While silicon nitride (Si3N4) is an antimicrobial and
osseosintegrative orthopaedic biomaterial, the contribution of surface topography to these
properties is unknown. Using a methicillin-resistant strain of Staphylococcus
aureus (MSRA), this study evaluated Si3N4 implants
in vitro via scanning electron microscopy (SEM) and colony forming unit
(CFU) assays, and later in an established in vivo murine tibia model of
implant-associated osteomyelitis. In vitro, the
“as-fired” Si3N4 implants displayed significant
reductions in adherent bacteria versus machined Si3N4
(2.6×104 vs. 8.7×104 CFU, respectively;
p< 0.0002). Moreover, SEM demonstrated that MRSA cannot
directly adhere to native “as fired” Si3N4.
Subsequently, a cross-sectional study was completed in which sterile or MRSA contaminated
“as-fired” and machined Si3N4 implants were inserted
into the tibiae of 8-week old female Balb/c mice, and harvested on day 1, 3, 5, 7, 10, or
14 post-op for SEM. The findings demonstrated that the antimicrobial activity of the
“as-fired” implants resulted from macrophage clearance of the bacteria
during biofilm formation on day 1, followed by osseointegration via the apparent
recruitment of mesenchymal stem cells (MSC) on days 3–5, which differentiated into
osteoblasts on days 7–14. In contrast, the antimicrobial behavior of the machined
Si3N4 was due to repulsion of the bacteria, a phenomenon that also
limited osteogenesis, as host cells were also unable to adhere to the machined surface.
Taken together, these results suggest that the in vivo biological
behavior of Si3N4 orthopaedic implants is driven by critical
features of their surface nanotopography.