Evidence map›Paper›PMID 42405122›Full record

ArticleRSC advances2026

Sustainable electrocatalysis: overcoming signal convolution of dopamine and paracetamol at a pristine graphene interface.

Lê Thi Kim Dung, Do Mai Nguyen, Nguyen Truong Son, Nguyen Minh Quang, Dinh Tuan, Tran Thanh Tam Toan, Vo Chau Ngoc Anh

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Lê Thi Kim DungUniversity of Medicine and Pharmacy, Hue University 530000 Vietnam vcnanh@hueuni.edu.vn.ORCID https://orcid.org/0000-0002-2674-4900
Do Mai NguyenUniversity of Science and Education, Danang University Danang City 550000 Vietnam.ORCID https://orcid.org/0000-0002-8474-0449
Nguyen Truong SonUniversity of Medicine and Pharmacy, Hue University 530000 Vietnam vcnanh@hueuni.edu.vn.ORCID https://orcid.org/0009-0002-2259-1908
Nguyen Minh QuangFaculty of Chemical Engineering, Industrial University of Ho Chi Minh City Ho Chi Minh City 700000 Vietnam.ORCID https://orcid.org/0000-0002-2418-9253
Dinh TuanFaculty of Pharmacy, Nam Can Tho University 168 Nguyen Van Cu Street An Binh Ward Can Tho City Vietnam.ORCID https://orcid.org/0000-0002-2000-5509
Tran Thanh Tam ToanPhu Xuan University Hue City 530000 Vietnam toan.tran@pxu.edu.vn.ORCID https://orcid.org/0000-0001-5426-2880
Vo Chau Ngoc AnhUniversity of Medicine and Pharmacy, Hue University 530000 Vietnam vcnanh@hueuni.edu.vn.ORCID https://orcid.org/0009-0007-2657-3682

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Simultaneous electrochemical quantification of dopamine and paracetamol is often hindered by overlapping oxidation potentials and severe surface passivation. To address this analytical gap, a completely reagent-free fabrication approach was developed to construct an electrochemically reduced graphene oxide (ERGO) modified glassy carbon electrode (GCE). The reliance on toxic reducing agents was entirely eliminated by utilizing a direct cathodic potential scan. Through this green process, the conductive carbon network was restored, yielding a highly active electrocatalytic interface. Complete baseline separation between the two target analytes was successfully achieved. Under optimized acidic conditions at pH 3.0, a broad linear dynamic range from 0.1 to 20 µM was obtained for both compounds. Furthermore, the limits of detection (LOD) were 0.008 µM for dopamine (DOP) and 0.016 µM for paracetamol (PAR). Excellent target selectivity was demonstrated even when the sensor was challenged with highly concentrated biological interferents such as ascorbic acid and uric acid. Finally, the platform's practical reliability was validated by analysing commercial pharmaceutical formulations, yielding recovery rates of 96.1-104.1%. These findings were statistically equivalent to standard chromatographic measurements, confirming that a highly accurate, eco-friendly tool is provided for routine clinical monitoring.

Identifiers

PMID42405122
PMCPMC13329819

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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.