Two different types of heterogeneous fluoridated hydroxyapatites previ
ously synthesized at 80 degrees C and pH 7.4, which might be composed
of hydroxyapatite covered with fluorapatite (H-FAp) and fluorapatite c
overed with hydroxyapatite (F-HAp), were observed by high-resolution t
ransmission electron microscopy. The transverse-sectional shapes of bo
th apatites were clearly hexagonal. This confirmed that both apatites
were highly crystallized. However, their shapes differed slightly from
each other in detail:H-FAp was more slender and F-HAp was typically h
exagonal, probably reflecting the shapes of the original core apatites
, hydroxyapatite and fluorapatite. The portions thought to be synthesi
zed with fluoride-free solution showed clear electron beam damage. The
expanded lattice image observed at the edge of the F-HAp crystal coin
cided approximately with the a-axis dimension of 0.9443 nm obtained fr
om the X-ray diffraction data of synthetic hydroxyapatite. After incub
ation in 0.5 mol l(-1) acetate buffer solution (37 degrees C, pH 4.0)
for one month, the fluorapatite-covered H-FAp maintained its sharp cor
ners, while the hydroxyapatite-covered F-HAp showed rounded corners.