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1.
Clin Oral Implants Res ; 24(9): 1035-43, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22587025

RESUMO

OBJECTIVES: A better understanding of the biological processes controlling osseointegration at the bone-to-implant interface is needed. The aim of this study was to examine which are the molecular and biochemical variables that are significantly related to osseointegration, using multiple regression analysis. MATERIALS AND METHODS: Titanium coins were placed into the tibial cortical bone of New Zealand White rabbits and evaluated using pull-out test after 4 and 8 weeks of healing. Correlations between pull-out and several markers from tissue fluid (Lactate dehydrogenase [LDH] and Alkaline phosphatase [ALP] activities and total protein content) and peri-implant bone tissue (total protein, RNA and DNA content, implant area covered with bone and gene expression of osteoblast, osteoclast and inflammation markers) were used to assess the importance of these parameters in bone healing and in relation to implant performance. RESULTS: Our results showed a negative correlation between the content of DNA, RNA and total protein at the peri-implant bone tissue and the pull-out force, indicating that as bone matures and implant becomes more osseointegrated, the organic content of bone decreases. The negative correlation found between pull-out force and ALP activity pointed to a delayed healing in implants with lower pull-out values and primary mineralization still ongoing. LDH activity and total protein content in the tissue fluid were as well negatively correlated with the pull-out force. Finally, a positive correlation was observed between the pull-out force and the expression of the osteoblast and the bone resorption markers, being osteocalcin and collagen-I the best predictive markers for osseointegration after 4 and 8 weeks of healing respectively. CONCLUSIONS: These results suggest that the evaluation of these markers could be relevant for the assessment of new implant surfaces for rapid bone healing and improved implant performance.


Assuntos
Biomarcadores/metabolismo , Implantes Dentários , Osseointegração/fisiologia , Tíbia/metabolismo , Titânio/metabolismo , Fosfatase Alcalina/metabolismo , Animais , Densidade Óssea , DNA/metabolismo , Feminino , Implantes Experimentais , L-Lactato Desidrogenase/metabolismo , Teste de Materiais , Proteínas/metabolismo , RNA/metabolismo , Coelhos , Propriedades de Superfície , Tíbia/cirurgia , Titânio/química , Cicatrização
2.
Dent Mater J ; 30(5): 739-48, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21946496

RESUMO

The aim of this study was to establish a wear model for testing composite filling materials with abrasion properties closer to a clinical situation. In addition, the model was used to evaluate the effect of filler volume and particle size on surface roughness and wear resistance. Each incisor tooth was prepared with nine identical standardized cavities with respect to depth, diameter, and angle. Generic composite of 3 different filler volumes and 3 different particle sizes held together with the same resin were randomly filled in respective cavities. A multidirectional wet-grinder with molar cusps as antagonist wore the surface of the incisors containing the composite fillings in a bath of human saliva at a constant temperature of 37°C. The present study suggests that the most wear resistant filling materials should consist of medium filling content (75%) and that particles size is not as critical as earlier reported.


Assuntos
Resinas Compostas/química , Materiais Dentários/química , Desgaste de Restauração Dentária , Acetofenonas/química , Condicionamento Ácido do Dente , Bis-Fenol A-Glicidil Metacrilato/química , Preparo da Cavidade Dentária/classificação , Polimento Dentário , Restauração Dentária Permanente , Humanos , Incisivo , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Ácidos Fosfóricos/química , Polietilenoglicóis/química , Polimerização , Ácidos Polimetacrílicos/química , Saliva/fisiologia , Silanos/química , Dióxido de Silício/química , Espectroscopia de Infravermelho com Transformada de Fourier , Propriedades de Superfície , Temperatura , Abrasão Dentária/fisiopatologia , Microtomografia por Raio-X , Zircônio/química
3.
Acta Biomater ; 6(3): 1025-32, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19778643

RESUMO

Previous studies have shown that bone-to-implant attachment of titanium implants to cortical bone is improved when the surface is modified with hydrofluoric acid. The aim of this study was to investigate if biological factors are involved in the improved retention of these implants. Fluoride was implemented in implant surfaces by cathodic reduction with increasing concentrations of HF in the electrolyte. The modified implants were placed in the cortical bone in the tibias of New Zealand white rabbits. After 4 weeks of healing, wound fluid collected from the implant site showed lower lactate dehydrogenase activity and less bleeding in fluoride-modified implants compared to control. A significant increase in gene expression levels of osteocalcin and tartrate-resistant acid phosphatase (TRAP) was found in the cortical bone attached to Ti implants modified with 0.001 and 0.01 vol.% HF, while Ti implants modified with 0.1% HF showed only induced TRAP mRNA levels. These results were supported by the performed micro-CT analyses. The volumetric bone mineral density of the cortical bone hosting Ti implants modified with 0.001% and 0.01% HF was higher both in the newly woven bone (<100 microm from the interface) and in the older Haversian bone (>100 microm). In conclusion, the modulation of these biological factors by surface modification of titanium implants with low concentrations of HF using cathodic reduction may explain their improved osseointegration properties.


Assuntos
Calcificação Fisiológica/fisiologia , Galvanoplastia/métodos , Fluoretos/química , Osteogênese/fisiologia , Próteses e Implantes , Tíbia/cirurgia , Titânio/química , Animais , Cristalização/métodos , Teste de Materiais , Desenho de Prótese , Coelhos , Propriedades de Superfície , Tíbia/patologia
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