

Semiquantitative assessment of the distribution of microplastic particles in the body during acute exposure
https://doi.org/10.47470/0016-9900-2025-104-5-643-647
EDN: drfrem
Abstract
Introduction. Microplastics pose a significant health threat due to their toxicity and capacity for bioaccumulation. Although studies have confirmed their detrimental effects on biological systems, the mechanisms governing particle accumulation and particle distributions have not been sufficiently studied.
The aim of our study was to develop and experimentally validate a semi-quantitative method to assess these processes on the base of investigation of the distribution of plastic microparticles in the organism under acute in vivo experimental conditions using a semi-quantitative method.
Materials and methods. Twelve female Wistar rats were divided into four groups. Animals received intracardiac injections of polystyrene microparticle suspensions (100, 500, and 1000 nm in diameter) or physiological saline solution. The accumulation of microparticles in six organs was evaluated using a semi-quantitative scoring method based on fluorescence microscopy and a rank-scale assessment. Data were analyzed using bootstrap methods with Holm–Bonferroni corrections, and differences were considered significant at p < 0.05.
Results. Following intracardiac administration, polystyrene microparticles measuring 100, 500, and 1000 nm were detected in the liver, kidneys, and lungs. They localized primarily in hepatic triads, the renal cortex, and the acinar regions and alveolar ducts of the lungs. The highest levels were observed upon administration of 1000-nm particles. Semi-quantitative analysis revealed liver and lung tissues to accumulate significantly more microparticles of the 1000-nm in size, while the kidneys showed greater accumulation of the 100-nm particles.
Limitations. This study was limited to examining the distribution of three microparticle size groups in a single animal model (laboratory rats, only 3 animals in each group) under acute toxicological conditions.
Conclusion. The intensity and abundance of fluorescent tissue elements depend on particle size and may be associated with the formation of microparticle conglomerates. While the semi-quantitative method allowed identifying certain distribution patterns, further research involving quantitative approaches is required to enhance the accuracy and specificity of these findings.
Compliance with ethical standards. All experiments in this study were conducted in accordance with European Convention standards for the protection of vertebrate animals used for research and other scientific purposes. The study protocol was approved by the local ethics committee (Approval No. 01-10 from October 9, 2024).
Contribution:
Ahmadeev A.R. – conducting the experiment, data collection and processing, writing the text, preparing figures;
Ryabova Yu.V. – research concept and design, writing the text;
Karimov D.O. – research concept and design, scientific editing of the text; Khusnutdinova N.Yu. – conducting the experiment; Kudoyarov E.R. – data collection and processing, writing the text; Valova Ya.V. – research concept and design, data collection and processing. All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version
Conflict of interest. The authors declare no conflict of interest.
Funding. The study was carried out within the framework of the sectoral research program of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing for 2021–2025.
Received: December 23, 2024 / Revised: January 15, 2025 / Accepted: March 26, 2025 / Published: June 27, 2025
About the Authors
Aidar R. AhmadeevRussian Federation
Junior Researcher, Laboratory of Toxicology, Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
e-mail: dgaar87@gmail.com
Yuliya V. Ryabova
Russian Federation
PhD (Medicine), Head of the Laboratory of Toxicology, Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa research institute of occupational health and human ecology, Ufa, 450106, Russian Federation
e-mail: ryabovayuvl@yandex.ru
Denis O. Karimov
Russian Federation
PhD (Medicine), Head of the Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa research institute of occupational health and human ecology, Ufa, 450106, Russian Federation
e-mail: karimovdo@gmail.com
Nadezhda Yu. Khusnutdinova
Russian Federation
Researcher, Laboratory of Toxicology, Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
e-mail: h-n-yu@yandex.ru
Eldar R. Kudoyarov
Russian Federation
Junior Researcher, Laboratory of Genetics, Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
e-mail: e.kudoyarov@yandex.ru
Yana V. Valova
Russian Federation
PhD (Biology), Head of the Laboratory of Genetics, Department of Toxicology and Genetics with an experimental laboratory animal clinic, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
e-mail: Q.juk@yandex.ru
References
1. Farag A.A., Youssef H.S., Sliem R.E., El Gazzar W.B., Nabil N., Mokhtar M.M., et al. Hematological consequences of polyethylene microplastics toxicity in male rats: Oxidative stress, genetic, and epigenetic links. Toxicology. 2023; 492: 153545. https://doi.org/10.1016/j.tox.2023.153545
2. Zhang Z., Chen W., Chan H., Peng J., Zhu P., Li J., et al. Polystyrene microplastics induce size-dependent multi-organ damage in mice: Insights into gut microbiota and fecal metabolites. J. Hazard. Mater. 2024; 461: 132503. https://doi.org/10.1016/j.jhazmat.2023.132503
3. Ma S., Xiao Y., Zhang X., Xu Y., Zhu K., Zhang K., et al. Dietary exposure to polystyrene microplastics exacerbates liver damage in fulminant hepatic failure via ROS production and neutrophil extracellular trap formation. Sci. Total Environ. 2024; 907: 167403. https://doi.org/10.1016/j.scitotenv.2023.167403
4. Deng Y., Zhang Y., Lemos B., Ren H. Tissue accumulation of microplastics in mice and biomarker responses suggest widespread health risks of exposure. Sci. Rep. 2017; 7: 46687. https://doi.org/10.1038/srep46687
5. Lee S., Kang K.K., Sung S.E., Choi J.H., Sung M., Seong K.Y., et al. Toxicity study and quantitative evaluation of polyethylene microplastics in ICR mice. Polymers. 2022; 14(3): 402. https://doi.org/10.3390/polym14030402
6. Leslie H.A., van Velzen M.J.M., Brandsma S.H., Vethaak A.D., Garcia-Vallejo J.J., Lamoree M.H. Discovery and quantification of plastic particle pollution in human blood. Environ. Int. 2022; 163: 107199. https://doi.org/10.1016/j.envint.2022.107199
7. Zhu L., Zhu J., Zuo R., Xu Q., Qian Y., An L. Identification of microplastics in human placenta using laser direct infrared spectroscopy. Sci. Total Environ. 2023; 856(Pt. 1): 159060. https://doi.org/10.1016/j.scitotenv.2022.159060
8. Huang S., Huang X., Bi R., Guo Q., Yu X., Zeng Q., et al. Detection and analysis of microplastics in human sputum. Environ. Sci. Technol. 2022; 56(4): 2476–86. https://doi.org/10.1021/acs.est.1c03859
9. Hillery A.M., Jani P.U., Florence A.T. Comparative, quantitative study of lymphoid and non-lymphoid uptake of 60 nm polystyrene particles. J. Drug Target. 1994; 2(2): 151–6. https://doi.org/10.3109/10611869409015904
10. Braakhuis H.M., Park M.V., Gosens I., De Jong W.H., Cassee F.R. Physicochemical characteristics of nanomaterials that affect pulmonary inflammation. Part. Fibre. Toxicol. 2014; 11: 18. https://doi.org/10.1186/1743-8977-11-18
11. Powell J.J., Faria N., Thomas-McKay E., Pele L.C. Origin and fate of dietary nanoparticles and microparticles in the gastrointestinal tract. J. Autoimmun. 2010; 34(3): J226–33. https://doi.org/10.1016/j.jaut.2009.11.006
12. Carr K.E., Smyth S.H., McCullough M.T., Morris J.F., Moyes S.M. Morphological aspects of interactions between microparticles and mammalian cells: intestinal uptake and onward movement. Prog. Histochem. Cytochem. 2012; 46(4): 185–252. https://doi.org/10.1016/j.proghi.2011.11.001
13. Romano J.P., Wolf M. Multiple testing of one-sided hypotheses: combining bonferroni and the bootstrap. In: Kreinovich V., Sriboonchitta S., Chakpitak N., eds. Predictive Econometrics and Big Data. TES 2018. Studies in Computational Intelligence, vol 753. Cham: Springer; 2017. https://doi.org/10.1007/978-3-319-70942-0_4
14. Kijasov A.P., Sozinov A.S., Gumerova A.A., Fatkheeva L.S. Method for producing semi-quantitative estimates of changes in chronic viral hepatitis-injured liver bioptates. Patent RF № 2227298; 2002. https://elibrary.ru/nhkqga (in Russian)
15. Guschin Ya.A. Application of morphometry methods to assess histopathology in preclinical studies. Laboratornye zhivotnye dlya nauchnykh issledovanii. 2024; (1): 32–41. https://doi.org/10.57034/2618723X-2024-01-04 https://elibrary.ru/mzmdwj (in Russian)
16. Levin F.B. Test system for determining protein in urine. Patent RF № 94012324 A1; 1996. (in Russian)
17. Rubtsov V.A., Keruchenko M.A., Shimanskaya A.G., Parygina M.N., Mozgovoj S.I., Pomorgajlo E.G., et al. Method for semiquantitative evaluation of pdcd4 protein by immunohistochemical method. Patent RF № 2706005 C1; 2018. https://elibrary.ru/ujjcus (in Russian)
Review
For citations:
Ahmadeev A.R., Ryabova Yu.V., Karimov D.O., Khusnutdinova N.Yu., Kudoyarov E.R., Valova Ya.V. Semiquantitative assessment of the distribution of microplastic particles in the body during acute exposure. Hygiene and Sanitation. 2025;104(5):643-647. (In Russ.) https://doi.org/10.47470/0016-9900-2025-104-5-643-647. EDN: drfrem