Evidence map›Paper›PMID 41952217›Full record

ArticleParticle and fibre toxicology2026

A simple and reliable method for the qualitative and quantitative analysis of nano- and microplastics in organs for controlled preclinical studies.

Soyeon Jeon, Gyuri Kim, Jun Hui Jeon, Sung Ik Yang, Kyuhong Lee, June-Woo Park, Wan-Seob Cho

Abstract read
In one paragraph

Article in Particle and fibre toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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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

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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

2 citing papers in PubMed.

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4 · The record

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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

7 authors.

Soyeon JeonLab of Toxicology, Department of Health Sciences, The Graduate School of Dong-A University, 37, Nakdong-daero 550 beon-gil, Saha-gu, Busan, 49315, Republic of Korea. 203780@donga.ac.kr.
Gyuri KimLab of Toxicology, Department of Health Sciences, The Graduate School of Dong-A University, 37, Nakdong-daero 550 beon-gil, Saha-gu, Busan, 49315, Republic of Korea.
Jun Hui JeonDepartment of Applied Chemistry, Kyung Hee University, Yongin-si, 17104, Republic of Korea.
Sung Ik YangDepartment of Applied Chemistry, Kyung Hee University, Yongin-si, 17104, Republic of Korea.
Kyuhong LeeInhalation Toxicology Center for Airborne Risk Factor, Korea Institute of Toxicology, 30 Baehak1-gil, Jeongeup, Jeollabuk-do, 56212, Republic of Korea.
June-Woo ParkFuture Environmental Impact Research Center, Korea Institute of Toxicology (KIT), 17, Jaegok-gil, Jinju, 52834, Republic of Korea.
Wan-Seob ChoLab of Toxicology, Department of Health Sciences, The Graduate School of Dong-A University, 37, Nakdong-daero 550 beon-gil, Saha-gu, Busan, 49315, Republic of Korea. wcho@dau.ac.kr.

Funding

National Research Foundation of Korea RS-2024-00336383National Research Foundation of Korea RS-2024-00354246
6 · The paper itself

Abstract

backgroundToxicity studies of microplastics increasingly emphasize the importance of particle retention, transformation, and physicochemical properties within biological systems, as these factors critically influence hazard identification and dose-response interpretation. However, quantitative and qualitative analyses of microplastics in biological matrices remain technically challenging, and many existing digestion-based methods can alter particle properties, thereby confounding toxicological outcomes. Herein, we propose a novel methodology to provide quick, easy, non-destructive, cost-efficient, and reliable outcomes by offering a particle collection method for microplastics as-present in organs using proteinase K (PK) digestion and a simple quantification method based on ultraviolet-visible (UV-Vis) spectrophotometry.

resultsThe test microplastic samples comprised three spherical polystyrene (0.1, 1, and 100 μm), two fragmented polystyrene (1 and 100 μm), one spherical polyethylene (10 μm), one fragmented polyethylene (100 μm), and two fragmented polypropylene (1 and 100 μm). Particles as-present in organs were successfully collected by conducting PK tissue digestion at 5 µg PK per mg dried tissue. The collected particles were then quantified using a standard curve, with absorbance measured at 750 nm. Spiking experiments with microplastics in mouse lung and mussel tissues showed > 90% accuracy and recovery for all test particles. Because the PK-based particle collection method is non-destructive, the collected particles can be further used to evaluate their physicochemical properties, such as size, shape, composition, and oxidative potential. However, the plastics treated with both acids and alkalis exhibited significant morphological, optical, and chemical changes, indicating that these methods are destructive to particles.

conclusionTherefore, this simple, non-destructive approach enables quantitative and qualitative analyses for laboratory toxicological studies and qualitative identification of microplastics in unknown biological samples, providing a valuable tool for future toxicity and environmental research.

Indexed as

MicroplasticsNanoparticlesAnimalsEndopeptidase KMaleMiceParticle SizePolyethylenePolystyrenesReproducibility of ResultsSpectrophotometry, UltravioletTissue DistributionEndopeptidase KMicroplasticsPolyethylenePolystyrenesBiokineticsBiological tissuesMicroplasticsProteinase KQualitative analysisQuantitative analysis

Identifiers

PMID41952217
PMCPMC13104356

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LicenceCC BY-NC-ND
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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.