“…The use of commercially available fluorescently labeled polystyrene (PS) particles has been a prevalent technique so far to characterize the uptake, tissue distribution and translocation of MNPs in aquatic organisms . However, there are many disadvantages limiting its application, including autofluorescence of the organism, high background fluorescence signal interference, high detection limit, and false positive results caused by fluorophore release. , In addition, due to the internal light diffraction and scattering of tissues, the resolution of biological imaging and the range of applicable organisms was limited (e.g., phytoplankton, zooplankton, fish larval, cell, and transparent organisms), and the deep tissue cannot be realistically measured. , A more recent approach is to measure the metal-doped plastic particle (e.g., palladium-doped NPs) after digesting the tissue of organisms, but the loss of latent spatial information is not conducive to in situ observation of the behavior of MNPs in vivo . To date, the challenge of tracking MNPs in vivo and the need for low detection limits have hindered their measurement at environmentally relevant concentrations.…”