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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Detection Methods Environmental Sources Gut & Microbiome Human Health Effects Policy & Risk Sign in to save

Unveiling Hidden Threats: Introduction of a Routine Workflow for Label-Free and Non-destructive Detection of Microplastics in Human FFPE Tissue Sections

2025 2 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 58 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Elisabeth S. Gruber, Verena Karl, Kristina Duswald, Mukund S. Bhamidipalli, Michaela Schlederer, Michaela Schlederer, Tanja Limberger, Béla Teleky, Lukas Kenner, Markus Brandstetter

Summary

Researchers developed a new workflow using mid-infrared photothermal microscopy to detect and identify microplastic particles directly in preserved human colon tissue sections. The method allows non-destructive, label-free identification of polymer types within tissue without special sample preparation. The study introduces a practical approach that could enable routine screening for microplastics in human tissues during standard medical examinations.

ABSTRACT Microplastic (MP) pollution has emerged as a significant environmental and health concern. This study aimed at developing a novel method for detecting MP particles in deparaffinized formalin-fixed paraffin-embedded (FFPE) routine tissue sections of human colon samples. By utilizing mid-infrared photothermal (MIP) microscopy, also known as optical photothermal infrared (OPTIR) spectroscopy, we here aimed to establish a work-flow representing a non-destructive infrared spectroscopic approach for distinct identification and localization of polymers in FFPE colon tissue sections by respecting standardized protocols well integrated into clinical routine. After OPTIR analysis, samples were processed to H&E staining for histopathological analysis at defined regions of interest. By using OPTIR spectroscopy, we succeeded in localizing polyethylene (PE), polystyrene (PS), and polyethylene terephthalate (PET) MPs in distinct regions of interest (21 PE particles, 1 PS particle, 1 PET fiber) and clearly identifying the embedded polymers in the respective colon tissue sections. Subsequent H&E analysis confirmed characteristic histopathological features of inflammation spatially associated with the respective MP polymers. We present here for the first time a diagnostic workflow that has the potential to enhance our understanding of MP accumulation in routine organ tissue slides and allows for exploration of its implications for human health. The observed morphological H&E features in proximity to the identified MPs could possibly indicate a link between MP exposure and colon inflammation.

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