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61 Evaluation of the Toxicity, Alveolar Cell Accumulation and Clearance of PET and PS Nanoplastics in Mouse Lungs

Annals of Work Exposures and Health 2023 3 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 45 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Julia Catalán, Aliro Villacorta, Adriana Rodríguez-Garraus, Ricard Marcos, Aswin Kuttykattil, Aswin Kuttykattil, Thomas Loret, Adriana Rodríguez-Garraus, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aswin Kuttykattil, Julia Catalán, Aliro Villacorta, Alba Hernández, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, Alba Hernández, Alba Hernández, Aliro Villacorta, Aliro Villacorta, Aliro Villacorta, S. Alexander Holme, S. Alexander Holme, Aswin Kuttykattil, Aswin Kuttykattil, Aswin Kuttykattil, Aliro Villacorta, Ricard Marcos, Ricard Marcos, Aswin Kuttykattil, Alba Hernández, Aswin Kuttykattil, Aliro Villacorta, Tom Venus, Aswin Kuttykattil, Aliro Villacorta, Ricard Marcos, Aliro Villacorta, Aliro Villacorta, Tom Venus Alba Hernández, Alba Hernández, Aswin Kuttykattil, Alba Hernández, Alba Hernández, Alba Hernández, Aliro Villacorta, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Ricard Marcos, Ricard Marcos, Tom Venus, Ricard Marcos, Cyrill Bussy, Tom Venus Alba Hernández, Ricard Marcos, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Ricard Marcos, Alba Hernández, Alba Hernández, Aliro Villacorta, Alba Hernández, Alba Hernández, Aliro Villacorta, Alba Hernández, Alba Hernández, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Julia Catalán, Julia Catalán, Cyrill Bussy, Cyrill Bussy, Adriana Rodríguez-Garraus, Adriana Rodríguez-Garraus, Ricard Marcos, Tom Venus Alba Hernández, Ricard Marcos, Alba Hernández, Alba Hernández, Ricard Marcos, Tom Venus, Ricard Marcos, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Ricard Marcos, Aliro Villacorta, Ricard Marcos, Julia Catalán, Ricard Marcos, Ricard Marcos, Alba Hernández, Irina Irina Estrela-Lopis, Alba Hernández, Irina Irina Estrela-Lopis, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Ricard Marcos, Alba Hernández, Ricard Marcos, Ricard Marcos, Tom Venus, Alba Hernández, Alba Hernández, Alba Hernández, Julia Catalán, Alba Hernández, Alba Hernández, Alba Hernández, Tom Venus Ricard Marcos, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Ricard Marcos, Ricard Marcos, Alba Hernández, Ricard Marcos, Alba Hernández, Alba Hernández, Ricard Marcos, Alba Hernández, Alba Hernández, Alba Hernández, Alba Hernández, Cyrill Bussy, Ricard Marcos, Ricard Marcos, Alba Hernández, Alba Hernández, Julia Catalán, Tom Venus, Tom Venus Aliro Villacorta, Tom Venus, Tom Venus

Summary

Pharyngeal aspiration of PET and polystyrene nanoplastics in mice triggered immune cell infiltration in lungs, with 50 nm PS nanoplastics causing significantly greater neutrophil recruitment at day 1 and eosinophil recruitment at day 7 compared to 200 nm particles or PET, highlighting size-dependent pulmonary toxicity.

Polymers
Models

Abstract Airborne micro and nano-plastics (MNPs) have been detected in both indoor and outdoor settings, raising concerns about potential adverse effects upon inhalation. Yet, their potential pulmonary toxicity has not been studied extensively. Herein, we evaluated the pulmonary toxicity and clearance of nanometric Poly-Ethylene Terephthalate (PET; ~50-200 nm) fragments from plastic bottles and two nanometric polystyrene (PS; 50 and 200 nm) beads. Adult mice were exposed to a unique dose of 50 ug in 30uL/mouse of PET, PS-50, PS-200, or vehicle by pharyngeal aspiration. The lungs, broncho-alveolar lavage fluids (BALF) and lymph nodes were collected at 1, 7 and 28 days after exposure. MNPs presence in lung tissue, accumulation in alveolar cells, and clearance from the alveolar cavity and lungs were assessed using confocal Raman microscopy (CRM). Inflammation and tissue damages were evaluated by histology, immunostaining and ELISA. PET and PS nanoplastics were detected by CRM in lungs and alveolar phagocytes. Evaluation of MNPs elimination and translocation to lymph nodes is underway. Pulmonary exposure to MNPs induced immune cell infiltration respective of MNP type or size. Recruitment of neutrophils at day 1 and eosinophils at day 7 was more pronounced for the PS-50 than for the other two MNPs. Recruitment of lymphocytes was noted at day 7, yet only for PS-50 nm. Potential long-term impact (genotoxicity, fibrosis) is under investigation. These results will inform the design of future chronic low-dose exposure studies, and path the way to new policies about the impact of MNPs on human health.

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