Quantifying nanoplastic cellular interactions and uptake pathways by label-free plasmonic imaging

  • J Hazard Mater. 2026 Jul 1:512:142290. doi: 10.1016/j.jhazmat.2026.142290.
Yachong Zhao  1 Peng Lin  2 Peiqi Cao  3 Guangzhong Ma  4
Affiliations
  • 1. Jinan Chengquan Biotechnology Co., Ltd., Jinan 250100, China.
  • 2. Zhejiang Key Laboratory of Excited-State Energy Conversion and Energy Storage, Department of Chemistry, Zhejiang University, Hangzhou 310058, China.
  • 3. Jinan Chengquan Biotechnology Co., Ltd., Jinan 250100, China. Electronic address: [email protected].
  • 4. Zhejiang Key Laboratory of Excited-State Energy Conversion and Energy Storage, Department of Chemistry, Zhejiang University, Hangzhou 310058, China. Electronic address: [email protected].
Abstract

Nanoplastics are increasingly detected in environmental and biological systems, yet quantitative understanding of their cellular interactions and uptake pathways remains limited, particularly under label-free conditions. Here, we employ surface plasmon resonance microscopy (SPRM) to investigate nanoplastic-cell interactions in real time with single-cell resolution. Using 200 nm polystyrene nanoparticles and HEK293 cells as a model system, we quantify the relative contributions of nanoplastic association with cells, including surface adsorption (8.47%), passive uptake (5.95%), and active internalization (85.58%), the latter further comprising clathrin-mediated (44.35%), caveolae-mediated (46.26%), and macropinocytosis-mediated pathways (9.39%). This study establishes SPRM as a label-free platform for quantitatively analyzing nanoplastic-cell interactions and provides a foundation for extending such analyses to more complex and environmentally relevant nanoparticle systems. SYNOPSIS: A label-free surface plasmon resonance microscopy approach quantitatively dissects nanoplastic-cell interaction pathways at the single-cell level.

Keywords
Endocytosis pathways; Label-free imaging; Nanoplastics; Single-cell analysis.
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