An Electrochemical Pipette for the Study of Drug Metabolite

14 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Electrochemistry offers an effective means of mimicking enzymatic metabolite pathways, particularly the oxidative pathways catalyzed by the cytochrome P450 superfamily. The electrochemical generation and identification of metabolites are time-sensitive, necessitating adjustable cell designs for accurate mechanistic interpretation. We present a thin-layer electrode (TLE) that addresses the needs of both analytical and synthetic electrochemical generation of drug metabolites. The TLE’s ability to conduct experiments on a minute-to-hour timescale allows for detailed observation of reaction mechanisms for metabolites not easily identified by traditional methods. The utility of the TLE for drug metabolite was benchmarked for electrochemical oxidation of acetaminophen, acebutolol, and 2-acetyl-4-butyramidophenol, known to produce quinone imine metabolites, i.e., NAPQI, upon oxidation. When combined with a microelectrode (µE), the TLE enables probing the concentration pro-files for metabolic oxidation of these drugs. The micromole scale and pipette-type structure of the TLE facilitate comprehen-sive structural elucidation of intermediates and products using chromatographic and spectroscopic techniques.

Keywords

Drug metabolites
Thin-layer electrochemistry
Microelectrode
Electrolysis
Electroanalysis

Supplementary materials

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Supporting Information
Description
Additional figures illustrating details of TLE and µE fabrication, more electrochemical experiments, spectra, and chromatograms of the compounds.
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