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Making fluorescent nylon, polypropylene, and polystyrene microplastics for in-vivo and in-vitro imaging
Summary
Researchers developed methods for making fluorescent nylon, polypropylene, and polystyrene microplastics by incorporating fluorescent dyes during fabrication, enabling reliable tracking in live-cell and in vivo imaging studies. The fluorescent MPs retained their physical properties while allowing visualization of cellular uptake, tissue distribution, and biological interactions.
Microplastics (MPs) are synthetic environmental pollutants increasingly linked to adverse human health effects. To study their biological impact, researchers require access to environmentally relevant MPs that can be accurately tracked in biological systems. However, most ambient MPs are composed of non-conjugated polymers that lack intrinsic fluorescence, limiting their utility in live-cell or in vivo imaging. To address this challenge, we present two alternative labeling approaches that enable visualization, distribution tracking, and quantification of MPs. First, we stained nylon and polypropylene MPs with Rhodamine 6G, a fluorescent dye known for its stability and compatibility with in vivo applications. These labeled MPs retained strong fluorescence in murine lung tissue for up to one week, as confirmed by fluorescent microscopy. Second, we conjugated aminated polystyrene microspheres with IRDye 800CW, a near-infrared fluorophore that reduces tissue autofluorescence and enables high-resolution imaging via IVIS and confocal microscopy. In vivo experiments revealed organ-specific accumulation of IRDye-labeled MPs, with a 2.8-fold increase in the liver and a 5-fold increase in the spleen compared to controls, detectable up to 72 hours post-injection. These labeling strategies provide re-searchers with practical tools to visualize and study the biodistribution of MPs in biological systems, advancing efforts to understand their health implications.