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Название: Flow-Through Acetylcholinesterase Sensor with Replaceable Enzyme Reactor
Авторы: Ivanov, A.
Stoikov, D.
Shafigullina, I.
Shurpik, D.
Stoikov, I.
Evtugyn, G.
Дата публикации: 2022
Издатель: MDPI
Библиографическое описание: Ivanov, A, Stoikov, D, Shafigullina, I, Shurpik, D, Stoikov, I & Evtugyn, G 2022, 'Flow-Through Acetylcholinesterase Sensor with Replaceable Enzyme Reactor', Biosensors, Том. 12, № 9, 676, стр. 676. https://doi.org/10.3390/bios12090676
Ivanov, A., Stoikov, D., Shafigullina, I., Shurpik, D., Stoikov, I., & Evtugyn, G. (2022). Flow-Through Acetylcholinesterase Sensor with Replaceable Enzyme Reactor. Biosensors, 12(9), 676. [676]. https://doi.org/10.3390/bios12090676
Аннотация: Fast and reliable determination of enzyme inhibitors are of great importance in environmental monitoring and biomedicine because of the high biological activity and toxicity of such species and the necessity of their reliable assessment in many media. In this work, a flow-through biosensor has been developed and produced by 3D printing from poly(lactic acid). Acetylcholinesterase from an electric eel was immobilized on the inner walls of the reactor cell. The concentration of thiocholine formed in enzymatic hydrolysis of the substrate was monitored amperometrically with a screen-printed carbon electrode modified with carbon black particles, pillar[5]arene, electropolymerized Methylene blue and thionine. In the presence of thiocholine, the cathodic current at −0.25 V decreased because of an alternative chemical reaction of the macrocycle. The conditions of enzyme immobilization and signal measurements were optimized and the performance of the biosensor was assessed in the determination of reversible (donepezil, berberine) and irreversible (carbofuran) inhibitors. In the optimal conditions, the flow-through biosensor made it possible to determine 1.0 nM–1.0 μM donepezil, 1.0 μM–1.0 mM berberine and 10 nM to 0.1 μM carbofuran. The AChE biosensor was tested on spiked samples of artificial urine for drugs and peanuts for carbofuran. Possible interference of the sample components was eliminated by dilution of the samples with phosphate buffer. Easy mounting, low cost of replaceable parts of the cell and satisfactory analytical and metrological characteristics made the biosensor a promising future application as a point-of-care or point-of-demand device outside of a chemical laboratory. © 2022 by the authors.
Ключевые слова: ACETYLCHOLINESTERASE SENSOR
ELECTROPOLYMERIZATION
FLOW-THROUGH ANALYSIS
INHIBITOR DETERMINATION
PILLAR[5]ARENE
ACETYLCHOLINESTERASE
BERBERINE
BIOSENSING TECHNIQUES
CARBOFURAN
CARBON
DONEPEZIL
ELECTRODES
ENZYMES, IMMOBILIZED
METHYLENE BLUE
PHOSPHATES
SOOT
THIOCHOLINE
3D PRINTING
AROMATIC COMPOUNDS
BIOACTIVITY
CARBON BLACK
ELECTRODES
ELECTROPOLYMERIZATION
ENZYMATIC HYDROLYSIS
ENZYME ELECTRODES
ACETYLCHOLINESTERASE
BERBERINE
CARBOFURAN
DONEPEZIL
MACROCYCLIC COMPOUND
PHOSPHATE BUFFERED SALINE
THIOCHOLINE
ACETYLCHOLINESTERASE
BERBERINE
CARBOFURAN
CARBON
IMMOBILIZED ENZYME
METHYLENE BLUE
PHOSPHATE
ACETYLCHOLINESTERASE
ACETYLCHOLINESTERASE SENSOR
CARBOFURANS
DONEPEZIL
ELECTROPOLYMERISATION
FLOW-THROUGH ANALYSIS
FLOWTHROUGH
INHIBITOR DETERMINATION
PILLAR[5]ARENE
THIOCHOLINE
ARTICLE
CHEMICAL REACTION
CONTROLLED STUDY
DILUTION
ELECTRIC CURRENT
ENZYME IMMOBILIZATION
ENZYME INHIBITION
NONHUMAN
PEANUT
POINT OF CARE TESTING
SPIKE
URINE
ELECTRODE
GENETIC PROCEDURES
SOOT
ENZYME IMMOBILIZATION
URI: http://elar.urfu.ru/handle/10995/131424
Условия доступа: info:eu-repo/semantics/openAccess
cc-by
Текст лицензии: https://creativecommons.org/licenses/by/4.0/
Идентификатор SCOPUS: 85138417567
Идентификатор WOS: 000858633100001
Идентификатор PURE: 30945438
551f2c10-3e5f-4677-b6ca-28adaf054186
ISSN: 2079-6374
DOI: 10.3390/bios12090676
Сведения о поддержке: Russian Foundation for Basic Research, РФФИ, (20-33-90107)
This research was funded by the Russian Foundation for Basic Research (grant 20-33-90107).
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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Лицензия на ресурс: Лицензия Creative Commons Creative Commons