The biocompatibility of two implantable materials, zirconia and alumina cer
amics, was investigated in vitro using human osteoblast cell cultures. The
viability of osteoblast cells with the materials was evaluated by the methy
lthiazole sulfate test that revealed an absence of any cytostatic or cytoto
xic effect. Cell proliferation kinetic and total protein synthesis in osteo
blasts with zirconia or alumina were similar to that observed in control ce
lls cultured on glass coverslips. Light and scanning electron microscopic e
xaminations showed an intimate contact between osteoblasts and the substrat
es; well-spread cells were observed on the surfaces of both materials. Adhe
sion ability and morphological characteristics were preserved in osteoblast
cultures with these substrates. Moreover, immunohistochemical staining in
osteoblasts with zirconia and alumina showed the capacity of these cells to
elaborate the extracellular matrix composed of types I and V collagen, ost
eocalcin, osteonectin, bone sialoprotein, and cellular fibronectin. Finally
, DNA image cytometry and interphase silver-nucleolar organizer regions qua
ntification were applied as complementary biocompatibility tests to detect
any changes in DNA synthesis and cell proliferation, respectively The resul
ts showed that neither material altered cell ploidy or cell growth rate in
accordance with the absence of any inducing effect on DNA synthesis or prol
iferation. (C) 1999 John Wiley & Sons, Inc.