Evidence map›Paper›PMID 42100459›Full record

ArticleRSC advances2026

Heteroatom-doped reduced graphene oxide electrochemical sensor for sensitive dopamine detection with preliminary clinical evaluation of neurotransmitter dysregulation in pediatric epilepsy.

Fatma Besbes, Zouhour Hsine, Said Galai, Ichraf Kraoua, Rym Mlika, Hafsa Korri-Youssoufi

Abstract read
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Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Fatma BesbesUniversité Paris-Saclay, UMR-CNRS, Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO, ECBB, Bât Henri Moisson 17 Avenue des Sciences 91400 Orsay France hafsa.korri-youssoufi@universite-paris-saclay.fr +33-169157440.ORCID https://orcid.org/0009-0000-4118-3411
Zouhour HsineLaboratory of Interfaces and Advanced Materials, Faculty of Science of Monastir, University of Monastir 5019 Monastir Tunisia.
Said GalaiResearch Laboratory of Neurological Diseases of the Child (LR18SP04), Department of Clinical Biology, National Institute Mongi Ben Hmida of Neurology at Tunis La Rabta 1007 Tunis Tunisia.ORCID https://orcid.org/0000-0003-1232-5120
Ichraf KraouaResearch Laboratory of Neurological Diseases of the Child (LR18SP04), Department of Clinical Biology, National Institute Mongi Ben Hmida of Neurology at Tunis La Rabta 1007 Tunis Tunisia.ORCID https://orcid.org/0000-0001-6942-5662
Rym MlikaLaboratory of Interfaces and Advanced Materials, Faculty of Science of Monastir, University of Monastir 5019 Monastir Tunisia.ORCID https://orcid.org/0000-0003-0382-9562
Hafsa Korri-YoussoufiUniversité Paris-Saclay, UMR-CNRS, Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO, ECBB, Bât Henri Moisson 17 Avenue des Sciences 91400 Orsay France hafsa.korri-youssoufi@universite-paris-saclay.fr +33-169157440.ORCID https://orcid.org/0000-0002-5858-5385

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring dopamine (DA) levels in biological fluids is highly informative for the early diagnosis and therapeutic management of neurological disorders such as Parkinson's disease, schizophrenia, attention-deficit/hyperactivity disorder (ADHD), and epilepsy, which represents a major pediatric neurological condition with wide clinical heterogeneity. In this study, we report a preliminary clinical evaluation of an electrochemical sensor developed for DA detection in the blood of pediatric epilepsy patients. The sensing platform is based on screen-printed carbon electrodes (SPCEs) modified with nitrogen-doped reduced graphene oxide (N-RGO) and nitrogen/sulfur co-doped reduced graphene oxide (S/N-RGO) to enhance electrocatalytic performance. Heteroatom incorporation into RGO significantly improved electron transfer kinetics, electroactive surface area, and sensing activity. Using chronoamperometry (CA) and differential pulse voltammetry (DPV), the N-RGO sensor achieved low detection limits of 6.8 nM and 7.9 nM, respectively, in buffer, with excellent selectivity in the presence of common interferents such as ascorbic acid and uric acid. High recovery rates (∼100%) were obtained in commercial plasma and fresh human serum samples, including those collected from pediatric epilepsy patients. Notably, DA plasma concentrations were found to be lower in this heterogeneous group of epileptic patients, reflecting neurotransmitter dysregulation associated with epilepsy subtype and antiepileptic treatment (valproate). This work presents a sensitive electrochemical sensor capable of detecting and monitoring DA in blood and highlights its potential as a minimally invasive point-of-care tool for pediatric epileptic patients. With further development, this device could also be applied to assess DA levels in other neurological disorders.

Identifiers

PMID42100459
PMCPMC13147507

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.