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- W3215667069 abstract "Nanoparticles in biological systems such as the bloodstream are exposed to a complex solution of biomolecules. A corona monolayer of proteins has historically been thought to form on nanoparticles upon introduction into such environments. To examine the first steps of protein binding, Fluorescence Correlation/Cross Correlation Spectroscopy and Fluorescence Resonance Energy Transfer were used to directly analyze four different nanoparticle systems. CdSe/ZnS core/shell quantum dots, 100 nm diameter polystyrene fluospheres, 200 nm diameter polystyrene fluospheres, and 200 nm diameter PEG-grafted DOTAP liposomes were studied with respect to serum protein binding, using bovine serum albumin as a model. Surface heterogeneity is found to be a key factor in protein binding to these nanoparticles, and as such we present a novel conceptualization of the early hard corona as low-ratio, non-uniform binding rather than a uniform monolayer." @default.
- W3215667069 created "2021-12-06" @default.
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- W3215667069 date "2021-01-01" @default.
- W3215667069 modified "2023-09-23" @default.
- W3215667069 title "Serum proteins on nanoparticles: early stages of the “protein corona”" @default.
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- W3215667069 doi "https://doi.org/10.1039/d1nr06137b" @default.
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