I have observed the presence of Gold NPs in cells by TEM analysis. The nanoparticles enter into the cells, but many are located on the outside of the cells membrane. Analysis by confocal microscopy (scattering 633nm) show the presence of nanoparticles around the nucleus but the same cells analyzed by TEM do not present NPs around the nucleus. The increased number of particles scattering around the nucleus of cells treated with Gold NPs is due to some biological effect, probably they are microvesicles. By ICP-MS analysis of cells treated with Gold NPs is impossible to understand if the amount of gold detected derives from NPs adhering to the cell membrane (external side) or not. Furthermore, it is difficult to assess the presence of gold ions in the solutions, in fact analyzing solutions after centrifugation or filtration by TEM can be observed NPs. Centrifugation and filtration are not able to completely eliminate the NPs from a solution. Finally, gold is unaffected by air, moisture and most corrosive reagents, and is therefore well suited for use in coins and jewelry and as a protective coating on other, more reactive, metals. However, it is not chemically inert. Gold is almost insoluble, but can be dissolved in aqua regia.
Common oxidation states of gold include +1 (gold(I) or aurous compounds) and +3 (gold(III) or auric compounds). Gold ions in solution are readily reduced and precipitated out as gold metal by adding any other metal as the reducing agent. The added metal is oxidized and dissolves allowing the gold to be displaced from solution and be recovered as a solid precipitate. Gold first ionization energy 1st: 890.1 kJ·mol−1