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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Human Health Effects Nanoplastics Sign in to save

Assessment of Nanoplastic-Induced Disruption in Cellular Glutathione Metabolism Using a Bubble-Assisted Photothermal Capture SERS Sensor

Analytical Chemistry 2025 1 citation ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 53 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Ruili Li, Ruili Li, Ruili Li, Ruili Li, Qi Liu, Shuting Huang, Xiaoqing Chen Shenghong Liu, Qi Liu, Shenghong Liu, Xiaoqing Chen Qi Liu, Shenghong Liu, Xiaoqing Chen Qi Liu, Qi Liu, Xiaoqing Chen Xiaoqing Chen

Summary

Researchers developed a novel sensor using bubble-assisted photothermal capture and SERS technology to measure how nanoplastics disrupt cellular glutathione metabolism, a key indicator of oxidative stress. They found that nanoplastic exposure depleted total glutathione levels and reduced the GSH/GSSG ratio in a dose-dependent manner, with environmentally aged nanoplastics causing more pronounced oxidative damage than pristine ones. The study provides a rapid method for assessing nanoplastic toxicity and suggests that environmental aging increases the health risks of nanoplastic exposure.

Nanoplastics (NPs) and their aged counterparts (aNPs) pose growing environmental and health risks; however, their impact on cellular redox homeostasis remains poorly understood due to the difficulty in simultaneously assessing the amounts of cellular glutathione (GSH) and corresponding glutathione disulfide (GSSG) using traditional methods. Here, under NP and aNP postexposure, we introduce a photothermal convective capture SERS strategy to directly assess total glutathione (GSHt) and the GSH/GSSG ratio─critical biomarkers of oxidative stress. This method leverages laser-induced bubble formation on Au nanoisland (AuNIs) substrates to concentrate analytes via convective flow without the need for specific linkers or templates, enabling label-free, one-step detection with high sensitivity. Our results demonstrate that NP exposure dose-dependently depletes GSHt and reduces the GSH/GSSG ratio in cells, indicating exacerbated oxidative damage. Notably, aNPs led to a more pronounced decline in GSHt levels and a faster reduction in the GSH/GSSG ratio than nonaged NPs, with prolonged aging, further amplifying cellular sensitivity. Our findings indicate that aNPs introduce additional oxygenated groups into cells, disrupting key biological processes and highlighting the potential risks associated with NP exposure. In conclusion, this study provides a rapid and direct approach to enhance our understanding of NP toxicity in real-world scenarios.

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