The nature of the orthopedic implant surface affects the interaction betwee
n cells and subsequent bone formation. The bone/cement interface in cement-
held prostheses is considered to be the main cause of fracture leading to i
mplant revision. It is thought that the introduction of a bioactive phase,
such as hydroxyapatite (HA), to cement may permit a stronger implant by enc
ouraging direct bone apposition rather than encapsulation of the implant by
fibrous tissue. Thus, a poly(methylmethacrylate) (PMMA) cement incorporati
ng 17.5% HA by weight has been investigated. In this study, in order to ana
lyze the interaction at the cellular level, the in vitro biological respons
e of the HA/PMMA to a similar PMMA without HA incorporation has been studie
d. Primary human osteoblast-like cells (HOB) were used as they are a model
of the cell type the cements might encounter in vivo. Cell proliferation an
d growth were assessed by measurement of total cellular DNA and tritiated t
hymidine ([H-3]-TdR) incorporation. Alkaline phosphatase (ALP) production w
as measured as an indicator of HOB phenotype upon the cements. The results
showed that HA/PMMA was a better substrate for HOB cells, resulting in incr
eased proliferation and ALP activity. Scanning electron microscopy (SEM) an
d transmission electron microscopy (TEM) showed that HOB cells cultured on
the HA-filled PMMA preferentially anchored to HA particles exposed at the c
ement surface, with a close intimacy observed between HA and HOB cells. (C)
1999 Kluwer Academic Publishers.