained. Results obtained with this electrochemical immunosensor were compared with those determined by HPLC-fluorescence detection, obtaining a very good correlation. The proposed immunosensor is a valuable alternative tool to determine ZEA in maize samples. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1271 / 1277
页数:7
相关论文
共 53 条
[1]   ELECTROCHEMICAL ACTIVATION OF CARBON ELECTRODES IN BASE - MINIMIZATION OF DOPAMINE ADSORPTION AND ELECTRODE CAPACITANCE [J].
ANJO, DM ;
KAHR, M ;
KHODABAKHSH, MM ;
NOWINSKI, S ;
WANGER, M .
ANALYTICAL CHEMISTRY, 1989, 61 (23) :2603-2608
[2]  
[Anonymous], 1980, ANAL CHEM, V52, P2242
[3]  
[Anonymous], 2007, 3022007 SAGPYA MIN A
[4]  
[Anonymous], 1993, IARC MONOGRAPHS EVAL, V56
[5]   Surface modification for enhancing antibody binding on polymer-based microfluidic device for enzyme-linked immunosorbent assay [J].
Bai, Yunling ;
Koh, Chee Guan ;
Boreman, Megan ;
Juang, Yi-Je ;
Tang, I-Ching ;
Lee, L. James ;
Yang, Shang-Tian .
LANGMUIR, 2006, 22 (22) :9458-9467
[6]   Quantum dot based rapid tests for zearalenone detection [J].
Beloglazova, N. V. ;
Speranskaya, E. S. ;
De Saeger, S. ;
Hens, Z. ;
Abe, S. ;
Goryacheva, I. Yu. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2012, 403 (10) :3013-3024
[7]  
BENNETT GA, 1985, J ASSOC OFF ANA CHEM, V68, P958
[8]   Rapid simultaneous determination of major type A- and B-trichothecenes as well as zearalenone in maize by high performance liquid chromatography-tandem mass spectrometry [J].
Berthiller, F ;
Schuhmacher, R ;
Buttinger, G ;
Krska, R .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1062 (02) :209-216
[9]  
Bianchini A., 2014, MYCOTOXINS CLASSIFIC, V2, P854
[10]   Development of a multicomponent method for Fusarium toxins using LC-MS/MS and its application during a survey for the content of T-2 toxin and deoxynivalenol in various feed and food samples [J].
Biselli, S ;
Hummert, C .
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2005, 22 (08) :752-760