Porous titanium granules in critical size defects of rabbit tibia with or without membranes.
- Author:
Rafael Arcesio DELGADO-RUIZ
1
;
Jose Luis CALVO-GUIRADO
2
;
Marcus ABBOUD
1
;
Maria Piedad RAMIREZ-FERNÁNDEZ
2
;
Jose Eduardo MATÉ-SÁNCHEZ
2
;
Bruno NEGRI
2
;
Alex WON
1
;
Georgios ROMANOS
1
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Male; Membranes, Artificial; Rabbits; Tibia; abnormalities; Titanium; chemistry
- From: International Journal of Oral Science 2014;6(2):105-110
- CountryChina
- Language:English
- Abstract: Recently, porous titanium granules (PTGs) have been indicated for the preservation of the dimensions of post-extraction sockets, as a filler in sinus lift procedures and for the treatment of peri-implant and periodontal defects, based on the osteoconductivity and dimensional stability of the titanium granules. However, there is a lack of information regarding the use of this material in larger defects and in conjunction with membranes. The objective of this study is to test the behavior of PTGs used to fill critical size defects in rabbit tibiae, with and without membranes. Critical defects were created in both tibiae of rabbits, divided randomly into three groups: Group A (defect filled with PTG), Group B (defect filled with PTG+collagen membrane) and a control group (empty defect). After six weeks, histomorphometric analysis was performed. The results showed more defect closures at the cortical area (87.37%±2.2%) and more bone formation at the marrow area (57.6%±1.3%) in Group B, in comparison with the other groups (P<0.05); the use of membranes improved the material stability expressed as more percentages of the original material when membranes were used (P<0.05). Finally, inflammatory reactions were observed when the granules were not protected by membranes. In spite of the limitations of this animal study, it may be concluded that PTG particles are osteoconductive and allow bone growth. The PTG particles must be covered by a membrane, especially when grafting larger defects, in order to control particle migration, promote clot stabilization and separate the PTG graft from undesired soft tissue cells.
