Inkjet-printed electrochemically reduced graphene oxide microelectrode as a platform for HT-2 mycotoxin immunoenzymatic biosensing
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32275576
DOI
10.1016/j.bios.2020.112109
PII: S0956-5663(20)30106-8
Knihovny.cz E-zdroje
- Klíčová slova
- 2D material, Antibody, Biosensor, Electrochemistry, Graphene oxide,
- MeSH
- biosenzitivní techniky přístrojové vybavení MeSH
- design vybavení MeSH
- elektrochemické techniky přístrojové vybavení MeSH
- grafit chemie MeSH
- imobilizační protilátky chemie MeSH
- imunoenzymatické techniky přístrojové vybavení MeSH
- mikroelektrody MeSH
- oxidace-redukce MeSH
- reagenční papírky analýza MeSH
- T-2 toxin analogy a deriváty analýza MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- grafit MeSH
- graphene oxide MeSH Prohlížeč
- HT-2 toxin MeSH Prohlížeč
- imobilizační protilátky MeSH
- reagenční papírky MeSH
- T-2 toxin MeSH
The design and application of an inkjet-printed electrochemically reduced graphene oxide microelectrode for HT-2 mycotoxin immunoenzymatic biosensing is reported. A water-based graphene oxide ink was first formulated and single-drop line working microelectrodes were inkjet-printed onto poly(ethylene 2,6-naphthalate) substrates, with dimensions of 78 μm in width and 30 nm in height after solvent evaporation. The printed graphene oxide microelectrodes were electrochemically reduced and characterized by Raman and X-ray photoelectron spectroscopies in addition to microscopies. Through optimization of the electrochemical reduction parameters, differential pulse voltammetry were performed to examine the sensing of 1-naphthol (1-N), where it was revealed that reduction times had significant effects on electrode performance. The developed microelectrodes were then used as an immunoenzymatic biosensor for the detection of HT-2 mycotoxin based on carbodiimide linking of the microelectrode surface and HT-2 toxin antigen binding fragment of antibody (anti-HT2 (10) Fab). The HT-2 toxin and anti-HT2 (10) Fab reaction was reported by anti-HT2 immune complex single-chain variable fragment of antibody fused with alkaline phosphatase (anti-IC-HT2 scFv-ALP) which is able to produce an electroactive reporter - 1-N. The biosensor showed detection limit of 1.6 ng ∙ mL-1 and a linear dynamic range of 6.3 - 100.0 ng ∙ mL-1 within a 5 min incubation with 1-naphthyl phosphate (1-NP) substrate.
Citace poskytuje Crossref.org
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