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Advisor(s)
Abstract(s)
Molecular imprinting undergone a substantial boost driven by the awareness of molecularly imprinted polymers
(MIPs)-ligand recognition skills. In particular, the introduction of natural-based compounds like cyclodextrins
into the structural scaffold of synthetic recognition elements attracted great importance as a novel route to design
more friendly-environments for protein binding, while promoting higher selectivity features. Herein, carbon
electrodes doped with platinum nanoparticles supported on multiwalled carbon nanotubes and functionalized
with polyallylamine (MWCNTs-PAH/Pt) were electrochemically modified with an imprinted sensing layer of
poly(β-cyclodextrin-pyrrole) (poly(β-CD-Py)) towards interleukin 6 (IL-6) monitoring. The analytical performance
of the biosensor was evaluated by using Cyclic Voltammetry and Electrochemical Impedance Spectroscopy
techniques. Along the assembly, experimental parameters like nanomaterial deposition, monomer-protein
concentrations and template removal solutions were carefully optimized and discussed. Furthermore, the electrodeposited
film was characterized in terms of composition, morphology and structure using scanning electron
microscopy (SEM) and Raman spectroscopy. Under optimal conditions, the developed sensor was able to rebind
IL-6 over a wide linear range [1 pg/mL – 100 ng/mL], displaying high sensitivity, quick electrochemical
response, and specific binding of the target molecule. Overall, this work reported the relevance of using hostguest
complexes directly embedded in polymeric chains to generate newly controlled electrochemical sensors
holding great potential for protein biosensing.
Description
Keywords
Cyclodextrins Electropolymerization Molecular imprinting Electrochemical Interleukin-6
Citation
Bianca Ferreira, Miguel Correa-Duarte, Arcelina Marques, Felismina Moreira, Gabriela Martins, Bioinspired host-tailored polymers based on molecular imprinting for cytokine assessment, Microchemical Journal, Volume 200, 2024, 110345, ISSN 0026-265X, https://doi.org/10.1016/j.microc.2024.110345.
Publisher
Elsevier