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Quantitative Tracking of Nanoplastic Uptake and Distribution in Zebrafish by Single-Particle Inductively Coupled Plasma Mass Spectrometry
Summary
Researchers developed a new method to track nanoplastics at the single-particle level in zebrafish using europium-doped polystyrene particles and mass spectrometry. They found that while most nanoplastics accumulated in the intestine, particles continuously penetrated into internal organs including the brain, demonstrating the ability to cross the blood-brain barrier. The study suggests that nanoplastics pose a systemic exposure risk, though the chorion of fish eggs appears to block their entry.
Tracking the uptake, distribution, and accumulation of nanoplastics (NPs) in biological organisms is important to understand their fate and effects but remains a major challenge. Herein, a novel framework was proposed for quantitatively tracking of NP fate in zebrafish at single-particle level by employing polystyrene NPs (PS NPs) doped with the europium chelate as the spiking material and using the single-particle inductively coupled plasma-mass spectrometry (sp-ICP-MS) technique. To ensure the sp-ICP-MS analysis, a critical pretreatment method was developed based on tetramethylammonium hydroxide (TMAH) digestion, allowing for the extraction of NPs from zebrafish tissues with a recovery rate ranging from 89.4% to 104.2% under optimal conditions. Benefiting from this method, it is found that though it mainly accumulated in the intestine (81.3-93.3%), NPs can further continuously penetrate into internal organs (3.3-13.6%) with a maximal concentration of 1.14 × 10<sup>5</sup> particles/mg and a maximal bioconcentration factor (BCF) of 5.5. More importantly, NPs were detected in the brain with a concentration of 2.14 × 10<sup>4</sup> particles/mg at day 7, demonstrating that it is able to cross the blood-brain barrier. On the contrary, NPs have been found to hardly penetrate into eggs due to the barrier function of the chorion. Furthermore, a similar evidence and conclusion were obtained by confocal laser scanning microscopy (CLSM) characterization. We hope that this work can provide a new paradigm for investigating the fate of trace NPs in organisms even in different environmental scenarios.
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