Development and Characterization of an Electroless Plated Silver/Cysteine Sensor Platform for the Electrochemical Determination of Aflatoxin B1
| Autor: | Mathew Ocheng, Deborah Wendiro, Alex Paul Wacoo, Joseph F. Hawumba, Peter C. Vuzi |
|---|---|
| Přispěvatelé: | Molecular Cell Physiology |
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
Aflatoxin
Article Subject Inorganic chemistry 02 engineering and technology Electrochemistry 01 natural sciences Horseradish peroxidase Redox lcsh:Technology (General) Electrical and Electronic Engineering Instrumentation Detection limit chemistry.chemical_classification biology Chemistry 010401 analytical chemistry food and beverages 021001 nanoscience & nanotechnology 0104 chemical sciences Control and Systems Engineering biology.protein Thiol lcsh:T1-995 Cyclic voltammetry 0210 nano-technology Cysteine Nuclear chemistry |
| Zdroj: | Journal of Sensors, Vol 2016 (2016) JOURNAL OF SENSORS. Hindawi Publishing Corporation Wacoo, A P, Ocheng, M, Wendiro, D, Vuzi, P C & Hawumba, J F 2016, ' Development and Characterization of an Electroless Plated Silver/Cysteine Sensor Platform for the Electrochemical Determination of Aflatoxin B-1 ', JOURNAL OF SENSORS . https://doi.org/10.1155/2016/3053019 |
| ISSN: | 1687-725X |
| DOI: | 10.1155/2016/3053019 |
| Popis: | An electroless plated silver/cysteine sensor platform [Glass|silver|cysteine|aflatoxin B1|horseradish peroxidase] for the Electrochemical detection of aflatoxin B1was developed and characterized. This involved four major steps: (1) an electroless deposition of silver (plating) onto a glass slide, (2) immobilization of cysteine; (3) conjugation of aflatoxin B1to cysteine groups; and (4) blocking of free cysteine groups with horseradish peroxidase (HRP). The binding of cysteine to the silver was demonstrated by the disappearance of thiol (S-H) groups at 2500 cm−1using Fourier transmittance infrared spectra (FT-IR), while the subsequent steps in the assembly of sensor platform were monitored using both FT-IR and cyclic voltammetry, respectively. The sensor platform exhibited a broadened nonsymmetrical redox couple as indicated by cyclic voltammetry. The platform was further characterized for sensitivity and limit of detection. The indirect competitive immunoassay format, whereby free and immobilized aflatoxin B1on the sensor competed for the binding site of free anti-aflatoxin B1antibody, was used at various concentrations of aflatoxin B1. The sensor generated differential staircase voltammogram that was inversely proportional to the concentration of aflatoxin B1and aflatoxin B1in the range of 0.06–1.1 ng/mL with a detection limit of 0.08 ng/mL could be detected. |
| Databáze: | OpenAIRE |
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