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Abstracts Book - IMRC 2018

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• SE2-O034<br />

IN VITRO BIOACTIVITY OF A DIOPSIDE-TRICALCIUM PHOSPHATE<br />

BIOCERAMIC SYNTHESIZED BY THE GLASS-CERAMIC METHOD<br />

Jorge López Cuevas 1 , Claudia López Badillo 2 , Juan Méndez Nonell 3 , Carlos Alberto Gutiérrez<br />

Chavarría 1<br />

1 Centro de Investigación y de Estudios Avanzados del IPN - CINVESTAV, Ceramics Engineering,<br />

Mexico. 2 Universidad Autónoma de Coahuila, Facultad de Ciencias Químicas, Mexico. 3 Centro<br />

de Investigación en Materiales Avanzados, S.C., , Mexico.<br />

A bioactive material induces the formation of apatite in contact with<br />

physiological fluids. This phase is very similar to hydroxyapatite, Ca 10 (PO 4 ) 6 (OH) 2 ,<br />

which is considered as a model for the mineral constituent of animal and human<br />

bones. On the other hand, a resorbable material can be broken down and<br />

assimilated by the human body. Diopside (CaO·MgO·2SiO 2 ) is a bioactive and<br />

resorbable material, whose bending and compressive strengths are higher than<br />

those of the human cortical bone, and Tricalcium Phosphate (3CaO·P 2 O 5 ) is a<br />

resorbable material. These properties make both materials useful for the<br />

fabrication of implants. In this work, a biomaterial based on the eutectic<br />

composition of the Diopside -Tricalcium Phosphate binary system,<br />

corresponding to 61 and 39 wt.% of these phases, respectively, was synthesized<br />

and characterized. The material was synthesized by using the so-called “glassceramic”<br />

or “vitroceramic” process, in which a parent glass with the desired<br />

composition is first obtained by melting and quenching a suitable mixture of raw<br />

materials, and then subjected to a crystallization heat treatment. A thermal<br />

treatment comprising a single heating and cooling cycle was employed in this<br />

work. The cooling rate, holding time and treatment temperature were varied.<br />

Then, all materials were soaked in a simulated body fluid (SBF) for 7, 14 and 21<br />

days, and characterized by X-ray diffraction (XRD), scanning electron microscopy<br />

(SEM), Vickers microhardness and chemical analysis by ICP. The synthesized<br />

materials developed an apatite surface layer in contact with the SBF. The most<br />

bioactive material was the one crystallized at 800 ºC, in which the diopside and<br />

tricalcium phosphate equilibrium phases were absent, and which had low<br />

mechanical properties. The best mechanical properties were obtained for the<br />

materials treated at 1000 ºC/ 7 h and at 1100 ºC for 2, 5 or 7 h. This was due to<br />

a larger development of the diopside phase. Under the latter conditions, the<br />

apatite surface layer achieved a Ca/P molar ratio very close to that of<br />

stoichiometric hydroxyapatite. Finally, the mechanicals properties, the Ca/P

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