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Ingested Polystyrene Nanospheres Translocate to Placenta and Fetal Tissues in Pregnant Rats: Potential Health Implications

Nanomaterials 2023 74 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 65 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Phoebe A. Stapleton, Glen M. DeLoid, Philip Demokritou, Chelsea M. Cary, Michael Goedken, Marianne Polunas, Zhenning Yang, Brian Buckley, Dimitrios Bitounis, Byron Cheatham

Summary

In a study on pregnant rats, researchers found that ingested nanoplastics (tiny 25-nanometer plastic spheres) crossed both the intestinal barrier and the placental barrier to reach every fetal organ examined, including the brain, heart, liver, kidneys, and lungs. This is the first study to directly demonstrate that swallowed nanoplastics can travel from a mother's gut to developing fetal tissues. The findings raise serious concerns about potential health effects of nanoplastic exposure during human pregnancy.

Recent studies in experimental animals found that oral exposure to micro- and nano-plastics (MNPs) during pregnancy had multiple adverse effects on outcomes and progeny, although no study has yet identified the translocation of ingested MNPs to the placenta or fetal tissues, which might account for those effects. We therefore assessed the placental and fetal translocation of ingested nanoscale polystyrene MNPs in pregnant rats. Sprague Dawley rats (N = 5) were gavaged on gestational day 19 with 10 mL/kg of 250 µg/mL 25 nm carboxylated polystyrene spheres (PS25C) and sacrificed after 24 h. Hyperspectral imaging of harvested placental and fetal tissues identified abundant PS25C within the placenta and in all fetal tissues examined, including liver, kidney, heart, lung and brain, where they appeared in 10-25 µm clusters. These findings demonstrate that ingested nanoscale polystyrene MNPs can breach the intestinal barrier and subsequently the maternal-fetal barrier of the placenta to access the fetal circulation and all fetal tissues. Further studies are needed to assess the mechanisms of MNP translocation across the intestinal and placental barriers, the effects of MNP polymer, size and other physicochemical properties on translocation, as well as the potential adverse effects of MNP translocation on the developing fetus.

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