TMDC-Coated Electrodes for Selective Hydroxyurea Detection

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Solution Overview

Problem

Current methods for determining hydroxyurea concentrations in biofluids, such as blood or plasma, face challenges due to interfering electro-active species like uric acid and ascorbic acid, which mask the electrochemical signature of hydroxyurea, necessitating the development of highly selective working electrodes.

Innovation Solution

The use of transition metal dichalcogenide (TMDC)-coated working electrodes, specifically MoS2-coated gold electrodes, in combination with differential pulse voltammetry and chemometrics, to enhance the detection and quantification of hydroxyurea by resolving complex electrochemical signals.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If standard electrochemical detection methods are used, then the detection process is simple, but interfering species mask the hydroxyurea signal resulting in poor measurement precision

Engineering Contradiction:
Improvedetection precisionVSAvoidelectrode structure complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent applies composite materials by coating the working electrode with transition metal dichalcogenide (TMDC) materials such as MoS2, WS2, or WSe2. This composite structure combines the electrochemical activity of the base electrode material with the selective catalytic properties of TMDC, enabling the electrode to distinguish hydroxyurea signals from interfering species like ascorbic acid and uric acid while maintaining structural integrity and electrochemical performance

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent implements local quality by modifying only the surface of the working electrode with TMDC coating rather than changing the entire electrode structure. This localized modification concentrates the selective detection capability at the electrode-solution interface where the electrochemical reactions occur, improving measurement precision without requiring complex changes to the overall device architecture

Inventive Principle:
Principle #3Local quality

2Measurement precision

If chromatographic analysis methods are used, then measurement precision is improved, but the detection process becomes time-consuming and less suitable for rapid monitoring

Engineering Contradiction:
Improveconcentration determination accuracyVSAvoidanalysis time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent replaces the mechanical separation processes inherent in chromatographic methods with an electrochemical detection approach using TMDC-coated electrodes. Instead of physically separating components through columns and mobile phases, the TMDC coating provides selective electrocatalytic activity that directly generates distinguishable electrochemical signals for hydroxyurea, enabling rapid concentration determination without time-consuming separation steps while maintaining accurate measurement

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Reliability

If electrode arrays with multiple coatings are used, then selectivity toward hydroxyurea is improved, but device complexity increases

Engineering Contradiction:
ImproveselectivityVSAvoidelectrode array complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies parameter changes by systematically varying the TMDC material composition (MoS2, WS2, WSe2), coating thickness, and electrochemical measurement parameters (potential range, scan rate) to optimize selectivity for hydroxyurea. This approach achieves high reliability through material and parameter optimization rather than requiring complex multi-electrode arrays, simplifying the device while maintaining superior selectivity compared to uncoated electrodes or those with conventional coatings

Inventive Principle:
Principle #35Parameter changes

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The TMDC-coated electrodes improve the limit of detection and sensitivity for hydroxyurea, enabling accurate quantification across a broad potential range, including clinical concentrations, and allow for precise determination in small biofluid samples using microfabricated sensors.

Implementation Method 1

Some drugs lend themselves to electrochemical detection e.g., in blood or urine samples, owing to their ability to undergo oxidation-reduction reaction to produce concentration-dependent electrochemical signal

Methodology Applied
Scientific EffectOxidation-reduction reaction: Redox Reactions

Implementation Method 2

When electroactive species are present in the tested sample, they undergo oxidation (or reduction) when the potential on the working electrode is sufficiently positive (or negative). The oxidation/reduction electrochemical reactions are indicated by an increase in the current (anodic or cathodic) measured

Methodology Applied
Scientific EffectElectrochemical oxidation: Oxidation

Data Source

PatentUS12535458B2Electrochemical sensor and determination of hydroxyurea
Publication Date: 2026.01.27 BG NEGEV TECHNOLOGIES & APPLICATIONS LTD
  • US12535458B2 patent drawing
  • US12535458B2 patent drawing
  • US12535458B2 patent drawing

AI summary

An electrochemical sensor comprising an array of working electrodes made of noble metals, wherein the array includes: one or more bare working electrode(s); and a first set of working electrodes coated with a first transition metal dichalcogenide, the first set comprises at least subset A and subset B, wherein working electrodes of subset B show the presence of hydroxide form(s) and/or high oxidation state oxide forms(s) of the noble metal, whereas working electrodes of subset A are free of such forms; and/or working electrodes of subset B show higher capacitive currents and lower charge transfer resistance compared to working electrodes of subset A, as determined by electrochemical impedance spectroscopy.