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Hydrogen bonding-mediated interaction underlies the enhanced membrane toxicity of chemically transformed polystyrene microplastics by cadmium

Journal of Hazardous Materials 2024 12 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Wanqing Zhao, Jianwen Zhou, Lixin Wang Hong Zhang, Xuan Zhang, Hong Zhang, Tong Ye, Hong Zhang, Hong Zhang, Hong Zhang, Shuping Zhang, Xuan Zhang, Jianwen Zhou, Xuan Zhang, Xuan Zhang, Jiansheng Cui, Ke Wang, Hong Zhang, Shuping Zhang, Ke Wang, Wanqing Zhao, Hong Zhang, Hong Zhang, Hong Zhang, Shuping Zhang, Shuping Zhang, Hong Zhang, Ke Wang, Hong Zhang, Jiansheng Cui, Jiansheng Cui, Jiansheng Cui, Jiansheng Cui, Jiansheng Cui, Shuping Zhang, Shuping Zhang, Shuping Zhang, Jiansheng Cui, Lixin Wang

Summary

This study found that cadmium, a toxic heavy metal, makes polystyrene microplastics more damaging to cell membranes by changing the plastic's surface properties. Cadmium-treated microplastics formed stronger hydrogen bonds with cell membrane fats, disrupting cells more effectively than untreated microplastics. Since both cadmium and microplastics are common environmental pollutants, their combined effect could be more harmful to human health than either one alone.

Polymers

The global attention on microplastic pollution and its implications for human health has grown in recent years. Additionally, the co-existence of heavy metals may significantly alter microplastics' physicochemical characteristics, potentially amplifying their overall toxicity-a facet that remains less understood. In this study, we focused the membrane toxicity of modified polystyrene microplastics (PS-MPs) following cadmium (Cd) pretreatment. Our findings revealed that Cd-pretreated PS-MPs exacerbated their toxic effects, including diminished membrane integrity and altered phase fluidity in simulated lipid membrane giant unilamellar vesicles (GUVs), as well as heightened membrane permeability, protein damage, and lipid peroxidation in red blood cells and macrophages. Mechanistically, these augmented membrane toxicities can be partially ascribed to modifications in the surface roughness and hydrophilicity of Cd-pretreated PS-MPs, as well as to interactions between PS-MPs and lipid bilayers. Notably, hydrogen bonds emerged as a crucial mechanism underlying the enhanced interaction of PS-MPs with lipid bilayers.

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