Electrochemical and morphological layer-by-layer characterization of electrode interfaces during a label-free impedimetric immunosensor build-up: The case of ochratoxin A

被引:28
作者
Cancelliere, Rocco [1 ,2 ]
Albano, David [1 ]
Brugnoli, Benedetta [1 ,3 ]
Buonasera, Katia [1 ]
Leo, Gabriella [4 ]
Margonelli, Andrea [1 ]
Rea, Giuseppina [1 ]
机构
[1] CNR, Inst Crystallog, Via Salaria Km 29,300, I-00015 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Chem Sci & Technol, Via Ric Sci 1, I-00133 Rome, Italy
[3] Sapienza Univ Rome, Dept Chem, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[4] CNR, Inst Study Nanostruct Mat, Via Salaria Km 29,300, I-00015 Rome, Italy
关键词
Electron transfer kinetics; Diffusivity process; Label-free immunosensors; Ochratoxin A immunosensor; Contact angle; SELF-ASSEMBLED MONOLAYERS; IMPEDANCE SPECTROSCOPY; MONOCLONAL-ANTIBODY; GOLD OXIDE; REDUCTION; OXIDATION; SURFACE; NANOPARTICLES; BIOSENSORS; DIFFUSION;
D O I
10.1016/j.apsusc.2021.150791
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this paper, we provide an in-depth electrochemical characterization of a label-free impedimetric immunosensor for rapid detection of ochratoxin A. The sensor was based on a carbodiimide-mediated amide coupling reaction to immobilize a specific ochratoxin A antibody onto 4-mercaptobenzoic acid-modified commercial screen-printed gold electrode. Different variables affecting the performance of the developed sensor were optimized. Cyclic voltammetry and electrochemical impedance spectroscopy were used to analyse modifications of the interfacial properties occurring at each step of the biosensor assembly. The free electrode surface area, the diffusion coefficient, the peak-to-peak separation, the heterogeneous electron transfer constant, and charge transfer resistance have been calculated and compared. The decrease of charge transfer resistance values was linearly proportional to the ochratoxin A concentration in the range of 0.37- 2.86 ng/mL, with a detection limit of 0.19 ng/mL, a limit of quantification of 0.40 ng/mL, very good selectivity, reproducibility, and storage stability in the absence of antifouling agents. Surface morphology and topographic data at each step of the immunosensor assembly were studied by Atomic Force Microscopy, which also provided information on the specific binding of ochratoxin A. Finally, contact angle measurements revealed the hydrophilicity evolution of the surface during sensor assembly enabling OTA binding.
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页数:12
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