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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. Detection Methods Environmental Sources Food & Water Human Health Effects Nanoplastics Policy & Risk Sign in to save

Accumulation of nanoplastics in human cells as visualized and quantified by hyperspectral imaging with enhanced dark-field microscopy

Environment International 2023 23 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Hongjie Zhang, Hongjie Zhang, Haoran Zhou, Martin Tsz‐Ki Tsui, Martin Tsz‐Ki Tsui, Wei Pan, Liuyan Yang, Yueyue Liu, Liuyan Yang, Chuan Wang, Martin Tsz‐Ki Tsui, Liuyan Yang, Yueyue Liu, Ai‐Jun Miao Ai‐Jun Miao Ai‐Jun Miao Ai‐Jun Miao Ai‐Jun Miao Martin Tsz‐Ki Tsui, Ai‐Jun Miao Ai‐Jun Miao Liuyan Yang, Ai‐Jun Miao Ai‐Jun Miao Ai‐Jun Miao Martin Tsz‐Ki Tsui, Ai‐Jun Miao Ai‐Jun Miao Liuyan Yang, Hongjie Zhang, Ai‐Jun Miao

Summary

Researchers developed a label-free imaging technique to visualize and count nanoplastic particles that accumulate inside human cells, using enhanced dark-field microscopy combined with hyperspectral imaging. The method successfully tracked polystyrene nanoplastics entering cells over time and measured accumulation rates without needing fluorescent labels. This tool could improve the accuracy of future studies assessing how nanoplastics build up in human tissue and what concentration levels may pose health risks.

Polymers

Nanoplastic (NP) pollution is receiving increasing attention regarding its potential effects on human health. The identification and quantification of intracellular NPs are prerequisites for an accurate risk assessment, but appropriate methods are lacking. Here we present a label-free technique to simultaneously visualize and quantify the bioaccumulation of NPs based on hyperspectral imaging with enhanced dark-field microscopy (HSI-DFM). Using polystyrene NPs (PS NPs) as representative particles, the construction of a hyperspectral library was optimized first with more accurate NP identification achieved when the library was based on intracellular instead of extracellular PS NPs. The PS NPs used herein were labeled with a green fluorescent dye so that the accuracy of HSI-DFM in identifying and quantifying intracellular NPs can be evaluated, by comparing the results with those obtained by fluorescence microscopy and flow cytometry. The validation of HSI-DFM for use in determinations of the NP concentration at the single-cell level allows analyses of the accumulation kinetics of NPs in single living cells. The utility of HSI-DFM in different cell lines and with NPs differing in their chemical composition was also demonstrated. HSI-DFM therefore provides a new approach to studies of the accumulation and distribution of NPs in human cells.

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