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Sep 2026

Comparing Suspect and Nontargeted Screening Workflows for Perinatal Chemical Exposome Analysis: A European Interlaboratory Study from the PARC-EU Project

Early-life chemical exposures may contribute to adverse health outcomes later in life. However, conventional chemical analyses typically cover only a limited subset of the chemical exposureome. Suspect and nontargeted screening (SS/NTS) using high-resolution mass spectrometry (HRMS) workflows provides a powerful framework for comprehensive assessments of exposure, with the potential to detect a broad range of environmental contaminants and emerging chemicals. An interlaboratory assay involving 12 laboratories was performed to evaluate the comparability and complementarity of SS/NTS approaches for maternal urine, serum, and milk, based on reversed-phase (RPLC), hydrophilic interaction liquid chromatography (HILIC), and gas chromatography (GC) with HRMS. Participants used in-house methods to possibly detect a predefined and shared list of 50 compounds with varying polarities spiked at three concentrations. The overall detection rates ranged from 4% to 72% for all three techniques, with RPLC-HRMS covering compounds with log P 0–6, while HILIC-HRMS and GC-HRMS extended this coverage. Univariate and multivariable analyses of RPLC-HRMS results for serum and urine identified sample preparation steps as key factors influencing detection rates. Workflow performances were additionally benchmarked by using the S-score. These findings demonstrate the complementarity of SS/NTS platforms for extending chemical-space coverage for the most comprehensive exposure characterization. Therefore, efforts should be made for harmonized QA/QC provisions while conserving the added value of different workflows for exposure data for risk assessments.

Tarek Moufawad, K. Ayeni, E. Baira et al. · 0 citations
Open access Sep 2026

Nontargeted Analysis of the Chemical Exposome in Preterm Birth: A Pilot Study of Placenta and Maternal Serum

Preterm birth is a leading cause of neonatal morbidity and mortality, yet the role of chemical exposures in its etiology remains poorly understood. We hypothesized that untargeted chemical profiling of paired maternal serum and placenta would reveal distinct exposure signatures and metabolic disruptions associated with preterm birth. We analyzed paired maternal serum and placenta samples from 83 pregnant women in New York City, USA, including 30 who delivered preterm (<37 weeks), by non-targeted analysis (NTA) using ultrahigh-performance liquid chromatography coupled to Orbitrap high-resolution mass spectrometry (UHPLC-Orbitrap HRMS). We confirmed 29 chemicals (Level 1), 28 of them exogenous, tentatively identified 1012 peak features (Level 2), and annotated 1180 peak features via in silico simulation (Level 3). Five Level 1 confirmed exogenous chemicals (i.e., dodecyltrimethylammonium, N,N-dimethyldecylamine oxide, rimsulfuron, triphenylphosphine oxide, and 2,6-dichlorobenzamide) and 208 tentatively identified Level 2 chemicals detected in this study appear not to have been previously detected in human blood samples. We identified 119 and 170 significantly differentially enriched features in serum and placenta, respectively (BH-corrected p < 0.05). Serum samples showed changes in glutathione, tryptophan, pyruvate, arachidonic acid, and phospholipid pathways in preterm birth. Our data suggest that chemical exposures might collectively amplify metabolic vulnerabilities in oxidative stress, lipid metabolism, and amino acid catabolism relevant to preterm birth.

Xiao-Wen Ji, Mathusa Lakuleswaran, Wenjie Lyu et al. · 0 citations

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