Development of an apatitic calcium phosphate bone cement is reported. 100 m
u Particles of tetracalcium phosphate (TTCP) and dicalcium phosphate dihydr
ate (DCPD) were mixed in equimolar ratio to form the cement powder. The wet
ting medium used was distilled water with Na2HPO4 as accelerator to manipul
ate the setting time. The cement powder, on wetting with the medium, formed
a workable putty. The setting times of the putty were measured using a Vic
at type apparatus and the compressive strength was determined with a Univer
sal Testing Machine. The nature of the precipitated cement was analyzed thr
ough X-ray diffraction (XRD), fourier transform infrared spectrometry (FTIR
) and energy dispersive electron microprobe (EDAX). The results shelved the
phase to be apatitic with a calcium-to-phosphorous ratio close to that of
hydroxyapatite. The microstructure analysis using scanning electron microsc
opy (SEM) showed hydroxyapatite nanocrystallite growth over particulate mat
rix surface. The structure has an apparent porosity of similar to 52%. Ther
e were no appreciable dimensional or thermal changes during setting, The ce
ment passed the ill vitro toxicological screening (cytotoxicity and haemoly
sis) tests, Optimization of the cement was done by manipulating the acceler
ator concentration so that the setting time, hardening time and the compres
sive strength had clinically relevant values.