Evidence map›Paper›PMID 41495198›Full record

ArticleScientific reports2026

Pulmonary toxicity of polymethyl methacrylate nanoplastics via intratracheal intubation in mice.

Changsic Youn, Yu-Jin Jo, Jeongwoo Kwon, Seung-Bin Yoon, Hyeong-Ju You, Ji-Su Kim

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Changsic Youn *Primate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea.
Yu-Jin Jo *Primate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea.
Jeongwoo KwonPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea.
Seung-Bin YoonPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea.
Hyeong-Ju YouPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea.
Ji-Su KimPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), 351-33, Neongme-gil, Ibam-myeon, Jeongeup-Si, Jeollabuk-Do, 56216, Republic of Korea. kimjs@kribb.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plastics, ubiquitous in daily life and industry, are released into the environment in substantial quantities. Instead of complete biodegradation, plastic waste fragments into smaller particles, accumulating as nanoplastics (NPs; < 1 μm). Humans are exposed to NPs through inhalation and ingestion of contaminated water and food, which can induce cytotoxicity through physical and chemical pathways. Polymethyl methacrylate (PMMA), commonly used in implants and artificial bones, has been identified in human lungs and associated with pulmonary embolism. While PMMA NP toxicity has been reported in vitro, their in vivo effects, as well as the underlying mechanism, remain poorly understood. In this study, we investigated the pulmonary effects of inhaled PMMA NPs in mice. Mice received 20 or 100 μg of PMMA NPs (25 nm) via intratracheal intubation for 28 days. PMMA-NP preparation and characterization are described in the Methods section. Exposed mice exhibited body weight loss and pulmonary accumulation of PMMA NPs. Bronchoalveolar lavage fluid (BALF) analysis revealed increased cell count and elevated inflammatory cytokines in serum and BALF. Histopathology (H&E staining) revealed abnormalities in lung tissue and alterations in protein and RNA expression. The findings demonstrate that respiratory exposure to PMMA NPs induces lung inflammation, tissue damage, and molecular dysregulation.

Indexed as

LungMicroplasticsNanoparticlesPolymethyl MethacrylateAnimalsBronchoalveolar Lavage FluidCytokinesIntubation, IntratrachealMaleMiceCytokinesMicroplasticsPolymethyl MethacrylateInflammationIntratracheal intubationLung toxicityNanoplasticPMMA

Identifiers

PMID41495198
PMCPMC12808127

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.