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In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice
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 en...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182653/ https://www.ncbi.nlm.nih.gov/pubmed/35683896 http://dx.doi.org/10.3390/polym14112220 |
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author | Lee, Sijoon Kang, Kyung-Ku Sung, Soo-Eun Choi, Joo-Hee Sung, Minkyoung Seong, Keum-Yong Lee, Jian Kang, Subin Yang, Seong Yun Lee, Sunjong Lee, Kyeong-Ryoon Seo, Min-Soo Kim, KilSoo |
author_facet | Lee, Sijoon Kang, Kyung-Ku Sung, Soo-Eun Choi, Joo-Hee Sung, Minkyoung Seong, Keum-Yong Lee, Jian Kang, Subin Yang, Seong Yun Lee, Sunjong Lee, Kyeong-Ryoon Seo, Min-Soo Kim, KilSoo |
author_sort | Lee, Sijoon |
collection | PubMed |
description | 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 (LD(50)) 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. |
format | Online Article Text |
id | pubmed-9182653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91826532022-06-10 In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice Lee, Sijoon Kang, Kyung-Ku Sung, Soo-Eun Choi, Joo-Hee Sung, Minkyoung Seong, Keum-Yong Lee, Jian Kang, Subin Yang, Seong Yun Lee, Sunjong Lee, Kyeong-Ryoon Seo, Min-Soo Kim, KilSoo Polymers (Basel) Article 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 (LD(50)) 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. MDPI 2022-05-30 /pmc/articles/PMC9182653/ /pubmed/35683896 http://dx.doi.org/10.3390/polym14112220 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lee, Sijoon Kang, Kyung-Ku Sung, Soo-Eun Choi, Joo-Hee Sung, Minkyoung Seong, Keum-Yong Lee, Jian Kang, Subin Yang, Seong Yun Lee, Sunjong Lee, Kyeong-Ryoon Seo, Min-Soo Kim, KilSoo In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title | In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title_full | In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title_fullStr | In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title_full_unstemmed | In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title_short | In Vivo Toxicity and Pharmacokinetics of Polytetrafluoroethylene Microplastics in ICR Mice |
title_sort | in vivo toxicity and pharmacokinetics of polytetrafluoroethylene microplastics in icr mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182653/ https://www.ncbi.nlm.nih.gov/pubmed/35683896 http://dx.doi.org/10.3390/polym14112220 |
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