ArticleACS omega2026
Rapid Point-of-Care Assessment of Paracetamol Intoxication via an Integrated Electrochemical-Colorimetric Method.
Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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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.
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Who cites it
1 citing paper in PubMed.
- Metal nanocrystals and nanoclusters with paracetamol passivation and for paracetamol detection: a critical review.Nanoscale advances · 2026Review
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This work addresses the detection and quantification of paracetamol (PAR) in human serum using a point-of-care approach, an essential assessment for intoxication cases in clinical analysis. Electrochemical and colorimetric methods have been widely reported for simple and fast determination of PAR in biological samples. However, most of these previous portable methods have neglected some aspects for a real-world clinical application of PAR intoxication, such as its toxic concentration range and a proper interference study in biological matrices. To fill this gap, we introduce a novel integrated sensing approach, combining colorimetric and electrochemical techniques for determining PAR. In contrast to other sensors, this work employs a simple screen-printed graphite electrode (SPE-Gr) combined with a colorimetric reagent (CR) for the rapid and selective detection of PAR in human serum. Analysis occurs via dual confirmation: after reaction between PAR and CR, first a color change can indicate intoxication levels, and the generated product is subsequently accurately quantified by square-wave adsorptive stripping voltammetry using a SPE-Gr. A wide linear range (4.5 to 1000 mg L
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Registered trials
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