KUDR, J., L. ZHAO, E.P. NGUYEN, H. AROLA, T.K. NEVANEN, V. ADAM, O. ZITKA and A. MERKOCI. Inkjet-printed electrochemically reduced graphene oxide microelectrode as a platform for HT-2 mycotoxin immunoenzymatic biosensing. BIOSENSORS & BIOELECTRONICS. OXFORD: ELSEVIER ADVANCED TECHNOLOGY, 2020, vol. 156, MAY, p. 112109-112116. ISSN 0956-5663. Available from: https://dx.doi.org/10.1016/j.bios.2020.112109.
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Basic information
Original name Inkjet-printed electrochemically reduced graphene oxide microelectrode as a platform for HT-2 mycotoxin immunoenzymatic biosensing
Authors KUDR, J., L. ZHAO, E.P. NGUYEN, H. AROLA, T.K. NEVANEN, V. ADAM, O. ZITKA and A. MERKOCI.
Edition BIOSENSORS & BIOELECTRONICS, OXFORD, ELSEVIER ADVANCED TECHNOLOGY, 2020, 0956-5663.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10403 Physical chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 10.618
RIV identification code RIV/00216224:14740/20:00121453
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.bios.2020.112109
UT WoS 000523557300005
Keywords in English 2D material; Antibody; Biosensor; Electrochemistry; Graphene oxide
Tags CF SAXS, ne MU, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 29/4/2021 12:23.
Abstract
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 mu m in width and 30 nm in height after solvent evaporation. The printed graphene oxide microelectmdes 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 microelectmde 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 electmactive 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.
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