Abstract
The combined impact of trace metals and polystyrene (PS) microplastics is extremely concerning for human health because PS microplastics can serve as a vehicle for other contaminants. Herein, we investigated the combined effect of copper ions (Cu2+) on the toxicity of PS nanoplastics in vivo and in vitro. The pristine PS (PPS) and ultraviolet irradiated oxidized PS (OPS) nanoplastics with 50 nm-size were conjugated with Cu2+ (13–27 mg/g) for 4 days to get four types of samples: PPS, OPS, PPS/Cu, and OPS/Cu. The comparative toxic potentials of test samples were evaluated using a mouse pharyngeal aspiration model and relevant human cell lines (A549 and differentiated THP-1 cells). The results showed an antagonistic effect in vivo and in vitro by the presence of Cu ions: PPS > PPS/Cu; OPS > OPS/Cu. Furthermore, the OPS produced significantly increased toxic potentials compared to the corresponding PPS: OPS > PPS; OPS/Cu > PPS/Cu. The antagonistic effect of Cu2+ on the toxicity of PS was due to the transformation of Cu2+ and balanced the surface charge of the nanoplastics, which inhibited the oxidative potential of corresponding nanoplastics. These antagonistic effects may provide a better understanding of the combined effects of metals on the intrinsic toxic potential of microplastics under natural conditions.
| Original language | English |
|---|---|
| Article number | 143288 |
| Journal | Chemosphere |
| Volume | 364 |
| DOIs | |
| Publication status | Published - Sept 2024 |
Bibliographical note
Publisher Copyright:© 2024 Elsevier Ltd
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Combined effect
- Heavy metals
- Microplastics
- Polystyrene
- transformation
Fingerprint
Dive into the research topics of 'Mitigated toxicity of polystyrene nanoplastics in combination exposure with copper ions by transformation into copper (I) oxide: Inhibits the oxidative potential of nanoplastics'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver