Evidence map›Paper›PMID 41145562›Full record

ArticleScientific reports2025

Sonochemically enhanced activated charcoal with improved oral palatability for efficient in vitro detoxification of acetaminophen.

Forough Riahimanesh, Ahmad Alahabadi, Mehdi Salari, Samad Nazemi

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Forough RiahimaneshCellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Ahmad AlahabadiDepartment of Environmental Health Engineering, School of Public Health, Sabzevar University of Medical Sciences, Sabzevar, Iran. ahmad_health@yahoo.com.
Mehdi SalariDepartment of Environmental Health Engineering, School of Public Health, Sabzevar University of Medical Sciences, Sabzevar, Iran. Msalari_22@yahoo.com.
Samad NazemiDepartment of Physiology and Pharmacology, School of Medical Sciences, Sabzevar University of Medical Sciences, Sabzevar, Iran.

Funding

Sabzevar University of Medical Sciences 403115
6 · The paper itself

Abstract

Acetaminophen (APAP) overdose is a major cause of drug-induced liver injury, underscoring the urgent need for detoxification agents that are both effective and suitable for oral administration. In this study, we developed a novel activated charcoal (UA-AChar) derived from Calligonum comosum wood, employing ammonium chloride-assisted chemical activation combined with ultrasonic treatment. The resulting material demonstrated an exceptionally high specific surface area (1531 m²/g), a mesoporous structure with a pore size of 2.20 nm, and a rich functional group composition containing both oxygen and nitrogen, all of which significantly enhance its adsorption performance. UA-AChar demonstrated high adsorption efficiency, achieving 89% and 86% removal of APAP within 15 min at pH 1.2 and 7.5, respectively, with a dosage of 0.4 g/L and an initial APAP concentration of 50 mg/L. In equilibrium studies at higher concentrations (500 mg/L), the maximum adsorption capacities reached 787.5 mg/g at pH 1.2 and 725 mg/g at pH 7.5. The experimental data were best described by the Freundlich isotherm, indicating multilayer adsorption on heterogeneous surfaces. Kinetic analysis revealed that the adsorption process followed a pseudo-second-order model. UA-AChar was incorporated into yogurt, ice cream, and honey to improve its oral acceptability. The addition of these flavoring agents preserved the adsorption efficiency within a clinically acceptable range (≤ 7% reduction), underscoring their potential to enhance palatability. Consequently, UA-AChar presents a promising and effective solution for managing APAP overdose, offering a patient-friendly approach to oral detoxification.

Indexed as

AcetaminophenCharcoalAdministration, OralAdsorptionHumansHydrogen-Ion ConcentrationInactivation, MetabolicAcetaminophenCharcoalAcetaminophenActivated charcoalAdsorptionDrug poisoningPalatability enhancementUltrasonic

Identifiers

PMID41145562
PMCPMC12559426

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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.