Bs. Sires et al., OSTEOGENIN-ENHANCED BONE-SPECIFIC DIFFERENTIATION IN HYDROXYAPATITE ORBITAL IMPLANTS, Ophthalmic plastic and reconstructive surgery, 13(4), 1997, pp. 244-251
Hydroxyapatite orbital implants undergo early ingrowth of fibrovascula
r tissue after enucleation. This animal study determined whether contr
ol and osteogenin-impregnated hydroxyapatite orbital implants vary in
their osteogenic response at 6 and 52 weeks. Rabbits underwent enuclea
tion with implantation of control or osteogenin-impregnated hydroxyapa
tite spheres. Light microscopy determined fibrovascular ingrowth, and
histomorphometry quantitated the amount of bone produced. Osteogenin i
mplants vascularized at a faster rate and contained bony foci by 6 wee
ks that became confluent at 1 year. Spontaneous osteogenesis was not s
een in control animals at 6 weeks. After 1 year they contained bone, a
lthough less than in the osteogenin implants. Mixed cell inflammation
was observed at the hydroxyapatite-tissue interface in both groups. No
inflammation was noted at the interface of hydroxyapatite and bone. T
hese are the first controlled observations that bone-specific differen
tiation occurs in the pores of spherical hydroxyapatite implants withi
n the soft tissues of the socket. This vascularized process can be enh
anced with osteogenin to occur earlier and more uniformly in the impla
nts at one year.