Microfluidic-based thrombosis model for studying microplastics toxicity

The potential impact of microplastics (MPs) on health has caused great concern, and a toxicology platform that realistically reproduces the system behaviour is urgently needed to further explore and validate MP-related health issues. Herein, we introduce an optically assisted thrombus platform to re...

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Veröffentlicht in:Lab on a chip 2022-03, Vol.22 (7), p.1344-1353
Hauptverfasser: Chen, Longfei, Zheng, Yajing, Liu, Yantong, Tian, Pengfu, Yu, Le, Bai, Long, Zhou, Fuling, Yang, Yi, Cheng, Yanxiang, Wang, Fubing, Zheng, Li, Jiang, Fenghua, Zhu, Yimin
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Zusammenfassung:The potential impact of microplastics (MPs) on health has caused great concern, and a toxicology platform that realistically reproduces the system behaviour is urgently needed to further explore and validate MP-related health issues. Herein, we introduce an optically assisted thrombus platform to reveal the interaction of MPs with the vascular system. The risk of accumulation has also been evaluated using a mouse model, and the effect of MPs on the properties of the thrombus are validated via in vitro experiments. The microfluidic system is endothelialized, and the regional tissue injury-induced thrombosis is then realized through optical irradiation. Whole blood is perfused with MPs, and the invasion process visualized and recorded. The mouse model shows a cumulative risk in the blood with continuous exposure to MPs ( P -value < 0.0001). The on-chip results show that MP invasion leads to decreased binding of fibrin to platelets ( P -value < 0.0001), which is consistent with the results of the in vitro experiments, and shows a high risk of thrombus shedding in real blood flow compared with normal thrombus. This work provides a new method to further reveal MP-related health risks. Regionalized optical irradiation of "endothelialized" micro-channels induced thrombosis on a microfluidic toxicology platform demonstrating the realistic reproduction of invasion of microplastics.
ISSN:1473-0197
1473-0189
DOI:10.1039/d1lc00989c