“…After the experimental conditions, as reported above, the culture medium was removed and the viable cells that remained adhered to the glass substrate were fixed in 1 mL of buffered 2.5% glutaraldehyde for 24 hours and post-fixed with 1% osmium tetroxide for 1 hour. The cells adhered to the glass substrate were then dehydrated in a series of increasing ethanol concentrations (30,50,70,95, and 100%) and immersed in 1,1,1,3,3,3-hexamethyldisilazane (HMDS; Acros Organics, Springfield, NJ, USA) for 90 min, as described elsewhere (C.A. de Souza Costa et al, 2008) and stored in a desiccator for 24 h. The cover glasses were then mounted on metallic stubs, sputter-coated with gold and the morphology of the surface-adhered L929 and MDPC-23 cells was examined with a scanning electron microscope (JEOL-JMS-T33A Scanning Microscope, Tokyo, Japan).…”