Metal-Ligand Interface and Internal Structure of Ultrasmall Silver Nanoparticles (2 nm).
Oliver WetzelShabnam HosseiniKateryna LozaMarc HeggenOleg PrymakPeter BayerChristine BeuckTorsten SchallerFelix NiemeyerClaudia WeidenthalerMatthias EpplePublished in: The journal of physical chemistry. B (2021)
Ultrasmall silver nanoparticles were prepared by reduction with NaBH4 and surface-terminated with glutathione (GSH). The particles had a solid core diameter of 2 nm as shown by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS). NMR-DOSY gave a hydrodynamic diameter of 2 to 2.8 nm. X-ray photoelectron spectroscopy (XPS) showed that silver is bound to the thiol group of the central cysteine in glutathione under partial oxidation to silver(+I). In turn, the thiol group is deprotonated to thiolate. X-ray powder diffraction (XRD) together with Rietveld refinement confirmed a twinned (polycrystalline) fcc structure of ultrasmall silver nanoparticles with a lattice compression of about 0.9% compared to bulk silver metal. By NMR spectroscopy, the interaction between the glutathione ligand and the silver surface was analyzed, also with 13C-labeled glutathione. The adsorbed glutathione is fully intact and binds to the silver surface via cysteine. In situ 1H NMR spectroscopy up to 85 °C in dispersion showed that the glutathione ligand did not detach from the surface of the silver nanoparticle, i.e. the silver-sulfur bond is remarkably strong. The ultrasmall nanoparticles had a higher cytotoxicity than bigger particles in in vitro cell culture with HeLa cells with a cytotoxic concentration of about 1 μg mL-1 after 24 h incubation. The overall stoichiometry of the nanoparticles was about Ag∼250GSH∼155.
Keyphrases
- silver nanoparticles
- high resolution
- electron microscopy
- fluorescent probe
- photodynamic therapy
- iron oxide
- living cells
- gold nanoparticles
- magnetic resonance
- induced apoptosis
- oxidative stress
- cell cycle arrest
- computed tomography
- magnetic resonance imaging
- nitric oxide
- positron emission tomography
- optic nerve
- hydrogen peroxide
- highly efficient
- iron oxide nanoparticles
- endoplasmic reticulum stress
- contrast enhanced
- pet ct