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In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice

Polymers 2022 29 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Sijoon Lee, Kyung‐Ku Kang, Soo‐Eun Sung, Joo-Hee Choi, Min Kyung Sung, Keum‐Yong Seong, Ji-An Lee, Hyun‐Han Kwon, Subin Kang, Seong Yun Yang, Sunjong Lee, Sunjong Lee, Kyeong‐Ryoon Lee, Min‐Soo Seo, Kil‐Soo Kim

Summary

Researchers investigated the in vivo toxicity and pharmacokinetics of polytetrafluoroethylene (PTFE) microplastics in mice, finding that these particles accumulated in organs and caused dose-dependent inflammatory responses and oxidative stress.

Polymers
Study Type In vivo

The increased use of plastics has led to severe environmental pollution, particularly by microplastics-plastic particles 5 mm or less in diameter. These particles are formed by environmental factors such as weathering and ultraviolet irradiation, thereby making environmental pollution worse. This environmental pollution intensifies human exposure to microplastics via food chains. Despite potential negative effects, few toxicity assessments on microplastics are available. In this study, two sizes of polytetrafluoroethylene (PTFE) microplastics, approximately 5 μm and 10-50 μm, were manufactured and used for single and four-week repeated toxicity and pharmacokinetic studies. Toxicological effects were comprehensively evaluated with clinical signs, body weight, food and water consumption, necropsy findings, and histopathological and clinical-pathological examinations. Blood collected at 15, 30 60, and 120 min after a single administration of microplastics were analyzed by Raman spectroscopy. In the toxicity evaluation of single and four-week repeated oral administration of PTFE microplastics, no toxic changes were observed. Therefore, the lethal dose 50 (LD50) and no-observed-adverse-effect-level (NOAEL) of PTFE microplastics in ICR mice were established as 2000 mg/kg or more. PTFE microplastics were not detected in blood, so pharmacokinetic parameters could not be calculated. This study provides new insight into the long-term toxicity and pharmacokinetics of PTFE microplastics.

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