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Molecular displacement approach for the electrochemical detection of protein-bound propofol

Ferrier, David; Kiely, Janice; Luxton, Richard

Molecular displacement approach for the electrochemical detection of protein-bound propofol Thumbnail


Authors

David Ferrier David.Ferrier@uwe.ac.uk
Research Fellow- Biosensing/ Health Technology

Janice Kiely Janice.Kiely@uwe.ac.uk
Professor in Bio-electronics/Res In CoDi

Richard Luxton Richard.Luxton@uwe.ac.uk
Research Centre Director-IBST/Professor



Abstract

Propofol is one of the principal drugs used for the sedation of patients undergoing mechanical ventilation in intensive care units. The correct dosage of such sedative drugs is highly important, but current methods of determining infusion rates are limited and there is a lack of suitable methods for directly determining patient blood propofol concentrations. A significant challenge for the development of propofol sensors is that propofol demonstrates very high protein binding, leading to a low free fraction in blood. Here we present a method for improving the efficacy of an electrochemical propofol sensor by increasing the free fraction via a molecular displacement approach. When used in conjunction with a carbon nanotube/graphene oxide/iron oxide nanoparticle functionalised screen-printed electrode, it was found that this approach dramatically improved the sensor’s sensitivity towards propofol. Ibuprofen was found to be the most effective displacement agent, with an optimal concentration of 30 mM. The resultant sensitivity was 2.82 nA/µg/ml/mm2 with a coefficient of variation of 0.07, and the limit of detection was 0.2 µg/ml. This approach demonstrates high specificity towards drugs commonly administered to intensive care patients.

Journal Article Type Article
Acceptance Date Nov 5, 2024
Online Publication Date Nov 7, 2024
Publication Date Dec 31, 2024
Deposit Date Nov 29, 2024
Publicly Available Date Nov 29, 2024
Print ISSN 2214-1804
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 46
Article Number 100710
DOI https://doi.org/10.1016/j.sbsr.2024.100710
Public URL https://uwe-repository.worktribe.com/output/13471605

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