Yang Zhenning, DeLoid Glen M, Baw Joshua, Zarbl Helmut, Demokritou Philip
Nanoscience and Advanced Materials Center, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ 08854, USA.
Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USA.
Nanomaterials (Basel). 2024 May 6;14(9):807. doi: 10.3390/nano14090807.
Micro- and nanoplastics (MNPs) have become ubiquitous contaminants of water and foods, resulting in high levels of human ingestion exposure. MNPs have been found in human blood and multiple tissues, suggesting that they are readily absorbed by the gastrointestinal tract (GIT) and widely distributed. Growing toxicological evidence suggests that ingested MNPs may pose a serious health threat. The potential genotoxicity of MNPs, however, remains largely unknown. In this study, genotoxicity of primary and environmentally relevant secondary MNPs was assessed in a triculture small intestinal epithelium (SIE) model using the CometChip assay. Aqueous suspensions of 25 and 1000 nm carboxylated polystyrene spheres (PS25C and PS1KC), and incinerated polyethylene (PEI PM) were subjected to simulated GIT digestion to create physiologically relevant exposures (digestas), which were applied to the SIE model at final MNP concentrations of 1, 5, and 20 μg/mL for 24 or 48 h. PS25C and PS1KC induced DNA damage in a time- and concentration-dependent manner. To our knowledge, this is one of the first assessment of MNP genotoxicity in an integrated in vitro ingestion platform including simulated GIT digestion and a triculture SIE model. These findings suggest that ingestion of high concentrations of carboxylated PS MNPs could have serious genotoxic consequences in the SIE.
微塑料和纳米塑料(MNPs)已成为水和食物中普遍存在的污染物,导致人类摄入大量此类物质。已在人体血液和多种组织中发现MNPs,这表明它们易于被胃肠道(GIT)吸收并广泛分布。越来越多的毒理学证据表明,摄入的MNPs可能对健康构成严重威胁。然而,MNPs的潜在遗传毒性在很大程度上仍不为人所知。在本研究中,使用彗星芯片分析法在三培养小肠上皮(SIE)模型中评估了原生和与环境相关的次生MNPs的遗传毒性。将25纳米和1000纳米的羧化聚苯乙烯球(PS25C和PS1KC)以及焚烧后的聚乙烯(PEI PM)的水悬浮液进行模拟胃肠道消化,以产生生理相关的暴露物(消化物),然后将其以最终MNPs浓度1、5和20微克/毫升应用于SIE模型24或48小时。PS25C和PS1KC以时间和浓度依赖性方式诱导DNA损伤。据我们所知,这是首次在包括模拟胃肠道消化和三培养SIE模型的综合体外摄入平台中对MNPs遗传毒性进行的评估之一。这些发现表明,摄入高浓度的羧化PS MNPs可能会在SIE中产生严重的遗传毒性后果。