Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/103198
Title: Flexible sensing devices integrating molecularly-imprinted polymers for the detection of 3-nitrotyrosine biomarker
Authors: Martins, G. V. 
Riveiro, A.
Chiussi, S.
Sales, M. G. F. 
Keywords: Molecularly-imprinted polymer; Flexible substrate; Gold-based electrodes; Electrochemical (bio)sensor; Oxidative stress biomarker
Issue Date: 2022
Project: IBEROS project (Instituto de Bioingeniería en Red para el Envejecimiento Saludable, INTERREG POCTEP/0245_IBEROS_1_E) supported by FEDER, also within the cooperation region of Galicia/Spain and North of Portugal 
FCT - UIDB/04469/2020 
Serial title, monograph or event: Biosensors and Bioelectronics: X
Volume: 10
Abstract: In recent years, the development of flexible and wearable devices for healthcare and biomedical applications has become an emerging technological goal, particularly with personalized medicine on the rise. As a response to the increasing demand for in-situ sensing platforms that fulfil some essential requirements like sensitivity, reproducibility and high stability, electrochemical sensors have boosted their way for innovative approaches. So, highquality flexible sensing strategies are still a demand for local monitoring. Herein, a flexible three-electrode system was fabricated on transparent polymeric sheet substrate through physical deposition of gold as working, counter, and reference electrodes. Along the fabrication process, the electrochemical performance of these electrodes was assessed by means of cyclic voltammetry (CV) while gold adherence to the plastic material was continuously improved. Afterwards, a high-performance molecularlyimprinted sensing film inspired by natural recognition mechanism was assembled through electropolymerization of phenol monomer, in the presence of 3-nitrotyrosine (3-NT), directly on the gold surface. Under the optimized conditions, the flexible (bio)sensor platform was able to detect the presence of 3-NT over the concentration range 10 pg/mL – 1 μg/mL, enabling one of the lower limits of detection found in the literature (1.13 pg/mL or 24.9 pM). The obtained (bio)sensor displayed good reproducibility, stability and selectivity over the chosen interfering substances. Overall, the developed electrochemical device may serve as a flexible, miniaturized, and reliable platform, with potential to be applied in the future as wearable sensing technology.
URI: https://hdl.handle.net/10316/103198
ISSN: 25901370
DOI: 10.1016/j.biosx.2022.100107
Rights: openAccess
Appears in Collections:FCTUC Eng.Química - Artigos em Revistas Internacionais

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