The present material is a non-sintered porous synthetic carbonate in its me
tastable modification under ambient pressure, i.e. aragonite, for bone reco
nstruction and drug carrying. The crystal structure, density, morphology an
d granulometry of the synthetic aragonite are characterized. Thr powdered a
ragonite is used for processing non-sintered porous ceramics. The influence
of process parameters on porosity is investigated. In vivo biocompatibilit
y, resorption and bone formation have been evaluated after implantation of
selected materials in femurs of sheep. Preliminary results show a mineraliz
ation of the implant sites and the complete resorption of implants at 6 mon
ths. Two antibiotics Metronidazole and Gentamicin were incorporated into ma
terials without alteration or degradation. This incorporation of therapeuti
c agents in the first stages of the process, and particularly before compac
tion, allows a controlled drug loading of the biomaterial. (C) 2001 Elsevie
r Science Ltd. All rights reserved.