Evidence map›Paper›PMID 41286311›Full record

ArticleScientific reports2025

Occurrence, distribution, and risk assessment of selected pharmaceuticals in municipal biosolids from the four wastewater treatment plants in Gauteng Province, South Africa.

Matome Peter Ngoetjana, Eyob Habte Tesfamariam, Sally Brown, Madelien Wooding

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. 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

4 authors.

Matome Peter NgoetjanaDepartment of Plant and Soil Sciences, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0003-4554-7037
Eyob Habte TesfamariamDepartment of Plant and Soil Sciences, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa. eyob.tesfamariam@up.ac.za.ORCID http://orcid.org/0000-0003-0724-9864
Sally BrownSchool of Environmental and Forest Sciences, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0002-9405-571X
Madelien WoodingDepartment of Chemistry, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0003-3869-7467

Funding

Water Research Commission Project number: C2022/2023-00880
6 · The paper itself

Abstract

The presence of pharmaceutical residues in municipal biosolids is an emerging environmental concern due to their potential accumulation in agricultural soils following land application. While parent compounds like sulfamethoxazole and carbamazepine are frequently studied, data on their transformation products in biosolids remain limited. This study assessed the occurrence, distribution, and environmental risks of sulfamethoxazole, carbamazepine, and two of their selected metabolites in biosolids collected from four wastewater treatment plants (WWTPs) in Gauteng Province, South Africa. A single biosolid sampling campaign was conducted across the four WWTPs, each characterized by varying operational parameters. Sulfamethoxazole and its two metabolites were not detected in any of the samples. In contrast, carbamazepine and its metabolites-carbamazepine-10,11-epoxide and carbamazepine diol-were detected, with maximum concentrations of 150.67, 601.95, and 89.18 ng/g dry weight, respectively. Carbamazepine and carbamazepine-10,11-epoxide occurred in all samples, while carbamazepine diol appeared in 50% of the samples. The concentration patterns varied across WWTPs and were significantly correlated with biosolid pH, organic carbon content, and oxidation-reduction potential. Risk quotient analysis indicated that the predicted soil concentrations of carbamazepine (0.50 ng/g dry weight) pose negligible ecological risk (RQ = 0.003). However, due to a lack of ecotoxicological data, environmental risks associated with carbamazepine-10,11-epoxide and carbamazepine diol could not be fully assessed. Overall, the findings highlight the persistence of carbamazepine and its metabolites in biosolids and underscore the importance of optimizing sludge treatment processes and generating toxicity data for pharmaceutical metabolites to support safe land application practices.

Indexed as

SewageWastewaterWater Pollutants, ChemicalCarbamazepineEnvironmental MonitoringPharmaceutical PreparationsRisk AssessmentSouth AfricaSulfamethoxazoleWaste Disposal, FluidCarbamazepinePharmaceutical PreparationsSewageSulfamethoxazoleWastewaterWater Pollutants, ChemicalBiosolidsDistributionEnvironmental riskMetabolitesOccurrencePharmaceuticals

Identifiers

PMID41286311
PMCPMC12748950

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LicenceCC BY-NC-ND
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Registered trials

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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.