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Plasmonic nanoshells have been acknowledged as efficient nanomaterials for laser desorption/ionization mass spectrometry (LDI-MS) detection of a wide range of small molecules, whereas their applications in mass spectrometry imaging (MSI) are less developed. In this work, we constructed and optimized SiO 2 @Au nanoshells with tailor-made shell structures and compositions for high-sensitivity LDI-MS analysis and a wide range of MSI applications. Owing to the synergistic effects of plasmonic shells with nanoscale roughness and specific crevice space for the selective trapping of small molecules and cations, SiO 2 @Au core−shell nanoparticles exhibit superior performance for the detection of a vast diversity of small molecules, including amino acids, oligosaccharides, dyestuff and drugs, peptides, nucleosides, and poly(ethylene glycols). Compared with organic matrices, this method affords a high reduction in matrix interference, higher analyte coverage, lower detection limits ranging from fmol to pmol, and good repeatability with relative standard deviation (RSD) below 5%. Due to the nanoscale size and homogeneous deposition of SiO 2 @Au nanoshells, the spatial distribution of various smallmolecule metabolites can be visualized in strawberry tissues at a pixel size of 100 μm without imaging artifacts. More valuably, the universality of SiO 2 @Au-assisted LDI-MSI is further demonstrated for mapping the lipid distribution within the whole-body tissues of zebrafish (Danio rerio), honeybees (Apis cerana), and mouse brain tissues in a spatially resolved manner at pixel sizes of 55, 30, and 50 μm, respectively. These results facilitate the expansion of the abilities of plasmonic core−shell nanoparticles in real-case MSI applications. Taken together, the results indicate that the SiO 2 @Au nanoshells are expected to be promising and efficient nanomaterials with superior DI efficiency and imaging capabilities, especially in the environmental science and life science fields.

Food safety issues caused by pesticide residue have exerted far-reaching impacts on human daily life, yet the available detection methods normally focus on surface residue rather than pesticide penetration to the internal area of foods. Herein, we demonstrated gold nanoparticle (AuNP)-immersed paper imprinting mass spectrometry imaging (MSI) for monitoring pesticide migration behaviors in various fruits and vegetables (i.e., apple, cucumber, pepper, plum, carrot, and strawberry). By manually stamping food tissues onto AuNP-immersed paper, this method affords the spatiotemporal visualization of insecticides and fungicides within fruits and vegetables, avoiding tedious and time-consuming sample preparation. Using the established MSI platform, we can track the migration of insecticides and fungicides into the inner region of foods. The results revealed that both the octanol-water partition coefficient of pesticides and water content of garden stuffs could influence the discrepancy in the migration speed of pesticides into food kernels. Taken together, this nanopaper imprinting MSI is poised to be a powerful tool because of its simplicity, rapidity, and easy operation, offering the potential to facilitate further applications in food analysis. Moreover, new perspectives are given to provide guidelines for the rational design of novel pesticide candidates, reducing the risk of food safety issues caused by pesticide residue.