Initially, implant surface analyses were performed on 10 machined implants
and on 10 sandblasted and acid-etched implants. Subsequently, sandblasted a
nd acid-etched implant cytotoxicity (using L929 mouse fibroblasts), morphol
ogic differences between cells (osteoblast-like cells MG63) adhering to the
machined implant surfaces, and cell anchorage to sandblasted and acid-etch
ed implant surfaces were evaluated. Results indicated that acid etching wit
h 1% hydrofluoric acid/30% nitric acid after sandblasting eliminated residu
al alumina particles. The average roughness (R-a) of sandblasted and acid-e
tched surfaces was about 2.15 mum. Cytotoxicity tests showed that sandblast
ed and acid-etched implants had non-cytotoxic cellular effects and appeared
to be biocompatible. Scanning electron microscopic examination showed that
the surface roughness produced by sandblasting and acid etching could affe
ct cell adhesion mechanisms. Osteoblast-like cells adhering to the machined
implants presented a very flat configuration, while the same cells adherin
g to the sandblasted and acid-etched surfaces showed an irregular morpholog
y and many pseudopodi. These morphologic irregularities could improve initi
al cell anchorage, providing better osseointegration for sandblasted and ac
id-etched implants.